منابع مشابه
Discovery of a rare ileocecal plasmacytoma
Here we report the discovery of an extramedullary ileocecal plasmacytoma, a rare entity reported only ∼60 times in the literature. This finding occurred during management of a patient who had sustained an occult perforation during diagnostic colonoscopy. We explored the patient finding a large ileocecal perforation, and thus a right hemicolectomy was performed. Interestingly, the pathology of t...
متن کاملSolitary Plasmacytoma of the Mandible: Report of a Rare Case
Solitary bone plasmacytoma belongs to a group of lymphoproliferative clinical disorders typified by clonal proliferation of plasma cells. Solitary plasmacytoma typically involves a single bone or extramedullary site. It commonly occurs in the vertebrae or thorax, and rarely involves the mandible. The aim of this report is to present a rare case of solitary plasmacytoma of the jaws mimicking per...
متن کاملPrimary pancreatic plasmacytoma: a rare case report
BACKGROUND Extramedullary plasmacytoma is a very rare tumor derived from plasma cells and found outside the bone marrow. Most have been identified in patients with the more aggressive anaplastic form of the disease. Only a few cases of primary pancreatic plasmacytoma have been reported. CASE PRESENTATION We present a case of a 56-year-old man in whom a pancreatic mass was found incidentally. ...
متن کاملAtresia of ileocecal junction, ileocecal valve: Rare variants of bowel atresia
Atresia of ileocecal junction and isolated atresia of ileocecal valve are rare types of intestinal atresia with very few reports in literature. We report two such cases. Radiology showed dilated ileal segment and distal micro colon in both the cases. At laparotomy there was atresia of ileocecal junction in the first case and isolated ileocaecal valve atresia with normal ileocecal junction in th...
متن کاملPlasmacytoma of the Breast: A Report of a Rare Disease.
BACKGROUND Extramedullary plasma cells tumours are rare. Much more rarer is their occurance in the breast tissue. Our aim is to report a single case of this very rare lesion (at least from an African perspective) that we incidentally diagnosed histopathologically as a primary extramedullary lesion in a 53 year old woman. CASE DETAILS Clinical records of a 53 year old postmenopausal woman was ...
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ژورنال
عنوان ژورنال: Journal of Surgical Case Reports
سال: 2014
ISSN: 2042-8812
DOI: 10.1093/jscr/rju016