Bilateral Renal Parenchymal Malacoplakia Presenting as Fever and Acute Renal Failure / 대한신장학회잡지
Korean Journal of Nephrology
; : 530-534, 2001.
Article
en Ko
| WPRIM
| ID: wpr-137348
Biblioteca responsable:
WPRO
ABSTRACT
Malacoplakia is a rare, chronic inflammatory disorder characterized by abnormal macrophage function and cell infiltration into normal tissues. We report a 72 year old male with bilateral renal parenchymal malacoplakia who presented with high fever and acute renal failure. The patient had anemia, leukocytosis, thrombocytopenia and bilateral nephromegaly with reduced renal function. Blood and urine cultures showed no micro-organisms. A kidney biopsy revealed diffuse interstitial histiocytic infiltration with intracellular inclusion bodies(Michaelis-Gutmann body). He was treated with antibiotics, and bethanechol, ascorbic acid without improvement. Following treatment with an intravenous methylprednisolone pulse therapy, clinical improvement was made. Renal parenchymal malacoplakia should be considered in the differential diagnosis when presented with high fever, enlarged kidneys and acute renal failure.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Ácido Ascórbico
/
Trombocitopenia
/
Biopsia
/
Metilprednisolona
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Betanecol
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Diagnóstico Diferencial
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Lesión Renal Aguda
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Fiebre
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Anemia
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Riñón
Tipo de estudio:
Diagnostic_studies
Límite:
Aged
/
Humans
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Male
Idioma:
Ko
Revista:
Korean Journal of Nephrology
Año:
2001
Tipo del documento:
Article