This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-NoDerivatives License 4.0 (CC BY-NC-ND 4.0) where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. AbstractPeritoneal flanges on virgin abdomen are of uncommon etiology of occlusive syndrome. In particular, congenital bridles represent 0.7 to 2% of small bowel and colon occlusions, from all causes. We report a case of a pelvic occlusion in a 22-year-old patient. ÖzAmeliyatsız batındaki peritoneal flanşlar tıkayıcı sendromun nadir bir etiyolojisidir. Özellikle, konjenital bridler, tüm nedenlerden % 0,7 ila % 2 ince bağırsak ve kolon oklüzyonunu temsil eder. Biz 22 yaşında bir hastada pelvik oklüzyon olgusunu sunuyoruz.

Hepatic hydatid cyst is a rare parasitic affection which constitutes a major health problem in countries endemic to hydatidosis. Rupture of hydatid cyst into gallbladder is an exceptional complication first described in 1952 by Atlas and Kamenear. We report the case of a hepatic hydatid cyst rupture into gallbladder in a 31-year-old patient with no history of disease.

Neuroendocrine tumors (NET) of the gallbladder are a rare entity with only 0.2% of all NET located in the gall bladder. Well-differentiated NETs occur at a relatively lower age group unlike other gallbladder tumors, whereas neuroendocrine carcinoma (NEC) occurs in an older category of patients. The aim of our study is to discuss the current level of evidence regarding this pathological entity by means of a rare case report on a neuroendocrine carcinoma of the gall bladder in a 63-year-old patient with a history of diabetes. Patient underwent cholecystectomy for acute cholecystitis. Pathology findings on surgical specimen came back for neuroendocrine tumour.

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