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1.
Indian J Pathol Microbiol ; 65(3): 673-675, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35900499

RESUMO

Intestinal neuronal dysplasia type B in the gastrointestinal tract is a rare occurrence and may occur alone or in combination with Hirschsprung disease. Distal colon seems to be a frequent site for isolated IND-B cases; however, small bowel involvement is scarcely reported. We report a case of 9 years old boy presenting with features of intestinal pseudo-obstruction for 5 years. Exploratory laparotomy revealed narrowed distal ileum with huge proximal dilatation. Histopathology of the resected terminal ileum revealed giant submucosal ganglion, hyperplastic submucosal nerves, and ectopic ganglion cells in the lamina propria suggestive of IND-B. Although IND-B involving ileum in isolation is a rare occurrence, suspicion should be kept in cases of intestinal obstruction with minimal response to conventional treatment.


Assuntos
Doença de Hirschsprung , Obstrução Intestinal , Criança , Doença de Hirschsprung/diagnóstico , Doença de Hirschsprung/patologia , Doença de Hirschsprung/cirurgia , Humanos , Íleo/patologia , Obstrução Intestinal/etiologia , Obstrução Intestinal/cirurgia , Masculino
2.
Indian J Surg Oncol ; 13(4): 731-740, 2022 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-36687231

RESUMO

A 44-year-old female presented with dull upper abdominal pain. Contrast-enhanced computed tomography (CECT) of the abdomen revealed a well-distended gallbladder with multiple foci of minimally enhancing, intraluminal, soft tissue lesion, and hyperdensity on non-contrast scan measuring 4.3 × 3.5 cm in the fundus with few calculi embedded in it. There was no evidence of extraluminal extension. The patient underwent extended cholecystectomy with liver wedge resection. Histologically, the tumor showed both carcinomatous and sarcomatous components, with prominent osteosarcomatous differentiation. We report this unusual case and present a review of all cases of carcinosarcoma of the gallbladder with sarcomatous differentiation. Despite curative resection, CSGB prognosis remains poor, and thus, the authors recommend to focus their efforts to improve the surgical outcomes.

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