학술논문
Unique Case of a Rare Mesenchymal Tumor Harboring a Somatic c.119delC VHL Mutation.
Document Type
Case Study
Author
Source
Subject
*VON Hippel-Lindau disease
*LIVER tumors
*FOLLICULAR dendritic cells
*SOMATIC mutation
*NUCLEOTIDE sequencing
*DIAGNOSTIC immunohistochemistry
*
*
*
*
*
Language
ISSN
2473-4284
Abstract
The article presents a case study of a 29-year-old female with a large abdominal mass and hepatic lesions. Topics mentioned include the histologic biopsy performed to her, the development of von Hippel-Lindau (VHL) disease, and the results of her immunohistochemistry (IHC). Also mentioned are the analysis of whole-genome sequencing (WGS) and DNA.