Severe Thrombocytopenia Due to Bone Marrow Failure in Children With Dyskeratosis Congenita Does Not Respond to Eltrombopag Treatment: Case Series

Author:

Pramanik-Jonsson Lotta12,Borssén Magnus34,Vonlanthen Sofie5,Nilsson Frans34,Sundin Mikael12

Affiliation:

1. Division of Pediatrics, Department of Clinical Science, Intervention and Technology, Karolinska Institutet

2. Section of Pediatric Hematology, Immunology and HCT, Astrid Lindgren Children’s Hospital

3. Department of Medical Biosciences, Umeå University

4. Section of Pediatric Hematology and Oncology, Child and Adolescent Medical Center, University Hospital of Umeå, Umeå, Sweden

5. Department of Clinical Immunology and Transfusion Medicine, Medical Diagnostics Center, Karolinska University Hospital, Stockholm

Abstract

Dyskeratosis congenita is a rare inherited disease with classic cutaneous symptoms, sometimes accompanied with more severe extracutaneous manifestations such as bone marrow failure, which can be lethal. Eltrombopag is an orally available thrombopoietin receptor agonist in clinical use for increasing platelet levels in patients with immune thrombocytopenia and aplastic anemia. Here, 3 pediatric patients with dyskeratosis congenita are presented with varying disease severity, in which off-label eltrombopag treatment had no clinical effect on bone marrow failure. This, in addition to the negative results in a previous case report, supports the preclusion of eltrombopag use in dyskeratosis congenita.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference18 articles.

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5. Dyskeratosis congenita: a combined immunodeficiency with broad clinical spectrum—a single-center pediatric experience;Jyonouchi;Pediatr Allergy Immunol,2011

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