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| =Other= | | =Other= |
| ==Neurofibromatosis==
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| Comes in two flavours:
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| #NF1 (peripheral).
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| #NF2 (central).
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|
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| ===NF1===
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| Features (need 2/7 to diagnose):<ref>URL: [http://emedicine.medscape.com/article/1177266-overview http://emedicine.medscape.com/article/1177266-overview]. Accessed on: 3 May 2010.</ref>
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| *Two or more neurofibromas or one plexiform neurofibroma.
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| *Café-au-lait spots.
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| *Freckles in axilla or inguinal area.
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| *Optic nerve glioma.
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| *Iris hamartomas (Lisch nodules).
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| *Sphenoid dysplasia or typical long-bone abnormalities (e.g. bowing).
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| *First-degree relative with NF1.
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|
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| ===NF2===
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| Features (need 1/3 to diagnose):<ref>URL: [http://emedicine.medscape.com/article/1178283-overview http://emedicine.medscape.com/article/1178283-overview]. Accessed on: 3 May 2010.</ref>
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| #Bilateral CNVIII masses on imaging.
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| #Unilateral CNVIII mass + first-degree relative with NF2.
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| #First-degree relative with NF2 ''and'' 2/4 of the following:
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| ## Meningioma.
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| ## Glioma.
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| ## Schwannoma.
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| ## Juvenile cataract.
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| ==Small round blue cell tumours (SRBCT)== | | ==Small round blue cell tumours (SRBCT)== |
| A group of tumours that has a similar histologic appearance. It is a group of tumours that is seen more often in childhood than adulthood. | | A group of tumours that has a similar histologic appearance. It is a group of tumours that is seen more often in childhood than adulthood. |