A clinicopathological and immunohistochemical study of malignant peripheral nerve sheath tumors.
dc.contributor.author | Sasidharan, Siny Vellukara | |
dc.contributor.author | Kumar, Vinu | |
dc.contributor.author | Pai, Radha R | |
dc.contributor.author | Vasudevan, Sheela | |
dc.date.accessioned | 2015-11-10T06:11:45Z | |
dc.date.available | 2015-11-10T06:11:45Z | |
dc.date.issued | 2014-10 | |
dc.description.abstract | Background: Malignant Peripheral Nerve Sheath Tumor (MPNST) is a rare aggressive sarcoma that develops within a peripheral nerve and forms a diagnostic challenge in view of its varied histomorphology. This short series highlights the clinicopathological spectrum of 11 cases of MPNST and the incidence of neurofibromatosis 1 (NF1) association. Methods: This retrospective and descriptive study on MPNST was done in the department of pathology, Kasturba medical college Mangalore (Manipal University), India over a period of three years from January 2008 to December 2010. Cases which were histopathologically diagnosed as MPNST were reviewed & immunostains was done where ever indicated to rule out the differentials. Results: A total of 11 cases of MPNST were documented with a wide age range of 17-85 years. Male:female ratio was 2.6:1. Extremities (63.64%) were found to be the most common site. Location wise most of the tumors were deep seated (63.64%) and maximum cases were high grade (54.55%). NF1 association was seen in 2 cases. Heterologous elements in the form of chondroid differentiation was seen in one case. Immunostain with S-100 was focally positive in all the cases. Conclusion: MPNST is a highly aggressive sarcoma with poor prognosis characterized by a challenge in its diagnosis as it has several mimics. Its diagnosis necessitates the incorporation of clinicopathological features and IHC with S-100 protein. | en_US |
dc.identifier.citation | Sasidharan Siny Vellukara, Kumar Vinu, Pai Radha R, Vasudevan Sheela. A clinicopathological and immunohistochemical study of malignant peripheral nerve sheath tumors. International Journal of Research in Medical Sciences. 2014 Oct-Dec; 2(4): 1307-1312. | en_US |
dc.identifier.issn | 2320-6071 | |
dc.identifier.issn | 2320-6012 | |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/165433 | |
dc.language.iso | en | en_US |
dc.source.uri | https://www.msjonline.org/?mno=164291 | en_US |
dc.subject | Malignant peripheral nerve sheath tumor | en_US |
dc.subject | Neurofibromatosis (NF-1), | en_US |
dc.subject | Heterologous differentiation | en_US |
dc.title | A clinicopathological and immunohistochemical study of malignant peripheral nerve sheath tumors. | en_US |
dc.type | Article | en_US |
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