Stonecipher M R, Jorizzo J L, White W L, Walker F O, Prichard E
Department of Dermatology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, NC 27157.
J Am Acad Dermatol. 1993 Jun;28(6):951-6. doi: 10.1016/0190-9622(93)70136-h.
Dermatomyositis sine myositis may have various connotations. Controversy exists as to nomenclature, degree of evaluation required, therapy, and course (e.g., does true dermatomyositis of the skin only exist?).
The purpose of this study was to assess prospectively patients with the clinicopathologic features of dermatomyositis and normal muscle enzyme serum levels to determine their course in terms of the onset of muscle disease.
Thirteen patients were studied by complete history and clinical examination, laboratory studies, electromyography, and skin and muscle biopsy. They were observed for 1 to 6 years.
Patients were classifiable into three groups: (1) cutaneous changes only, (2) cutaneous changes only at baseline with subsequent development of myositis, and (3) cutaneous changes with normal muscle enzyme serum levels at baseline but with myositis demonstrated by electromyography and/or muscle biopsy specimens.
Significantly different prognostic and therapeutic implications are present in patients with dermatomyositis with normal muscle enzyme serum levels depending on the results of electromyography, muscle biopsy, and clinical observation.
无肌病性皮肌炎可能有多种含义。在命名、所需评估程度、治疗及病程方面(例如,是否仅存在真正的皮肤性皮肌炎?)存在争议。
本研究旨在前瞻性评估具有皮肌炎临床病理特征且肌肉酶血清水平正常的患者,以确定其肌肉疾病发病方面的病程。
通过完整病史、临床检查、实验室检查、肌电图以及皮肤和肌肉活检对13例患者进行研究。对他们进行了1至6年的观察。
患者可分为三组:(1)仅皮肤改变;(2)基线时仅皮肤改变,随后出现肌炎;(3)基线时皮肤改变且肌肉酶血清水平正常,但肌电图和/或肌肉活检标本显示有肌炎。
根据肌电图、肌肉活检和临床观察结果,肌肉酶血清水平正常的皮肌炎患者存在显著不同的预后和治疗意义。