Clinical Case Reports (Mar 2022)

Familial essential thrombocythemia: 6 cases from a mono‐institutional series

  • Vincenzo Accurso,
  • Marco Santoro,
  • Salvatrice Mancuso,
  • Giorgia Vajana,
  • Riccardo Tomasello,
  • Cristina Rotolo,
  • Giulia Camarda,
  • Marta Mattana,
  • Sergio Siragusa

DOI
https://doi.org/10.1002/ccr3.5525
Journal volume & issue
Vol. 10, no. 3
pp. n/a – n/a

Abstract

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Abstract Rarely essential thrombocythemia (ET) is diagnosed in more than one person within a family. Familial myeloproliferative neoplasms are underdiagnosed. In this report, we describe 6 couples of familial ET, evaluating the heterogeneity of the mutational state and the clinical presentation.

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