Soft Tissue Sarcomas Mimicking Benign Inflammatory Processes: A Diagnostic Dilemma.

Q4 Medicine Mediterranean Journal of Rheumatology Pub Date : 2023-08-27 eCollection Date: 2023-12-01 DOI:10.31138/mjr.270823.sts
Cleofina Furtado, Rania Zeitoun, Jonathan Wilkes, Vaiyapuri Sumathi, George Tony
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Abstract

Background: Soft tissue sarcomas are rare and often go undetected until a later stage, particularly when they present as intra-articular or tenosynovial lesions mimicking benign synovial pathologies. The failure to distinguish between malignant and benign synovial disease can have a significant impact on patient outcomes and limit alternatives for local control surgery and limb salvage.

Case description: In this case series, we present two cases of soft tissue sarcomas, one being an intraarticular synovial chondrosarcoma, and the other a pleomorphic spindle cell sarcoma centred along tendon sheaths. Radiologically, the initial clinical presentation of these cases resembled benign synovial pathologies, leading to a delay in diagnosis and treatment.

Conclusion: Our study underscores the importance of maintaining a low threshold of suspicion for surveillance, a multidisciplinary approach, and early histological diagnosis to ensure appropriate timely treatment and a favourable prognosis for patients with soft tissue sarcomas.

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模仿良性炎症过程的软组织肉瘤:诊断难题。
背景:软组织肉瘤非常罕见,而且往往在晚期才被发现,尤其是当它们以关节内或腱鞘内病变的形式出现,并模仿良性滑膜病变时。未能区分恶性和良性滑膜病会对患者的预后产生重大影响,并限制了局部控制手术和肢体挽救的选择:在本病例系列中,我们介绍了两例软组织肉瘤,一例是关节内滑膜软骨肉瘤,另一例是以腱鞘为中心的多形性纺锤形细胞肉瘤。从放射学角度看,这些病例最初的临床表现与良性滑膜病变相似,导致诊断和治疗延误:我们的研究强调了保持低怀疑阈值监测、多学科方法和早期组织学诊断的重要性,以确保软组织肉瘤患者得到适当及时的治疗和良好的预后。
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CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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