Difference between revisions of "Von Hippel-Lindau disease"
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[[Image:Clear_cell_renal_cell_carcinoma_-_2_--_intermed_mag.jpg|thumb|right|[[Clear cell renal cell carcinoma]] a tumour seen in von Hippel-Lindau disease. [[H&E stain]].]] | |||
The '''von Hippel-Lindau disease''', also '''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 disease''', also '''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> | ||
*[[Hemangioblastoma]]s. | *[[Hemangioblastoma]]s. | ||
*Increased [[Kidney_tumours#Hereditary_RCC|renal cancer]] ([[clear cell renal cell carcinoma]]). | *Increased [[Kidney_tumours#Hereditary_RCC|renal cancer]] ([[clear cell renal cell carcinoma]]). | ||
*[[Pheochromocytoma]]. | *[[Pheochromocytoma]], [[pancreatic neuroendocrine tumour]]s<ref name=pmid22370733>{{Cite journal | last1 = Charlesworth | first1 = M. | last2 = Verbeke | first2 = CS. | last3 = Falk | first3 = GA. | last4 = Walsh | first4 = M. | last5 = Smith | first5 = AM. | last6 = Morris-Stiff | first6 = G. | title = Pancreatic Lesions in von Hippel-Lindau Disease? A Systematic Review and Meta-synthesis of the Literature. | journal = J Gastrointest Surg | volume = | issue = | pages = | month = Feb | year = 2012 | doi = 10.1007/s11605-012-1847-0 | PMID = 22370733 }}</ref> and [[papillary cystadenoma of the epididymis]].<ref name=pmid23708309>{{Cite journal | last1 = Toutziaris | first1 = C. | last2 = Kampantais | first2 = S. | last3 = Perdikis | first3 = I. | last4 = Gourvas | first4 = V. | last5 = Laskaridis | first5 = L. | last6 = Gkagkalidis | first6 = K. | last7 = Lakis | first7 = S. | last8 = Ioannidis | first8 = S. | title = Papillary cystadenoma of epididymis: Is there a need for further investigation in unilateral cases? | journal = Int J Surg Case Rep | volume = 4 | issue = 7 | pages = 616-8 | month = | year = 2013 | doi = 10.1016/j.ijscr.2013.03.038 | PMID = 23708309 }}</ref><ref name=pmid20367315>{{Cite journal | last1 = Odrzywolski | first1 = KJ. | last2 = Mukhopadhyay | first2 = S. | title = Papillary cystadenoma of the epididymis. | journal = Arch Pathol Lab Med | volume = 134 | issue = 4 | pages = 630-3 | month = Apr | year = 2010 | doi = 10.1043/1543-2165-134.4.630 | PMID = 20367315 }}</ref> | ||
*Port-wine stains, skin lesion - looks like spilled wine; think [http://commons.wikimedia.org/wiki/File:Gorbatschow_DR-Forum_129_b2.jpg ''Mikhail Gorbachev'']. | *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 and Endolymphatic sac | *Eye dysfunction and [[Endolymphatic sac tumour]]s.<ref name=Ref_PSNP440>{{Ref PSNP|440}}</ref> | ||
**Eye dysfunction = retinal angiomas,<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> (or ''retinal hemangioblastomas''<ref name=Ref_PSNP440>{{Ref PSNP|440}}</ref> -- depending on the source) . | **Eye dysfunction = retinal angiomas,<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> (or ''retinal hemangioblastomas''<ref name=Ref_PSNP440>{{Ref PSNP|440}}</ref><ref name=pmid17057815>{{Cite journal | last1 = Chew | first1 = EY. | title = Ocular manifestations of von Hippel-Lindau disease: clinical and genetic investigations. | journal = Trans Am Ophthalmol Soc | volume = 103 | issue = | pages = 495-511 | month = | year = 2005 | doi = | PMID = 17057815 | PMC = 1447586 | URL = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1447586/ }}</ref> -- depending on the source) . | ||
*[[Liver]] cysts, [[pancreas]] cysts ([[serous microcystic adenoma]]), pancreatic islet cell tumours & [[kidney]] cysts. | *[[Liver]] cysts, [[pancreas]] cysts ([[serous microcystic adenoma]]), pancreatic islet cell tumours & [[kidney]] cysts. | ||
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*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> | *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> | ||
==Pancreatic islet cell | ==Pancreatic neuroendocrine tumour== | ||
{{Main|Pancreatic neuroendocrine tumour}} | |||
*[[AKA]] ''pancreatic islet cell tumour'' | |||
In VHL these have distinct morphology: | In VHL these have distinct morphology: | ||
