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1.
Afr J Paediatr Surg ; 21(4): 242-246, 2024 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-39279616

RESUMO

BACKGROUND: Ureteropelvic junction obstruction (UPJO) is the most common cause of antenatal hydronephrosis. Although majority of them improve with time, none of the existing diagnostic modalities can accurately predict which hydronephrotic kidney is at the risk of progressive renal damage and will benefit from early surgery. Postural variations in the anteroposterior pelvic diameter (APPD) of the hydronephrotic kidney in children during follow-up postnatal ultrasonography (USG) reflect the intrapelvic tension, which might help in predicting the need of surgery amongst these patients. MATERIALS AND METHODS: We designed this prospective observational study in all unilateral UPJO patients on postural variation in the APPD of renal pelvis on ultrasonography. The mean age of all patients were 2.15 years (0-5 years) and managed at our institute at All India Institute of Medical Sciences, Bhubaneswar. The study duration was from July 2019 to May 2021. The management of these patients was done as per the standard institutional protocol and there was no deviation due to inclusion in this study. We documented the variations in postural APPD both amongst the conservatively managed group and the surgically managed group of patients. Linear correlation between two continuous variables was explored using Pearson's correlation (if the data were normally distributed) and Spearman's correlation (for non-normally distributed data). RESULTS: We found a higher prone APPD than supine APPD in all these patients indicating the obstruction at ureteropelvic junction. However, in the surgical group, there was less variation in the postural APPD compared to the conservative group, and when there was no variation in the postural APPD, the need of surgery was 100%. The limitation of our study was the small sample size (n = 36). A study involving a larger population or involving multiple institutions may further add significance to our findings. CONCLUSION: We found less postural variation in APPD on USG to be more likely associated with severe UPJO requiring early surgery. This may indicate a non-compliant renal pelvis. However, it was statistically not significant.


Assuntos
Hidronefrose , Pelve Renal , Ultrassonografia , Obstrução Ureteral , Humanos , Pelve Renal/diagnóstico por imagem , Obstrução Ureteral/cirurgia , Obstrução Ureteral/diagnóstico por imagem , Estudos Prospectivos , Lactente , Feminino , Masculino , Pré-Escolar , Recém-Nascido , Hidronefrose/diagnóstico por imagem , Hidronefrose/etiologia , Hidronefrose/cirurgia , Índia , Valor Preditivo dos Testes , Postura/fisiologia
3.
Afr J Paediatr Surg ; 21(2): 138-140, 2024 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-38546253

RESUMO

ABSTRACT: Gastric teratomas are very rare tumours. They present with upper abdomen distension which can easily be confused with other common conditions with mass per abdomen in the paediatric age group. Surgical excision is curative for gastric teratomas. The diagnosis is confirmed by radiological evaluation followed by histopathological analysis of excised specimen. We are reporting two such cases of gastric teratomas who presented with complaints of upper abdomen distension. They were evaluated with radiological imaging and successfully managed by surgical excision.


Assuntos
Teratoma , Humanos , Criança , Radiografia , Teratoma/diagnóstico por imagem , Teratoma/cirurgia
4.
Afr J Paediatr Surg ; 21(1): 73-74, 2024 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-38259026

RESUMO

ABSTRACT: Male congenital urethrocutaneous fistula is an extremely rare anomaly that is commonly associated with chordee or anorectal malformations. It is characterised by an abnormal urethral opening on the ventral aspect of the penis with well-formed distal urethra and meatus at the tip of the glans. The treatment is individualised according to the site of the fistula, associated anomalies and condition of the distal urethra. The principles of hypospadias surgery should be strictly followed.


Assuntos
Malformações Anorretais , Hipospadia , Masculino , Humanos , Hipospadia/complicações , Hipospadia/cirurgia , Malformações Anorretais/complicações , Malformações Anorretais/diagnóstico , Malformações Anorretais/cirurgia , Uretra/cirurgia
5.
J Indian Assoc Pediatr Surg ; 28(4): 342-344, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37635885

RESUMO

Anorectal malformations (ARMs) are common congenital anomalies in neonates. Colonic perforation is very rare in ARMs. Delay in diagnosis of neonate with ARM results in colonic perforations and life-threatening morbidity. Colonic perforation due to ARM may not be completely avoided; however, early diagnosis and management are essential in assuring better outcomes.

6.
Afr J Paediatr Surg ; 20(3): 243-244, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37470565

RESUMO

The cystic dilatation of the common bile duct (CBD) is a rare pathology in an infant. It is the second-most common surgical cause of cholestatic jaundice in infants after biliary atresia. A 4-month-old female child was admitted to our department with complaints of abdominal distension. The physical examination revealed the presence of a huge palpable mass involving the right hypochondrium up to the right iliac fossa and umbilical region. Ultrasound abdomen revealed a large intra-abdominal cyst but unable to comment on the organ of origin of the cyst due to its huge size. Multidetector computed tomography of the abdomen was suggestive of possible origin of the cyst from CBD extending from porta hepatis to pelvis. At laparotomy, there was a huge choledochal cyst extending from porta hepatis to pelvis. The choledochal cyst was excised, followed by Roux-en-Y hepaticojejunostomy.


Assuntos
Cisto do Colédoco , Feminino , Humanos , Lactente , Cisto do Colédoco/diagnóstico , Cisto do Colédoco/diagnóstico por imagem , Fígado/patologia
8.
J Indian Assoc Pediatr Surg ; 27(6): 778-780, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36714471

RESUMO

We report a case of colonic agenesis with anorectal malformation in a newborn girl. The patient also presented with congenital heart disease. We are presenting the clinical features, intraoperative findings, and treatment plan.

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