Anoftalmia bilateral em cão associada à malformação peniana congênita / Bilateral anophthalmia in dog associated with congenital penile malformation

Background: Anophthalmia refers to the complete absence of an eyeball. It is a very rare congenital condition that affects all breeds of dogs, which may be unilateral or bilateral. Anophthalmia results from a severe developmental deficiency in the primitive forebrain, prior to the formation of the optic sulcus. This condition has a complex etiology, and chromosomal, monogenic, and environmental causes have already been identified. There might be an association between anophthalmia and other congenital abnormalities. This case report aimed to report the case of a male dog with bilateral anophthalmia associated with penile malformation. Case: A 3-year-old male mongrel dog was evaluated in a clinical consultation at the Veterinary Medical Teaching Hospital of the Federal University of Piauí (UFPI) - Teresina - Brazil, with signs of anemia and diarrhea. His vaccinations were not up to date (multiple and anti-rabies), presented ectoparasites (ticks), and showed inappetence. The owner reported that the animal was blind from birth, was already well adapted to its environment, had the company of other animals, and had no access to the street. On clinical examination, the animal had a good body score. The eyelids were bilaterally present with normally developed eyelashes. Both the head and face had a symmetrical appearance, without structural abnormalities, and the palpebral fissures were narrow. When opening the eyelids manually, the presence of the conjunctiva was observed bilaterally, the orbits were shallow, and neither orbit contained the eyeball. Further inspection with an ophthalmic clinical flashlight did not reveal any other ocular structures. The initial diagnosis was suggestive of bilateral anophthalmia. Ultrasound examination of the ocular region confirmed the presence of bilateral anophthalmia. A general physical examination revealed a malformed penis with a persistent penile frenulum. Regarding systemic clinical signs (apathy, inappetence, diarrhea, and anemia), clinical and laboratory examinations led to the suspicion of verminosis. Discussion: The dog in this report had a good body score; however, this type of malformation can generate non-viable puppies. Anophthalmia is an extremely rare congenital ocular malformation, both in humans and companion animals, in which there are no ocular structures in the orbits, and these structures (orbits) in affected individuals are generally small and shallow, as seen in the dog in this report. Ultrasonographic examination confirmed the bilateral anophthalmic condition, being the most accurate method of diagnosing this congenital condition. The animal in this report presented with anophthalmia associated with penile malformation. This type of association until this case report has only been described in humans and mice, and is probably caused by a mutation in the SOX2 gene, which is responsible for the protein of the same name, which makes the maturation of ocular tissues in the primitive forebrain. Thus, it is likely that such congenital alterations are the cause of the malformations observed in this animal. Maternal vitamin A deficiency, a factor known to cause ocular malformations, may also be involved in the etiology of congenital diseases. Nutritional imbalances in dogs are common in the animal's region of origin The dog in this report had a normal life. Although it is a condition that causes blindness, dogs can have a normal life and welfare, even with bilateral anophthalmia.

Surgical correction of bilateral ectopic ureter using the neoureterocystostomy technique / Correção cirúrgica de ureter ectópico bilateral utilizando a técnica de neoureterocistostomia

Ureteral ectopy is a rare disorder in the small animals' clinic. It is characterized as a congenital anomaly, resulting from the ducts differentiation failure during embryogenesis. In this scenario, the ureters present themselves outside the anatomical site, being inserted into the uterus, urethra, urinary vesicle neck, or vagina. The clinical signs are urinary incontinence and perivulvar dermatitis. Surgery is the accepted treatment to correct the anomaly. The surgical procedure is based on relocating the ectopic ureter and treating associated modifications. This report describes a case of intramural bilateral ureteral ectopy, corrected surgically through the neoureterocystostomy technique, making it possible to control the animal's urinary incontinence.(AU)

A ectopia ureteral é uma afecção de incidência rara na clínica de pequenos animais, sendo caracterizada como anomalia congênita resultante de falha na diferenciação dos ductos durante a embriogênese. Neste cenário, os ureteres se apresentam fora do seu local anatômico, sendo inseridos no útero, no colo da vesícula urinária, na uretra ou na vagina. Os sinais clínicos comumente apresentados são a incontinência urinária bem como a dermatite perivulvar. O tratamento de eleição para correção da anomalia é o procedimento cirúrgico, no qual a técnica de escolha é baseada na relocação do ureter ectópico e tratamento das alterações associadas. Neste contexto, o presente relato descreve um caso de ectopia ureteral bilateral intramural, corrigido cirurgicamente por meio da técnica neoureterocistostomia, o que possibilitou controle da incontinência urinária do paciente.(AU)

Surgical correction of bilateral ectopic ureter using the neoureterocystostomy technique / Correção cirúrgica de ureter ectópico bilateral utilizando a técnica de neoureterocistostomia

Ureteral ectopy is a rare disorder in the small animals' clinic. It is characterized as a congenital anomaly, resulting from the ducts differentiation failure during embryogenesis. In this scenario, the ureters present themselves outside the anatomical site, being inserted into the uterus, urethra, urinary vesicle neck, or vagina. The clinical signs are urinary incontinence and perivulvar dermatitis. Surgery is the accepted treatment to correct the anomaly. The surgical procedure is based on relocating the ectopic ureter and treating associated modifications. This report describes a case of intramural bilateral ureteral ectopy, corrected surgically through the neoureterocystostomy technique, making it possible to control the animal's urinary incontinence.(AU)

