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2019, Number 3

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Rev Hematol Mex 2019; 20 (3)

Primary renal lymphoma

Recinos-Money E, Zepeda-Castilla E, Pérez-Castro J, Escobar-Alfaro G, Aragón-Castro M
Full text How to cite this article

Language: Spanish
References: 14
Page: 231-234
PDF size: 207.20 Kb.


Key words:

Lymphoma, Renal, Rituximab.

ABSTRACT

The primary renal lymphoma is a rare disease whose etiology and pathogenesis are not yet well defined, so much so, its existence is in doubt. This explains the multiple ways to treat it. This paper reports the case of a male patient of 56 years old who consulted for incidental finding of creatinine 2 mg/dL. Abdominal US showed a left renal tumor. Thoracic and abdomino-pelvic tomography corroborated a left renal tumor. Left radical nephrectomy was performed. The pathology report was a diffuse non-Hodgkin large cell type B lymphoma. Bone marrow aspiration was negative. Patient received six cycles of chemotherapy with cyclophosphamide, doxorubicin, vincristine, prednisone and rituximab scheme, in addition, maintenance for 2 years with rituximab bimonthly. The patient is disease-free after 96 months of follow-up and has normal creatinine. Primary renal lymphoma affects 60 years old men with highly variable symptoms. The diagnosis is very difficult by clinic or images and is usually performed by the histology of nephrectomy. Diffuse non-Hodgkin large cell type B lymphoma is the most common subtype. Currently, treatment consists of systemic chemotherapy and rituximab and survival has improved greatly with this scheme.


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Rev Hematol Mex. 2019;20