Finan M C, Winkelmann R K
Arch Dermatol. 1983 May;119(5):419-22.
A patient had clinical findings of asthma, peripheral eosinophilia, multisystem abnormalities, and cutaneous extravascular granulomas, consistent with a diagnosis of allergic granulomatosis. In addition, a well-differentiated lymphocytic lymphoma was diagnosed on the basis of bone marrow findings, and a monoclonal gammopathy was demonstrated by serum immunoelectrophoresis. Clinically, the skin lesions appeared as erythematous papules or nodules on the extremities, and some of them showed central ulceration. Histologically, there were dermal extravascular necrotizing granulomas embedded in a granulomatous and inflammatory cell infiltrate. These lesions bore a striking resemblance to those described by Churg and Strauss in patients with allergic granulomatosis, although tissue eosinophilia was significantly less prominent.
一名患者有哮喘、外周血嗜酸性粒细胞增多、多系统异常及皮肤血管外肉芽肿等临床表现,符合变应性肉芽肿病的诊断。此外,根据骨髓检查结果诊断为高分化淋巴细胞淋巴瘤,血清免疫电泳显示单克隆丙种球蛋白病。临床上,皮肤损害表现为四肢的红斑丘疹或结节,部分有中央溃疡。组织学上,真皮血管外坏死性肉芽肿包埋于肉芽肿性和炎性细胞浸润中。这些损害与Churg和Strauss描述的变应性肉芽肿病患者的损害极为相似,尽管组织嗜酸性粒细胞增多不那么明显。