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职业性硬皮病。一项为期17年的随访研究。

Occupational scleroderma. A 17-year follow-up study.

作者信息

Ishikawa O, Warita S, Tamura A, Miyachi Y

机构信息

Department of Dermatology, Gunma University School of Medicine, Japan.

出版信息

Br J Dermatol. 1995 Nov;133(5):786-9. doi: 10.1111/j.1365-2133.1995.tb02757.x.

Abstract

Two patients with a scleroderma-like disorder induced by epoxy resins were reported from the Department of Dermatology, Gunma University School of Medicine, Japan in 1980. Here, we describe the clinical and laboratory characteristics of these patients after 17 years' follow-up from 1976 to 1993. Their systemic manifestations and indurated sclerotic skin changes disappeared within 5 years. No internal organ involvement has developed during the period of follow-up. On routine laboratory tests, no abnormalities have been found in the peripheral blood or in the blood chemistry or serology. Histological examination revealed atrophy of the dermis and restoration of the normal pattern of fine collagen bundles, when compared with the previous skin biopsy specimens. This scleroderma-like disorder induced by epoxy resins is considered to be different from systemic sclerosis: it has an acute onset and a fairly good prognosis, and does not show involvement of the internal organs.

摘要

1980年,日本群马大学医学院皮肤科报告了两名因环氧树脂引发硬皮病样病症的患者。在此,我们描述了从1976年至1993年对这些患者进行17年随访后的临床和实验室特征。他们的全身表现和硬结性硬化皮肤改变在5年内消失。随访期间未出现内脏器官受累情况。在常规实验室检查中,外周血、血液化学或血清学均未发现异常。与之前的皮肤活检标本相比,组织学检查显示真皮萎缩,细胶原束恢复正常形态。这种由环氧树脂引发的硬皮病样病症被认为与系统性硬化症不同:它起病急,预后较好,且不表现出内脏器官受累。

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