A ectopia ureteral é uma afecção de incidência rara na clínica de pequenos animais, sendo caracterizada como anomalia congênita resultante de falha na diferenciação dos ductos durante a embriogênese. Neste cenário, os ureteres se apresentam fora do seu local anatômico, sendo inseridos no útero, no colo da vesícula urinária, na uretra ou na vagina. Os sinais clínicos comumente apresentados são a incontinência urinária bem como a dermatite perivulvar. O tratamento de eleição para correção da anomalia é o procedimento cirúrgico, no qual a técnica de escolha é baseada na relocação do ureter ectópico e tratamento das alterações associadas. Neste contexto, o presente relato descreve um caso de ectopia ureteral bilateral intramural, corrigido cirurgicamente por meio da técnica neoureterocistostomia, o que possibilitou controle da incontinência urinária do paciente.(AU)

Hipoplasia renal bilateral em felino / Bilateral renal hypoplasia in feline

A hipoplasia renal ocorre quando há o desenvolvimento incompleto do rim, resultando em um menor número de néfrons, lóbulos e cálices ao nascimento do animal. A gravidade dessa anomalia depende do nível de acometimento. Quando unilateral, ocorre a hipertrofia compensatória do rim saudável e, em casos bilaterais, é frequente a ocorrência de insuficiência renal e infecções. Foi retratada como uma afecção hereditária em algumas raças puras ou mestiças de suínos, potros, caprinos, bovinos e cães, contudo, é incomum em felinos. O presente trabalho tem como objetivo relatar o caso de uma felina, sem raça definida, de dois meses de idade, com queixa de apatia, anorexia e êmes por três dias. No exame físico, foi observada desidratação estimada em 10%, tempo de preenchimento capilar de três segundos, hipotermia, hipoglicemia e letargia. Frente a essas alterações, foram solicitados exames complementares para melhor elucidação do quadro. Os exames bioquímicos revelaram azotemia e hiperfosfatemia grave, bem como hipercalcemia e hipercalemia leve. Já a urinálise, indicou redução da densidade urinária associada à presença de cilindros hialinos e céreos. A ultrassonografia abdominal evidenciou perda de diferenciação córtico-medular e diminuição de ambos os rins, alterações essas compatíveis com nefropatia. Instituiu-se tratamento paliativo visando minimizar complicações secundárias da injúria renal aguda, contudo, a paciente veio a óbito. Na necropsia, os rins apresentavam tamanho reduzido bilateralmente e o exame histopatológico revelou a presença de moderados glomérulos primitivos multifocais associados à distensão do espaço glomerular. A avaliação clínica e as lesões histopatológicas foram consistentes com o diagnóstico de hipoplasia renal congênita.

Renal hypoplasia occurs when there is incomplete development of the kidney, resulting in fewer nephrons, lobes and calyces at birth. The severity of this anomaly depends on the level of involvement. When unilateral, compensatory hypertrophy of the healthy kidney occurs and, in bilateral cases, renal failure and infections are frequent. It has been portrayed as an inherited condition in some pure or mixed breeds of pigs, foals, goats, cattle and dogs, however, it is uncommon in felines. This paper aims to report the case of a feline, mixed breed, two months old, with complaints of apathy, anorexia and emesis for three days. Physical examination showed an estimated dehydration of 10%, capillary refilling time of three seconds, hypothermia, hypoglycemia and lethargy. In view of these changes, complementary exams were requested to better clarify the condition. Biochemical examinations revealed severe azotemia and hyperphosphatemia, as well as hypercalcemia and mild hyperkalemia. Urinalysis, on the other hand, indicated a reduction in urinary density associated with the presence of hyaline and brain cylinders. Abdominal ultrasound showed a loss of corticomedullary differentiation and a decrease in both kidneys, changes compatible with nephropathy. Palliative treatment was instituted in order to minimize secondary complications of acute kidney injury, however, the patient died. At necropsy, the kidneys were bilaterally reduced in size and histopathological examination revealed the presence of moderate multifocal primitive glomeruli associated with distention of the glomerular space. Clinical evaluation and histopathological lesions were consistent with the diagnosis of congenital renal hypoplasia.

Hypoplasia of ribs associated with cleft palate, cleft lip, and unilateral renal agenesis in a neonate dog of undefined breed / Hipoplasia de costelas associada a fenda palatina, lábio leporino e agenesia renal unilateral em cão neonato sem raça definida

Congenital defects can cause changes in the normal function or morphology of organs, thus contributing to neonatal mortality. Malformations in dogs occur as a result of genetic factors or by the action of teratogenic agents during pregnancy. Genetic defects can be inherited from one or both parents. These defects are more common in purebred puppies or can even be the result of consanguinity. Teratogenic agents, such as toxins, drugs, infectious diseases, mechanical influences, and irradiation, may affect the litters during gestational development. Hypoplasia of ribs has been described in human newborns. It is a rare and lethal malformation of autosomal recessive inheritance that prevents thoracic expansion and reduces pulmonary compliance, causing respiratory failure. A pregnant bitch of undefined breed was submitted to caesarean section. At birth, a neonate exhibited respiratory distress, and the palpation of the thorax indicated absence of ribs. In addition, the newborn had cleft palate and cleft lip, which led to perform the euthanasia of the animal. Post-mortem examination indicated hypoplasia of ribs and unilateral renal agenesis. As in the canine neonate, hypoplasia of ribs in human newborns is also associated with other malformations, such as cleft lip, cleft palate, and urogenital defects. The present report describes the first case of hypoplasia of ribs associated with other malformations in a canine neonate, the cause being possibly related to a genetic hereditary factor.(AU)

