Right hypochondrial abscess: A rare consequence of supportive cholecystitis

Right hypochondrial abscess: A rare consequence of supportive cholecystitis

INTRODUCTION Spontaneous cholecystocutaneous abscess is an extremely uncommon complication of acute suppurative cholecystitis. Over the past century very few cases of spontaneous cholecystocutaneous fistulas have been described in the medical literature. We, here, report a case of abdominal wall abscess secondary to cholecystocutaneous fistula. CASE REPORT A 78 -year-old male presented as an ...

Torsion of a fatty fringe of the falciform ligament, a rare cause of right hypochondrial pain.

Brucellar spondylitis presenting as right hypochondrial pain.

A 24 year old Yugoslavian woman, who had lived in Britain for 18 months, presented with right loin pain, dysuria, and frequency of micturition of two months' duration. After collection of a urine sample co-trimoxazole tablets were prescribed. No bacterial growth was obtained from the urine culture. Six days later she was admitted to a surgical ward with intense right hypochondrial pain of a col...

A Rare Case of Eosinophilic Cholecystitis Presenting in a Patient with Thalassemia Intermedia; a Case Report

Eosinophilic cholecystitis is a rare inflammatory condition encountered in surgical cholecystectomy specimens. In terms of histopathology, it is defined by transmural infiltration of eosinophils composing more than 90% of leukocytes. We here report a case of 19-year-old male admitted with thalassemia intermedia and with severe left upper quadrant pain. The patient underwent open splenectomy and...

Agenesis of Right Lung: A Rare Congenital Disorder

  Pulmonary agenesis is a rare congenital anomaly in which there is absence of pulmonary parenchyma as well as its bold vessels. It is an unusual cause of respiratory distress in newborn. Unilateral agenesis of lung is often associated with other congenital anomalies. The condition may lead to diagnostic difficulties.   Right pulmonary agenesis has poor prognosis. Here we present a case of fem...