Umbert I J, Winkelmann R K
Department of Dermatology, Mayo Clinic, Rochester, MN 55905.
Br J Dermatol. 1991 Mar;124(3):291-5. doi: 10.1111/j.1365-2133.1991.tb00578.x.
We report two patients with chronic, recurrent, nodular panniculitis lesions that later developed areas of lipoatrophy. Histologically, there was a consistent lobular lipophagic replacement of fat cells with lipophagic giant cells. The clinical appearance was that of tender, erythematous, superficial or subcutaneous, symmetrical nodules and plaques of 1-2 weeks' duration. The lesions could occur with episodes of fever. One patient had hepatomegaly and the other had an increased sedimentation rate and leucocytosis. The histology and the clinical pattern of the panniculitus syndrome resembled those of lipophagic lipoatrophy of childhood. This is a panniculitis of unknown cause in which the principal inflammatory cell response in the subcutaneous tissue is the macrophage.
我们报告了两名患有慢性复发性结节性脂膜炎病变的患者,这些病变后来出现了脂肪萎缩区域。组织学上,脂肪细胞出现一致的小叶性噬脂性替代,伴有噬脂性巨细胞。临床表现为持续1 - 2周的触痛性、红斑性、浅表或皮下对称结节和斑块。病变可伴有发热发作。一名患者有肝肿大,另一名患者血沉加快和白细胞增多。脂膜炎综合征的组织学和临床模式类似于儿童期噬脂性脂肪萎缩。这是一种病因不明的脂膜炎,其中皮下组织主要的炎症细胞反应是巨噬细胞。