Difference between revisions of "Neurofibromatosis"
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* † One could include ''paraganglioma'' here. | * † One could include ''paraganglioma'' here. | ||
===Images=== | |||
<gallery> | |||
File:Early_neurofibromatosis.jpg | Café-au-lait spot (WC/Haymanj) | |||
File:NF-1-Tache_cafe-au-lait.jpg | Café-au-lait spot (WC/Accrochoc) | |||
File:Lisch_nodules.gif | Lisch nodule (iris hamartoma) in the eye (WC/filip em) | |||
File:Neurofibroma03.jpg | Multiple neurofibromas of the skin in NF1 (WC/Enigma51) | |||
File:Neurofibroma02.jpg | Multiple neurofibromas of the skin in NF1 (WC/Enigma51) | |||
File:Neurofibroma_large_NF1.jpg | Large neurofibroma in a NF1 case (WC/jensflorian) | |||
File:Neurofibromatosis,_bowel.jpg | Neurofibromatosis in the bowel (WC/Dr. Robertson) | |||
File:MPNST Pathology gross.jpg | Malignant peripheral nerve sheath tumor of the forearm (WC/drbloodmoney) | |||
</gallery> | |||
===Others=== | ===Others=== |
Revision as of 10:32, 28 April 2015
Neurofibromatosis is a genetic conditions, also known as von Recklinghausen's disease. It is abbreviated as NF.
It comes in two flavours:
- Neurofibromatosis type 1 - NF1 (peripheral).
- Neurofibromatosis type 2 - NF2 (central).
Neurofibromatosis type 1
- Autosomal dominant.
Diagnosis
Features (need 2/7 to diagnose):[1]
- Two or more neurofibromas or one plexiform neurofibroma.
- May give rise to a malignant peripheral nerve sheath tumour.
- Café-au-lait spots.
- Freckles in axilla or inguinal area.
- Optic nerve glioma.
- Iris hamartomas (Lisch nodules).
- Sphenoid dysplasia or typical long-bone abnormalities (e.g. bowing).
- First-degree relative with NF1.
Mnemonic
Diagnostic criteria CAFE SPOT:[2]
- Café-au-lait spots.
- Axillary or inguinal freckling.
- neuroFibroma (two or more) or plexiform neurofibroma (one).
- Eye hamartomas (Lisch nodules).
- Skeletal abnormalities, e.g. sphenoid dysplasia, leg bowing.
- Positive family history. †
- Optic Tumour (optic nerve glioma).
Note:
- † One could include paraganglioma here.
Images
Others
Possible association
Neurofibromatosis type 2
Diagnosis
Features (need 1/3 to diagnose):[8]
- Bilateral CNVIII masses on imaging.
- Unilateral CNVIII mass + first-degree relative with NF2.
- First-degree relative with NF2 and 2/4 of the following:
- Meningioma (meningothelial meningioma).[9]
- Glioma.
- Schwannoma.
- Juvenile cataract.
Mnemonic MISME:[10]
- Multiple Inherited Schwannomas.
- Meningiomas.
- Ependymomas.
See also
References
- ↑ URL: http://emedicine.medscape.com/article/1177266-overview. Accessed on: 3 May 2010.
- ↑ URL: http://www.paeds.co.uk/wiki/index.php?title=Mnemonics#Neurofibromatosis_Type_1_diagnostic_criteria. Accessed on: 30 May 2011.
- ↑ Alexakis, N.; Connor, S.; Ghaneh, P.; Lombard, M.; Smart, HL.; Evans, J.; Hughes, M.; Garvey, CJ. et al. (2004). "Hereditary pancreatic endocrine tumours.". Pancreatology 4 (5): 417-33; discussion 434-5. doi:10.1159/000079616. PMID 15249710.
- ↑ Agaimy A, Hartmann A (October 2010). "[Hereditary and non-hereditary syndromic gastointestinal stromal tumours]" (in German). Pathologe 31 (6): 430–7. doi:10.1007/s00292-010-1354-6. PMID 20848108.
- ↑ Castoldi, L.; De Rai, P.; Marini, A.; Ferrero, S.; De Luca, V.; Tiberio, G. (2001). "Neurofibromatosis-1 and Ampullary Gangliocytic Paraganglioma Causing Biliary and Pancreatic Obstruction.". Int J Gastrointest Cancer 29 (2): 93-98. PMID 12754392.
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 101000
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 607379
- ↑ URL: http://emedicine.medscape.com/article/1178283-overview. Accessed on: 3 May 2010.
- ↑ URL: http://moon.ouhsc.edu/kfung/jty1/neurotest/Q13-Ans.htm. Accessed on: 26 October 2010.
- ↑ URL: http://emedicine.medscape.com/article/342667-overview. Accessed on: 20 February 2012.