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

JCEM case reports Pub Date : 2024-08-12 eCollection Date: 2024-08-01 DOI:10.1210/jcemcr/luae138
Hisanori Goto, Iyo Tanimura, Yujiro Nakano, Yumie Takeshita, Toshinari Takamura
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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.

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遗传性出血性远端血管扩张症中的甲状腺动静脉畸形:无创成像的成功启示。
遗传性出血性毛细血管扩张症(HHT)会导致多个器官出现动静脉畸形(AVM)。本报告首次对 HHT 并发甲状腺动静脉畸形进行了记录和成像。一名 72 岁的 HHT 女性患者被转诊接受甲状腺结节评估。超声波检查显示右侧甲状腺叶有一个高血管化结节,起初怀疑是恶性的。然而,三维计算机断层扫描血管造影显示甲状腺动静脉畸形,甲状腺上动脉和甲状腺下静脉吻合异常。在甲状腺动静脉畸形的形成过程中,慢性甲状腺炎和甲状腺功能减退并发症可能是第二次发作,这是因为第一次发作的种系突变具有易感性。本报告揭示了HHT患者中被忽视的甲状腺病变,并提倡采用无创影像学方法诊断甲状腺动静脉畸形。此外,该病例还提示了人类HHT中AVM形成的潜在机制,可能支持二次突变假说。
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