Inherited Thrombocytopenia Caused by Germline ANKRD26 Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome

J Investig Med High Impact Case Rep. 2020 Jan-Dec:8:2324709620938941. doi: 10.1177/2324709620938941.

Abstract

Thrombocytopenia 2 (THC2) is an autosomal dominant disorder characterized by ankyrin repeat domain 26 mutation and moderate thrombocytopenia. THC2 exposes patients to a low risk of bleeding and an increased likelihood of myelodysplastic syndrome/acute myeloid leukemia. Germline evaluation for a genetic disorder should be considered when a patient presents with isolated thrombocytopenia and associated dysmegakaryopoiesis. In this case report, we present a male patient who presented with isolated thrombocytopenia but was ultimately confirmed to have an inherited THC2 thrombocytopenia/myelodysplastic syndrome. Given the rarity of the disease, no clear guidelines on how to follow THC2 patients over the long term have been established. We recommend a monthly complete blood count and clinical visits every 3 months at a minimum.

Keywords: ANKRD26; acute leukemia; germline mutations; myelodysplastic syndrome; thrombocytopenia 2.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Breakage
  • Chromosome Disorders / genetics*
  • Chromosome Disorders / pathology
  • Genetic Predisposition to Disease
  • Germ-Line Mutation
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Male
  • Middle Aged
  • Myelodysplastic Syndromes / diagnosis
  • Thrombocytopenia / congenital*
  • Thrombocytopenia / genetics
  • Thrombocytopenia / pathology

Substances

  • ANKRD26 protein, human
  • Intercellular Signaling Peptides and Proteins

Supplementary concepts

  • Thrombocytopenia chromosome breakage