Schirren C G, Eckert F
Dermatologische Klinik und Poliklinik, Ludwig-Maximilians-Universität München.
Hautarzt. 1991 Feb;42(2):107-11.
We report a 40-year-old patient, who presented with a nodular tumor at the scalp. The histological diagnosis was angiolymphoid hyperplasia with eosinophils (ALHE). Immunohistochemical staining of the proliferating vessels was characteristic for endothelial cells. The perivascular inflammatory infiltrate mainly consisted of CD4-positive lymphocytes. Recently it has become clear that Kimura disease, which was thought to be a variant of ALHE, can be distinguished from ALHE by clinical, histological and immunohistochemical criteria and constitutes its own clinical identity. While ALHE is a localized proliferation of endothelial cells, Kimura disease is a proliferation of lymphoid cells characterized by invasive growth and possibly lymphadenopathy.
我们报告了一名40岁的患者,其头皮出现了一个结节性肿瘤。组织学诊断为伴有嗜酸性粒细胞的血管淋巴样增生(ALHE)。增殖血管的免疫组织化学染色显示为内皮细胞的特征性表现。血管周围的炎性浸润主要由CD4阳性淋巴细胞组成。最近已经明确,曾被认为是ALHE一种变体的木村病,可以通过临床、组织学和免疫组织化学标准与ALHE区分开来,并构成其自身的临床特征。虽然ALHE是内皮细胞的局限性增殖,但木村病是一种以浸润性生长和可能伴有淋巴结病为特征的淋巴细胞增殖。