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Von Hippel-Lindau disease
Classification & external resources

ICD-10	Q85.8
ICD-9	759.6
OMIM	193300
DiseasesDB	14000
eMedicine	ped/2417  oph/354
MeSH	C10.562.400

Von Hippel-Lindau disease (VHL) is a rare inherited genetic condition involving the abnormal growth of tumors in parts of the body which are particularly rich in blood supply.

Contents 1 Features 2 Types 3 Genetics 4 History 5 Nomenclature 6 See also 7 References 8 External links

Features of VHL are:

• angiomatosis - little knots of capillaries in the retina and various organs.
• hemangioblastomas - tumors of the central nervous system (CNS, especially the cerebellum, brain stem, and spinal cord).
• pheochromocytoma - tumors of the adrenal medulla that often produce catecholamines
• renal cell carcinoma - malignant tumors on the kidneys
• pancreas - cysts and tumors of the pancreas, which may be neuroendocrine tumors

Untreated, VHL may result in blindness and permanent brain damage; death is usually caused by complications of tumors in the brain or kidney, cardiovascular disease secondary to pheochromocytoma. With early detection and appropriate treatment, there is more hope today for people with VHL than ever before.

There are various subtypes:

• Type 1 (angiomatosis without pheochromocytoma)
• Type 2 (angiomatosis with pheochromocytoma)
  • Type 2A (low risk of renal cell carcinoma)
  • Type 2B (high risk of renal cell carcinoma)
  • Type 2C (only pheochromocytoma and no angiomatosis or renal cell carcinoma)

The disease is caused by mutations of the Von Hippel-Lindau tumor suppressor (VHL) gene on the short arm of third chromosome.

VHL is an autosomal dominant disorder, but there is a wide variation in the age of onset of the disease, the organ system affected and the severity of effect. Most people with von Hippel-Lindau syndrome inherit an altered copy of the gene from one parent. In about 20 percent of cases, however, the altered gene is the result of a new mutation that occurred during the formation of reproductive cells (eggs or sperm) or early in fetal development.

As long as one copy of the VHL gene is producing functional VHL protein in each cell, tumors do not form. If a mutation occurs in the second copy of the VHL gene during a person's lifetime, the cell will have no working copies of the gene and will produce no functional VHL protein. A lack of this protein allows tumors characteristic of von Hippel-Lindau syndrome to develop.

Eugen von Hippel described the angiomas in the eye in 1904.^[1]. Arvid Lindau described the angiomas of the cerebellum and spine in 1927.^[2]

In an article appearing in the Associated Press, it has been speculated by a Vanderbilt University endocrinologist that the hostility underlying the Hatfield-McCoy feud may have been partly due to the consequences of Von Hippel-Lindau disease. The article suggests that the McCoy family was pre-disposed to bad tempers because many of them had a pheochomocytoma, which produced excess adrenaline and a tendency toward explosive tempers.^[3] Pheochromocytomas produce surges of adrenaline which are more often perceived as panic attacks than rage attacks. Left untreated, they will cause serious cardiovascular disease, heart attack, and stroke. Only about 20% of people with VHL get pheochromocytomas.^[4]

Other names are: angiomatosis retinae, angiophakomatosis retinae et cerebelli, familial cerebello-retinal angiomatosis, cerebelloretinal hemangioblastomatosis, Hippel Disease, Hippel-Lindau syndrome, HLS, Lindau disease or retinocerebellar angiomatosis.

• Von Hippel Lindau Binding protein 1

1. ^ Von Hippel E. Ueber eine sehr seltene Erkrankung der Netzhaut. Albrecht von Graefes Arch Ophthal 1904;59:83-106.
2. ^ Lindau A. Zur Frage der Angiomatosis Retinae und Ihrer Hirncomplikation. Acta Ophthal 1927;4:193-226.
3. ^ "Hatfield-McCoy feud blamed on ‘rage’ disease", MSNBC.com, 2007-04-05. Retrieved on 2007-04-05. 
4. ^ "'Pheochromocytoma Information'", vhl.org, 2007-04-05. Retrieved on 2007-04-05. 

• Clinical Description of VHL
• The VHL Handbook
• Von Hippel-Lindau Disease (VHL) at NINDS
• Von Hippel-Lindau syndrome at NLM Genetics Home Reference
• von Hippel-Lindau syndrome at CHORUS
• Hippel-Lindau disease at Who Named It
• Online 'Mendelian Inheritance in Man' (OMIM) 608537 (VHL gene)

v • d • e Phakomatoses and other congenital malformations not elsewhere classified (Q85-Q89, 759)
Phakomatoses	Neurofibromatosis (type I, type II) - Tuberous sclerosis - Sturge-Weber syndrome - Von Hippel-Lindau disease - Incontinentia pigmenti - Ataxia telangiectasia
Due to known exogenous causes	Fetal alcohol syndrome - Phocomelia (via Thalidomide)
Affecting multiple systems	facial (Mobius syndrome, Goldenhar syndrome, Cyclopia, Apert syndrome) short stature (Aarskog-Scott syndrome, Cockayne syndrome, Cornelia de Lange Syndrome, Dubowitz syndrome, Noonan syndrome, Robinow syndrome, Silver-Russell dwarfism, Seckel syndrome, Smith-Lemli-Opitz syndrome) limbs (Holt-Oram syndrome, Klippel-Trenaunay-Weber syndrome, Nail-patella syndrome, Rubinstein-Taybi syndrome, Sirenomelia, VACTERL association) overgrowth (Beckwith-Wiedemann syndrome, Sotos syndrome, Weaver syndrome) Marfan syndrome - Alport syndrome - Bardet-Biedl syndrome - Zellweger syndrome
Other	Asplenia - Splenomegaly - Persistent thyroglossal duct - Thyroglossal cyst - Situs inversus - Conjoined twins - Cowden syndrome - Hamartoma - Peutz-Jeghers syndrome