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1.
Medicine (Baltimore) ; 103(8): e37093, 2024 Feb 23.
Artigo em Inglês | MEDLINE | ID: mdl-38394506

RESUMO

BACKGROUND: Situs inversus is a rare congenital anatomical variant that involves a group of anomalies regarding the arrangement of intrathoracic and intraabdominal organs. Being able to find in the abdominal region the liver, gallbladder, inferior vena cava, and head of the pancreas and ascending colon on the left side of the abdomen, while on the right side there is the spleen, the stomach, the body of the pancreas, the ligament of Treitz, descending colon among others. In this same way, the thoracic organs, lungs and heart, are changed in their position in a mirror translocation. METHODS: We systematically searched MEDLINE, Web of Science, Google Scholar, CINAHL, Scopus, and LILACS; the search strategy included a combination of the following terms: "Situs inversus," "Situs inversus totalis," "Cancer," "Neoplasm," "Abdominopelvic regions," and "clinical anatomy." RESULTS: Within the 41 included studies, 46 patients with situs inversus who had cancer, in addition to being found in this organ and in these regions, we also found as a result that the majority of the studies in the research were in stage II; finally, no one study could assert the direct relationship between the situs inversus totalis and the cancer. CONCLUSION: If our hallmarks could make us think that more exhaustive follow-up of the stomach and other organs should be carried out in these patients, there could also be other predisposing factors for cancer, which is why more studies are suggested to give future diagnostic and treatment guidelines treatment.


Assuntos
Dextrocardia , Neoplasias , Situs Inversus , Humanos , Situs Inversus/complicações , Situs Inversus/diagnóstico , Abdome/anormalidades , Baço/anormalidades
2.
Cir. pediátr ; 37(1): 37-41, Ene. 2024. ilus, tab
Artigo em Espanhol | IBECS | ID: ibc-228970

RESUMO

Introducción: El abdomen hostil es una patología quirúrgica caracterizada por una pérdida de espacio entre los órganos y estructuras del abdomen. La terapia de presión negativa se ha descrito de manera extensa en adultos, pero no así en pacientes pediátricos. El objetivo de este estudio es presentar los resultados a corto plazo de la terapia de presión negativa en pacientes pediátricos con abdomen hostil debido a distintas etiologías. Material y métodos: Identificación y análisis retrospectivo de los pacientes pediátricos con abdomen hostil (< 18 años) tratados con terapia de presión negativa ABTHERA. Resultados: Se incluyó a 7 pacientes. La mediana de edad fue de 16 años (rango: 9-17). 5 (71,4%) eran niños y 2 (28,6%) niñas. 3 (43%) presentaban antecedentes médico-quirúrgicos de interés (lupus eritematoso sistémico, apendicectomía complicada y derivación ventriculoperitoneal). El dispositivo se empleó a presión constante, entre–50 y –125 mmHg. Los hallazgos preoperatorios y postoperatoriosse notificaron mediante la clasificación de Bjork. Los dispositivos sesustituyeron cada 4-7 días (mediana de 5 días). La cantidad total dereemplazos fue de 1-4 (mediana de 3). 5 (71,4%) pacientes precisaronventilación mecánica invasiva durante la terapia de presión negativadebido al estado clínico. 4 (57%) pacientes recibieron nutrición enteral.1 (14%) paciente requirió reintervención posterior al cierre definitivopor el desarrollo de un absceso retroperitoneal. El resultado, evaluadoen base a la tolerancia oral, el movimiento intestinal y la ausencia dedolor, fue favorable en todos los pacientes.Conclusión: Los dispositivos de terapia de presión negativa aportanresultados favorables en los pacientes pediátricos con abdomen hostil,aunque se necesita más información para evaluar los ajustes de presióny la frecuencia de reemplazo del dispositivo.(AU)