Os defeitos congênitos podem causar alterações na função ou na morfologia normal de órgãos, contribuindo para a mortalidade neonatal canina. As malformações em cães podem ocorrer devido a fatores genéticos ou por ação de agentes teratogênicos durante a gestação. Os defeitos genéticos podem ser herdados de um ou ambos os pais, sendo mais comum em filhotes de raça pura, ou ainda ocorrerem por consaguinidade. Já os agentes teratogênicos como toxinas, fármacos, doenças infecciosas, influências mecânicas e irradiação, podem afetar a ninhada durante o desenvolvimento gestacional. A hipoplasia de costelas é relatada em recém-nascidos humanos, é uma malformação rara e letal de herança autossômica recessiva que impede a expansão torácica e reduz a complacência pulmonar, causando insuficiência respiratória. Uma cadela prenhe sem raça definida foi submetida à cesariana, ao nascimento um neonato apresentou sofrimento respiratório, à palpação do tórax presumiu-se ausência de costelas, o recém-nascido apresentava ainda fenda palatina e lábio leporino, e optou-se pela eutanásia do animal. No exame post-mortem foi diagnosticado hipoplasia de costelas e agenesia renal unilateral. Assim como encontrado no neonato canino, em recém-nascidos humanos a hipoplasia de costelas também está associada com outras malformações, como fenda labial e do palato e defeitos urogenitais. O presente relato descreve o primeiro caso de hipoplasia de costelas em neonato canino, associada com outras malformações, sendo a causa possivelmente relacionada a um fator genético hereditário.(AU)

Experimental reproduction of congenital anomalies in the progeny of cows fed apple pomace during pregnancy / Reprodução experimental de anomalias congênitas na progênie de vacas alimentadas com bagaço de maçã durante a gestação

This study aimed to describe and discuss the results of an experiment carried out in two stages with pregnant cows fed 25kg/apple pomace/day. The first stage involved 16 pregnant Holstein Friesian cows divided into four groups: Group 0 - Control (5 cows); Group I - 1 month-gestation (4 cows); Group II - 3 month-gestation (4 cows); Group III - 6 month-gestation (3 cows) and was performed from September to December 2015. The second stage comprised 12 pregnant Holstein Friesian cows divided into three groups: Group 0 - Control (6 cows), Group I - 1 month-gestation (3 cows), and Group II - 3 month-gestation (3 cows) and was conducted from April 2016 to February 2017. All study animals received apple pomace at a dose of 25kg/day. As for the first experiment stage, a cow in Group III bred a calf with complete absence of the coccygeal vertebrae and tail, slight bending of the hind limbs, scoliosis in the thoracic spine, and limited mobility. At 30 days, it presented with diarrhea and underdevelopment, and was euthanized for necropsy. At gross examination, malformations were observed in the thoracic spine, coxofemural joint, and genitourinary tract. Regarding the second experiment stage, a cow in Group I gave birth to a calf with curved pelvic and thoracic limbs with thick joints and flattening hooves. Microscopic examination of the femur showed disorganized, irregular hypertrophic zone and scarce growth zone, in addition to primary spongy zone with short, slightly mineralized trabeculae. Samples of the apple pomace used in this study were frozen and sent for laboratory evaluation of pesticide residues, which showed a positive result for the fungicide carbendazim.(AU)

O presente trabalho tem por finalidade descrever e discutir os resultados do experimento realizado em vacas prenhes que foram alimentadas com 25kg/dia de bagaço de maçã. Experimentos foram conduzidos em duas etapas, a primeira no ano de 2015, de setembro a dezembro onde foram utilizadas 16 vacas prenhes da raça holandês. Estas foram divididas em quatro grupos: Grupo 0, Controle (5 vacas); Grupo I, 1 mês gestação (4 vacas); Grupo II, 3 meses gestação (4 vacas); Grupo III, 6 meses gestação (3 vacas). A segunda etapa foi realizada em abril de 2016 a fevereiro de 2017. Foram utilizadas 12 vacas prenhes da raça holandês, divididas em três grupos: Grupo 0, Controle (6 vacas); Grupo I, 1 mês gestação (3 vacas); Grupo II, 3 meses gestação (3 vacas). Todas as vacas receberam bagaço de maçã na dose de 25kg/dia/vaca. Para o primeiro experimento, uma vaca do Grupo III pariu uma bezerra, com ausência completa das vértebras coccígeas e cauda, encurvamento leve dos membros posteriores, escoliose na coluna torácica e dificuldade de locomoção. Decorridos 30 dias do nascimento, manifestou diarreia e pouco desenvolvimento, sendo eutanasiada para necropsia. Na macroscopia, havia malformações na coluna torácica, articulação coxofemoral e no aparelho urogenital. Em relação ao segundo experimento uma vaca do Grupo I pariu uma bezerra com membros pélvicos e torácicos, curvos e com articulações consideravelmente grossas e "achinelamento" de cascos. Na microscopia do fêmur foi observado na placa epifisária, zona hipertrófica desorganizada, irregular e zona de crescimento escassa. Na zona esponjosa primária observou-se trabéculas curtas e pouco mineralizadas. Amostras do bagaço de maçã utilizado na experimentação foram congeladas e enviadas para avaliação de resíduos agrotóxicos, onde foi encontrado resultado positivo para o fungicida carbendazim.(AU)

Experimental reproduction of congenital anomalies in the progeny of cows fed apple pomace during pregnancy / Reprodução experimental de anomalias congênitas na progênie de vacas alimentadas com bagaço de maçã durante a gestação

This study aimed to describe and discuss the results of an experiment carried out in two stages with pregnant cows fed 25kg/apple pomace/day. The first stage involved 16 pregnant Holstein Friesian cows divided into four groups: Group 0 - Control (5 cows); Group I - 1 month-gestation (4 cows); Group II - 3 month-gestation (4 cows); Group III - 6 month-gestation (3 cows) and was performed from September to December 2015. The second stage comprised 12 pregnant Holstein Friesian cows divided into three groups: Group 0 - Control (6 cows), Group I - 1 month-gestation (3 cows), and Group II - 3 month-gestation (3 cows) and was conducted from April 2016 to February 2017. All study animals received apple pomace at a dose of 25kg/day. As for the first experiment stage, a cow in Group III bred a calf with complete absence of the coccygeal vertebrae and tail, slight bending of the hind limbs, scoliosis in the thoracic spine, and limited mobility. At 30 days, it presented with diarrhea and underdevelopment, and was euthanized for necropsy. At gross examination, malformations were observed in the thoracic spine, coxofemural joint, and genitourinary tract. Regarding the second experiment stage, a cow in Group I gave birth to a calf with curved pelvic and thoracic limbs with thick joints and flattening hooves. Microscopic examination of the femur showed disorganized, irregular hypertrophic zone and scarce growth zone, in addition to primary spongy zone with short, slightly mineralized trabeculae. Samples of the apple pomace used in this study were frozen and sent for laboratory evaluation of pesticide residues, which showed a positive result for the fungicide carbendazim.(AU)

