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特发性多中心Castleman病亚型的计算机断层扫描结果

Computed tomography findings of idiopathic multicentric Castleman disease subtypes.

作者信息

Iguchi Toshihiro, Nishikori Asami, Sato Yasuharu, Nishimura Midori Filiz, Iwaki Noriko, Kojima Katsuhide, Asahara Takashi, Otsuka Fumio, Maeda Yoshinobu, Hiraki Takao

机构信息

Department of Radiological Technology, Faculty of Health Sciences, Okayama University, Okayama, Japan.

Department of Radiology, Okayama University Hospital, Okayama, Japan.

出版信息

J Clin Exp Hematop. 2024;64(4):292-296. doi: 10.3960/jslrt.24053.

Abstract

This study retrospectively evaluated the computed tomography (CT) findings of idiopathic multicentric Castleman disease (iMCD) at a single center and compared the CT findings of iMCD-TAFRO with those of iMCD-non-TAFRO. CT images obtained within 30 days before diagnostic confirmation were reviewed for 20 patients with iMCD (8 men and 12 women, mean age 52.8 ± 12.3 years, range 25-74 years). Twelve patients were diagnosed with iMCD-TAFRO, five with iMCD-idiopathic plasmacytic lymphadenopathy, and three with iMCD-not otherwise specified. CT images revealed anasarca and lymphadenopathy in all 20 patients. The iMCD-TAFRO group showed significantly higher frequencies of ascites (100% vs. 37.5%, P = 0.004), gallbladder wall edema (75.0% vs. 12.5%, P = 0.020), periportal collar (91.7% vs. 25.0%, P = 0.004), and anterior mediastinal lesions (non-mass-forming infiltrative lesions) (66.7% vs. 12.5%, P = 0.028). Para-aortic edema tended to be more frequent in patients with the iMCD-TAFRO group (83.3% vs. 37.5%, P = 0.062), while the absence of anterior mediastinal lesions tended to be more frequent in the iMCD-non-TAFRO group (16.7% vs. 62.5%, P = 0.062). These CT findings may have clinical implications for improving the accuracy and speed of iMCD diagnosis and differentiating iMCD-TAFRO from other subtypes.

摘要

本研究回顾性评估了单中心特发性多中心Castleman病(iMCD)的计算机断层扫描(CT)表现,并比较了iMCD-TAFRO与iMCD-非TAFRO的CT表现。对20例iMCD患者(8例男性和12例女性,平均年龄52.8±12.3岁,范围25-74岁)诊断确认前30天内获得的CT图像进行了回顾。12例患者被诊断为iMCD-TAFRO,5例为iMCD-特发性浆细胞性淋巴结病,3例为iMCD-未另行指定。CT图像显示所有20例患者均有全身性水肿和淋巴结病。iMCD-TAFRO组腹水(100%对37.5%,P=0.004)、胆囊壁水肿(75.0%对12.5%,P=0.020)、门静脉周围套袖征(91.7%对25.0%,P=0.004)和前纵隔病变(非肿块形成浸润性病变)(66.7%对12.5%,P=0.028)的发生率显著更高。iMCD-TAFRO组患者腹主动脉旁水肿倾向于更常见(83.3%对37.5%,P=0.062),而iMCD-非TAFRO组无前纵隔病变倾向于更常见(16.7%对62.5%,P=0.062)。这些CT表现可能对提高iMCD诊断的准确性和速度以及将iMCD-TAFRO与其他亚型区分开来具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9068/11786149/5c8fbccb6471/jslrt-64-292-g001.jpg

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