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遗传性出血性毛细血管扩张症中的甲状腺动静脉畸形:无创成像成功的见解

Thyroid Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia: Insights on Successful Noninvasive Imaging.

作者信息

Goto Hisanori, Tanimura Iyo, Nakano Yujiro, Takeshita Yumie, Takamura Toshinari

机构信息

Department of Endocrinology and Metabolism, Kanazawa University Graduate School of Medical Sciences, Kanazawa, 920-8640, Japan.

Department of Radiology, Kanazawa University Hospital, Kanazawa, 920-8641, Japan.

出版信息

JCEM Case Rep. 2024 Aug 12;2(8):luae138. doi: 10.1210/jcemcr/luae138. eCollection 2024 Aug.

Abstract

Hereditary hemorrhagic telangiectasia (HHT) causes arteriovenous malformations (AVMs) in several organs. This report is the first to document and image a thyroid AVM complication in HHT. A 72-year-old woman with HHT was referred for thyroid nodule evaluation. Ultrasonography showed a hypervascularized nodule in the right thyroid lobe which was initially suspected to be malignant. However, 3-dimensional computed tomography angiography demonstrated a thyroid AVM with abnormal anastomosis of the superior thyroid artery and the inferior thyroid vein. In the formation of thyroid AVM, here, chronic thyroiditis and hypothyroidism complications may have been a second hit, due to the predisposing first-hit germline mutation. This report sheds light on overlooked thyroid lesions in HHT and advocates a noninvasive imaging approach in diagnosing thyroid AVMs. Furthermore, this case suggests a potential mechanism of AVM formation in human HHT, possibly supporting the second-hit hypothesis.

摘要

遗传性出血性毛细血管扩张症(HHT)可导致多个器官出现动静脉畸形(AVM)。本报告首次记录并成像了HHT患者的甲状腺AVM并发症。一名72岁的HHT女性因甲状腺结节评估前来就诊。超声检查显示右甲状腺叶有一个血管丰富的结节,最初怀疑为恶性。然而,三维计算机断层血管造影显示为甲状腺AVM,甲状腺上动脉与甲状腺下静脉存在异常吻合。在甲状腺AVM的形成过程中,由于最初的胚系突变易感性,慢性甲状腺炎和甲状腺功能减退并发症可能是第二次打击。本报告揭示了HHT中被忽视的甲状腺病变,并提倡采用非侵入性成像方法诊断甲状腺AVM。此外,该病例提示了人类HHT中AVM形成的潜在机制,可能支持二次打击假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b895/11317758/3b2131a49dcf/luae138f1.jpg

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