Introduction: Hostile abdomen is a surgical condition characterized by loss of space between organs and structures in the abdomen. Negative pressure therapy use has been widely described in adults; the case is not the same for pediatric patients. The goal of this study is to present short-term results of negative pressure therapy use in pediatric patients with hostile abdomen due to different etiologies. Materials and methods: Pediatric hostile abdomen patients (< 18 years) who were treated Negative pressure therapy using ABTHERA were identified and retrospectively reviewed. Results: 7 patients were included in this study. Median age was 16 (range: 9-17 yo). 5 (71.4%) were male and 2 (28.6%) females. 3 (43%) had significant past medical/surgical history (Systemic Lupus Erythematosus, complicated appendectomy and ventriculoperitonealshunt). The device was set at a continuous pressure ranging from –50 to –125 mmHg. Pre and post-surgical findings were reported using Bjork’s classification. Devices were replaced every 4-7 days (median 5 days). Total amount of replacements was 1-4 (median 3). 5 (71.4%) patients required invasive mechanical ventilation during use of Negative pressure therapy based on clinical status. 4 (57%) patients received enteral nutrition. 1 (14%) patient required re-intervention posterior to definitive closure due to retroperitoneal abscess development. Outcome, evaluated by (oral tolerance, bowel movement and absence of pain), was favorable in all patients. Conclusion: Negative pressure therapy devices generate favorable results in hostile abdomen in pediatric population but further information is needed to assess pressure settings and device replacement frequency.(AU)


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , /métodos , Técnicas de Fechamento de Ferimentos Abdominais , Abdome/cirurgia , Tratamento de Ferimentos com Pressão Negativa , Peritonite/cirurgia , Apendicite/cirurgia , Estudos Retrospectivos , Pediatria , Cirurgia Geral , Abdome/anormalidades , Estados Unidos
4.
Cir. pediátr ; 34(3): 164-167, Jul. 2021. ilus
Artigo em Espanhol | IBECS | ID: ibc-216762

RESUMO

Introducción: La eventroplastia con malla retromuscular de Rives-Stoppa ha demostrado en adultos tener los mejores resultados en lareparación de las grandes eventraciones de la línea media. Presentamosel primer caso pediátrico tratado exitosamente con esta técnica. Caso clínico: Varón de 9 años con eventración tras laparotomíamedia urgente. Los principios básicos de la corrección fueron: aperturadel saco herniario y adhesiolisis, incisión longitudinal sobre la vainaposterior del músculo recto y tallado del espacio retromuscular, cierrede la vaina posterior, colocación de una malla sobre este plano aloján-dola en el espacio retromuscular creado y cierre sin tensión del colgajomusculo-aponeurótico anterior, reconstruyendo así la línea media. Norecidiva tras 2 años de seguimiento. Comentarios: La técnica de Rives-Stoppa implica una reconstruc-ción por planos más anatómica que restaura las propiedades anatomo-fisiológicas de la pared abdominal. Consideramos que puede ser unaalternativa útil en el tratamiento de las eventraciones pediátricas.(AU)


Introduction: Retromuscular mesh hernia repair using Rives-Stoppatechnique has demonstrated the best results when it comes to repairinglarge midline hernias. We present the first pediatric case successfullytreated with this technique. Clinical case: This is the case of a 9-year-old male patient with her-nia following urgent midline laparotomy. Basic repair principles includedopening of the hernia sac and adhesiolysis, longitudinal incision on the posterior sheath of the rectus muscle and division of the retromuscularspace, closure of the posterior sheath, placement of a mesh on this planein the brand-new retromuscular space, and tension-free closure of theanterior musculo-aponeurotic flap, thus reconstructing the midline. Norecurrences have been noted after a 2-year follow-up. Discussion: Rives-Stoppa technique allows for a more anatomicallayered reconstruction, which helps restore the anatomical and physi-ological properties of the abdominal wall. In our view, this could be auseful alternative for pediatric hernia treatment.(AU)


Assuntos
Humanos , Masculino , Criança , Pacientes Internados , Exame Físico , Abdome/anormalidades , Abdome/cirurgia , Hérnia Incisional , Pediatria , Cirurgia Geral
5.
Clín. investig. ginecol. obstet. (Ed. impr.) ; 48(1): 33-35, ene.-mar. 2021. ilus
Artigo em Espanhol | IBECS | ID: ibc-201988

