Difference between revisions of "Von Hippel-Lindau disease"

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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>
*Hemanigoblastomas.  
*[[Hemanigoblastoma]]s.  
*Increased renal cancer (clear cell RCC).
*Increased [[renal cancer]] (clear cell RCC).
*Pheochromocytoma.  
*Pheochromocytoma.  
*Port-wine stains.  
*Port-wine stains.  
*Eye dysfunction.
*Eye dysfunction.
*Liver cysts, pancreas cysts & kidney cysts.
*Liver cysts, pancreas cysts (serous microcystic adenoma) & kidney cysts.


Bare bones version:  
Bare bones version:  
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==References==
==References==
{{reflist}}
{{reflist}}
[[Category:Syndromes]]

Revision as of 04:06, 25 August 2010

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

  • Hemanigoblastomas.
  • Increased renal cancer (clear cell RCC).
  • Pheochromocytoma.
  • Port-wine stains.
  • Eye dysfunction.
  • Liver cysts, pancreas cysts (serous microcystic adenoma) & kidney cysts.

Bare bones version:

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

See also

References