O presente trabalho tem por finalidade descrever e discutir os resultados do experimento realizado em vacas prenhes que foram alimentadas com 25kg/dia de bagaço de maçã. Experimentos foram conduzidos em duas etapas, a primeira no ano de 2015, de setembro a dezembro onde foram utilizadas 16 vacas prenhes da raça holandês. Estas foram divididas em quatro grupos: Grupo 0, Controle (5 vacas); Grupo I, 1 mês gestação (4 vacas); Grupo II, 3 meses gestação (4 vacas); Grupo III, 6 meses gestação (3 vacas). A segunda etapa foi realizada em abril de 2016 a fevereiro de 2017. Foram utilizadas 12 vacas prenhes da raça holandês, divididas em três grupos: Grupo 0, Controle (6 vacas); Grupo I, 1 mês gestação (3 vacas); Grupo II, 3 meses gestação (3 vacas). Todas as vacas receberam bagaço de maçã na dose de 25kg/dia/vaca. Para o primeiro experimento, uma vaca do Grupo III pariu uma bezerra, com ausência completa das vértebras coccígeas e cauda, encurvamento leve dos membros posteriores, escoliose na coluna torácica e dificuldade de locomoção. Decorridos 30 dias do nascimento, manifestou diarreia e pouco desenvolvimento, sendo eutanasiada para necropsia. Na macroscopia, havia malformações na coluna torácica, articulação coxofemoral e no aparelho urogenital. Em relação ao segundo experimento uma vaca do Grupo I pariu uma bezerra com membros pélvicos e torácicos, curvos e com articulações consideravelmente grossas e "achinelamento" de cascos. Na microscopia do fêmur foi observado na placa epifisária, zona hipertrófica desorganizada, irregular e zona de crescimento escassa. Na zona esponjosa primária observou-se trabéculas curtas e pouco mineralizadas. Amostras do bagaço de maçã utilizado na experimentação foram congeladas e enviadas para avaliação de resíduos agrotóxicos, onde foi encontrado resultado positivo para o fungicida carbendazim.(AU)

Aplasia uterina total em cadela com atrofia segmentar de vagina / Total uterine aplasia in bitch with segmental atrophy of vagina

Background: Congenital uterine malformations are rarely identified in domestic and human animals and are related to problems during the embryonic formation of the paramesonephric ducts. Cases of agenesis and segmental aplasia or unicorn uterus have been described in bitches, but there are no reports of total uterine aplasia in this specie. The report of a case of total uterine aplasia and segmental atrophy of the cranial vagina, accidentally diagnosed is reported herein.Case: An adult female bitch without defined breed in bad general condition was attended in the emergency service in a Veterinary Hospital. During anamnesis the information was restricted because it was an errant animal rescued for the consultation, but accompanied for at least 12 months in the environment in which it lived. Data related to the estrous cycle were unknown, but no gestation was observed in the last year. Investigations detected anemia and intense thrombocytopenia, azotemia and increased alanine aminotransferase. Two days later, with no progression, images suggestive of hemometra/ mucometra were observed during abdominal ultrasonography, and the patient underwent emergency ovariohysterectomy despite the general poor condition. Before the procedure the uterus was not routinely identified, but a fibromuscular, nontubular and thin structure occupied the region corresponding to the horns and uterine body, thickening in the cervix region. Death four days after surgery and sent to necropsy. During necropsy it was observed that the vulva and the vestibule of the vagina did not present macroscopic alterations, however there was a marked digitiform narrowing of the cranial region of the vagina, which ended in blind bottom. The mucosa in this narrowing was smooth, without folds. The microscopic structure of the ovaries, uterine tubes and caudal vagina were preserved.[...]

Aplasia uterina total em cadela com atrofia segmentar de vagina / Total uterine aplasia in bitch with segmental atrophy of vagina

Background: Congenital uterine malformations are rarely identified in domestic and human animals and are related to problems during the embryonic formation of the paramesonephric ducts. Cases of agenesis and segmental aplasia or unicorn uterus have been described in bitches, but there are no reports of total uterine aplasia in this specie. The report of a case of total uterine aplasia and segmental atrophy of the cranial vagina, accidentally diagnosed is reported herein.Case: An adult female bitch without defined breed in bad general condition was attended in the emergency service in a Veterinary Hospital. During anamnesis the information was restricted because it was an errant animal rescued for the consultation, but accompanied for at least 12 months in the environment in which it lived. Data related to the estrous cycle were unknown, but no gestation was observed in the last year. Investigations detected anemia and intense thrombocytopenia, azotemia and increased alanine aminotransferase. Two days later, with no progression, images suggestive of hemometra/ mucometra were observed during abdominal ultrasonography, and the patient underwent emergency ovariohysterectomy despite the general poor condition. Before the procedure the uterus was not routinely identified, but a fibromuscular, nontubular and thin structure occupied the region corresponding to the horns and uterine body, thickening in the cervix region. Death four days after surgery and sent to necropsy. During necropsy it was observed that the vulva and the vestibule of the vagina did not present macroscopic alterations, however there was a marked digitiform narrowing of the cranial region of the vagina, which ended in blind bottom. The mucosa in this narrowing was smooth, without folds. The microscopic structure of the ovaries, uterine tubes and caudal vagina were preserved.[...](AU)

