下颌下Castleman病的单中心浆细胞型:一例报告和文献复习

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Yuusuke Fujiwara , Yuu Tanizawa , Kenta Shinoda , Tomoya Nagai , Atsushi Mamiya , Sohichi Aizawa , Shigehiro Abe , Hisataka Kitano
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引用次数: 0

摘要

Castleman病(CD)通常发生在纵隔,很少发生在头颈部。头颈部几乎所有的CD都是透明血管(HV)型,浆细胞(PC)型CD相对罕见。一位82岁的女性,左下颌下区有一个明确的、有弹性的、坚硬的、可触摸的无痛肿瘤。肿瘤的磁共振成像显示T1加权图像上的低信号强度,T2加权图像上显示中等至高信号强度。进行了细针抽吸,未发现发育不良。肿瘤切除术在全身麻醉下进行。组织病理学诊断为PC型CD,术后10个月随访无复发。在此,我们报告了第一例女性和年龄最大的PC型下颌下CD病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unicentric plasma cell type of Castleman’s disease in the submandibular: A case report and literature review

Castleman’s disease(CD)usually occurs in the mediastinum and rarely occurs in the head and neck region. Almost all CD in the head and neck region is hyaline vascular (HV) type, and plasma cell (PC) type of CD is relatively rare. An 82-year-old woman with a well-defined, elastic, hard, and palpable painless tumor in the left submandibular area was referred to our division. Magnetic resonance imaging of the tumor revealed low signal intensity on T1-weighted images, moderate to high signal intensity on T2-weighed images. Fine needle aspiration was performed, and no dysplasia was detected. Tumorectomy was performed under general anesthesia. The histopathological diagnosis was PC type of CD. There was no recurrence at follow-up 10 months after surgery. Herein, we present the first female and the oldest case of PC type of CD in the submandibular.

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CiteScore
0.80
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83 days
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