Synovial Chondromatosis of Distal Radioulna Joint with Features of Lytic Lesion in a 29 years Male: A Case Report and Review of Literature

N. Kumar, J. Mukhopadhaya, O. Anand
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引用次数: 1

Abstract

Background: Synovial chondromatosis is a rare, benign condition characterized by proliferation of synovial lining and metaplasia. The disease is usually mono articular and commonly involves knee joint, but it can also occur in shoulder, elbow, hip, ankle and wrist joints. A review of the literature produced 30 case reports of synovial chondromatosis of the wrist with only five cases showing recurrence (5/30, 17%). Because of its low prevalence and nonspecific symptoms, it can present diagnostic difficulties and lead to a delay in treatment. Case: We report a 6 month follow up case of a 29 year old right hand dominant male who presented with complaint of pain and swelling in right wrist joints of four months duration. Plain X-ray revealed lytic lesion at distal end of right ulna with multiple radio opaque deposits. MRI and FNAC were in favour of Synovial chondromatosis. Patient underwent synovectomy and excision of calcific lesion through a dorsoulnar approach and a separate incision over radial styloid under general anaesthesia. Histopathology confirmed the diagnosis of Synovial chondromatosis. Patient had no recurrence till last follow up (6 Month). Conclusion: Synovial chondromatosis of wrist joint is extremely rare. A close coordination between the clinician, radiologist and pathologist is essential for accurate diagnosis and management.
29岁男性桡尺骨远端关节滑膜软骨瘤病伴溶解性病变1例报告及文献复习
背景:滑膜软骨瘤病是一种罕见的良性疾病,以滑膜内膜增生和化生为特征。这种疾病通常发生在单关节,通常累及膝关节,但也可发生在肩、肘、髋、踝关节和腕关节。文献回顾发现30例腕部滑膜软骨瘤病报告,其中只有5例复发(5/ 30,17 %)。由于其低患病率和非特异性症状,它可能带来诊断困难并导致治疗延误。病例:我们报告了一个29岁的右手主导型男性的6个月的随访病例,他提出了疼痛和肿胀在右手腕关节持续4个月的投诉。平片示右侧尺骨远端溶解性病变伴多发放射性不透明沉积。MRI和FNAC提示滑膜软骨瘤病。患者在全身麻醉下经背神经入路及桡骨茎突上单独切口行滑膜切除术及钙化病灶切除术。组织病理学证实滑膜软骨瘤病的诊断。最后一次随访(6个月)无复发。结论:腕关节滑膜软骨瘤病极为罕见。临床医生、放射科医生和病理学家之间的密切协调是准确诊断和管理的必要条件。
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