厚皮性:青春期一种未被诊断的疾病——一例报告及文献复习。

Q3 Medicine
Case Reports in Dermatological Medicine Pub Date : 2025-05-08 eCollection Date: 2025-01-01 DOI:10.1155/crdm/5560071
Mishari T Alrubaiaan, Yousef H Alharthi, Suliman Alfaraj
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引用次数: 0

摘要

厚皮畸形(PDD)是一种罕见的,未被诊断的良性疾病,其特征是手部近端指间关节(PIP)的不对称,双侧梭状肿胀。在这种类型的指状纤维瘤病中,皮肤增厚被认为是由于重复的机械刺激而发生的。此外,由于其显著的临床表现,PDD常被忽视或误诊为其他炎性关节病或厚皮骨膜增生。此外,由于其难以捉摸的性质和相似的更严重的条件,临床医生应该意识到这种情况。在此,我们报告一个PDD的病例,并讨论鉴别诊断,以提高识别和防止误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pachydermodactyly: An Underdiagnosed Condition in Adolescence-A Case Report and Literature Review.

Pachydermodactyly (PDD) is a rare, underdiagnosed benign condition characterized by asymmetrical, bilateral fusiform swellings of the hands' proximal interphalangeal (PIP) joints. In this type of digital fibromatosis, cutaneous thickening is thought to occur due to repetitive mechanical irritation. Furthermore, due to its striking clinical appearance, PDD is commonly overlooked or misdiagnosed as other inflammatory arthropathies or pachydermoperiostosis. In addition, because of its elusive nature and resemblance to more serious conditions, clinicians should be aware of this condition. Herein, we present a case of PDD and discuss the differential diagnoses to improve recognition and prevent misdiagnosis.

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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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