Literature DB >> 33462008

Pachydermodactyly presenting as juvenile idiopathic arthritis in an adolescent man.

Ameen Jubber1, Dushyanth Gnanappiragasam2, Maumer Durrani1, Alison Kinder1, Karen E Harman1.   

Abstract

We present the case of a 17-year-old Asian man diagnosed with pachydermodactyly, a rare digital fibromatosis. Although this is a non-inflammatory periarticular soft tissue disorder, the clinical appearance can mimic inflammatory arthritis. The patient had a 2-year history of fusiform swelling of multiple proximal interphalangeal joints. He was initially diagnosed with juvenile idiopathic arthritis and treated with methotrexate, but a lack of clinical response led to the diagnosis of pachydermodactyly. Recognising this rare condition can prevent unnecessary and potentially harmful treatment. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  dermatology; drugs: musculoskeletal and joint diseases; radiology; skin

Year:  2021        PMID: 33462008     DOI: 10.1136/bcr-2020-237214

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  1 in total

1.  Unilateral pachydermodactyly misdiagnosed as juvenile idiopathic arthritis: A case report.

Authors:  Roaa Aljohani
Journal:  Medicine (Baltimore)       Date:  2022-01-21       Impact factor: 1.889

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.