Abstract
Germline mutations in GATA2 are associated with a complex immunodeficiency and cancer predisposition syndrome. Somatic GATA2mut in myeloid malignancies may impart a similar phenotype. We reviewed adult patients with a diagnosis of GATA2mut hematological malignancy who were referred to our HHMC for genetic testing, and identified to have somatic GATA2mut. Nine patients with a median age of 63 years were included. Six patients (66.7%) were males. Atypical CML and acute myeloid leukemia were the most common initial presentation. The median overall VAF was 47.14%. Monocytopenia was pronounced when the GATA2mut involved the C-terminal ZFD. GATA2 N-terminal ZFD mutations tend to be co-mutated with biCEBPAmut. Unlike germline GATA2 mutations, monocytopenia associated with somatic GATA2 mutations often resolved at remission. We concluded that similar to germline GATA2 mutations, a subset of somatic GATA2 mutations can impart a germline phenotype.
| Original language | English |
|---|---|
| Pages (from-to) | 2025-2033 |
| Number of pages | 9 |
| Journal | Leukemia and Lymphoma |
| Volume | 60 |
| Issue number | 8 |
| DOIs | |
| State | Published - 3 Jul 2019 |
| Externally published | Yes |
Keywords
- Emberger syndrome
- GATA2
- MonoMAC syndrome
- immunodeficiency
- pulmonary alveolar proteinosis