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Thyroid Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia: Insights on Successful Noninvasive Imaging.
Goto, Hisanori; Tanimura, Iyo; Nakano, Yujiro; Takeshita, Yumie; Takamura, Toshinari.
Affiliation
  • Goto H; Department of Endocrinology and Metabolism, Kanazawa University Graduate School of Medical Sciences, Kanazawa, 920-8640, Japan.
  • Tanimura I; Department of Radiology, Kanazawa University Hospital, Kanazawa, 920-8641, Japan.
  • Nakano Y; Department of Endocrinology and Metabolism, Kanazawa University Graduate School of Medical Sciences, Kanazawa, 920-8640, Japan.
  • Takeshita Y; Department of Endocrinology and Metabolism, Kanazawa University Graduate School of Medical Sciences, Kanazawa, 920-8640, Japan.
  • Takamura T; Department of Endocrinology and Metabolism, Kanazawa University Graduate School of Medical Sciences, Kanazawa, 920-8640, Japan.
JCEM Case Rep ; 2(8): luae138, 2024 Aug.
Article in En | MEDLINE | ID: mdl-39135960
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JCEM Case Rep Year: 2024 Document type: Article Affiliation country: Japan Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: JCEM Case Rep Year: 2024 Document type: Article Affiliation country: Japan Country of publication: United kingdom