Disease heterogeneity in IgG4-related hypophysitis: report of two histopathologically proven cases and review of the literature-Reference-Cited by-同舟云学术

Disease heterogeneity in IgG4-related hypophysitis: report of two histopathologically proven cases and review of the literature

Published:2019-03-25 Issue:3 Volume:475 Page:373-381
ISSN:0945-6317
Container-title:Virchows Archiv
language:en
Short-container-title:Virchows Arch

Author:

Uccella Silvia^ORCID,Amaglio Cristina,Brouland Jean-Philippe,Bianconi Eleonora,Ippolito Silvia,Messerer Mahmoud,Rouiller Nathalie,Tanda Maria Laura,Sessa Fausto,La Rosa Stefano

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,General Medicine,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00428-019-02564-2.pdf

Reference25 articles.

1. Faje A (2016) Hypophysitis: evaluation and management. Clin Diabetes Endocrinol 2:15

2. Deshpande V, Zen Y, Chan JK, Yi EE, Sato Y (2012) Consensus statement on the pathology of IgG4-related disease. Mod Pathol 25:1181–1192

3. Leporati P, Landek-Salgado MA, Lupi I, Chiovato L, Caturegli P (2011) IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. J Clin Endocrinol Metab 96:1971–1980

4. Wong S, Lam WY, Wong WK, Lee KC (2007) Hypophysitis presents as inflammatory pseudotumor in immunoglobulin G4-related systemic disease. Hum Pathol 38:1720–1723

5. Osawa S, Ogawa Y, Watanabe M, Tominaga T (2009) Hypophysitis presenting with atypical rapid deterioration: with special reference to immunoglobulin G4 related disease-case report. Neurol Med Chir 49:622–625

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