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儿童膝关节创伤性含铁血黄素沉着性滑膜炎 MRI 表现酷似色素绒毛结节性滑膜炎 1 例报告

Post-Traumatic Hemosiderotic Synovitis of the Knee Mimicking Pigmented Villonodular Synovitis on Magnetic Resonance Imaging (MRI) in a Child: A Case Report.

机构信息

Department of Diagnostic Radiology and Nuclear Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.

Division of Orthopedic, Department of Special Surgery, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.

出版信息

Am J Case Rep. 2021 Jun 29;22:e931992. doi: 10.12659/AJCR.931992.

Abstract

BACKGROUND Hemosiderotic synovitis (HS) is a rare proliferative synovial disorder with incompletely understood pathophysiology. It mainly affects the knee joint. It can be confused with pigmented villonodular synovitis (PVNS), both clinically and radiologically. HS has not been previously reported in children, and this rare incidence may lead to difficulties in early clinical and radiological diagnosis, possibly affecting the patient's outcome. CASE REPORT A 13-year-old boy presented with progressive right knee pain, swelling, and limitation of movement 2 months after a traumatic injury in a soccer game. His past medical and family history was unremarkable. His physical exam showed right knee effusion, fullness in the popliteal fossa, and painful restriction in active and passive knee motion. Laboratory tests showed a mildly elevated erythrocyte sedimentation rate. Knee X-rays showed joint effusion. Knee MRI showed large knee joint effusion with diffuse low signal intensity villous synovial hypertrophy in all sequences in addition to a large popliteal cyst with the same imaging characteristics, consistent with diffuse-form PVNS. Total arthroscopic synovectomy was performed without complications. Intraoperatively, there was a large effusion containing yellow clots. The histopathological diagnosis was post-traumatic HS with no evidence of PVNS or malignancy. The patient showed significant clinical and radiological improvement postoperatively with no evidence of recurrence. CONCLUSIONS Post-traumatic HS is a very rare entity that should always be considered in the differential diagnosis of synovitis in active, non-hemophilic children. Radiologists' familiarity with this rare condition is important to guide correct and early diagnosis, and to avoid unnecessary invasive intervention.

摘要

背景

血色沉着性滑膜炎(HS)是一种罕见的增生性滑膜疾病,其发病机制尚未完全阐明。它主要影响膝关节。它在临床上和影像学上都可能与色素绒毛结节性滑膜炎(PVNS)相混淆。HS 在儿童中尚未有报道,这种罕见的发病率可能导致早期临床和影像学诊断困难,从而可能影响患者的预后。

病例报告

一名 13 岁男孩在足球比赛中受伤后 2 个月出现右膝关节进行性疼痛、肿胀和活动受限。他的既往病史和家族史无明显异常。体格检查显示右膝关节积液,腘窝饱满,主动和被动膝关节活动受限且疼痛。实验室检查显示红细胞沉降率轻度升高。膝关节 X 线片显示关节积液。膝关节 MRI 显示大量膝关节积液,所有序列均弥漫性低信号强度绒毛状滑膜增生,同时还伴有具有相同影像学特征的大型腘窝囊肿,符合弥漫型 PVNS。行全关节镜滑膜切除术,无并发症。术中可见大量含有黄色血凝块的渗出液。组织病理学诊断为创伤后 HS,无 PVNS 或恶性肿瘤的证据。术后患者的临床和影像学均有显著改善,无复发迹象。

结论

创伤后 HS 是一种非常罕见的疾病,在活跃、非血友病儿童的滑膜炎鉴别诊断中应始终考虑到这种疾病。放射科医生对这种罕见疾病的熟悉程度对于正确和早期诊断以及避免不必要的侵入性干预至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0096/8255086/464b370f6cbd/amjcaserep-22-e931992-g001.jpg

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