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重新探讨莫蒂默氏病:一例多形性皮肤和系统性肉样瘤病。

Mortimer's Malady revisited: a case of polymorphic cutaneous and systemic sarcoidosis.

机构信息

Department of Dermatology and STD, University College of Medical Sciences and GTB Hospital, University of Delhi, New Delhi, 110 095, India.

出版信息

Indian J Dermatol Venereol Leprol. 2010 Jul-Aug;76(4):448. doi: 10.4103/0378-6323.66606.

Abstract

Sarcoidosis is a systemic disorder with prominent cutaneous component. Skin lesions are of diverse morphology, of which few are specific for the disease. We describe a 30-year-old woman with polymorphic skin lesions including papules, plaques, and nodules, as well as uncommon variants like eyelid papules, palmar and digital nodules, tattoo sarcoid, as well as scar sarcoid. The patient also had stage II pulmonary sarcoidosis, and articular as well as reticulo-endothelial system involvement manifested by enlarged mediastinal and abdominal lymph nodes and hepatosplenomegaly. The presentation of polymorphic skin lesions with involvement of multiple extra-cutaneous systems is uncommon in a single patient.

摘要

结节病是一种以皮肤表现突出的全身性疾病。皮肤损害形态多样,其中少数具有疾病特异性。我们描述了一位 30 岁女性,其皮肤损害呈多形性,包括丘疹、斑块和结节,以及不常见的变异型,如眼睑丘疹、手掌和手指结节、纹身样结节病以及瘢痕样结节病。该患者还患有 II 期肺结节病,关节和网状内皮系统受累,表现为纵隔和腹部淋巴结肿大以及肝脾肿大。在单个患者中,多形性皮肤损害伴多个皮肤外系统受累的表现并不常见。

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