Eltrombopag in Good’s Syndrome

Joint Authors

Kristiansen, Håvard Anton
Spetalen, Signe
Heldal, Dag
Fløisand, Yngvar

Source

Case Reports in Hematology

Issue

Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-3, 3 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2014-10-19

Country of Publication

Egypt

No. of Pages

3

Main Subjects

Diseases

Abstract EN

Good’s syndrome is a rare acquired immunodeficiency associated with thymoma.

Eltrombopag is a thrombopoietin receptor agonist and has been shown to be a valuable supplement to the treatment of several types of refractory cytopenias.

In this paper, we describe a male patient suffering from Good’s syndrome with immune-mediated T-cell driven pancytopenia and absence of megakaryopoiesis.

He was successfully treated with eltrombopag resulting in a multilineage clinical response.

American Psychological Association (APA)

Kristiansen, Håvard Anton& Spetalen, Signe& Fløisand, Yngvar& Heldal, Dag. 2014. Eltrombopag in Good’s Syndrome. Case Reports in Hematology،Vol. 2014, no. 2014, pp.1-3.
https://search.emarefa.net/detail/BIM-1034742

Modern Language Association (MLA)

Kristiansen, Håvard Anton…[et al.]. Eltrombopag in Good’s Syndrome. Case Reports in Hematology No. 2014 (2014), pp.1-3.
https://search.emarefa.net/detail/BIM-1034742

American Medical Association (AMA)

Kristiansen, Håvard Anton& Spetalen, Signe& Fløisand, Yngvar& Heldal, Dag. Eltrombopag in Good’s Syndrome. Case Reports in Hematology. 2014. Vol. 2014, no. 2014, pp.1-3.
https://search.emarefa.net/detail/BIM-1034742

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1034742