两例正中神经纤维脂肪瘤:具有病理磁共振特征的罕见病例

Q4 Medicine
Antonios Michailidis MD , Ioannis Tsifountoudis MD, PhD , Ola Furmaga-Rokou MD , Anastasia Theocharidou MD , Evangelos Petsatodis MD, PhD
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引用次数: 0

摘要

正中神经纤维脂肪瘤是一种罕见的良性肿瘤,其特征是神经鞘内纤维脂肪组织过度生长,通常会导致神经受压。本报告介绍了两例病例:一名 33 岁的男性,腕部肿块逐渐增大;一名 48 岁的女性,最初因桡骨疼痛被诊断为德-夸尔文氏腱鞘炎,但在核磁共振检查中发现偶发纤维脂肪瘤。在这两个病例中,核磁共振成像在诊断中都发挥了关键作用,它显示出的特征性特点使诊断得以明确、无创。早期识别这些核磁共振成像结果对于指导治疗和避免不必要的手术干预至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two cases of fibrolipomatous hamartomas of the median nerve: A rare entity with pathognomonic MRI features
Fibrolipomatous hamartomas of the median nerve are rare, benign tumors characterized by the overgrowth of fibro-fatty tissue within the nerve sheath, often leading to nerve compression. This report presents 2 cases: a 33-year-old man with a gradually enlarging wrist mass and a 48-year-old woman, initially diagnosed with De Quervain's tenosynovitis for radial pain, who was found to have an incidental fibrolipomatous hamartoma on MRI. In both cases, MRI played a pivotal role in diagnosis, revealing characteristic features that enabled a definitive, noninvasive diagnosis. Early recognition of these MRI findings is essential for guiding management and preventing unnecessary surgical interventions.
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来源期刊
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
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