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Von Hippel-Lindau Disease (Angiomatosis)What is Von Hippel-Lindau Disease (VHL)? von Hippel-Lindau disease (VHL) is a rare, genetic multi-system disorder characterised by the abnormal growth of tumours in certain parts of the body (angiomatosis). The tumours of the central nervous system (CNS) are benign and are comprised of a nest of blood vessels and are called haemangioblastomas (or angiomas in the eye). Haemangioblastomas may develop in the brain, the retina of the eyes, and other areas of the nervous system. Other types of tumours develop in the adrenal glands, the kidneys, or the pancreas. Symptoms of VHL vary among patients and depend on the size and location of the tumours. Symptoms may include headaches, problems with balance and walking, dizziness, weakness of the limbs, vision problems, and high blood pressure. Cysts (fluid-filled sacs) and/or tumours (benign or cancerous) may develop around the haemangioblastomas and cause the symptoms listed above. Individuals with VHL are also at a higher risk than normal for certain types of cancer, especially kidney cancer. Is there any treatment? What is the prognosis?
Page last modified: September 2006 Source: NINDS/NIH |
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