A new species of phlebotomine sandfly, Pintomyia (Pifanomyia) duckei (Diptera: Psychodidae) from Manaus, State of Amazonas, Brazil / Uma nova espécie de flebotomíneo, Pintomyia (Pifanomyia) duckei (Diptera: Psychodidae) de Manaus, Estado do Amazonas, Brasil

Pintomyia (Pifanomyia) duckei Oliveira, Alencar and Freitas sp. n. from Adolpho Ducke Reserve, Manaus, Amazonas state, Brazil, is described and illustrated based on three male specimens, the holotype and two paratypes. The paratypes have abnormalities in the external genitalia, one with asymmetric bilateral anomaly (different anomalies in each of certain paired structures) and the other with unilateral anomaly (anomaly in one of the paired structures). The new species probably belongs to the Serrana Series, integrating the list of the species whose males possess gonostylus with two stout spines (one apical and other subapical), as well as a small and very thin spine on the inner surface of the basal half.

Pintomyia (Pifanomyia) duckei Oliveira, Alencar e Freitas sp. n. da Reserva Florestal Adolpho Ducke, Manaus, Estado do Amazona, Brasil, é descrita e ilustrada com base em três espécimes machos, o holótipo e dois parátipos. Os parátipos possuem anomalias na genitália externa, sendo um com anomalia bilateral assimétrica (anomalias diferentes em cada uma das estruturas pareadas) e outro com anomalia unilateral (anomalia em uma das estruturas pareadas). A nova espécie provavelmente pertence à Série Serrana, integrando a lista das espécies, cujos machos possuem gonóstilo com dois espinhos robustos (um apical e outro subapical), bem como um espinho delgado e muito curto na superfície interna da metade basal.

A new species of phlebotomine sandfly, Pintomyia (Pifanomyia) duckei (Diptera: Psychodidae) from Manaus, State of Amazonas, Brazil / Uma nova espécie de flebotomíneo, Pintomyia (Pifanomyia) duckei (Diptera: Psychodidae) de Manaus, Estado do Amazonas, Brasil

Pintomyia (Pifanomyia) duckei Oliveira, Alencar and Freitas sp. n. from Adolpho Ducke Reserve, Manaus, Amazonas state, Brazil, is described and illustrated based on three male specimens, the holotype and two paratypes. The paratypes have abnormalities in the external genitalia, one with asymmetric bilateral anomaly (different anomalies in each of certain paired structures) and the other with unilateral anomaly (anomaly in one of the paired structures). The new species probably belongs to the Serrana Series, integrating the list of the species whose males possess gonostylus with two stout spines (one apical and other subapical), as well as a small and very thin spine on the inner surface of the basal half.(AU)

Pintomyia (Pifanomyia) duckei Oliveira, Alencar e Freitas sp. n. da Reserva Florestal Adolpho Ducke, Manaus, Estado do Amazona, Brasil, é descrita e ilustrada com base em três espécimes machos, o holótipo e dois parátipos. Os parátipos possuem anomalias na genitália externa, sendo um com anomalia bilateral assimétrica (anomalias diferentes em cada uma das estruturas pareadas) e outro com anomalia unilateral (anomalia em uma das estruturas pareadas). A nova espécie provavelmente pertence à Série Serrana, integrando a lista das espécies, cujos machos possuem gonóstilo com dois espinhos robustos (um apical e outro subapical), bem como um espinho delgado e muito curto na superfície interna da metade basal.(AU)

Remaining uterine mesonephric duct cyst in female dog (Canis familiaris) first case report in Brazil / Cisto de ducto mesonéfrico uterino remanescente em cadela (Canis familiaris) - primeiro relato de caso no Brasil / Quiste remaneciente del ducto mesonéfrico uterino en perra (Canis familiaris) primero relato del caso en Brasil

The aim of work was to describe a remaining uterine mesonephric duct cyst in female Pinscher dog, with 8 years old. The main complaint of the owner was no heat at least 18 months. Clinical examination revealed presence of cysts in all teats, confirmed by cytopathologic exam. Haemogram, serum biochemical exams, urinalysis, radiographs of the thorax and abdominal ultrasound were performed and no changes were observed. During the ovaryhysterectomy was observed endometrial hyperplasia and the histopathologic diagnosis was remaining uterine mesonephric duct cyst associated with discrete endometrial hyperplasia. Was concluded that adequate histopathologycal identification of the uterine mesonephric duct cyst is crucial so do not mistake with neoplasia.(AU)

O objetivo do trabalho foi descrever um caso de cisto de ducto mesonéfrico remanescente uterino em cadela da raça Pinscher, 8 anos de idade. A principal queixa do proprietário foi ausência de cio com duração de 18 meses. No exame físico evidenciou-se presença de cistos em todos os tetos, confirmado pelo exame citopatológico. Foi realizado hemograma, exames de bioquímica sérica, urinálise, exame radiográfico do tórax e ultrassom abdominal, e não foram observadas alterações. Durante o procedimento de ovário-histerectomia, foi observada hiperplasia endometrial e o diagnóstico histopatológico foi de cisto de ducto mesonéfrico remanescente uterino associado à hiperplasia endometrial discreta. Concluiu-se que a identificação histopatológica adequada do cisto de ducto mesonéfrico uterino é crucial para que o mesmo não seja confundido com neoplasia.(AU)

