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1.
Med J Malaysia ; 77(Suppl 1): 59-61, 2022 07.
Artigo em Inglês | MEDLINE | ID: mdl-35899891

RESUMO

INTRODUCTION: Pediatric cholelithiasis (PC) is relatively rare when compared to adult cholelithiasis. This study is aimed to describe the clinical characteristics of pediatric cholelithiasis treated at Hasan Sadikin General Hospital (HSGH), Bandung, Indonesia. MATERIALS AND METHODS: This is a descriptive study of children aged 0-18 years who were diagnosed with and treated for cholelithiasis at the HSGH over 4-5 years. Variables collected during this study were sex, age, chief complaint, previous medical history, diagnostic test, definitive management, and clinical outcomes. RESULTS: There were 12 cases of pediatric cholelithiasis during the study period, including those of 5 boys (41.7%) and 7 girls (58.3%). The mean and median age of the patients was 10.75 years and 12 years, respectively. The most prevalent complaint of the patients was abdominal pain (75%), followed by jaundice (16.6%) and abdominal distension (8.4%). Thalassemia was the most frequently associated disorder among the patients (25%). Ultrasonography was diagnostic imaging used on 66.6% of patients. Fifty-eight percent of patients have performed the surgery. The most frequently used surgical technique to manage the patients included laparoscopic cholecystectomy (33.3%), followed by laparotomic cholecystectomy (16.7%). CONCLUSION: PC is an uncommon disorder, but easier to diagnose reasonably with the development of imaging study. Minimally invasive procedures using laparoscopic cholecystectomy were the most frequently performed surgical treatment in this study.


Assuntos
Colecistectomia Laparoscópica , Colelitíase , Dor Abdominal , Adulto , Criança , Colecistectomia , Colecistectomia Laparoscópica/métodos , Colelitíase/diagnóstico , Colelitíase/cirurgia , Feminino , Humanos , Laparotomia , Masculino , Estudos Retrospectivos
2.
J Fr Ophtalmol ; 43(7): 604-610, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32631693

RESUMO

INTRODUCTION: Childhood ocular trauma is a preventable cause of visual impairment and blindness worldwide. The purpose of our study was to determine demographic, etiologic, and clinical characteristics, visual outcome, and factors affecting visual prognosis in children with open globe injuries (OGI) and to analyze the predictive value of ocular trauma scoring systems for OGI in children. METHODS: We conducted a retrospective study enrolling 120 pediatric patients hospitalized for OGI from January 2010 to March 2017. Age, gender, date of trauma, time between trauma and presentation, place and circumstances of injury, etiology, visual acuity (VA), wound location and type of injury based on the Birmingham Eye Trauma Terminology, and the clinical signs were recorded. We recorded the number of surgical procedures performed, complications and visual outcomes. RESULTS: The mean age was 7.38 years. In all, 62.5% of the patients were male, and 37.5% were female. The gender ratio was observed to decrease with increasing age. The mean time interval between injury and consultation was 22.80±42.68hours. Injuries usually occurred at home (80%) followed by playgrounds and sports venues (8.3%), the street (6.7%) and school (5%). All of the OGI's were accidental, and the main context was play (70%). The most common traumas were penetrating injury (60.8%) and metal (30%) objects. Penetrating trauma accounted for 68.3% of cases, followed by rupture (27.5%) and intraocular foreign body (IOFB) (7.5%). Initial VA was<1/10 in 59.2% of cases, and the point of entry was the cornea in 65.8% of cases. Final VA was<1/10 in 39.69% of all cases. FVA was significantly correlated with BCVA prior to the surgery, mechanism of the trauma, wound location and size, and other associated lesions. The Ocular Trauma Score (OTS) and the Pediatric Ocular Trauma Score (POTS) were significantly correlated with final VA. CONCLUSION: OGI's in children occurs most frequently in school-age boys. Prognosis is determined by presenting visual acuity, trauma score, and wound severity and location.


Assuntos
Ferimentos Oculares Penetrantes/diagnóstico , Ferimentos Oculares Penetrantes/epidemiologia , Adolescente , Cegueira/diagnóstico , Cegueira/epidemiologia , Cegueira/etiologia , Criança , Pré-Escolar , Corpos Estranhos no Olho/diagnóstico , Corpos Estranhos no Olho/epidemiologia , Corpos Estranhos no Olho/etiologia , Ferimentos Oculares Penetrantes/patologia , Feminino , Humanos , Lactente , Masculino , Prognóstico , Estudos Retrospectivos , Ruptura/diagnóstico , Ruptura/epidemiologia , Ruptura/etiologia , Índices de Gravidade do Trauma , Tunísia/epidemiologia , Baixa Visão/diagnóstico , Baixa Visão/epidemiologia , Baixa Visão/etiologia , Acuidade Visual
3.
Int J Surg Case Rep ; 65: 48-51, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31689627