RESUMO

El descenso de estructuras inicialmente intraabdominales hacia la región inguinal arrastra consigo una evaginación de peritoneo parietal: el canal de Nuck. Su obliteración incompleta permitirá el paso de líquido o estructuras abdominales originando un hidrocele de dicho canal o hernias inguinales indirectas. El quiste del canal de Nuck se presenta como una masa fluctuante, elástica y no reductible, ecográficamente quística, bien delimitada, de pared ecogénica fina y contenido anecoico, sin señal Doppler color. El diagnóstico diferencial incluye hernias, adenomegalias, enfermedad vascular, tumoral, etc. Aunque el diagnóstico definitivo es histopatológico, la ecografía es una técnica accesible, eficiente y fiable, que permite el estudio dinámico y en tiempo real


The descent of initially intra-abdominal structures towards the inguinal region leads to an evagination of the parietal peritoneum, and is called the canal of Nuck. Its incomplete obliteration will allow the passage of liquid or abdominal structures, leading to a hydrocele of the said canal or indirect inguinal hernias. The canal of Nuck cyst appears as a fluctuating, elastic and non-reducible mass, cystic in the ultrasound, and well-defined with a thin echogenic wall and an anechoic content, with no colour Doppler signal. The differential diagnosis includes hernias, adenomegalies, vascular pathology, and tumours. Although the definitive diagnosis is histopathological, ultrasound is an accessible, efficient and reliable technique, which allows dynamic and real-time study


Assuntos
Humanos , Feminino , Adulto , Cavidade Peritoneal/anormalidades , Anormalidades Urogenitais/diagnóstico por imagem , Canal Inguinal/anormalidades , Diagnóstico Diferencial , Abdome/anormalidades , Cavidade Peritoneal/diagnóstico por imagem , Abdome/diagnóstico por imagem , Canal Inguinal/cirurgia
7.
Autops. Case Rep ; 11: e2021329, 2021. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1339248

RESUMO

Primary hepatic gas gangrene is a form of primary abdominal gas gangrene. The condition is caused by Clostridium perfringens, other clostridia, and non-clostridia bacterial species producing gas. Unlike classical gas gangrene or myonecrosis, the disease develops without a wound or a port of entry. Instead, gas-producing bacteria in the gastrointestinal tract colonize an underlying pathological process with foci of necrosis, producing excessive gas and spreading hematogenously to other organs. Herein we present two autopsy cases of primary hepatic gas gangrene diagnosed on autopsy, with the gross and histological changes that can be considered specific for this rare condition. Both patients had severe underlying liver disease-prone for this entity development. The gross changes in the cases are postmortem subcutaneous emphysema, skin bullae with pooled blood, pneumothorax, pneumoabdomen, abundant gas in the circulatory system, porous structure of the internal organs (tissue gas bubbles), and advanced tissue lysis, not corresponding to the post mortem time. Histology showed optically empty areas of varying size in the internal organs, which weave the structure of the organs and rod-shaped bacteria with scarcity or complete absence of inflammatory reaction.


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Gangrena Gasosa/patologia , Abdome/anormalidades , Autopsia , Clostridium perfringens , Hepatopatias
8.
Sci Rep ; 10(1): 21170, 2020 12 03.
Artigo em Inglês | MEDLINE | ID: mdl-33273483

RESUMO

Incisional hernia (IH) in children could result in life-threatening complications, including incarceration and bowel strangulation. The incidence and risk factors of IH in infants are scarcely reported. Since IH-correction may require extensive surgery and a long recovery program, identifying infants and birth defects at risk, may lead to a different approach during the primary surgery. Therefore, the aim of this review is to systematically review the available data on the incidence of IH following surgery for congenital anomalies in infants. All studies describing IH were considered eligible. PubMed and Embase were searched and risk of bias was assessed. Primary outcome was the incidence of IH, secondary outcomes were difference in IH occurrence between disease severity (complex vs simple) and closure method (SILO vs primary closure) in gastroschisis patients. A meta-analysis was performed to pool the reported incidences in total and per congenital anomaly separately. Subgroup analysis within gastroschisis articles was performed. The 50 included studies represent 3140 patients. The pooled proportion of IH was 0.03 (95% CI 0.02-0.05; I2 = 79%, p ≤ 0.01) all anomalies combined. Gastroschisis (GS) reported highest pooled proportion 0.10 (95% CI 0.06-0.17; n = 142/1273; I2 = 86%; p ≤ 0.01). SILO closure (OR 3.09) and simple gastroschisis, i.e. without additional anomalies, (OR 0.18) were of significant influence. This review reports the incidence of IH in infants with different congenital abdominal anomalies, of which gastroschisis reported the highest risk. In GS patients, complex GS and SILO closure are risk factors for IH development.


