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皮肤松弛症:两例有趣病例报告。

Cutis laxa: a report of two interesting cases.

作者信息

Mitra Subhabrata, Agarwal Amit Amit, Das Jayanta Kumar, Gangopadhyay Asok

机构信息

Consultant Dermatologist, Berhampur, West Bengal, India.

出版信息

Indian J Dermatol. 2013 Jul;58(4):328. doi: 10.4103/0019-5154.113986.

Abstract

Cutis laxa is a rare disease that may be either inherited or acquired. The acquired form is rarer than the inherited form. Pathogenesis of this disease is largely unknown. Two cases of acquired cutis laxa are reported here and neither of them had any systemic involvement or any history of drug intake. One of them had localized disease with history of preceding cutaneous inflammation. The other patient with generalized lesion lacked any history of preceding illness. The patient with localized lesion was treated satisfactorily by reconstructive surgery. The other patient had generalized involvement, for which no satisfactory treatment could be offered.

摘要

皮肤松弛症是一种罕见疾病,可分为遗传性或获得性。获得性形式比遗传性形式更罕见。该疾病的发病机制在很大程度上尚不清楚。本文报告了两例获得性皮肤松弛症病例,两例均无全身受累情况或任何药物摄入史。其中一例为局限性疾病,有先前皮肤炎症史。另一例有全身性病变的患者没有任何先前疾病史。局限性病变患者通过重建手术得到了满意的治疗。另一例患者有全身性受累,对此无法提供满意的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b274/3726908/d14aecca9b97/IJD-58-328c-g001.jpg

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