Villers A, Lami M-C, Filoche P, Milinkevitch S, Goujon J-M, Guillet G
Service de Dermatologie et d'Allergologie, CHU de Poitiers.
Ann Dermatol Venereol. 2006 Jun-Jul;133(6-7):573-6. doi: 10.1016/s0151-9638(06)70966-8.
Dermatomyositis is a rare and serious inflammatory connective tissue disease characterized by a typical cutaneous rash and myopathy. Amyopathic dermatomyositis is a particular form of dermatomyositis involving only cutaneous signs and without myopathy present for over 2 years.
A 48 year-old woman presented with a 3-year history of cutaneous rash without myopathy characteristic of amyopathic dermatomyositis. Clinical examination revealed extensive axillary adenopathy, histological examination of which suggested secondary melanoma. The patient reported a black nevus in the axillary area that had disappeared 1 year earlier. Curettage of the lymph node was negative and the patient was treated with interferon (3M 3 times a week). Regression of the cutaneous signs was noted.
The data, there have been no other reports of paraneoplastic amyopathic dermatomyositis associated with regression of primary melanoma. The literature contains few reports of dermatomyositis associated with melanoma. Amyopathic dermatomyositis may be associated with malignancy.
皮肌炎是一种罕见且严重的炎症性结缔组织病,其特征为典型的皮肤皮疹和肌病。无肌病性皮肌炎是皮肌炎的一种特殊形式,仅累及皮肤体征,且在2年以上无肌病表现。
一名48岁女性,有3年皮肤皮疹病史,无无肌病性皮肌炎特征性的肌病。临床检查发现广泛腋窝淋巴结肿大,组织学检查提示继发性黑色素瘤。患者报告腋窝区有一黑痣,已于1年前消失。淋巴结刮除术结果为阴性,患者接受干扰素治疗(每周3次,每次300万单位)。皮肤体征消退。
据资料显示,此前尚无原发性黑色素瘤消退相关的副肿瘤性无肌病性皮肌炎的其他报道。文献中关于皮肌炎与黑色素瘤相关的报道很少。无肌病性皮肌炎可能与恶性肿瘤有关。