Gimferrer-Arriaga Josep-Oriol, Gascó-Adrien Javier, Perelló-Moreno Laura, Esteras-Serrano Matías J
Department of Trauma and Orthopaedic Surgery, Hospital Universitari Son Llàtzer,Ctra. Manacor km 4, 07198, Palma de Mallorca, Spain.
J Orthop Case Rep. 2019;9(5):55-58. doi: 10.13107/jocr.2250-0685.1532.
Synovial osteochondromatosis is a rare condition characterized by the formation of multiple cartilaginous nodules, which involves metaplastic changes of the synovium and is commonly found in larger joints. Occurrence in foot and ankle is uncommon, even less in metatarsophalangeal joints.
A 54-year-old woman with primary synovial osteochondromatosis in the first metatarsophalangeal joint was treated by complete excision plus synovectomy. After 8years of follow-up, the patient remains symptom free with no recurrence observed. A summary of the case and review of all published cases found in the current literature around this location is discussed.
Though rare, synovial chondromatosis should be considered as a differential diagnosis in a refractory synovitis and tumor mass in the metatarsophalangeal joint of the hallux.
滑膜骨软骨瘤病是一种罕见疾病,其特征为形成多个软骨结节,涉及滑膜的化生改变,常见于较大关节。发生于足踝部并不常见,在跖趾关节更为少见。
一名54岁女性,第一跖趾关节原发性滑膜骨软骨瘤病,接受了完整切除加滑膜切除术治疗。经过8年随访,患者无症状,未观察到复发。讨论了该病例总结以及对当前文献中此部位所有已发表病例的回顾。
尽管罕见,但滑膜软骨瘤病应被视为拇趾跖趾关节难治性滑膜炎和肿瘤肿块的鉴别诊断之一。