El objetivo del trábalo fue describir un caso de quiste remaneciente del ducto mesonéfrico uterino en perra da raza Pinscher, 8 años de edad. La principal queja del propietario fue ausencia del cio con duración de 18 meses. El examen físico reveló una presencia de quistes en los techos, confirmado por examen citopatológico. Se realizaron hemograma, pruebas bioquímicas sérica, análisis de orina, radiografías de tórax y ecografía abdominal, y no se observaron cambios. Durante ovario histerectomía se observó hiperplasia endometrial y el diagnóstico histopatológico se fue quiste remaneciente del ducto mesonéfrico uterina asociado a la hiperplasia endometrial discreta. Se concluyó que la identificación histopatológico adecuada del ducto mesonéfrico uterina es crucial para que no se confunda con neoplasia.(AU)

Remaining uterine mesonephric duct cyst in female dog (Canis familiaris) – first case report in Brazil / Cisto de ducto mesonéfrico uterino remanescente em cadela (Canis familiaris) - primeiro relato de caso no Brasil / Quiste remaneciente del ducto mesonéfrico uterino en perra (Canis familiaris) – primero relato del caso en Brasil

The aim of work was to describe a remaining uterine mesonephric duct cyst in female Pinscher dog, with 8 years old. The main complaint of the owner was no heat at least 18 months. Clinical examination revealed presence of cysts in all teats, confirmed by cytopathologic exam. Haemogram, serum biochemical exams, urinalysis, radiographs of the thorax and abdominal ultrasound were performed and no changes were observed. During the ovaryhysterectomy was observed endometrial hyperplasia and the histopathologic diagnosis was remaining uterine mesonephric duct cyst associated with discrete endometrial hyperplasia. Was concluded that adequate histopathologycal identification of the uterine mesonephric duct cyst is crucial so do not mistake with neoplasia.

O objetivo do trabalho foi descrever um caso de cisto de ducto mesonéfrico remanescente uterino em cadela da raça Pinscher, 8 anos de idade. A principal queixa do proprietário foi ausência de cio com duração de 18 meses. No exame físico evidenciou-se presença de cistos em todos os tetos, confirmado pelo exame citopatológico. Foi realizado hemograma, exames de bioquímica sérica, urinálise, exame radiográfico do tórax e ultrassom abdominal, e não foram observadas alterações. Durante o procedimento de ovário-histerectomia, foi observada hiperplasia endometrial e o diagnóstico histopatológico foi de cisto de ducto mesonéfrico remanescente uterino associado à hiperplasia endometrial discreta. Concluiu-se que a identificação histopatológica adequada do cisto de ducto mesonéfrico uterino é crucial para que o mesmo não seja confundido com neoplasia.

El objetivo del trábalo fue describir un caso de quiste remaneciente del ducto mesonéfrico uterino en perra da raza Pinscher, 8 años de edad. La principal queja del propietario fue ausencia del cio con duración de 18 meses. El examen físico reveló una presencia de quistes en los techos, confirmado por examen citopatológico. Se realizaron hemograma, pruebas bioquímicas sérica, análisis de orina, radiografías de tórax y ecografía abdominal, y no se observaron cambios. Durante ovario histerectomía se observó hiperplasia endometrial y el diagnóstico histopatológico se fue quiste remaneciente del ducto mesonéfrico uterina asociado a la hiperplasia endometrial discreta. Se concluyó que la identificación histopatológico adecuada del ducto mesonéfrico uterina es crucial para que no se confunda con neoplasia.

Congenital multiple arthrogryposis in bovine / Artrogripose congênita múltipla em bovino

This report describes an anal atresia, anatomical urethra alteration (slightly caudal to the udder), thickened joints, and changes in the pelvis in a newborn Holstein cow. Visualization of the final portion of the rectum was not possible by perineal access and laparotomy through the right flank was performed in order for abdominal exploration and colostomy attempt. During the surgical procedure visceral rupture and malformations incompatible with life were observed, so surgeons opted for euthanasia and necropsy. Alterations were confirmed in the genitourinary and gastrointestinal tract. The non-formation of the anus caused dilation of the distal portion of the rectum with fecal content retention, which was drained to the body of the uterus, with the presence of meconium. This amount of anatomical and clinical changes were diagnosed as congenital multiple arthrogryposis.(AU)

Este relato de caso descreve atresia anal, alteração anatômica da uretra (inserida caudalmente ao úbere), articulações espessadas e alterações na pelve em um neonato bovino da raça Holandesa. A visualização da porção final do reto não foi possível pelo acesso perineal, e laparotomia através do flanco direito foi feita para exploração abdominal e realização da colostomia. Durante o procedimento cirúrgico, foram observadas ruptura visceral e malformações incompatíveis com a vida, então os cirurgiões optaram pela eutanásia e necropsia. Alterações foram confirmadas nos tratos geniturinário e gastrointestinal. A não formação do ânus causou dilatação da porção distal do reto com retenção fecal, desviando ao corpo do útero, o qual possibilitou a entrada de mecônio nesse compartimento, além de outras alterações devido à ingestão e alteração no trânsito gastrointestinal. Essa quantidade de alterações anatômicas e clínicas foi diagnosticada como artrogripose congênita múltipla.(AU)

Congenital multiple arthrogryposis in bovine / Artrogripose congênita múltipla em bovino

This report describes an anal atresia, anatomical urethra alteration (slightly caudal to the udder), thickened joints, and changes in the pelvis in a newborn Holstein cow. Visualization of the final portion of the rectum was not possible by perineal access and laparotomy through the right flank was performed in order for abdominal exploration and colostomy attempt. During the surgical procedure visceral rupture and malformations incompatible with life were observed, so surgeons opted for euthanasia and necropsy. Alterations were confirmed in the genitourinary and gastrointestinal tract. The non-formation of the anus caused dilation of the distal portion of the rectum with fecal content retention, which was drained to the body of the uterus, with the presence of meconium. This amount of anatomical and clinical changes were diagnosed as congenital multiple arthrogryposis.(AU)

