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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease malignant peripheral nerve sheath tumor
Comorbidity C1261473|sarcoma
Sentences 3
PubMedID- 23161774 In the combined patient series from the 3 european sarcoma centers, 35% of the mpnst patients were diagnosed with nf1 (table 1)—33% in the norwegian series, 38% in the swedish series, and 36% in the italian series (supplementary tables 1–3).
PubMedID- 24131748 We caution readers against assuming any spindle cell tumor with epithelial immunolabeling to be synovial sarcoma, as 3/6 of our mpnst cases had ck and ema expression, which is comparable to previous studies and may have been due to cross-reactivity with schwannian components [12], and one must be cognizant of mpnst subtypes (epithelial and perineurial) with an epithelial immunophenotype.
PubMedID- 24618071 Differential diagnosis included synovial sarcoma, anaplastic meningioma with epithelial metaplasia, malignant peripheral nerve sheath tumor, and metastatic carcinosarcoma.

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