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World J Gastroenterol ; 11(39): 6221-4, 2005 Oct 21.
Article in English | MEDLINE | ID: mdl-16273656

ABSTRACT

We present the fourth case of a primary pancreatic anaplastic large cell lymphoma (ALCL), ALK-. An 80-year-old man was admitted to our clinic for further investigation of a fever of unknown origin. He noted anorexia, weight loss and fatigue. His laboratory tests showed anemia and a great elevation of ESR, LDH, and beta (2) microglobulin. In CT and MRI scan, a soft tissue mass in the pancreas was observed. A repeated endoscopy after his admission revealed an ulcerated mass-like deformity of the duodenal bulb. Explorative laparotomy confirmed a diffuse spread of an unresectable malignant pancreatic mass extending to the adjacent organs. Duodenal and surgical biopsies identified an ALCL of T-cell lineage, ALK-. The patient died in the Intensive Care Unit due to hemodynamic instability. Our case is the first one indicating that primary pancreatic lymphoma should be suspected in a patient with pancreatic mass and elevated serum LDH and beta(2) microglobulin.


Subject(s)
Lymphoma, Large B-Cell, Diffuse/pathology , Pancreatic Neoplasms/pathology , Protein-Tyrosine Kinases/metabolism , Aged, 80 and over , Anaplastic Lymphoma Kinase , Carcinoma/metabolism , Carcinoma/pathology , Fatal Outcome , Humans , Lymphoma, Large B-Cell, Diffuse/metabolism , Male , Pancreatic Neoplasms/metabolism , Receptor Protein-Tyrosine Kinases
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