Este relato de caso descreve atresia anal, alteração anatômica da uretra (inserida caudalmente ao úbere), articulações espessadas e alterações na pelve em um neonato bovino da raça Holandesa. A visualização da porção final do reto não foi possível pelo acesso perineal, e laparotomia através do flanco direito foi feita para exploração abdominal e realização da colostomia. Durante o procedimento cirúrgico, foram observadas ruptura visceral e malformações incompatíveis com a vida, então os cirurgiões optaram pela eutanásia e necropsia. Alterações foram confirmadas nos tratos geniturinário e gastrointestinal. A não formação do ânus causou dilatação da porção distal do reto com retenção fecal, desviando ao corpo do útero, o qual possibilitou a entrada de mecônio nesse compartimento, além de outras alterações devido à ingestão e alteração no trânsito gastrointestinal. Essa quantidade de alterações anatômicas e clínicas foi diagnosticada como artrogripose congênita múltipla.(AU)

Canine perineal hypospadias / Hipospadia perineal canina

Background: Hypospadias is a congenital malformation, rarely reported in dogs, caused by a failure of the urogenital folds to fuse during fetal development resulting in incomplete formation of the penile urethra. The inadequate production of fetal androgens is believed to be the etiology of this condition. It is characterized by urethra and corpus spongiosum deficiency, often accompanied by penile underdevelopment, and cryptorchidism. Classification is based on anatomical location of the urethral meatus opening as glandular, penile, perineal, anal, and scrotal. The aim of this paper is to report a case of perineal hypospadias in a male, six-month old French bulldog, describing the therapeutic approach. Case: A six month old male French bulldog, weighing 14.3 kg, was presented for a veterinarian appointment at the Department of Veterinary Medicine (Federal University of Sergipe, Brazil) due to a prolapsed nictitans gland and abnormalities of its genitalia. The medical records included recurrent urinary infection, presence of ectoparasites (thick) and ehrlichiosis, previously treated with doxycycline for 28 days (5 mg/kg/BID). During physical examination, the patient was bright and alert showing a good overall body condition. Temperature, pulse, respiration, thoracic auscultation and lymph nodes were within normal limits. Abdominal palpation was unremarkable. Inspection of the [...]

Canine perineal hypospadias / Hipospadia perineal canina

Background: Hypospadias is a congenital malformation, rarely reported in dogs, caused by a failure of the urogenital folds to fuse during fetal development resulting in incomplete formation of the penile urethra. The inadequate production of fetal androgens is believed to be the etiology of this condition. It is characterized by urethra and corpus spongiosum deficiency, often accompanied by penile underdevelopment, and cryptorchidism. Classification is based on anatomical location of the urethral meatus opening as glandular, penile, perineal, anal, and scrotal. The aim of this paper is to report a case of perineal hypospadias in a male, six-month old French bulldog, describing the therapeutic approach. Case: A six month old male French bulldog, weighing 14.3 kg, was presented for a veterinarian appointment at the Department of Veterinary Medicine (Federal University of Sergipe, Brazil) due to a prolapsed nictitans gland and abnormalities of its genitalia. The medical records included recurrent urinary infection, presence of ectoparasites (thick) and ehrlichiosis, previously treated with doxycycline for 28 days (5 mg/kg/BID). During physical examination, the patient was bright and alert showing a good overall body condition. Temperature, pulse, respiration, thoracic auscultation and lymph nodes were within normal limits. Abdominal palpation was unremarkable. Inspection of the [...](AU)

Agenesia renal unilateral e criptorquidismo ipsilateral em um felino: relato de caso / Unilateral renal agenesis and ipsilateral cryptorchidism in a cat: case report

A agenesia renal é uma afecção congênita rara na espécie felina, frequentemente associada a uma malformação reprodutiva. O presente trabalho relata o caso de um felino com agenesia renal unilateral associada a criptorquidismo ipsilateral, com ênfase no diagnóstico, tratamento e acompanhamento. O paciente foi conduzido ao Hospital de Clínicas Veterinárias da Universidade Federal do Rio Grande do Sul para avaliação de criptorquidismo. A agenesia renal foi um achado durante a ecografia abdominal do felino. Durante a laparotomia, foi confirmada a ausência do rim e ureter direito, hipertrofia do rim esquerdo e presença de um testículo ectópico. O paciente teve alta após a recuperação anestésica e se mantém clinicamente estável, transcorridos seis meses da cirurgia. A agenesia renal unilateral é uma condição compatível com a vida, contanto que o rim existente apresente funcionamento aceitável. Assim, sugere-se que a possibilidade de rim único em felinos criptorquidas deve ser investigada sempre que possível, tendo em vista a alta correlação entre essas malformações, e objetivando um acompanhamento da função renal do paciente ao longo da vida.(AU)

Renal agenesis is a rare disorder in feline species, commonly associated with reproductive malformation. This study aims to report the case of a cat with unilateral renal agenesis combined with ipsilateral cryptorchidism, emphasizing the diagnosis, treatment and patient follow up. The patient was taken to the Veterinary Hospital of the Federal University of Rio Grande do Sul to evaluate the cryptorchidism. The renal agenesis was an incidental finding during the abdominal ultrasound. At laparotomy, the absence of the right kidney and ureter was confirmed, hypertrophy of the left kidney and the presence of an ectopic testicle were found. The patient was discharged after recovering from anesthesia and remains clinically stable six months after surgery. The unilateral renal agenesis is a life compatible condition as long as the existing kidney has an acceptable performance. Therefore, it is suggested that the chance of a single kidney in cats whit cryptorchidism should be investigated, given the correlation between these malformations, and aiming to monitor renal function throughout the life of the patient.(AU)

Bilateral ureteral ectopia in female dogs: diagnosis, surgical treatment, and clinical outcomes / Ectopia ureteral bilateral em cadelas: diagnóstico, tratamento cirúrgico e evolução clínica

