Well differentiated neuroendocrine tumors (NETs) arising in the gastrointestinal and
pancreaticobiliary system are the most common neuroendocrine neoplasms. Studies of the …

Abstract von Hippel Lindau disease (vHL) is caused by a hereditary predisposition to
multiple neoplasms, especially hemangioblastomas in the retina and CNS, renal cell …

Simple Summary Von Hippel–Lindau (VHL) is a hereditary syndrome associated with
various tumors in the brain, spine, eyes, kidneys, adrenals, and in the pancreas …

Guidelines for surveillance of patients with von Hippel‐Lindau disease: Consensus statement of
the International VHL Surveilla Page 1 Received: 22 February 2023 Revised: 17 April 2023 …

Abstract Background/Aims Retinal haemangioblastomas (RH) remain a major cause of
visual impairment in patients with von Hippel‐Lindau (VHL) disease. Identification of …

Objective: Pheochromocytomas are a hallmark feature of von Hippel-Lindau disease (vHL).
To our knowledge, this is the first systematic review with meta-analysis evaluating the …

Simple Summary Von Hippel–Lindau is a rare endocrine (and other organ) multi-neoplasia
syndrome. A clinical diagnosis may be defined using different diagnostic criteria. However …

Purpose Von Hippel-Lindau (VHL) disease is a hereditary kidney cancer syndrome, with
which patients are more likely to get affected by renal cell carcinoma (RCC), pancreatic cyst …

Interventions: The patient underwent cerebellar mass resection surgery. Outcomes: The
patient recovered after surgical resection. Lessons: In this report, we emphasize the atypical …

Tumors of the endocrine glands are common. Knowledge of their molecular pathology has
greatly advanced in the recent past. This review covers the main molecular alterations of …