Igg4-Related Hypophysitis

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Igg4-Related Hypophysitis Publisher Pubmed

Amirbaigloo A¹ ; Esfahanian F² ; Mouodi M² ; Rakhshani N³ ; Zeinalizadeh M⁴

Source: Endocrine Published:2021

Abstract

Hypophysitis is a rare pituitary inflammatory disorder classified in different ways. Immunoglobulin G4-related disease (IgG4-RD), also a rare disease is a systemic fibro-inflammatory condition characterized by infiltration of tissue with IgG4-positive plasma cells; however prevalence of both of them probably is underestimated. In this paper, we present an Iranian patient with biopsy-proven IgG4-related hypophysitis and then review the clinical characteristics, laboratory, imaging, pathologic findings and therapeutic management as well as prognosis of 115 published cases of hypophysitis secondary to IgG4-related disease. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Style	Citing Format
MLA	Amirbaigloo A, et al.. "Igg4-Related Hypophysitis." Endocrine, vol. 73, no. 2, 2021, pp. 270-291.
APA	Amirbaigloo A, Esfahanian F, Mouodi M, Rakhshani N, Zeinalizadeh M (2021). Igg4-Related Hypophysitis. Endocrine, 73(2), 270-291.
Chicago	Amirbaigloo A, Esfahanian F, Mouodi M, Rakhshani N, Zeinalizadeh M. "Igg4-Related Hypophysitis." Endocrine 73, no. 2 (2021): 270-291.
Harvard	Amirbaigloo A et al. (2021) 'Igg4-Related Hypophysitis', Endocrine, 73(2), pp. 270-291.
Vancouver	Amirbaigloo A, Esfahanian F, Mouodi M, Rakhshani N, Zeinalizadeh M. Igg4-Related Hypophysitis. Endocrine. 2021;73(2):270-291.
BibTex	@article{ author = {Amirbaigloo A and Esfahanian F and Mouodi M and Rakhshani N and Zeinalizadeh M}, title = {Igg4-Related Hypophysitis}, journal = {Endocrine}, volume = {73}, number = {2}, pages = {270-291}, year = {2021} }
RIS	TY - JOUR AU - Amirbaigloo A AU - Esfahanian F AU - Mouodi M AU - Rakhshani N AU - Zeinalizadeh M TI - Igg4-Related Hypophysitis JO - Endocrine VL - 73 IS - 2 SP - 270 EP - 291 PY - 2021 ER -

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