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21 三体综合征年轻成人单发椎体浆细胞瘤 1 例报告

Vertebral solitary bone plasmacytoma in a young adult with Trisomy 21: A case report.

机构信息

Neurology's Department, Habib Bourguiba Hospital, Sfax, Tunisia.

Neurosurgery's Department, Habib Bourguiba Hospital, Sfax, Tunisia.

出版信息

J Spinal Cord Med. 2020 Nov;43(6):908-911. doi: 10.1080/10790268.2018.1557866. Epub 2018 Dec 17.

Abstract

Solitary bone plasmacytoma (SBP) are rare lesions, accounting for less than 5% of all plasma cell proliferations. We describe a case of a 21-year-old female with Trisomy 21 presenting with cauda equina compression from an SBP. Solitary bone plasmacytoma (SBP) is a rare primary bone tumor. It is characterized by monoclonal proliferation of malignant plasma cells localized to a bone segment, without signs of systemic invasion. The vertebral location is the most common. It preferentially affects men during their 5th or 6th decade. We report the first association between solitary bone plasmacytoma and Trisomy 21.

摘要

孤立性骨浆细胞瘤(SBP)是一种罕见的病变,占所有浆细胞增殖的不到 5%。我们描述了一例 21 岁女性患者,患有 21 三体,表现为马尾受压的孤立性骨浆细胞瘤。孤立性骨浆细胞瘤(SBP)是一种罕见的原发性骨肿瘤。其特征是恶性浆细胞单克隆增殖局限于骨段,无全身侵犯的迹象。脊柱部位最为常见。它主要发生在男性的 5 或 6 十年代。我们报告了首例孤立性骨浆细胞瘤与 21 三体之间的关联。

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[Solitary bony plasmocytoma of the mandible].[下颌骨孤立性骨浆细胞瘤]
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