*Clear cells<ref name=pmid10740008>{{Cite journal | last1 = Musso | first1 = C. | last2 = Paraf | first2 = F. | last3 = Petit | first3 = B. | last4 = Archambeaud-Mouveroux | first4 = F. | last5 = Valleix | first5 = D. | last6 = Labrousse | first6 = F. | title = [Pancreatic neuroendocrine tumors and von Hippel-Lindau disease]. | journal = Ann Pathol | volume = 20 | issue = 2 | pages = 130-3 | month = Mar | year = 2000 | doi = | PMID = 10740008 }}</ref> - unusual in [[neuroendocrine tumours]]. | *Clear cells<ref name=pmid10740008>{{Cite journal | last1 = Musso | first1 = C. | last2 = Paraf | first2 = F. | last3 = Petit | first3 = B. | last4 = Archambeaud-Mouveroux | first4 = F. | last5 = Valleix | first5 = D. | last6 = Labrousse | first6 = F. | title = [Pancreatic neuroendocrine tumors and von Hippel-Lindau disease]. | journal = Ann Pathol | volume = 20 | issue = 2 | pages = 130-3 | month = Mar | year = 2000 | doi = | PMID = 10740008 }}</ref> - unusual in [[neuroendocrine tumours]] otherwise. | ||
*Fibrosis. (???) | *Fibrosis. (???) | ||
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*[[Kidney tumours]]. | *[[Kidney tumours]]. | ||
*[[Neurocutaneous syndromes]]. | *[[Neurocutaneous syndromes]]. | ||
*[[Birt–Hogg–Dubé syndrome]]. | |||
*[[TCEB1-mutated renal cell carcinoma]]. | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
==External links== | |||
*[http://www.vhl.org/wordpress/medical-professionals/when-to-suspect-vhl/ When to suspect VHL (vhl.org)]. | |||
[[Category:Syndromes]] | [[Category:Syndromes]] |
Latest revision as of 18:21, 31 May 2016
The von Hippel-Lindau disease, also von Hippel-Lindau syndrome is characterized by (mnemonic: HIPPEL):[1]
- Hemangioblastomas.
- Increased renal cancer (clear cell renal cell carcinoma).
- Pheochromocytoma, pancreatic neuroendocrine tumours[2] and papillary cystadenoma of the epididymis.[3][4]
- Port-wine stains, skin lesion - looks like spilled wine; think Mikhail Gorbachev.
- Eye dysfunction and Endolymphatic sac tumours.[5]
- Liver cysts, pancreas cysts (serous microcystic adenoma), pancreatic islet cell tumours & kidney cysts.
Bare bones version:
- Hippel-Lindau, with H and L as above.
Prevalence
- 1 in 40,000 live births.[8]
Pancreatic neuroendocrine tumour
Main article: Pancreatic neuroendocrine tumour
- AKA pancreatic islet cell tumour
In VHL these have distinct morphology:
- Clear cells[9] - unusual in neuroendocrine tumours otherwise.
- Fibrosis. (???)
Trivia
VHL gene is found on chromosome 3.[10]
See also
- Adrenal gland.
- Kidney tumours.
- Neurocutaneous syndromes.
- Birt–Hogg–Dubé syndrome.
- TCEB1-mutated renal cell carcinoma.
References
- ↑ URL: http://www.medicalmnemonics.com/pdf/2002_09_full_abr_8x11.pdf. Accessed on: 11 September 2008.
- ↑ Charlesworth, M.; Verbeke, CS.; Falk, GA.; Walsh, M.; Smith, AM.; Morris-Stiff, G. (Feb 2012). "Pancreatic Lesions in von Hippel-Lindau Disease? A Systematic Review and Meta-synthesis of the Literature.". J Gastrointest Surg. doi:10.1007/s11605-012-1847-0. PMID 22370733.
- ↑ Toutziaris, C.; Kampantais, S.; Perdikis, I.; Gourvas, V.; Laskaridis, L.; Gkagkalidis, K.; Lakis, S.; Ioannidis, S. (2013). "Papillary cystadenoma of epididymis: Is there a need for further investigation in unilateral cases?". Int J Surg Case Rep 4 (7): 616-8. doi:10.1016/j.ijscr.2013.03.038. PMID 23708309.
- ↑ Odrzywolski, KJ.; Mukhopadhyay, S. (Apr 2010). "Papillary cystadenoma of the epididymis.". Arch Pathol Lab Med 134 (4): 630-3. doi:10.1043/1543-2165-134.4.630. PMID 20367315.
- ↑ 5.0 5.1 Perry, Arie; Brat, Daniel J. (2010). Practical Surgical Neuropathology: A Diagnostic Approach: A Volume in the Pattern Recognition series (1st ed.). Churchill Livingstone. pp. 440. ISBN 978-0443069826.
- ↑ 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.
- ↑ Chew, EY. (2005). "Ocular manifestations of von Hippel-Lindau disease: clinical and genetic investigations.". Trans Am Ophthalmol Soc 103: 495-511. PMC 1447586. PMID 17057815. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1447586/.
- ↑ Singh AD, Shields CL, Shields JA (2001). "von Hippel-Lindau disease". Surv Ophthalmol 46 (2): 117–42. PMID 11578646.
- ↑ Musso, C.; Paraf, F.; Petit, B.; Archambeaud-Mouveroux, F.; Valleix, D.; Labrousse, F. (Mar 2000). "[Pancreatic neuroendocrine tumors and von Hippel-Lindau disease].". Ann Pathol 20 (2): 130-3. PMID 10740008.
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 608537