Difference between revisions of "Von Hippel-Lindau disease"

From Libre Pathology
Jump to navigation Jump to search
(wikify)
(more, prevalence, eye dysfunction)
Line 1: Line 1:
The '''von Hippel-Lindau syndrome''' is characterized by (mnemonic: ''HIPPEL''):<ref>URL: [http://www.medicalmnemonics.com/pdf/2002_09_full_abr_8x11.pdf http://www.medicalmnemonics.com/pdf/2002_09_full_abr_8x11.pdf]. Accessed on: 11 September 2008.</ref>
The '''von Hippel-Lindau syndrome''' is characterized by (mnemonic: ''HIPPEL''):<ref>URL: [http://www.medicalmnemonics.com/pdf/2002_09_full_abr_8x11.pdf http://www.medicalmnemonics.com/pdf/2002_09_full_abr_8x11.pdf]. Accessed on: 11 September 2008.</ref>
*[[Hemanigoblastoma]]s.  
*[[Hemanigoblastoma]]s.  
*Increased [[renal cancer]] (clear cell RCC).
*Increased [[Kidney_tumours#Hereditary_RCC|renal cancer]] (clear cell RCC).
*Pheochromocytoma.  
*Pheochromocytoma.  
*Port-wine stains.  
*Port-wine stains, skin lesion - looks like spilled wine; think [http://commons.wikimedia.org/wiki/File:Gorbatschow_DR-Forum_129_b2.jpg ''Mikhail Gorbachev''].  
*Eye dysfunction.
*Eye dysfunction - retinal angioma.<ref name=pmid10804089>{{cite journal |author=Harris AL |title=von Hippel-Lindau syndrome: target for anti-vascular endothelial growth factor (VEGF) receptor therapy |journal=Oncologist |volume=5 Suppl 1 |issue= |pages=32–6 |year=2000 |pmid=10804089 |doi= |url=http://theoncologist.alphamedpress.org/cgi/content-nw/full/5/suppl_1/32/T1}}</ref>
*Liver cysts, pancreas cysts (serous microcystic adenoma) & kidney cysts.
*[[Liver]] cysts, [[pancrea]]s cysts (serous microcystic adenoma) & [[kidney]] cysts.


Bare bones version:  
Bare bones version:  
*Hippel-Lindau, with H and L as above.
*Hippel-Lindau, with H and L as above.
==Prevalence==
*1 in 40,000 live births.<ref name=pmid11578646>{{cite journal |author=Singh AD, Shields CL, Shields JA |title=von Hippel-Lindau disease |journal=Surv Ophthalmol |volume=46 |issue=2 |pages=117–42 |year=2001 |pmid=11578646 |doi= |url=}}</ref>


==See also==
==See also==
Line 15: Line 18:


==References==
==References==
{{reflist}}
{{reflist|2}}


[[Category:Syndromes]]
[[Category:Syndromes]]

Revision as of 12:36, 26 August 2010

The von Hippel-Lindau syndrome is characterized by (mnemonic: HIPPEL):[1]

Bare bones version:

  • Hippel-Lindau, with H and L as above.

Prevalence

  • 1 in 40,000 live births.[3]

See also

References

  1. ↑ URL: http://www.medicalmnemonics.com/pdf/2002_09_full_abr_8x11.pdf. Accessed on: 11 September 2008.
  2. ↑ Harris AL (2000). "von Hippel-Lindau syndrome: target for anti-vascular endothelial growth factor (VEGF) receptor therapy". Oncologist 5 Suppl 1: 32–6. PMID 10804089. http://theoncologist.alphamedpress.org/cgi/content-nw/full/5/suppl_1/32/T1.
  3. ↑ Singh AD, Shields CL, Shields JA (2001). "von Hippel-Lindau disease". Surv Ophthalmol 46 (2): 117–42. PMID 11578646.
Retrieved from "https://librepathology.org/w/index.php?title=Von_Hippel-Lindau_disease&oldid=1565"