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嗜酸性粒细胞增多性血管淋巴样增生:老年患者的不典型表现。

Angiolymphoid hyperplasia with eosinophilia: atypical appearance in an older patient.

作者信息

Karabudak Ozlem, Taskapan Oktay, Bozdogan Onder, Dogan Bilal

机构信息

Department of Dermatology, GATA Teaching Hospital, Tibbiye Street 81327 Kadikoy, Istanbul, Turkey.

出版信息

Indian J Dermatol. 2008;53(3):144-5. doi: 10.4103/0019-5154.43206.

Abstract

We describe a 76-year-old man presenting with a chronic, non-healing ulcer of six-year duration on his left zygomatic area. The skin biopsy specimen taken from the lesion, showed increased vascular proliferation, edematous endothelial cells in the dermal blood vessels and perivascular eosinophilic/lymphocytic infiltration. The routine and specific blood tests were unremarkable. On the basis of these features, the patient was diagnosed as having angiolymphoid hyperplasia with eosinophilia (ALHE). We present the case because of its rarity in older people, atypical clinical appearance; and stress the consideration of ALHE in the differential diagnosis of chronic non-healing superficial ulcers confined to face and neck.

摘要

我们描述了一名76岁男性,其左侧颧部有一个持续六年的慢性不愈合溃疡。从病变部位取下的皮肤活检标本显示血管增生增加、真皮血管内皮细胞水肿以及血管周围嗜酸性/淋巴细胞浸润。常规和特殊血液检查均无异常。基于这些特征,该患者被诊断为嗜酸性粒细胞增多性血管淋巴样增生症(ALHE)。我们呈现此病例是因其在老年人中罕见、临床表现不典型;并强调在局限于面部和颈部的慢性不愈合浅表溃疡的鉴别诊断中应考虑ALHE。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d5a/2763747/1f43aa197a45/IJD-53-144-g001.jpg

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