Margad Omar, Boukhris Jalal, Azriouil Ouahb, Daoudi Mohamed, Mortaji Aziz, Koulali Khalid
Service de Traumatologie Orthopédie de l'Hôpital Militaire Avicenne, Marrakech, Maroc.
Pan Afr Med J. 2017 Sep 27;28:86. doi: 10.11604/pamj.2017.28.86.9507. eCollection 2017.
Pigmented villonodular synovitis (PVNS) is a rare benign proliferation of synovial joints, serous bursa, tendinous sheaths of unknown etiopathogeny. We here report 20 cases of PVNS of the knee recorded at the Avicenne Military Hospital, Marrakech over a period of 9 years, from January 2000 to December 2009. This study aimed to identify the specific features of this lesion and to examine its anatomoclinic and prognostic aspects. Annual incidence was 2.2 cases per year: 15 men and 5 women. The average age was 32.5 years. It occurred in the right-hand in 55%, 18 patients had monoarticular presentation of the disease while 1 patient had biarticular presentation of the disease. 80% of cases had pain and swelling, palpable mass was detected in 1 case, meniscal syndrome in 1 case, monoseptic arthritis in 3 cases while popliteal cyst in 2 cases. 14 cases (70%) had diffuse involvement, 6 cases had localized involvement. MRI was evocative in 3 patients out of 5; 2 patients underwent diagnostic arthroscopy. Diagnosis was based on anatomo-pathological examination. Treatment was based on subtotal synovectomy in 15 cases and on tumor excision in patients with localized involvement. 2 cases with osteocartilaginous destruction underwent arthroplasty. Patients' evolution was marked by 2 diffuse recurrences after a mean follow-up of 3-7 years. 3 patients had stiffness associated with quadriceps atrophy, therefore arthrolysis was performed. One case of histologically confirmed PVNS had proved to be a monophasic synovial sarcoma invading the bone 5 months after total synovectomy. Hence, the indication for amputation.
色素沉着绒毛结节性滑膜炎(PVNS)是一种病因不明的滑膜关节、滑囊、腱鞘的罕见良性增生性疾病。我们在此报告2000年1月至2009年12月期间在马拉喀什阿维森纳军事医院记录的20例膝关节PVNS病例。本研究旨在确定该病变的具体特征,并探讨其解剖临床和预后方面。年发病率为每年2.2例:男性15例,女性5例。平均年龄为32.5岁。右侧发病占55%,18例患者为单关节发病,1例患者为双关节发病。80%的病例有疼痛和肿胀,1例可触及肿块,1例有半月板综合征,3例有单发性关节炎,2例有腘窝囊肿。14例(70%)为弥漫性受累,6例为局限性受累。5例患者中有3例MRI表现典型;2例患者接受了诊断性关节镜检查。诊断基于解剖病理学检查。15例患者的治疗基于滑膜次全切除术,局限性受累患者则行肿瘤切除术。2例有骨软骨破坏的患者接受了关节成形术。平均随访3至7年后,2例弥漫性复发显著影响了患者的病情进展。3例患者出现与股四头肌萎缩相关的僵硬,因此进行了关节松解术。1例经组织学证实为PVNS的病例在滑膜全切除术后5个月被证明是侵犯骨骼的单相滑膜肉瘤。因此,有截肢指征。