Difference between revisions of "Peripheral nerve sheath tumours"

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*p27.
*p27.
*MIB1.
*MIB1.
==Malignant triton tumour==
*Abbreviated ''MTT''.
*[[AKA]] ''malignant peripheral nerve sheath tumor with rhabdomyosarcomatous differentiation''.<ref name=pmid17149968>{{Cite journal  | last1 = Stasik | first1 = CJ. | last2 = Tawfik | first2 = O. | title = Malignant peripheral nerve sheath tumor with rhabdomyosarcomatous differentiation (malignant triton tumor). | journal = Arch Pathol Lab Med | volume = 130 | issue = 12 | pages = 1878-81 | month = Dec | year = 2006 | doi = 10.1043/1543-2165(2006)130[1878:MPNSTW]2.0.CO;2 | PMID = 17149968 }}</ref>
===General===
*Rare.
*Considered to be a variant of ''[[MPNST]]''.
*Prognosis worse that conventional MPNST.<ref name=pmid17149968/>
*Diagnosis may require clinical information, i.e. individual has a history of [[neurofibromatosis type 1]].
Note:
*A handful of ''benign triton tumours'' are reported; these are considered ''neuromuscular [[hamartoma]]s''.<ref name=pmid15814954>{{Cite journal  | last1 = Castro | first1 = DE. | last2 = Raghuram | first2 = K. | last3 = Phillips | first3 = CD. | title = Benign triton tumor of the trigeminal nerve. | journal = AJNR Am J Neuroradiol | volume = 26 | issue = 4 | pages = 967-9 | month = Apr | year = 2005 | doi =  | PMID = 15814954 }}
</ref>
===Microscopic===
Features - Woodruff criteria - all required:<ref name=pmid17149968/>
# (a) Tumour arise from a peripheral nerve ''or'' (b) individual has [[NF1]] ''or'' (c) lesion a metastasis arising in the context of (a) or (b).
# Schwann cell tumour characteristics.
# Rhabdomyoblasts.
DDx:
*[[Malignant peripheral nerve sheath tumour]].


==Morton neuroma==
==Morton neuroma==
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