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IgG4-Related Hypophysitis: Case Report and Literature Review

IgG4-related hypophysitis is a rare, inflammatory process of the pituitary that mimics more commonly seen pituitary tumors. We report a case of IgG4-related hypophysitis in a 16-year-old female with diabetes insipidus who was found to have IgG4-related hypophysitis based on tissue diagnosis. This en...

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Detalles Bibliográficos
Autores principales: Decker, Lauren, Crawford, Angela M, Lorenzo, Gamaliel, Stippler, Martina, Konstantinov, Konstantin N, SantaCruz, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5208633/
https://www.ncbi.nlm.nih.gov/pubmed/28083451
http://dx.doi.org/10.7759/cureus.907
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author Decker, Lauren
Crawford, Angela M
Lorenzo, Gamaliel
Stippler, Martina
Konstantinov, Konstantin N
SantaCruz, Karen
author_facet Decker, Lauren
Crawford, Angela M
Lorenzo, Gamaliel
Stippler, Martina
Konstantinov, Konstantin N
SantaCruz, Karen
author_sort Decker, Lauren
collection PubMed
description IgG4-related hypophysitis is a rare, inflammatory process of the pituitary that mimics more commonly seen pituitary tumors. We report a case of IgG4-related hypophysitis in a 16-year-old female with diabetes insipidus who was found to have IgG4-related hypophysitis based on tissue diagnosis. This entity has not been previously described in a pediatric patient. Recognition of certain inflammatory processes of the pituitary may lead to alternative means of diagnosis and medical management without a biopsy.
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spelling pubmed-52086332017-01-12 IgG4-Related Hypophysitis: Case Report and Literature Review Decker, Lauren Crawford, Angela M Lorenzo, Gamaliel Stippler, Martina Konstantinov, Konstantin N SantaCruz, Karen Cureus Pathology IgG4-related hypophysitis is a rare, inflammatory process of the pituitary that mimics more commonly seen pituitary tumors. We report a case of IgG4-related hypophysitis in a 16-year-old female with diabetes insipidus who was found to have IgG4-related hypophysitis based on tissue diagnosis. This entity has not been previously described in a pediatric patient. Recognition of certain inflammatory processes of the pituitary may lead to alternative means of diagnosis and medical management without a biopsy. Cureus 2016-12-01 /pmc/articles/PMC5208633/ /pubmed/28083451 http://dx.doi.org/10.7759/cureus.907 Text en Copyright © 2016, Decker et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pathology
Decker, Lauren
Crawford, Angela M
Lorenzo, Gamaliel
Stippler, Martina
Konstantinov, Konstantin N
SantaCruz, Karen
IgG4-Related Hypophysitis: Case Report and Literature Review
title IgG4-Related Hypophysitis: Case Report and Literature Review
title_full IgG4-Related Hypophysitis: Case Report and Literature Review
title_fullStr IgG4-Related Hypophysitis: Case Report and Literature Review
title_full_unstemmed IgG4-Related Hypophysitis: Case Report and Literature Review
title_short IgG4-Related Hypophysitis: Case Report and Literature Review
title_sort igg4-related hypophysitis: case report and literature review
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5208633/
https://www.ncbi.nlm.nih.gov/pubmed/28083451
http://dx.doi.org/10.7759/cureus.907
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