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眼睑淋巴瘤样丘疹病。

Lymphomatoid papulosis of the eyelid.

作者信息

Cloke Adam, Lim Lik Thai, Kumarasamy Manjula, Roberts Fiona, Kemp Ewan G

机构信息

Tennent Institute of Ophthalmology, Gartnavel General Hospital, Glasgow, UK.

出版信息

Semin Ophthalmol. 2013 Jan;28(1):1-3. doi: 10.3109/08820538.2012.680643.

Abstract

Lymphomatoid papulosis (LyP) is a chronic papulonecrotic or papulonodular skin disease, with histological features suggestive of malignant lymphoma. It was originally described by Macauley (1968) as a "self-healing paradoxical eruption, histologically malignant but clinically benign." Unless accompanied by systemic lymphoma, most patients have no constitutional symptoms, and physical findings are limited to the skin. The distribution of lesions is characteristically on the trunk or extremities, but the face, scalp, or oral mucosa may be involved. We report an unusual case of lymphomatoid papulosis of the eyelid. To the best of our knowledge, this is the first report of eyelid involvement by lymphomatous papulosis.

摘要

淋巴瘤样丘疹病(LyP)是一种慢性丘疹坏死性或丘疹结节性皮肤病,组织学特征提示为恶性淋巴瘤。它最初由麦考利(1968年)描述为“一种自愈性矛盾性皮疹,组织学上为恶性但临床上为良性”。除非伴有系统性淋巴瘤,大多数患者无全身症状,体格检查结果仅限于皮肤。皮损分布特征性地见于躯干或四肢,但面部、头皮或口腔黏膜也可能受累。我们报告一例罕见的眼睑淋巴瘤样丘疹病病例。据我们所知,这是淋巴瘤样丘疹病累及眼睑的首例报告。

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