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1.
World J Gastroenterol ; 11(39): 6221-4, 2005 Oct 21.
Artigo em Inglês | MEDLINE | ID: mdl-16273656

RESUMO

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.


Assuntos
Linfoma Difuso de Grandes Células B/patologia , Neoplasias Pancreáticas/patologia , Proteínas Tirosina Quinases/metabolismo , Idoso de 80 Anos ou mais , Quinase do Linfoma Anaplásico , Carcinoma/metabolismo , Carcinoma/patologia , Evolução Fatal , Humanos , Linfoma Difuso de Grandes Células B/metabolismo , Masculino , Neoplasias Pancreáticas/metabolismo , Receptores Proteína Tirosina Quinases
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