多发性皮肤网状组织细胞瘤
Multiple Cutaneous Reticulohistiocytoma.
作者信息
Hemmady Karishma D, Someshwar Shylaja S, Jerajani Hemangi R
机构信息
Department of Dermatology, Mahatma Gandhi Mission Hospital, Navi Mumbai, Maharashtra, India.
出版信息
Indian J Dermatol. 2016 Jan-Feb;61(1):121. doi: 10.4103/0019-5154.174130.
Multicentric reticulohistiocytosis is a rare non-Langerhans cell histiocytosis characterized in its full form by severe destructive arthritis, cutaneous nodules, and systemic manifestations. Cutaneous lesions may precede, accompany, or more commonly develop later than other features in this disease. We describe a case of multiple cutaneous reticulohistiocytoma without any systemic associations after thorough investigations.
多中心性网状组织细胞增生症是一种罕见的非朗格汉斯细胞组织细胞增生症，其典型表现为严重的破坏性关节炎、皮肤结节和全身症状。在这种疾病中，皮肤病变可能先于、伴随其他特征出现，或更常见地在其他特征之后出现。经过全面检查，我们报告一例无任何全身关联的多发性皮肤网状组织细胞瘤病例。
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