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