Midline brain hamartomatous lesions in fibrodysplasia ossificans progressiva with ACVR1 mutations.
Jesse Lee KresakMeggen WalshAnthony TuzzoloZehra OrduluJason GregoryPublished in: Neuropathology : official journal of the Japanese Society of Neuropathology (2023)
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by extensive heterotopic ossification of soft tissue structures leading to severe limitations in movement. FOP is caused by a germline mutation in the activating receptor type IA (ACVR1) gene. Worrisome is the fact that up to a third of diffuse intrinsic pontine gliomas (DIPG) also harbor the same point mutation in ACVR1. Radiological reports of central nervous system (CNS) involvement by FOP have described brainstem masses; however, the literature on the histopathology or pathogenesis of these lesions is scant. Here we present detailed neuropathologic findings of a brainstem mass in a patient with FOP and suggest that the tumor is hamartomatous in nature. This report, along with a literature review of radiographic and laboratory data, offers support for the idea that the ACVR1 mutation may incite CNS proliferation, predominantly in the brainstem, but is probably not an oncologic driver. These lesions may be seen at autopsy and are likely noncontributory to death.
Keyphrases
- case report
- soft tissue
- signaling pathway
- genome wide
- blood brain barrier
- copy number
- systematic review
- high grade
- low grade
- high resolution
- resting state
- prostate cancer
- white matter
- early onset
- dna repair
- gene expression
- dna methylation
- radical prostatectomy
- cerebral ischemia
- artificial intelligence
- ultrasound guided
- fine needle aspiration
- genome wide identification