Massa M C, Fretzin D F, Chowdhury L, Sweet D L
J Am Acad Dermatol. 1984 Aug;11(2 Pt 2):333-9. doi: 10.1016/s0190-9622(84)70168-x.
Since Kimura's original description of an unusual subcutaneous disorder with distinctive histologic features of vascular and lymphoid proliferation, numerous descriptions of diseases with similar features have been reported. A variety of descriptive labels, including Kimura's disease, angiolymphoid hyperplasia (ALH) with eosinophilia, atypical pyogenic granuloma, papular angioplasia, and histiocytoid hemangioma, have been applied to these diseases. Although this information has broadened our understanding of the clinical and pathologic spectrum of ALH, the etiology and/or pathogenesis remains unknown. Our case report illustrates the wide range of clinical features of ALH, demonstrating extensive lesions on skin and mucosa. The extreme histologic variability with regard to eosinophils, lymphoid infiltrates, and vascular alterations is also illustrated. Dramatic response to vinblastine sulfate treatment has not been previously reported and may provide a viable treatment alternative in selected patients.
自从木村首次描述了一种具有独特血管和淋巴样增生组织学特征的不寻常皮下疾病以来,已经报道了许多具有相似特征疾病的描述。多种描述性标签,包括木村病、嗜酸性粒细胞性血管淋巴样增生(ALH)、非典型化脓性肉芽肿、丘疹性血管形成和组织细胞样血管瘤,都被应用于这些疾病。尽管这些信息拓宽了我们对ALH临床和病理谱的理解,但其病因和/或发病机制仍然未知。我们的病例报告说明了ALH广泛的临床特征,展示了皮肤和黏膜上的广泛病变。还说明了在嗜酸性粒细胞、淋巴样浸润和血管改变方面组织学的极大变异性。硫酸长春碱治疗的显著反应此前尚未见报道,可能为部分患者提供一种可行的治疗选择。