Calreticulin Type 26 Mutation in Myelofibrosis: A Rare Variant With Diagnostic Challenges.

backgroundMyeloproliferative neoplasms (MPNs) are clonal hematologic disorders commonly driven by mutations in JAK2, MPL, or CALR. Because routine CALR assays are largely optimized for the canonical Type 1 and Type 2 exon 9 variants, rare noncanonical mutations may be missed, creating diagnostic challenges.

methodsWe report the case of a 78-year-old woman diagnosed with an MPN in 2016 and treated with hydroxyurea. Initial molecular testing included JAK2 V617F screening and PCR-based fragment-length analysis by capillary electrophoresis for CALR exon 9 indels, both of which yielded negative results. After clinical progression, in 2024, repeat hematologic evaluation, bone marrow biopsy, Sanger sequencing, cloning, and next-generation sequencing (NGS) were performed.

resultsDisease progression was associated with marked thrombocytosis, leukocytosis, microcytic anemia, and bone marrow findings consistent with primary myelofibrosis. Advanced molecular testing identified a heterozygous CALR c.1122delG frameshift mutation (Type 26), a rare exon 9 variant not detected by the initial assay. Cloning confirmed heterozygosity, and NGS demonstrated a variant allele frequency of 43%. An additional CBL splice-site mutation (VAF 17%) was also detected.

conclusionThis case highlights the limitations of routine assays focused on common CALR mutations and supports comprehensive sequencing-based approaches for detecting rare CALR variants. Expanded molecular testing may improve diagnostic accuracy and clinical classification in MPNs.