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1.
World J Clin Cases ; 3(7): 671-4, 2015 Jul 16.
Artículo en Inglés | MEDLINE | ID: mdl-26244160

RESUMEN

Gallbladder perforation (GBP) is a rare but serious complication of cholecystitis and needs to be managed promptly. Acalculus cholecystitis leading to GBP is frequently associated with enteric fever and found in critically ill patients, and a surgical approach is not always feasible in such patients. Use of percutaneous tube cholecystostomy (PTC) in such patients is a known entity but it is usually followed by interval cholecystectomy. Here we report a case of perforated gallbladder in a child managed conservatively and successfully with PTC as the definitive treatment wherein cholecystectomy was avoided. The functionality of the gallbladder was confirmed by a Tc99m-HIDA scan.

2.
Eur J Pediatr Surg ; 25(2): 189-94, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24683103

RESUMEN

BACKGROUND: Meningomyelocele is a defect of the spinal cord, vertebrae, and the overlying skin and is the most common form of open spinal dysraphism. Rapid closure of the back defect in the early postnatal period is mandatory to reduce the frequency of infection-related complications of the central nervous system. Majority of the cases present with small defects, which can be closed primarily, with or without subcutaneous dissection. However, direct closure is not possible in 25% of the cases. Different types of local flaps (skin or muscle flaps) are widely used for covering the skin defects; and with varying results. PATIENTS AND METHODS: A prospective nonrandomized study was conducted in the department of pediatric surgery at a tertiary hospital, from September 2007 to October 2011. Overall 35 patients with large meningomyelocele defects that could not be closed primarily were included in the study. All patients were treated using subcutaneous tissue based pedicle flap with bilateral V-Y advancement. RESULTS: There were 27 neonates, 7 infants, and 1 child, with a male:female ratio of 1.19:1. There were 3 thoracolumbar, 14 lumbar, 14 lumbosacral, 3 sacral, and 1 multiple meningomyelocele defects with an average size of 8.5 cm (range 6.5-11 cm). Average intraoperative blood loss was 8 mL (range 6-10.5 mL). Average operative time which included flap reconstruction time, after closure of dura, was 38.6 min. Total seven patients had wound complications viz. fat necrosis (n = 2), flap necrosis (n = 2), hematoma (n = 1), cerebrospinal fluid leak followed by wound dehiscence (n = 1), wound infection which led to meningitis (n = 1). Average healing time for flap repair was 7.52 days. Overall 80% (n = 28) of the patients had good flap texture and contour with satisfactory cosmesis. CONCLUSION: Closure of large meningomyelocele wound defects with subcutaneous based pedicle flap with bilateral V-Y advancement is an effective technique. The main advantages of this technique are its simplicity, short operative time, good tolerance, early healing, and good cosmetic outcome with an excellent flap texture and contour match with minimal complications.


Asunto(s)
Meningomielocele/cirugía , Procedimientos de Cirugía Plástica/métodos , Colgajos Quirúrgicos , Pérdida de Sangre Quirúrgica , Preescolar , Estética , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Tempo Operativo , Estudios Prospectivos , Procedimientos de Cirugía Plástica/efectos adversos , Colgajos Quirúrgicos/efectos adversos , Cicatrización de Heridas
3.
Urology ; 83(6): 1401-3, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24767515

RESUMEN

Urethral polyp is a rare cause of bladder outlet obstruction, voiding dysfunction, and hematuria in the pediatric age group. Urethral polyps are rarely associated with other congenital urinary tract anomalies. In this study, we report a case of solitary posterior urethral polyp with type I posterior urethral valve in a 7-day-old neonate presented with urinary retention and deranged renal function. The polyp was diagnosed on cystoscopy. Transurethral resection of the polyp with posterior urethral valve fulguration was performed. Pathologic assessment revealed a fibroepithelial lesion, which was consistent with congenital posterior urethral polyp.


Asunto(s)
Pólipos/diagnóstico , Uretra/anomalías , Neoplasias Uretrales/diagnóstico , Anomalías Urogenitales/diagnóstico , Anomalías Múltiples/diagnóstico , Anomalías Múltiples/cirugía , Biopsia con Aguja , Cistoscopía/métodos , Estudios de Seguimiento , Humanos , Inmunohistoquímica , Recién Nacido , Masculino , Procedimientos Quirúrgicos Mínimamente Invasivos/métodos , Pólipos/congénito , Pólipos/cirugía , Enfermedades Raras , Medición de Riesgo , Resultado del Tratamiento , Uretra/diagnóstico por imagen , Uretra/cirugía , Neoplasias Uretrales/congénito , Neoplasias Uretrales/cirugía , Retención Urinaria/diagnóstico , Retención Urinaria/etiología , Anomalías Urogenitales/cirugía , Urografía/métodos , Procedimientos Quirúrgicos Urológicos/métodos
4.
J Clin Neonatol ; 2(3): 140-2, 2013 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-24251260

RESUMEN

Solitary crossed renal ectopia (SCRE) is an exceedingly rare anomaly of the urinary tract. So far, only 34 cases have been reported in the literature. It usually presents after infancy. Most of these cases are diagnosed incidentally while patients are undergoing evaluation for associated genitourinary, cardiovascular, hematological or vertebral abnormalities. We report the first case of SCRE presenting in neonatal age with impaired renal function and vesico-ureteric reflux.

5.
Indian J Plast Surg ; 46(1): 127-9, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23960319

RESUMEN

Epigastric heteropagus is an extremely rare congenital anomaly, in which there is asymmetrical conjoined twinning, with the parasitic twin attached to the epigastrium. A 2-day-old male, with epigastric heteropagus and omphalocele, was operated in our institution. After excision of the parasitic twin, omphalocele was covered with a gluteal skin flap available from the parasitic twin. Post-operative course was uneventful, except for infection along the edges of the skin flaps, which was managed conservatively. Only 44 cases of epigastric heteropagus twins have been reported previously in world literature. We present a novel surgical approach for the repair of the omphalocele in a case of epigastric heteropagus twins, probably the 45(th) case to be reported in the world literature.

6.
J Pediatr Surg ; 47(11): e31-2, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23164027

RESUMEN

Defective closure of the pharyngeal apparatus during the second week of gestation results in pharyngeal arch anomalies. Although pharyngeal apparatus (branchial) anomalies are frequently seen, bilateral cases are rare (only 2% to 3%). Bilaterality has a familial predisposition. Our patients, a set of identical twins, presented with bilateral discharging cervical sinuses noticed at 3 months of age. Physical examination was suggestive of bilateral pharyngeal apparatus (branchial) sinuses. Both patients were managed with surgical excision in the same operative sitting. To the best of our knowledge, ours is the first case of bilateral pharyngeal apparatus (branchial) sinuses in a set of identical twins.


Asunto(s)
Región Branquial/anomalías , Enfermedades en Gemelos/diagnóstico , Gemelos Monocigóticos , Región Branquial/cirugía , Enfermedades en Gemelos/cirugía , Humanos , Lactante , Masculino
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