Valencia I C, Colsky A, Berman B
Department of Dermatology and Cutaneous Surgery, University of Miami School of Medicine, FL, USA.
J Am Acad Dermatol. 1998 Nov;39(5 Pt 2):864-6. doi: 10.1016/s0190-9622(98)70367-6.
Multicentric reticulohistiocytosis (MRH) is a rare systemic disorder that most often affects women in the fourth to fifth decades of life and is characterized by widespread cutaneous papules and nodules, often associated with a destructive arthritis. The characteristic histologic feature of the skin lesions, and of other affected organs, is the presence of histiocytes and multinucleated giant cells containing abundant eosinophilic cytoplasm with a "ground glass appearance." Approximately 30% of the patients have an underlying malignancy suggesting MRH may be a paraneoplastic phenomenon. We describe a case of MRH associated with recurrent, metastatic breast carcinoma.
多中心网状组织细胞增多症(MRH)是一种罕见的系统性疾病,最常影响40至50岁的女性,其特征为广泛的皮肤丘疹和结节,常伴有破坏性关节炎。皮肤病变以及其他受累器官的特征性组织学表现是存在组织细胞和多核巨细胞,这些细胞含有丰富的嗜酸性细胞质,呈“毛玻璃样外观”。约30%的患者存在潜在恶性肿瘤,提示MRH可能是一种副肿瘤现象。我们报告一例与复发性转移性乳腺癌相关的MRH病例。