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Von Hippel-Lindau disease is a rare multisystem disorder that shows autosomal dominant inheritance. It is a cancer syndrome that is characterized by the development of a variety of benign and malignant tumors-CNS hemangioblastomas, retinal angiomas, endolymphatic sac tumors, renal cysts and tumors, pancreatic cysts and tumors, adrenal pheochromocytomas, and epididymal cystadenomas. Here we present the 68 Ga-labeled DOTANOC scans of 2 siblings who show an interesting spectrum of findings consistent with Von Hippel-Lindau disease. Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

Citation

Priyanka G B, Nishikant Avinash Damle, Ravindranath Reddy K, Nikhil Tandon, Priyanka Naranje, Devasenathipathy Kandasamy, Kishan Subudhi. 68 Ga-DOTANOC PET/CT in 2 Siblings With Von Hippel-Lindau Disease. Clinical nuclear medicine. 2024 Jun 01;49(6):e266-e268

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PMID: 38537203

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