Filizoglu Nuh, Ozguven Salih
From the Department of Nuclear Medicine, Marmara University Pendik Training and Research Hospital, Istanbul, Turkey.
Clin Nucl Med. 2022 Nov 1;47(11):e700-e701. doi: 10.1097/RLU.0000000000004309. Epub 2022 Jun 11.
Von Hippel-Lindau (VHL) disease is an autosomal dominant hereditary cancer syndrome that is characterized by the presence of various malignant and benign tumors, including retinal and central nervous system hemangioblastomas. Hemangioblastomas are highly vascular tumors that can occur sporadically or within VHL disease. Herein, we present 68 Ga-DOTATATE PET/CT findings of a unique case of suprasellar hemangioblastoma in a 52-year-old man with VHL disease.
冯·希佩尔-林道（VHL）病是一种常染色体显性遗传性癌症综合征，其特征是存在各种恶性和良性肿瘤，包括视网膜和中枢神经系统血管母细胞瘤。血管母细胞瘤是高度血管化的肿瘤，可散发性发生或在VHL病患者中出现。在此，我们展示了一名52岁患有VHL病的男性鞍上血管母细胞瘤独特病例的68 Ga-DOTATATE PET/CT检查结果。
