Milam C P, Cohen L E, Fenske N A, Ling N S
Department of Internal Medicine, USF College of Medicine, Tampa 33612.
J Am Acad Dermatol. 1988 Sep;19(3):469-77. doi: 10.1016/s0190-9622(88)70199-1.
Scleromyxedema is a rare type of papular mucinosis that exhibits a generalized lichenoid pattern. A wide variety of clinical manifestations can occur in patients with this disease. Cutaneous involvement is characteristic, but neurologic, cardiovascular, renal, neoplastic, and other systemic manifestations have been described. A monoclonal gammopathy may be present. Many treatment modalities have been used in the past for scleromyxedema. None, however, have shown consistently favorable results. This report concerns the cases of three patients with scleromyxedema who were treated with isotretinoin.
硬化性黏液水肿是一种罕见的丘疹性黏蛋白病,表现为全身性苔藓样皮疹。该病患者可出现多种临床表现。皮肤受累是其特征,但也有神经、心血管、肾脏、肿瘤及其他全身表现的报道。可能存在单克隆丙种球蛋白病。过去曾对硬化性黏液水肿使用过多种治疗方法。然而,没有一种方法能始终显示出良好的效果。本报告涉及3例接受异维A酸治疗的硬化性黏液水肿患者的病例。