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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2016
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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. |
format | Online Article Text |
id | pubmed-5208633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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