Isolated renal intravascular lymphoma: a case report and review of the literature

Autor:	Cemil Tascioglu, Abdullah Ozkok, Irem Sarihan, Murat Kose, Timur Selcuk Akpinar, Duygu Batu
Rok vydání:	2014
Předmět:	Male Pathology medicine.medical_specialty Lymphoma B-Cell Nephrotic Syndrome urologic and male genital diseases Critical Care and Intensive Care Medicine Fever of Unknown Origin Nephritic syndrome medicine Humans Fever of unknown origin B-cell lymphoma Kidney medicine.diagnostic_test business.industry Acute kidney injury Combination chemotherapy General Medicine Acute Kidney Injury Middle Aged medicine.disease Kidney Neoplasms medicine.anatomical_structure Nephrology Renal biopsy business Nephrotic syndrome
Zdroj:	Renal Failure. 36:1125-1128
ISSN:	1525-6049 0886-022X
DOI:	10.3109/0886022x.2014.918829
Popis:	Intravascular large B-cell lymphoma (IVLBCL) is a very rare subtype of extranodal large B-cell lymphoma. It may involve various organ systems such as skin, liver, lung or kidney. Isolated kidney involvement of IVLBCL is also very rare. Herein we report a very rare case of isolated renal IVLBCL presented with fever of unknown origin, acute kidney injury and nephrotic syndrome. Diagnosis was suspected with isolated high renal (18)F fluorodeoxyglucose uptake in positron emission tomography and confirmed with renal biopsy. Complete remission was obtained with combined chemotherapy including rituximab. We reviewed the English literature in terms of IVLBCL with renal involvement and we could only find 16 such cases. Accordingly, fever, AKI and nephritic syndrome are the most common presenting symptoms in renal intravascular lymphoma.
Databáze:	OpenAIRE
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