An aggressive multifocal primary CNS histiocytosis with PTPN11 (Shp2) mutation

Neuropathol Appl Neurobiol. 2018 Feb;44(2):240-243. doi: 10.1111/nan.12404.

Authors

Q Zhang¹, A Shibani², B Sadikovic¹, C J Howlett¹, L-C Ang¹

Affiliations

¹ Department of Pathology and Laboratory Medicine, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.
² Brandon Regional Health Centre, Brandon, MB, Canada.

PMID: 28403515
DOI: 10.1111/nan.12404

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Cerebellar Neoplasms / genetics
Cerebellar Neoplasms / pathology*
Histiocytic Disorders, Malignant / genetics
Histiocytic Disorders, Malignant / pathology*
Humans
Male
Middle Aged
Mutation*
Protein Tyrosine Phosphatase, Non-Receptor Type 11 / genetics*

Substances

PTPN11 protein, human
Protein Tyrosine Phosphatase, Non-Receptor Type 11