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先天性全身性脂肪营养不良中囊性骨病变的不寻常磁共振成像表现。

Unusual magnetic resonance imaging findings of cystic bone lesions in congenital generalized lipodystrophy.

机构信息

Tesla Diagnostic Imaging, Brasilia, Brazil.

Base Hospital of the Federal District, Brasilia, Brazil.

出版信息

J Postgrad Med. 2022 Oct-Dec;68(4):236-238. doi: 10.4103/jpgm.jpgm_1031_21.

Abstract

Cystic bone lesions are the hallmark of skeletal abnormalities in patients with congenital generalized lipodystrophy (CGL). However, their pathophysiology is still unclear and theories about their origin remain largely speculative. This article reports on a patient with CGL and cystic bone lesions, some of them with unusual magnetic resonance imaging (MRI) findings that include elevated signal intensity on T1-weighted images and fluid-fluid levels, the latter evolving to a more "classic" cystic appearance on follow-up. Even though similar findings were first described almost 30 years ago, little attention was given to them back then; furthermore, other than the present report, no other study has performed sequential exams to follow their evolution in serial MRI. The authors conduct a review of the literature, hypothesizing that these remarkable findings may reflect an intermediate stage in the process of cystification of the abnormal bone marrow, incapable to perform adipose conversion, lending factual support to the modern theories about this issue.

摘要

囊性骨病变是先天性全身性脂肪营养不良(CGL)患者骨骼异常的标志。然而,其病理生理学仍不清楚,关于其起源的理论仍在很大程度上是推测性的。本文报道了一例 CGL 合并囊性骨病变的患者,其中一些病变具有不寻常的磁共振成像(MRI)表现,包括 T1 加权图像上的高信号强度和液-液水平,后者在随访中演变为更“典型”的囊性外观。尽管类似的发现早在近 30 年前就已首次描述,但当时并未引起太多关注;此外,除了本报告外,没有其他研究进行连续检查以跟踪其在连续 MRI 中的演变。作者对文献进行了回顾,假设这些显著的发现可能反映了异常骨髓囊性化过程中的一个中间阶段,无法进行脂肪转化,为关于这个问题的现代理论提供了实际支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/095c/9841538/cccf6e77747d/JPGM-68-236-g001.jpg

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