| Literature DB >> 14730391 |
George Mantzios1, Panagiotis Tsirigotis, Filio Veliou, Iosif Boutsikakis, Lillian Petraki, John Kolovos, Sotirios Papageorgiou, Yannis Robos.
Abstract
Primary adrenal lymphoma (PAL) is an extremely rare entity and adrenal insufficiency is a common complication. Bilateral enlargement of adrenal glands should raise the suspicion of lymphoma, especially in patients with clinical or laboratory features of adrenal insufficiency. Most of these cases are highly aggressive tumors and should be treated with multiagent chemotherapy. The role of bilateral adrenalectomy and/or radiotherapy cannot be estimated. Our patient with PAL was an 80-year-old man who presented with clinical and laboratory features of adrenal insufficiency. Combination chemotherapy plus rituximab was unsuccessful and our patient died from progressive disease.Entities:
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Year: 2004 PMID: 14730391 DOI: 10.1007/s00277-003-0838-3
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673