RESUMO

INTRODUCTION: Ballistic traumatology of the shoulder joint is uncommon. Usually, it is associated to comminuted fractures of the upper humerus. Total shoulder arthroplasty has been proposed to restore a good function. The indication of resurfacing hemi arthroplasty still controversial and is not commonly reported after ballistic traumatology. PRESENTATION OF CASE: We report the case of a 26-year-old soldier victim of a gunshot of the left shoulder entailing a comminuted complex fracture of the upper extremity of the humerus. After shoulder immobilization of 3 months joint mobility was very limited. Radiographs showed bone malunion with a total loss of the hemispherical form of the humeral head. Patient has undergone a resurfacing hemi arthroplasty. Surgery outcome was good. At five years of follow-up, there were no major functional complaints. Clinical and radiological result was satisfactory with a good shoulder mobility. DISCUSSION: Shoulder arthroplasty provided good functional outcome in case of post fracture sequelae. Difficulty was to choose between total arthroplasty and hemi arthroplasty. In young and active patients, authors disapproved total arthroplasty in post traumatic gleno-humeral arthrosis to prevent revision difficulties especially after glenoid erosion. CONCLUSION: Although follow-up still be limited, the indication of shoulder hemi arthroplasty was appropriate regarding functional outcome and patient satisfaction. Further clinical and radiological supervision still necessary to detect glenoid erosion.

5.
Ann Chir Plast Esthet ; 63(3): 234-239, 2018 Jun.
Artigo em Francês | MEDLINE | ID: mdl-29153869

RESUMO

Through a retrospective study of 70 cases of benign soft tissue tumors in the orthopedic traumatology department of the military hospital of Tunis over a 12-year period from January 2005 to December 2016, we have compared our findings to those of the literature in an attempt to identify epidemiological notions relevant to daily medical practice as epidemiological data on benign tumors of the soft parts of the hand remain few and sometimes discordant. The authors report a series of 70 active, young adults, mostly female, with a swelling at the level of the hand as the most common reason for consultation. The middle finger and index finger were the most affected fingers at equal frequencies. The key supplementary examination was the ultrasound of the soft parts. All patients were treated with a complete surgical biopsy of their tumor followed by a histological study of the surgical specimen. Three cases of recidivism were noted. Through this study, the frequency of tumors of the soft parts of the hand in a particular population (Tunisian military agents) is emphasized. Moreover, this study allowed us to confirm the data of the literature concerning the dominance of the digital localization. On the other hand, this study reports that the giant cell tumor is the most common histological type in the study population.


Assuntos
Mãos , Neoplasias de Tecidos Moles/cirurgia , Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Adulto Jovem
6.
Cell Tissue Res ; 314(3): 367-79, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14523643

RESUMO

Exposure to hyperglycemia in utero impairs rat nephrogenesis. The effect of maternal diabetes on insulin-like growth factors and their receptors in the fetal kidney is associated with an increase in both mRNA and protein of the insulin-like growth factor II/mannose 6-phosphate receptor. However, this receptor has never been localized in the fetal kidney. The spatial and temporal distribution of the three insulin-like growth factor receptors (insulin-like growth factor I receptor, insulin-like growth factor II/mannose 6-phosphate receptor and insulin receptor) in rat metanephros during both normal and streptozotocin-induced diabetic renal development was investigated using in situ hybridization and immunohistochemistry. All receptors were found in the fetal kidney from the start of nephrogenesis. Insulin-like growth factor I receptor expression was ubiquitous and continuously present during metanephric development. Insulin receptor expression was developmentally regulated during kidney maturation with an enhanced expression in proximal tubules at the late stages of development. Insulin-like growth factor II/mannose 6-phosphate receptor expression was ubiquitous in the early stages of development and was dramatically decreased at the late stages of normal kidney development. Insulin receptor and insulin-like growth factor I receptor expressions were unchanged in diabetic metanephroi. Although the spatial expression of insulin-like growth factor II/mannose 6-phosphate receptor was unaffected by hyperglycemia, its expression was not downregulated in the mesenchyme of the nephrogenic zone of diabetic fetuses on gestational day 20. This study suggests a crucial role of insulin-like growth factor II/mannose 6-phosphate receptor in the pathogenesis of the impaired nephrogenesis in fetuses of diabetic mothers.


Assuntos
Diabetes Mellitus Experimental/complicações , Rim/anormalidades , Rim/metabolismo , Organogênese/fisiologia , Gravidez em Diabéticas/complicações , Receptor IGF Tipo 1/metabolismo , Receptor IGF Tipo 2/metabolismo , Receptor de Insulina/metabolismo , Animais , Modelos Animais de Doenças , Regulação para Baixo/fisiologia , Feminino , Hiperglicemia/complicações , Imuno-Histoquímica , Rim/fisiopatologia , Gravidez , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-Dawley , Receptor IGF Tipo 1/genética , Receptor IGF Tipo 2/genética , Receptor de Insulina/genética
7.
Diabetes ; 50(5): 1069-75, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11334410

