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网状红斑性粘蛋白沉积症综合征的阳性光生物学研究。

Positive photobiological investigation in reticular erythematous mucinosis syndrome.

作者信息

Adamski H, Le Gall F, Chevrant-Breton J

机构信息

Department of Dermatology, CHU Pontchaillou, University of Rennes, Rue H. Le Guilloux, 35033 Rennes Cedex 9, France.

出版信息

Photodermatol Photoimmunol Photomed. 2004 Oct;20(5):235-8. doi: 10.1111/j.1600-0781.2004.00113.x.

Abstract

BACKGROUND

Reticular erythematous mucinosis (REM) syndrome is a rare disorder. Its clinical course is cyclic with remissions and exacerbations. In this disease, photosensitivity has previously been noticed but rarely demonstrated. We report three new cases with positive photobiological investigation.

CASE REPORTS

Three patients (two males, one female) with a mean age 47 years were seen with reticular erythematous papules on the upper chest and or back. After sun exposure, the lesions were exacerbated. Skin biopsies showed dermal lymphocytic perivascular infiltration with mucin deposition between collagen bundles. Direct immunofluorescence was negative. Antinuclear antibodies were absent. In cabin, ultraviolet (UV)A exposure reproduced clinically and histologically REM lesions in our cases. UVA and UVB provocating phototests were negative. In all patients treatment with oral antimalarials and external photoprotection was effective.

CONCLUSIONS

In our patients, we confirm the photosensitive feature of REM syndrome by provocative irradiation in UVA cabin. The mechanism of triggering is actually unclear. It is supposed that UV radiation, heat, and perspiration are necessary to reveal this affection.

摘要

背景

网状红斑性黏蛋白病(REM)综合征是一种罕见疾病。其临床病程呈周期性,有缓解期和加重期。此前已注意到该疾病存在光敏性,但鲜有相关证明。我们报告3例光生物学检查呈阳性的新病例。

病例报告

3例患者(2例男性,1例女性),平均年龄47岁,上胸部和/或背部可见网状红斑丘疹。日晒后,皮损加重。皮肤活检显示真皮血管周围淋巴细胞浸润,胶原束间有黏蛋白沉积。直接免疫荧光检查为阴性。抗核抗体阴性。在暗室中,紫外线A(UVA)照射在我们的病例中重现了临床上和组织学上的REM皮损。UVA和UVB激发光试验均为阴性。所有患者口服抗疟药及外用光防护治疗均有效。

结论

在我们的患者中,通过在UVA暗室中进行激发照射,我们证实了REM综合征的光敏特征。触发机制目前尚不清楚。据推测,紫外线辐射、热和出汗是引发这种疾病的必要条件。

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