Titlebook: Von Hippel-Lindau Disease; A Comprehensive Guid Dhaval Thakor Patel,Amit Tirosh Book 2024 The Editor(s) (if applicable) and The Author(s),

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Retinal Hemangioblastomas,aluation, diagnosis, and treatment of RHs. Other ophthalmic findings in patients with VHL, screening and surveillance guidelines, and special situations such as childhood and pregnancy, are covered as well.

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Pulmonary-Veins

Surgical Management of Pancreatic Neuroendocrine Tumors in von Hippel-Lindau Disease,PanNETs are almost uniformly nonfunctional with variable metastatic potential. Surgical treatment depends on the size of the lesion, tumor genotype, the location within the pancreas as well as patient-related factors. This chapter will outline the treatment options for patients with VHL disease and PanNETs.

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Pheochromocytomas: Surgical Approach,cal pheochromocytomas, as well as tumors in the nearby kidney and pancreas. Close coordination between medical, surgical, and anesthesia teams is crucial in the perioperative period. Following resection, patients undergo lifelong surveillance for recurrent pheochromocytoma.

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