RESUMO

We have recently demonstrated that the exposure to hyperglycemia in utero impairs nephrogenesis in rat fetuses (Amri K et al., Diabetes 48:2240-2245, 1999). Diabetic pregnancy is commonly associated with alterations in the IGF system in fetal tissues. It has also been shown that both IGF-I and IGF-II are produced within developing metanephros and promote renal organogenesis. Therefore, we investigated the effect of maternal diabetes on IGFs and their receptors in developing fetal rat kidney. Diabetes was induced in pregnant rats by a single injection of streptozotocin on day 0 of gestation. We measured the amounts of IGF and their receptors, both proteins and mRNAs, in the metanephroi of fetuses issued from diabetic subjects and in age-matched fetuses from control subjects (14-20 days of gestation). IGF-II was produced throughout fetal nephrogenesis, whereas IGF-I protein was not detected, suggesting a critical role of IGF-II in kidney development. Fetal exposure to maternal diabetes caused no change in IGF production in the early stages of nephrogenesis. Similarly, the amounts of IGF-I receptor and insulin receptor were not altered. By contrast, there was an increase in production of IGF-II/mannose-6-phosphate receptor throughout nephrogenesis. Because this receptor plays an essential role in regulating the action of IGF-II, the altered nephrogenesis in fetuses exposed to maternal diabetes may be linked to a decrease in IGF-II bioavailability.


Assuntos
Diabetes Mellitus Experimental/fisiopatologia , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Rim/embriologia , Gravidez em Diabéticas/fisiopatologia , Receptor IGF Tipo 2/genética , Animais , Desenvolvimento Embrionário e Fetal , Feminino , Idade Gestacional , Fator de Crescimento Insulin-Like I/análise , Fator de Crescimento Insulin-Like II/análise , Gravidez , Biossíntese de Proteínas , RNA Mensageiro/análise , Ratos , Ratos Sprague-Dawley , Transcrição Gênica
8.
Pediatr Res ; 49(5): 660-6, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11328949

RESUMO

IGFs and their binding proteins are important regulators of fetal development. We have previously reported that overexpression of the human IGF binding protein-1 in mice is associated with glomerulosclerosis. The aim of this study was to investigate whether, in that model, decreased bioavailability of IGFs also affected nephrogenesis. When the mothers expressed human IGF binding protein-1, pups were growth retarded and had a reduced number of nephrons. Even nontransgenic pups born to heterozygous mothers had a nephron reduction, indicating that renal hypoplasia was secondary to fetal growth retardation. When the transgene was expressed only in the fetus, pups had a normal birth weight and the kidney was normal at birth, as indicated by histologic studies. However, a significant reduction in the nephron number was observed at 3 mo of age. Because nephrogenesis continues for a few days after birth in the mouse, this indicated that human IGF binding protein-1 overexpression altered postnatal nephrogenesis. In addition, exogenously added IGF-II, but not IGF-I, was effective in stimulating in vitro nephrogenesis. Together these elements suggest that reduced amounts of circulating IGFs, presumably IGF-II, impair kidney development.


Assuntos
Proteínas de Ligação a Fator de Crescimento Semelhante a Insulina/fisiologia , Néfrons/embriologia , Animais , Animais Recém-Nascidos , Feminino , Heterozigoto , Homozigoto , Humanos , Proteínas de Ligação a Fator de Crescimento Semelhante a Insulina/genética , Camundongos , Camundongos Transgênicos , Néfrons/anatomia & histologia , Gravidez , Ratos , Ratos Sprague-Dawley
9.
Diabetes ; 48(11): 2240-5, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-10535460

RESUMO

Congenital malformations occur more frequently in the offspring of diabetic mothers. These in vivo and in vitro studies investigate the potential adverse effects of hyperglycemia on kidney development in the rat. Female rats were made hyperglycemic throughout gestation with a single injection of streptozotocin (STZ) on day 0 of gestation, or for a short period encompassing the early stage of renal organogenesis by infusing glucose from gestational days 12-16. Kidney development in the pups was assessed by determining the total number of nephrons formed in the kidney. The number of nephrons was significantly reduced (10-35%) in the pups from STZ-treated dams, as a function of hyperglycemia. There were also fewer nephrons in pups from dams given glucose infusion whose hyperglycemia was transiently higher on day 13 of gestation. The in vitro experiments were done on metanephroi removed from 14-day-old fetuses and grown for 6 days in medium containing 0, 6.9, 13.8, or 27.5 mmol/l glucose. The development of explants grown in 0, 13.8, and 27.5 mmol/l glucose was impaired compared with that of explants grown in the 6.9 mmol/l control medium, showing that the glucose concentration must be closely controlled to ensure optimum in vitro metanephros development. Thus, exposure to hyperglycemia in utero can cause a nephron deficit, which in turn may have renal consequences later in life.


Assuntos
Diabetes Mellitus Experimental/fisiopatologia , Hiperglicemia/fisiopatologia , Rim/embriologia , Rim/crescimento & desenvolvimento , Gravidez em Diabéticas/fisiopatologia , Efeitos Tardios da Exposição Pré-Natal , Envelhecimento , Animais , Animais Recém-Nascidos , Peso ao Nascer , Glicemia/metabolismo , Peso Corporal , Desenvolvimento Embrionário e Fetal , Feminino , Hiperglicemia/etiologia , Insulina/sangue , Néfrons/anatomia & histologia , Tamanho do Órgão , Gravidez , Ratos , Ratos Sprague-Dawley
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