SMARCA4-deficient central nervous system metastases: A case series and systematic review.
Meaghan O MorrisKerime AraratHannah CutshallMurat GokdenAnaliz RodriguezLisa M RooperMatthew LindbergJames Stephen NixPublished in: Journal of neuropathology and experimental neurology (2024)
SMARCA4 alterations can be encountered in a variety of human neoplasms, and metastases to the central nervous system (CNS) are rare, offering a challenge to neuropathologists despite not representing a distinct diagnostic entity. To better understand the clinical and histologic presentation of such neoplasms, we report an observational case series and systematic review of 178 unique articles that yielded 15 published cases and 7 cases from institutional files. In the systematic review, the median age was 58 years, the male-to-female ratio was 2:1, and the most common diagnosis was lung adenocarcinoma; all CNS metastases were discovered within 1 year of presentation. In the case series, the median age was 58 years, the male-to-female ratio was 6:1, and all known metastases originated from the lung. Most patients had a smoking history and died of disease. GATA-3 positivity was seen in most case series examples. Concurrent TP53 mutations (83.3%) and a high tumor mutation rate (60%) were common. To our knowledge, this is the only case series and systematic review in the English literature aimed at assessing SMARCA4-altered metastases in the CNS and vertebral column. We highlight the challenges of neuropathologic evaluation of such tumors and provide observational evidence of early metastases, histologic appearances, and immunohistochemical findings, including previously unreported GATA-3 positivity.
Keyphrases
- systematic review
- meta analyses
- end stage renal disease
- blood brain barrier
- healthcare
- chronic kidney disease
- transcription factor
- endothelial cells
- newly diagnosed
- squamous cell carcinoma
- bone mineral density
- mass spectrometry
- body composition
- postmenopausal women
- case report
- induced pluripotent stem cells
- wild type