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Bronchogenic cysts are congenital foregut malformations that develop due to abnormal budding of the embryonic foregut and tracheobronchial tree.
A 35-year-old healthy man presented with gradually progressive abdominal pain and distention, nausea, vomiting, early satiety, and 4.5-kg weight gain over 3-4 months resulting from a large gastric phytobezoar extending from gastric fundus to antrum.
A colonoscopy of an 18-year-old woman showed 2 cecae, each with its own appendicial orifice.
Liver ultrasound imaging may show the “comet tail” sign.
Idiopathic esophageal ulcer (IEU) secondary to AIDS in a 51-year-old white man with AIDS were completely resolved within 3 weeks of starting highly active anti-retroviral therapy (HAART).
This case highlights the novel endoscopic finding of a “moon surface mucosa” in the small bowel, which was a likely contributor in this case of gastrointestinal hemorrhage.
EPP manifests with recurrent cutaneous photosensitivity without typical bullae or vesicles, leading to chronic skin changes. A 63-year-old woman presented with a left buttock mass that had rapidly increased in size after a recent trauma. We propose that cylindrical batteries should be removed endoscopically as soon as possible after ingestion. A 50-year-old man underwent abdominal rectopexy with non-absorbable mesh for complete rectal prolapse 7 years ago with relief of symptoms for 2 months followed by gradual recurrence over more than 6 years. Cystectomy revealed a cyst containing hair and a tooth. ERCP has a higher sensitivity and should be used if imaging findings are uncertain. We report a case of a 41-year-old man with a mature cystic teratoma (MCT) of the pancreas, who presented with a 6-month history of dull, aching pain and tense, globular, ill-defined upper abdominal swelling. A gallbladder stricture can often be confused for a choledochal cyst on imaging, including MRCP. VBDS is a rare cause of jaundice in patients with Hodgkin’s and non-Hodgkin’s diseases such as ALCL. Splenic involvement secondary to acute pancreatitis is rare (approximately 2%). Intraductal papillary mucinous neoplasms (IPMN) arise from main pancreatic and/or branch ducts, and are characterized by intraductal papillary proliferation of mucin-producing epithelial cells exhibiting various degrees of dysplasia.
A 69-year-old man was admitted for painless jaundice and a 2-week history of pruritus, dark urine, and acholic stools, and represents the third case of an intracholedochal metastatic lesion without simultaneous liver involvement reported in the literature. Abdominal CT showed an intestinal obstruction caused by an 8 x 6 x 11 cm hematoma on the right lateral duodenal wall without signs of active bleeding.