Suppr超能文献

[浆细胞异常增生症与弥漫性特发性骨肥厚。这仅仅是偶然关联吗?]

[Plasma cell dyscrasias and diffuse idiopathic skeletal hyperostosis. Is it a merely accidental association?].

作者信息

Scutellari P N, Orzincolo C, Spanedda R, Piva N

机构信息

Instituto di Radiologia, Università degli Studi di Ferrara.

出版信息

Radiol Med. 1991 May;81(5):625-32.

PMID:2057587
Abstract

The radiologic staging of a series of 144 patients (88 males and 56 females) affected with plasma-cell dyscrasias and observed over a 26-month period, revealed both the well-known bone myeloma-related abnormalities and hyperostotic lesions similar to those described in diffuse idiopathic skeletal hyperostosis. The incidence of skeletal hyperostosis was 31.94%, much higher than that reported in literature for the general population (5%). Typically, the axial skeleton is the most common location for abnormalities in multiple myeloma (MM) as well as in DISH: involvement of the dorsal spine was observed in 65% of cases, the cervical spine was involved in 34.8% of patients, and the lumbar spine in 28.3%. Peripheral ossifying enthesopathy, considered as "whiskering" in the pelvis, was found in 12 cases (8.2%), 7 males and 5 females. DISH was indifferently present in both MM (23 cases), with severe osteolysis (stage III) or simple osteoporosis (stage I), and monoclonal gammopathy of undetermined significance (MGUS) (17 cases), usually without any myeloma-related bone lesions, and in Waldenström disease (4 cases). Many hypotheses are discussed as to the possible pathogenesis (e.g.: accidental, dysmetabolic, or degenerative) of hyperostosis in dysgammaglobulinemias, but, to date, they are no more than mere guesses. DISH is a disorder the etiology of which is still unknown: it is likely to be an ossifying diathesis, but its incidence in both illnesses--which are both plasma-cell dyscarsias--is too high for the association to be accidental. Thus, a pathogenetic factor produced by multiple myeloma can be hypothesized, capable of increasing the so-called idiopathic hyperostosis.

摘要

对144例(88例男性和56例女性)浆细胞异常增生症患者进行了为期26个月的观察,其放射学分期显示出既存在众所周知的与骨髓瘤相关的异常,也有类似于弥漫性特发性骨肥厚中所描述的骨质增生性病变。骨骼骨质增生的发生率为31.94%,远高于文献报道的普通人群的发生率(5%)。通常,轴向骨骼是多发性骨髓瘤(MM)以及弥漫性特发性骨肥厚中异常的最常见部位:65%的病例观察到胸椎受累,34.8%的患者颈椎受累,28.3%的患者腰椎受累。在12例(8.2%)患者中发现了周围骨化性附着点病,其中7例男性和5例女性,在骨盆中表现为“须状”。弥漫性特发性骨肥厚在伴有严重骨质溶解(III期)或单纯骨质疏松(I期)的MM(23例)以及意义未明的单克隆丙种球蛋白病(MGUS)(17例,通常无任何与骨髓瘤相关的骨病变)和华氏巨球蛋白血症(4例)中均有出现。关于球蛋白异常血症中骨质增生可能的发病机制(例如:偶然的、代谢紊乱的或退行性的)有很多假说进行了讨论,但迄今为止,它们都不过是猜测而已。弥漫性特发性骨肥厚是一种病因仍不明的疾病:它可能是一种骨化素质,但它在这两种均为浆细胞异常增生症的疾病中的发生率过高,以至于这种关联不太可能是偶然的。因此,可以推测存在一种由多发性骨髓瘤产生的致病因素,能够增加所谓的特发性骨质增生。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验