Colomb D, Weltert Y A, Brechard J L, de Rivoyre V
Dermatologica. 1981;163(1):94-104.
The authors have recently come across a female patient with pseudo-pyogenic granuloma and have taken this opportunity to recall the clinical and histological features of this disease which was described in 1969 by Wilson Jones and Bleehein. In this connection, they have studied the relationship of this disease with similar entities, i.e. subcutaneous angiolymphoid hyperplasia with eosinophilia (described by Wells and Whinster in 1969) on the one hand and kimura's disease (described by Kimura in 1948) on the other hand. Whereas subcutaneous angiolymphoid hyperplasia with eosinophilia seems to be an evolutive form developing from pseudopyogenic granuloma, Kimura's disease differs from it clinically and histologically and is considered as a borderline form.
作者最近遇到一名患有假性化脓性肉芽肿的女性患者,并借此机会回顾了1969年由威尔逊·琼斯和布莱欣描述的这种疾病的临床和组织学特征。就此,他们研究了这种疾病与类似疾病的关系,一方面是嗜酸性粒细胞增多性皮下血管淋巴样增生(1969年由韦尔斯和温斯特描述),另一方面是木村病(1948年由木村描述)。嗜酸性粒细胞增多性皮下血管淋巴样增生似乎是从假性化脓性肉芽肿发展而来的一种演进形式,而木村病在临床和组织学上与之不同,被认为是一种临界形式。