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脊柱原发性淀粉样瘤。病例报告及文献综述。

Primary amyloidoma of the spine. A case report and review of the literature.

作者信息

Leeson M C, Rechtine G R, Makley J T, Carter J R

出版信息

Spine (Phila Pa 1976). 1985 May;10(4):303-6. doi: 10.1097/00007632-198505000-00002.

Abstract

Primary amyloidosis of bone is a rare disease process. When amyloid lesions do occur in bone, they are often associated with myeloma or other plasma cell dyscrasias. Because of its rarity and its protean clinical and radiographic picture adequate biopsy tissue for histopathologic studies is essential for accurate diagnosis. This case presents a 43-year-old man with nondescript back pain and an impressive radiographic lesion in his lower thoracic spine demonstrating the need for careful diagnostic evaluation and a high incidence of suspicion. When occurring primarily in a localized anatomic area, the prognosis for survival is excellent, and cure can be expected by local excision and reconstruction, as necessary.

摘要

原发性骨淀粉样变性是一种罕见的疾病过程。当淀粉样病变确实发生在骨骼中时,它们通常与骨髓瘤或其他浆细胞发育异常相关。由于其罕见性以及其多样的临床和影像学表现,获取足够的活检组织进行组织病理学研究对于准确诊断至关重要。本病例介绍了一名43岁男性,他有难以描述的背痛,其下胸椎有一个令人印象深刻的影像学病变,这表明需要进行仔细的诊断评估且怀疑指数较高。当主要发生在局部解剖区域时,生存预后良好,必要时通过局部切除和重建有望治愈。

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