Case Report

Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report

Volume: 13 Number: 1 April 28, 2016
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Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic necrotizing vasculitis characterized by tissue and blood eosinophilia. Several drugs including leukotriene receptor antagonists (LTRAs) are suspected to trigger EGPAdevelopment. Here, we present a case of EGPAunrelated to LTRAs.

Keywords

References

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Details

Primary Language

English

Subjects

-

Journal Section

Case Report

Authors

Hakan Tanrıverdi * This is me

Fırat Uygur This is me

Ömer Yazgan This is me

Figen Atalay This is me

Publication Date

April 28, 2016

Submission Date

June 28, 2015

Acceptance Date

November 4, 2015

Published in Issue

Year 2016 Volume: 13 Number: 1

APA
Tanrıverdi, H., Uygur, F., Altınsoy, B., Erboy, F., Yazgan, Ö., & Atalay, F. (2016). Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report. Harran Üniversitesi Tıp Fakültesi Dergisi, 13(1), 84-87. https://izlik.org/JA46NS52GJ
AMA
1.Tanrıverdi H, Uygur F, Altınsoy B, Erboy F, Yazgan Ö, Atalay F. Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report. Harran Üniversitesi Tıp Fakültesi Dergisi. 2016;13(1):84-87. https://izlik.org/JA46NS52GJ
Chicago
Tanrıverdi, Hakan, Fırat Uygur, Bülent Altınsoy, Fatma Erboy, Ömer Yazgan, and Figen Atalay. 2016. “Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report”. Harran Üniversitesi Tıp Fakültesi Dergisi 13 (1): 84-87. https://izlik.org/JA46NS52GJ.
EndNote
Tanrıverdi H, Uygur F, Altınsoy B, Erboy F, Yazgan Ö, Atalay F (April 1, 2016) Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report. Harran Üniversitesi Tıp Fakültesi Dergisi 13 1 84–87.
IEEE
[1]H. Tanrıverdi, F. Uygur, B. Altınsoy, F. Erboy, Ö. Yazgan, and F. Atalay, “Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report”, Harran Üniversitesi Tıp Fakültesi Dergisi, vol. 13, no. 1, pp. 84–87, Apr. 2016, [Online]. Available: https://izlik.org/JA46NS52GJ
ISNAD
Tanrıverdi, Hakan - Uygur, Fırat - Altınsoy, Bülent - Erboy, Fatma - Yazgan, Ömer - Atalay, Figen. “Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report”. Harran Üniversitesi Tıp Fakültesi Dergisi 13/1 (April 1, 2016): 84-87. https://izlik.org/JA46NS52GJ.
JAMA
1.Tanrıverdi H, Uygur F, Altınsoy B, Erboy F, Yazgan Ö, Atalay F. Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report. Harran Üniversitesi Tıp Fakültesi Dergisi. 2016;13:84–87.
MLA
Tanrıverdi, Hakan, et al. “Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report”. Harran Üniversitesi Tıp Fakültesi Dergisi, vol. 13, no. 1, Apr. 2016, pp. 84-87, https://izlik.org/JA46NS52GJ.
Vancouver
1.Hakan Tanrıverdi, Fırat Uygur, Bülent Altınsoy, Fatma Erboy, Ömer Yazgan, Figen Atalay. Eosinophilic Granulomatosis With Polyangiitis (Churg Strauss Syndrome): Case Report. Harran Üniversitesi Tıp Fakültesi Dergisi [Internet]. 2016 Apr. 1;13(1):84-7. Available from: https://izlik.org/JA46NS52GJ

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