Assuntos
Abdome/anormalidades , Anormalidades Congênitas/cirurgia , Humanos , Hérnia Incisional/etiologia , Lactente , Viés de Publicação , Risco
9.
Mol Genet Genomic Med ; 8(10): e1465, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32856427

RESUMO

BACKGROUND: Precise diagnosis and classification of CBWA cases can be challenging. BSA are considered when there is a body wall anomaly, skeletal abnormalities, and the umbilical cord is anomalous, absent or rudimentary, and LBWC when there is a body wall and structural limb anomalies with or without craniofacial abnormalities. METHODS: PubMed was searched for body stalk anomalies, limb body wall complex, body stalk anomalies and amniotic band syndrome, and limb body wall complex and amniotic band syndrome. Sixty nine articles were selected and reviewed. This article systematically classifies the variants of CBWA in 218 cases, the study is based on the embryological and anatomical criteria established by Martín-Alguacil and Avedillo to study BSA in the pig. RESULTS: Eight different BSA presentation were defined. One hundred and eighty nine cases were classified as BSA, from which five were Type I, nine Type II, 20 Type III, 57 Type IV, 11Type V, 24 Type VI, 11 Type VII, and 52 Type VIII. Twenty six cases presented cranial phenotype, 114 abdominal phenotype, 42 cranio/abdominal overlapping phenotype, and five without defined phenotype. In addition, 52 BSA cases presented some kind of spinal dysraphism (SPDYS) and were classified as BSA/SPDYS, most of these cases did not show structural limb anomalies, except for three cases and were classified as LBWC/SPDYS. CONCLUSION: This morphology-based classification represents a useful tool for clinical diagnosis, it helps to quantify and to evaluate CBWA in a precise, objective manner.


Assuntos
Anormalidades Congênitas/patologia , Fenótipo , Abdome/anormalidades , Abdome/embriologia , Anormalidades Congênitas/classificação , Desenvolvimento Embrionário , Humanos , Crânio/anormalidades , Crânio/embriologia
10.
BMC Surg ; 20(1): 124, 2020 Jun 09.
Artigo em Inglês | MEDLINE | ID: mdl-32517682

RESUMO

BACKGROUND: Cocoon abdomen is a relatively rare abdominal disease characterized by the total or partial encasement of the small intestinal by a dense fibro-collagenous membrane. CASE PRESENTATION: We reported an unusual case of idiopathic cocoon abdomen with congenital colon malrotation. Laparotomy and sac release were performed on the patient. The patient was no recurrence 6 months after operation. A literature review was also performed. CONCLUSION: Preoperative diagnosis of abdominal cocoon is difficult. A careful history, physical examination and appropriate radiology may be helpful in making a definitive diagnosis. If conservative treatment can't relieve symptoms effectively, surgery is currently considered to be important in the management of this disease.


Assuntos
Abdome/anormalidades , Colo/anormalidades , Anormalidades do Sistema Digestório/diagnóstico , Volvo Intestinal/diagnóstico , Abdome/cirurgia , Colo/cirurgia , Humanos , Obstrução Intestinal/cirurgia , Intestino Delgado/cirurgia , Laparotomia/métodos , Masculino , Pessoa de Meia-Idade , Radiografia
11.
Mol Genet Genomic Med ; 8(6): e1227, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-32281290

RESUMO

The presence of body wall closing defects (abdominoschisis and thoracoabdominoschisis) in combination with other congenital malformations was studied in the pig (Sus scrofa domesticus). After clinical examination and literature review, body wall defects with multiple congenital anomalies in eight pigs were described, and classified using anatomical and embryological criteria. Several BSA presentations were identified and classified as follows: (a) BSA Type I: fetus with spinal and UC defects, thoracoabdominoschisis, anal atresia and/or other internal organs structural defects, and structural limb defects; (b) BSA Type II: fetus with spinal and UC defects, thoracoabdominoschisis, anal atresia and/or other internal organs structural defects, and nonstructural limb defects; (c) BSA Type III: fetus with spinal and UC defects, abdominoschisis, anal atresia and/or other internal organs structural defects, and structural limb defects; and (d) BSA Type IV: fetus with spinal and UC defects, abdominoschisis, anal atresia and/or other internal organs structural defects, and nonstructural limb defects. Two types of LBWC were differentiated: LBWC Type I: characterized by thoracoabdominoschisis and structural limb defects, and LBWC Type II: characterized by abdominoschisis and structural limb defects, corresponding to BSA type I and type III. This is the first report on BSA and LBWC in the pig.


