A Rare Case of Synovial Sarcoma with Bone Metastasis Mimicking Multiple Myeloma – Challenges of Management in a Nigerian Resource Constrained Setting

Nkpozi Mo, Eyichukwu . G, Ayogu . Bo
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Abstract

Background: Synovial sarcoma (SS), a rare carcinoma of soft tissues (including ligaments and muscles) around the big joints of the body, poses significant diagnostic and management challenges in low and middle income countries especially if it presented when metastasis had occurred. When there is metastasis to the bones, it mimics multiple myeloma on radiological skeletal survey. The objective of this report is to draw attention to this rare carcinoma which, usually, presents as a small painless nodule within the first three decades of life. We report this rare case of SS in a middle aged Nigerian lady who presented initially at National Orthopaedic Hospital (NOHE) with chronic severe right hip pain in which the initial radiological skeletal survey strongly suggested multiple myeloma. Definitive diagnosis and management of this case of synovial sarcoma was very challenging to the patient and managing unit. Conclusion: Early diagnosis of SS is critical at which point surgical excision or radiotherapy may be the preferred treatment option to achieve a favorable outcome. When metastasis is extensive, chemotherapy becomes the therapy of choice and it does not come cheap or easily available.
一例罕见的滑膜肉瘤伴骨转移的多发性骨髓瘤-在尼日利亚资源有限的情况下治疗的挑战
背景:滑膜肉瘤(SS)是一种罕见的身体大关节周围软组织(包括韧带和肌肉)癌,在低收入和中等收入国家,尤其是当它发生转移时出现,给诊断和治疗带来了重大挑战。当有骨转移时,它在放射骨骼调查上模仿多发性骨髓瘤。本报告的目的是引起人们对这种罕见的癌症的注意,这种癌症通常在生命的前三十年出现一个小的无痛结节。我们报告这个罕见的SS病例,一位中年尼日利亚女士最初在国家骨科医院(NOHE)表现为慢性严重右髋关节疼痛,最初的放射骨骼调查强烈提示多发性骨髓瘤。本例滑膜肉瘤的最终诊断和治疗对患者和治疗单位都是非常具有挑战性的。结论:SS的早期诊断至关重要,手术切除或放射治疗可能是获得良好预后的首选治疗方案。当转移范围广泛时,化疗成为治疗的选择,它并不便宜或容易获得。
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