FH enzyme is responsible for converting fumarate to malate in the Krebs cycle. Autosomal dominant FH mutations, which result in the accumulation of the oncometabolite fumarate, have been implicated in hereditary leiomyomatosis and renal cell cancer (HLRCC). Gliomas are not considered part of the HLRCC syndrome.
Patient A is a 24-year-old woman with history of resected FH-deficient uterine leiomyoma and a subsequent diagnosis of cerebellar high-grade glioma with IDH-WT and methylated MGMT. Subsequent germline testing revealed gene mutations in FH (R233C) and p53 (T125M).
Patient B is a 55-year-old woman with resected stage 1B cutaneous melanoma and pathogenic germline FH-mutation (p.Lys477dup), who subsequently developed a right frontal glioblastoma, (IDH-WT, methylated MGMT).
Compared to patient B, patient A’s high-grade astrocytoma had an earlier age of onset and demonstrated a significant element of pseudoprogression. Patient A’s DNA methylation profiling classified the tumor as a high-grade IDH-mutant astrocytoma, even though no IDH mutation was detected by sequencing from two separate reference laboratories. Analysis of FH mutations in gliomas from Foundation Medicine testing database will be reported.