Assuntos
Anormalidades Múltiplas/veterinária , Doenças dos Suínos/patologia , Abdome/anormalidades , Anormalidades Múltiplas/classificação , Anormalidades Múltiplas/patologia , Animais , Coluna Vertebral/anormalidades , Suínos , Doenças dos Suínos/classificação , Tórax/anormalidades
12.
Autops. Case Rep ; 10(1): 2020137, Jan.-Mar. 2020. ilus
Artigo em Inglês | LILACS | ID: biblio-1087663

RESUMO

Actinomycosis is an uncommon, endogenous, and chronic infection with varied and nonspecific clinical features such as abdominal, pelvic or cervical masses, ulcerative lesions, abscesses, draining fistula, fibrosis, and constitutional symptoms. The disease ensues when the bacteria disrupt the mucosal barrier, invade, and spread throughout interfascial planes. Currently, the diagnosis of actinomycosis is challenging because of its very low frequency and depending on the clinical presentation it may masquerade malignancies. Therapy consists initially in intravenous penicillin, followed by an oral regimen that may be extended until a year of treatment. A timely diagnosis is crucial to avoid extensive therapeutic attempt as surgery. However, a biopsy or drainage of abscesses and fistula's tract may be required not only as a diagnostic procedure as part of the therapy. We report the case of a 72-year-old woman with an abdominal mass initially misdiagnosed as a liposarcoma. A second biopsy of a skin lesion of the abdominal wall made the diagnosis of actinomycosis, avoiding a major surgical procedure. The patient was treated with a long-term course of antibiotics with favorable outcome. Liposarcoma was ruled out after the patient's full recovery with antibiotics and the misdiagnosis was credit to the overconfidence on the immunohistochemical positivity to MDM2.


Assuntos
Humanos , Feminino , Idoso , Actinomicose/diagnóstico , Abdome/anormalidades , Lipossarcoma/diagnóstico , Diagnóstico Diferencial
15.
J Med Case Rep ; 13(1): 366, 2019 Dec 12.
Artigo em Inglês | MEDLINE | ID: mdl-31829256

RESUMO

BACKGROUND: Autosomal recessive renal polycystic kidney disease occurs in 1 in 20,000 live births. It is caused by mutations in both alleles of the PKHD1 gene. Management of delivery in cases of suspected autosomal recessive renal polycystic kidney disease is rarely discussed, and literature concerning abdominal dystocia is extremely scarce. We present a case of a patient with autosomal recessive renal polycystic kidney disease whose delivery was complicated by abdominal dystocia, and we discuss the factors that determined the route and timing of delivery. CASE PRESENTATION: A 23-year-old Caucasian woman, G2 P0, with a prior unremarkable pregnancy was referred to our tertiary center at 31 weeks of gestation because of severe oligoamnios (amniotic fluid index = 2) and hyperechogenic, dedifferentiated, and enlarged fetal kidneys. She had no other genitourinary anomaly. Fetal magnetic resonance imaging showed enlarged, hypersignal kidneys and severe pulmonary hypoplasia. We had a high suspicion of autosomal recessive renal polycystic kidney disease, and after discussion with our multidisciplinary team, the parents opted for conservative care. Ultrasound performed at 35 weeks of gestation showed a fetal estimated weight of 3550 g and an abdominal circumference of 377 mm, both above the 90th percentile. Because of the very rapid kidney growth and suspected risk of abdominal dystocia, we proposed induction of labor at 36 weeks of gestation after corticosteroid administration for fetal lung maturation. Vaginal delivery was complicated by abdominal dystocia, which resolved by continuing expulsive efforts and gentle fetal traction. A 3300-g (P50-90) male infant was born with Apgar scores of 1-7-7 at 1, 5, and 10 minutes, respectively, and arterial and venous umbilical cord pH values of 7.23-7.33. Continuous peritoneal dialysis was started at day 2 of life because of anuria. Currently, the infant is 1 year old and is waiting for kidney transplant that should be performed once he reaches 10 kg. Molecular analysis of PKHD1 performed on deoxyribonucleic acid (DNA) from the umbilical cord confirmed autosomal recessive renal polycystic kidney disease. CONCLUSIONS: Management of delivery in cases of suspected autosomal recessive renal polycystic kidney disease needs to be discussed because of the risk of abdominal dystocia. The route and timing of delivery depend on the size of the fetal abdominal circumference and the gestational age. The rate of kidney growth must also be taken into account.


