Alrubaiaan Mishari T, Alharthi Yousef H, Alfaraj Suliman
College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Department of Dermatology and Dermatologic Surgery, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Case Rep Dermatol Med. 2025 May 8;2025:5560071. doi: 10.1155/crdm/5560071. eCollection 2025.
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.
厚皮性多指(趾)畸形(PDD)是一种罕见的、诊断不足的良性病症,其特征为手部近端指间(PIP)关节出现不对称的双侧梭形肿胀。在这种类型的指(趾)纤维瘤病中,皮肤增厚被认为是由于反复的机械刺激所致。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性骨膜病。此外,由于其难以捉摸的性质以及与更严重病症的相似性,临床医生应了解这种病症。在此,我们报告一例PDD病例,并讨论鉴别诊断方法,以提高识别率并防止误诊。