A Case of Malakoplakia with Duplex Kidney / 대한비뇨기과학회지
Korean Journal of Urology
;
: 250-255, 1989.
Artículo
en Coreano
| WPRIM
| ID: wpr-108818
ABSTRACT
Malakoplakia is a very rare disease which affects middle-aged women and usually involves the urinary tract. Of these, the bladder is the most common site and the renal parenchyme is involved in 16%. It is a type of granulomatous inflammation in which the histiocyte contains distinct basophilic inclusion called Michaelis-Gutmann bodies. It may be caused by a defect of phagocytic activity of the lysosome. We experienced a cases of malakoplakia with duplex kidney in a 59-year old female, which was treated successfully with left nephrectomy and antibiotics. Herein we report this case with a brief review of literature.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Sistema Urinario
/
Basófilos
/
Vejiga Urinaria
/
Enfermedades Raras
/
Histiocitos
/
Inflamación
/
Riñón
/
Lisosomas
/
Malacoplasia
/
Antibacterianos
Límite:
Femenino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Urology
Año:
1989
Tipo del documento:
Artículo
Similares
MEDLINE
...
LILACS
LIS