Assuntos
Abdome/anormalidades , Distocia/diagnóstico por imagem , Doenças Fetais/diagnóstico por imagem , Cabeça/diagnóstico por imagem , Nefrectomia/métodos , Rim Policístico Autossômico Recessivo/diagnóstico por imagem , Abdome/diagnóstico por imagem , Abdome/embriologia , Parto Obstétrico , Feminino , Doenças Fetais/cirurgia , Feto , Idade Gestacional , Cabeça/embriologia , Humanos , Recém-Nascido , Comunicação Interdisciplinar , Masculino , Diálise Peritoneal , Rim Policístico Autossômico Recessivo/embriologia , Rim Policístico Autossômico Recessivo/cirurgia , Gravidez , Resultado do Tratamento , Ultrassonografia Pré-Natal , Adulto Jovem
18.
World J Emerg Surg ; 14: 34, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31341511

RESUMO

Background: Timing and adequacy of peritoneal source control are the most important pillars in the management of patients with acute peritonitis. Therefore, early prognostic evaluation of acute peritonitis is paramount to assess the severity and establish a prompt and appropriate treatment. The objectives of this study were to identify clinical and laboratory predictors for in-hospital mortality in patients with acute peritonitis and to develop a warning score system, based on easily recognizable and assessable variables, globally accepted. Methods: This worldwide multicentre observational study included 153 surgical departments across 56 countries over a 4-month study period between February 1, 2018, and May 31, 2018. Results: A total of 3137 patients were included, with 1815 (57.9%) men and 1322 (42.1%) women, with a median age of 47 years (interquartile range [IQR] 28-66). The overall in-hospital mortality rate was 8.9%, with a median length of stay of 6 days (IQR 4-10). Using multivariable logistic regression, independent variables associated with in-hospital mortality were identified: age > 80 years, malignancy, severe cardiovascular disease, severe chronic kidney disease, respiratory rate ≥ 22 breaths/min, systolic blood pressure < 100 mmHg, AVPU responsiveness scale (voice and unresponsive), blood oxygen saturation level (SpO2) < 90% in air, platelet count < 50,000 cells/mm3, and lactate > 4 mmol/l. These variables were used to create the PIPAS Severity Score, a bedside early warning score for patients with acute peritonitis. The overall mortality was 2.9% for patients who had scores of 0-1, 22.7% for those who had scores of 2-3, 46.8% for those who had scores of 4-5, and 86.7% for those who have scores of 7-8. Conclusions: The simple PIPAS Severity Score can be used on a global level and can help clinicians to identify patients at high risk for treatment failure and mortality.


Assuntos
Abdome/fisiopatologia , Prognóstico , Sepse/diagnóstico , Abdome/anormalidades , Adulto , Idoso , Distribuição de Qui-Quadrado , Feminino , Mortalidade Hospitalar , Humanos , Escala de Gravidade do Ferimento , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Fatores de Risco , Sepse/fisiopatologia
19.
Medicine (Baltimore) ; 98(25): e16159, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-31232973

