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肩部原发性滑膜软骨肉瘤的罕见表现:一例报告

Rare presentation of primary synovial chondrosarcoma arising in the shoulder: a case report.

作者信息

Kawaguchi Kengo, Endo Makoto, Sagiyama Koji, Maekawa Akira, Nabeshima Akira, Fujiwara Toshifumi, Oda Yoshinao, Nakashima Yasuharu

机构信息

Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, 3-1-1, Maidashi, Higashi-Ku, Fukuoka, Japan.

Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, 3-1-1, Maidashi, Higashi-Ku, Fukuoka, Japan.

出版信息

Skeletal Radiol. 2025 Jun;54(6):1341-1346. doi: 10.1007/s00256-024-04811-3. Epub 2024 Oct 8.

Abstract

Synovial chondrosarcoma (CHS) is a rare malignant tumor arising from the synovial tissue and is often associated with synovial chondromatosis. Herein, we present a unique case of primary synovial CHS in the shoulder joint without evidence of synovial chondromatosis. A 60-year-old man presented to our hospital with a complain of left shoulder pain that persisted for 6 years, which was initially misdiagnosed as synovitis. Radiography revealed an osteolytic lesion involving the humerus and the scapula. Histologically, the tumor exhibited features of grade 2 synovial CHS, infiltrating the trabecular bones and intra-articular space. Wide resection led to a 9-year recurrence-free survival. This case underscores the challenges in diagnosing and managing synovial CHS, particularly in cases with atypical presentations lacking synovial chondromatosis, necessitating careful follow-up and adequate surgical intervention.

摘要

滑膜软骨肉瘤(CHS)是一种起源于滑膜组织的罕见恶性肿瘤,常与滑膜软骨瘤病相关。在此,我们报告一例独特的肩关节原发性滑膜CHS病例,无滑膜软骨瘤病证据。一名60岁男性因左肩疼痛持续6年就诊于我院,最初被误诊为滑膜炎。影像学检查显示肱骨和肩胛骨有溶骨性病变。组织学上,肿瘤表现为2级滑膜CHS特征,浸润小梁骨和关节内间隙。广泛切除导致9年无复发生存期。该病例强调了诊断和管理滑膜CHS的挑战,特别是在缺乏滑膜软骨瘤病的非典型表现病例中,需要仔细随访和充分的手术干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a8e/12000184/7ae02c719da2/256_2024_4811_Fig1_HTML.jpg

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