Background: Ectopic ureter is the most common cause of congenital urinary incontinence in dogs. Intramural ectopic ureter occurs when the ureter runs within the urinary bladder wall, while extramural ectopic ureter occurs when the distal ureter is not associated with the bladder wall. Ectopic ureters are diagnosed using different techniques and/or combinations of various imaging studies. Surgical correction is the standard treatment for dogs with an ectopic ureter, and these surgical techniques include neoureterostomy, ureteroneocystostomy, and nephroureterectomy. The aim of this report is to describe two cases of ectopic ureter successfully treated with surgery. Cases: In case 1, a 2-month-old female poodle, weighing 1.3 kg, with urinary incontinence since birth was presented to our veterinary service. Excretory urography revealed an ectopic ureter, and ureteroneocystostomy was performed. Abdominal ultrasonography performed 30 days after surgery revealed left renal pyelectasis and ureteral dilatation. Based on these fi ndings, nephrectomy was performed. In case 2, a 3-month-old Golden Retriever, weighing 13.5 kg, with urinary incontinence since birth was brought to our veterinary service. Abdominal ultrasonography revealed a small left kidney and left ureteral dilation. Laparotomy was performed and revealed bilateral intramural ectopic ureters. Based on these findings, bilater

Background: Ectopic ureter is the most common cause of congenital urinary incontinence in dogs. Intramural ectopic ureter occurs when the ureter runs within the urinary bladder wall, while extramural ectopic ureter occurs when the distal ureter is not associated with the bladder wall. Ectopic ureters are diagnosed using different techniques and/or combinations of various imaging studies. Surgical correction is the standard treatment for dogs with an ectopic ureter, and these surgical techniques include neoureterostomy, ureteroneocystostomy, and nephroureterectomy. The aim of this report is to describe two cases of ectopic ureter successfully treated with surgery. Cases: In case 1, a 2-month-old female poodle, weighing 1.3 kg, with urinary incontinence since birth was presented to our veterinary service. Excretory urography revealed an ectopic ureter, and ureteroneocystostomy was performed. Abdominal ultrasonography performed 30 days after surgery revealed left renal pyelectasis and ureteral dilatation. Based on these fi ndings, nephrectomy was performed. In case 2, a 3-month-old Golden Retriever, weighing 13.5 kg, with urinary incontinence since birth was brought to our veterinary service. Abdominal ultrasonography revealed a small left kidney and left ureteral dilation. Laparotomy was performed and revealed bilateral intramural ectopic ureters. Based on these findings, bilater

Ectopia ureteral bilateral em cadelas: diagnóstico, tratamento cirúrgico e evolução clínica / Bilateral Ureteral Ectopia in Female Dogs: Diagnosis, Surgical Treatment, and Clinical Outcomes

Background: Ectopic ureter is the most common cause of congenital urinary incontinence in dogs. Intramural ectopic ureter occurs when the ureter runs within the urinary bladder wall, while extramural ectopic ureter occurs when the distal ureter is not associated with the bladder wall. Ectopic ureters are diagnosed using different techniques and/or combinations of various imaging studies. Surgical correction is the standard treatment for dogs with an ectopic ureter, and these surgical techniques include neoureterostomy, ureteroneocystostomy, and nephroureterectomy. The aim of this report is to describe two cases of ectopic ureter successfully treated with surgery. Cases: In case 1, a 2-month-old female poodle, weighing 1.3 kg, with urinary incontinence since birth was presented to our veterinary service. Excretory urography revealed an ectopic ureter, and ureteroneocystostomy was performed. Abdominal ultrasonography performed 30 days after surgery revealed left renal pyelectasis and ureteral dilatation. Based on these findings, nephrectomy was performed. In case 2, a 3-month-old Golden Retriever, weighing 13.5 kg, with urinary incontinence since birth was brought to our veterinary service. Abdominal ultrasonography revealed a small left kidney and left ureteral dilation. Laparotomy was performed and revealed bilateral intramural ectopic ureters. Based on these findings, bilateral neoureterostomy was performed. Thirty days after surgery, patient presented with urinary infection that was controlled with antibiotics. Both dogs were continent one year after treatment. Discussion: Imaging results of the urinary tract can be useful in diagnosing ectopic ureter. Image modalities used for detecting ectopic ureter include excretory urography, pneumocystography, vaginography, retrograde urethrography, ultrasonography, computed tomography, and magnetic resonance imaging. The difference between extra and intramural ureteral ectopia, in some cases, can only be determined during exploratory laparotomy. Surgical complications vary due to several factors, such as whether the ureteral ectopia is uni- or bilateral, intra or extramural, and also the surgical treatment used. Ureteroneocystostomy complications include hydroureter, hydronephrosis, cystitis, transient stenosis, anastomotic dehiscence, persistent dysuria, and loss of normal ureteric peristalsis. Complications of neoureterostomy include persistent dysuria, cystitis, and reflex dyssynergia. Recanalization is a possible cause of postoperative incontinence if the distal ureter is not completely resected. Unilateral hydronephrosis was observed in the first reported case, and nephroureterectomy was performed. A nephroureterectomy is indicated when severe pathologic findings are present, such as severe hydronephrosis, hydroureter, or renal dysplasia and when the contralateral kidney and ureter are functioning normally. In the second case, bacterial cystitis was diagnosed during the post-operative period and was controlled with antibiotic therapy. After surgery, 44­67% of dogs had persistent urinary incontinence. Although residual incontinence can occur after incomplete intramural ureteral remnant or ureteral trough resection, incontinence has also been reported after ureteral reimplantation and nephroureterectomy. Bilateral disease and concurrent urogenital abnormalities often contribute to treatment failure. Therapeutic success was reported in both cases without signs of urinary incontinence one year after surgery.