| Literature DB >> 23796955 |
Ryckie G Wade1, Sachin Daivajna, Peter Chapman, Joseph G Murphy, Damodar Makkuni.
Abstract
INTRODUCTION: Multicentric Reticulohistiocytosis (MRH) is a rare non-Langerhans cell histiocytosis characterised by destructive polyarthritis and violaceous skin papules. PRESENTATION OF CASE: In 2010, a 70-year-old woman with Palindromic Rheumatism was diagnosed with MRH. Within a few months, she developed ankylosis of the small joints of both hands which resulted in severe fixed flexion deformities of the fingers and thumbs. The joint disease failed to respond to medical therapies and the palmar skin of her left hand was becoming increasingly macerated. Therefore, she elected to undergo arthrodesis of the metacarpophalangeal joints to allow hand hygiene. DISCUSSION: To-date, this is the first report of a surgical intervention for this rare condition and represents a novel avenue of potential therapy. Medical therapies for MRH are usually ineffective in preventing the debilitating small joint disease which often develops and there is on-going research into newer agents and alternative surgical techniques.Entities:
Keywords: ANA; Ankylosis; Arthritis; Arthrodesis; DIPJ; Dermatoarthritis; ENA; Fusion; Hand; Histiocytoma; Lipoid; MCPJ; Multicentric; PIPJ; Pitheliod; Reticulohistiocytoma; Reticulohistiocytosis; Review; Surgery; antinuclear antibodies; distal interphalangeal joint; extractable nuclear antigens; metacarphophalangeal joint; proximal interphalangeal joint
Year: 2013 PMID: 23796955 PMCID: PMC3710911 DOI: 10.1016/j.ijscr.2013.04.039
Source DB: PubMed Journal: Int J Surg Case Rep ISSN: 2210-2612