先天性间母细胞肾瘤1例报告。

Taiwan yi xue hui za zhi. Journal of the Formosan Medical Association Pub Date : 1989-08-01

C Y Kuo, Y K Tsau, K I Yau, S M Chuang

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引用次数: 0

摘要

摘要先天性间母细胞肾瘤(CMN)是一种罕见的肾脏肿瘤，具有独特的病理和独特的临床、治疗和预后模式。特征性病理表现为均匀的间充质梭形细胞交错排列。典型CMN仅行肾切除术预后良好。我们报告一个典型的先天性中胚层肾瘤，这是产前发现，并与母体羊水过多。

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Congenital mesoblastic nephroma: report of a case.

Congenital mesoblastic nephroma (CMN) is a rare renal tumor with a distinct pathology and a unique clinical, therapeutic, and prognostic pattern. The characteristic pathological feature is uniform mesenchymal spindle-shaped cells arranged in interlacing bundles. The prognosis of typical CMN is believed to be excellent by nephrectomy alone. We report a typical case of congenital mesoblastic nephroma which was prenatally detected, and was associated with maternal polyhydramnios.

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Taiwan yi xue hui za zhi. Journal of the Formosan Medical Association

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