RESUMO

RATIONALE: Computerized tomography (CT)-guided blue dye localization has been widely discussed for preoperative localization of pulmonary nodules. However, few studies have investigated this technique for intra-abdominal lesions. Although preoperative localization is not commonly required in laparotomy, it may assume importance with advancements in the field of laparoscopic surgery. PATIENT CONCERNS: Herein, we report the cases of 2 patients diagnosed with colon cancer who underwent hemicolectomy with extended lymphadenectomy and subsequent chemotherapy. DIAGNOSES: Follow-up CT scans showed newly developed metastatic lymphadenopathy and peritoneal tumor implants. INTERVENTIONS: Considering the difficulty in identification of and access to the target lesions during laparoscopic surgery, preoperative CT-guided blue dye localization was performed in both cases. OUTCOMES: All the target lesions were identified by the dye marker and removed successfully. The pathologic results revealed adenocarcinoma. LESSONS: We established the following strategy for preoperative CT-guided dye localization of intra-abdominal lesions:Intra-abdominal lesions that are hard to identify due to their size or morphology, and difficult to approach due to their location or surrounding structures, maybe the candidates for this procedure, especially in cases of laparoscopic surgery.Operators should adjust their localization planning based on the surgery method, cutting path, and location of port sites. The target dye marker should be clearly visible in the presumed intra-operative field of view.A second dye marker should be made to ensure surgical success when the target dye marker is obscured by the surrounding structures in the presumed intra-operative field of view.


Assuntos
Linfadenopatia/diagnóstico , Neoplasias Peritoneais/diagnóstico , Corantes de Rosanilina/uso terapêutico , Tomografia Computadorizada por Raios X/métodos , Abdome/anormalidades , Abdome/cirurgia , Corantes/uso terapêutico , Feminino , Humanos , Laparoscopia/métodos , Linfadenopatia/fisiopatologia , Pessoa de Meia-Idade , Tomografia Computadorizada por Raios X/normas
20.
Rev. bras. cir. plást ; 34(1): 38-44, jan.-mar. 2019. ilus, tab
Artigo em Inglês, Português | LILACS | ID: biblio-994542

RESUMO

Introdução: Na abdominoplastia convencional, a cicatriz do novo umbigo representa o ponto de maior desafio. Em sua execução, já foram descritas e utilizadas várias técnicas e táticas cirúrgicas, com resultados nem sempre satisfatórios, sob o ponto de vista do paciente e também do médico. O objetivo é demonstrar a aplicabilidade e satisfação com a onfaloplastia em triângulo isósceles e com dupla fixação na abdominoplastia. Métodos: Foram selecionadas 97 pacientes do sexo feminino, com idades entre 25 e 65 anos. Todas foram submetidas à dermolipectomia abdominal clássica associada à lipoaspiração moderada de todo abdome anterior e flancos e avaliadas com 90, 180 e 360 dias pós-operatórios, pelo mesmo cirurgião. Resultados: Observou-se um índice de resultados satisfatórios das cicatrizes umbilicais na maioria dos casos (92,8%). Algumas cicatrizes umbilicais apresentaram estenoses (3,1%) e outras, cicatrizes inestéticas (4,1%). Não se observaram necroses. Conclusão: A utilização desta técnica demonstrou ser eficaz, de fácil execução e com resultados muito satisfatórios na estética da cicatriz umbilical nas dermolipectomias abdominais.


Introduction: In conventional abdominoplasty, the creation of a new umbilical scar is challenging. Several surgical techniques and approaches have previously been described and applied, but not always with satisfactory results. The objective is to demonstrate the applicability and satisfaction with omphaloplasty based on an isosceles triangle with double fixation in abdominoplasty. Methods: The study included 97 female patients aged between 25 and 65 years. All underwent classic abdominal dermolipectomy with moderate abdominal liposuction of the entire anterior abdomen and flanks by the same surgeon and were evaluated at 90, 180, and 360 days postoperatively. Results: Patients were satisfied with the umbilicus in most cases (92.8%). Some umbilical scars had contracted (3.1%) and others appeared unsightly (4.1%). No necrosis was observed. Conclusion: This technique was effective and easy to perform, with satisfactory umbilical scar aesthetic outcomes in abdominal dermolipectomy.


Assuntos
Humanos , Feminino , Adulto , Pessoa de Meia-Idade , Umbigo/cirurgia , Lipectomia/métodos , Cicatriz , Abdominoplastia/efeitos adversos , Abdominoplastia/métodos , Abdominoplastia/reabilitação , Abdome/anormalidades , Abdome/cirurgia
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