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Case Reports in Orthopedics
Volume 2015 (2015), Article ID 242078, 4 pages
Case Report

Surgical Management of Unilateral Soft Tissue Swelling around the Proximal Interphalangeal Joint in an Adolescent: A Case Report of Pachydermodactyly

1Saitama Hand Surgery Institute, Saitama Seikeikai Hospital, 1721 Ishibashi, Higashimatsuyama City, Saitama 355-0072, Japan
2Department of Radiology, Saitama Medical University, 38 Morohongo, Moroyamacho, Iruma, Saitama 350-0451, Japan
3Department of Radiology, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe City, Saitama 350-8550, Japan
4Department of Pathology, Saitama International Center, Saitama Medical University, 1397-1 Yamane, Hidaka City, Saitama 350-1298, Japan

Received 11 October 2015; Revised 11 November 2015; Accepted 15 November 2015

Academic Editor: Paul E. Di Cesare

Copyright © 2015 Naoki Kato et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Pachydermodactyly (PDD) is a rare and benign acquired form of digital fibromatosis, characterized by asymptomatic fusiform soft tissue hypertrophy of the lateral aspect of the proximal interphalangeal (PIP) joints of the fingers. The etiology of PDD remains unknown, but it usually affects healthy males around the age of puberty. It can be misdiagnosed as inflammatory rheumatic diseases, especially as juvenile chronic arthritis. Here, we report a case of PDD in an 18-year-old man who had progressive fusiform swelling of the PIP joint on his left middle finger. Although he had no pain or functional limitation of movement, he chose to undergo surgical resection of the lesion to obtain a conclusive diagnosis and to rectify the deformity’s appearance. Histologically, the lesion was characterized by coarse fibrosis in the adipose tissue, peripheral nerve fibers, and eccrine glands; this is compatible with a diagnosis of PDD.