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肩色素绒毛结节性滑膜炎:病例报告及文献复习。

Pigmented Villonodular Synovitis of the Shoulder: A Case Report and Literature Review.

机构信息

Department of Orthopaedics, University of Patras, School of Medicine, University Hospital of Patras, Patras, Greece.

Department of Orthopaedic Surgery, National & Kapodistrian University of Athens, KAT General Hospital, Athens, Greece.

出版信息

Am J Case Rep. 2024 Aug 22;25:e944483. doi: 10.12659/AJCR.944483.

DOI:10.12659/AJCR.944483
PMID:39169602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11348819/
Abstract

BACKGROUND Pigmented villonodular synovitis is a rare clinical entity, with 2-3% of all PVNS cases affecting the shoulder. Diagnosis is challenging and can elude clinicians for years, with definitive treatment involving arthroscopic or open synovectomy. CASE REPORT A 50-year-old woman presented with left shoulder pain persisting for 2 years. She was initially conservatively treated by a rheumatologist, with corticosteroid schemes intra-articularly injected and per os, but no improvement of her symptoms was noted. Two years later, she was referred to the Orthopedics Department of our hospital with constant pain in her left shoulder, refractory to the conservative measures. Physical examination revealed tenderness of her shoulder on palpation and limited range of motion. The diagnosis of PVNS was established by preoperative magnetic resonance arthrography (MRA) and confirmed by biopsy from intra-operative tissue sampling. Arthroscopic debridement and synovectomy were performed, yielding good surgical results, and she now reports pain relief, improved function, and no recurrence of symptoms at 1-year follow-up. CONCLUSIONS The diagnosis of PVNS can be elusive for years. MRI and clinical suspicion along with tissue biopsy can set the diagnosis. Shoulder PVNS follows a similar natural history as knee PVNS, with conservative treatment failing and arthroscopic excision providing definite relief. We report a rare case of shoulder PVNS, underscoring the importance of considering PVNS in cases of shoulder pain refractory to conservative treatment.

摘要

背景

色素绒毛结节性滑膜炎是一种罕见的临床实体,约 2-3%的 PVNS 病例影响肩部。诊断具有挑战性,可能多年来一直被临床医生忽视,明确的治疗方法包括关节镜或开放性滑膜切除术。

病例报告

一名 50 岁女性因左肩部疼痛持续 2 年就诊。她最初由风湿病学家进行保守治疗,关节内和口服皮质类固醇方案,但她的症状没有改善。两年后,她因左肩部持续疼痛、保守治疗无效而被转诊至我院骨科。体格检查显示左肩触诊时有压痛,活动范围受限。术前磁共振关节造影术(MRA)和术中组织取样活检确定了色素绒毛结节性滑膜炎的诊断。关节镜下清创和滑膜切除术取得了良好的手术效果,患者现在报告疼痛缓解,功能改善,随访 1 年无症状复发。

结论

PVNS 的诊断可能多年来一直难以捉摸。MRI 和临床怀疑以及组织活检可以确定诊断。肩 PVNS 的自然病程与膝 PVNS 相似,保守治疗失败,关节镜切除可提供明确缓解。我们报告了一例罕见的肩 PVNS 病例,强调了在保守治疗无效的肩部疼痛病例中考虑 PVNS 的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/948de6237e6d/amjcaserep-25-e944483-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/9b5ca93a8b3e/amjcaserep-25-e944483-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/5066a3c13429/amjcaserep-25-e944483-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/72fe4e8db0e2/amjcaserep-25-e944483-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/948de6237e6d/amjcaserep-25-e944483-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/9b5ca93a8b3e/amjcaserep-25-e944483-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/5066a3c13429/amjcaserep-25-e944483-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/72fe4e8db0e2/amjcaserep-25-e944483-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6c/11348819/948de6237e6d/amjcaserep-25-e944483-g004.jpg

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BMC Musculoskelet Disord. 2022 Nov 29;23(1):1023. doi: 10.1186/s12891-022-05978-3.
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Pigmented Villonodular Synovitis of the Glenohumeral Joint and Biceps Tendon Sheath.盂肱关节和肱二头肌肌腱鞘的色素沉着绒毛结节性滑膜炎
Cureus. 2021 Apr 17;13(4):e14529. doi: 10.7759/cureus.14529.
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Subacromial pigmented villonodular synovitis: case report and review.肩峰下色素沉着绒毛结节性滑膜炎:病例报告及文献复习
J Surg Case Rep. 2021 Mar 8;2021(3):rjab019. doi: 10.1093/jscr/rjab019. eCollection 2021 Mar.
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Arthroscopy. 2020 Jun;36(6):1587-1598. doi: 10.1016/j.arthro.2020.01.059. Epub 2020 Feb 13.
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