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Renal Parenchymal Malakoplakia Presenting with Abscesses and Hepatic Extension Misdiagnosed as a Malignant Tumor: A Case Report / 대한내과학회지
Korean Journal of Medicine ; : 764-768, 2012.
Artículo en Coreano | WPRIM | ID: wpr-741100
ABSTRACT
Malakoplakia is a chronic inflammatory disorder that usually affects the urinary tract in immunocompromised patients and rarely extends to adjacent organs. Due to its mass-like presentation, malakoplakia is often clinically misdiagnosed as a neoplastic lesion. We describe the case of a 51-year-old female with renal malakoplakia and hepatic extension and large intraperitoneal abscesses that had been misdiagnosed as malignancy. She was diagnosed with myasthenia gravis 12 years prior and had been treated with oral corticosteroids and immunosuppressants. Radical nephrectomy concomitant with abscess drainage was performed. The final pathology was compatible with malakoplakia, and the patient was successfully treated with antibiotics. Although renal malakoplakia is a rare disease, it should be included in the differential diagnosis of patients with a renal mass who have a history of recurrent urinary tract infections or evidence of immunosuppression.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Sistema Urinario / Infecciones Urinarias / Drenaje / Terapia de Inmunosupresión / Huésped Inmunocomprometido / Corticoesteroides / Enfermedades Raras / Diagnóstico Diferencial / Absceso / Inmunosupresores Tipo de estudio: Estudio diagnóstico Límite: Femenino / Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2012 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Sistema Urinario / Infecciones Urinarias / Drenaje / Terapia de Inmunosupresión / Huésped Inmunocomprometido / Corticoesteroides / Enfermedades Raras / Diagnóstico Diferencial / Absceso / Inmunosupresores Tipo de estudio: Estudio diagnóstico Límite: Femenino / Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2012 Tipo del documento: Artículo