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Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities

Inflammatory disease of the pituitary gland is known as hypophysitis. There are multiple histological subtypes, the most common being lymphocytic, and the pathogenesis is variable and diverse. Hypophysitis can be primary and idiopathic or autoimmune related, or secondary to local lesions, systemic d...

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Autores principales: Rawanduzy, Cameron A., Winkler-Schwartz, Alexander, Couldwell, William T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057821/
https://www.ncbi.nlm.nih.gov/pubmed/36982990
http://dx.doi.org/10.3390/ijms24065917
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author Rawanduzy, Cameron A.
Winkler-Schwartz, Alexander
Couldwell, William T.
author_facet Rawanduzy, Cameron A.
Winkler-Schwartz, Alexander
Couldwell, William T.
author_sort Rawanduzy, Cameron A.
collection PubMed
description Inflammatory disease of the pituitary gland is known as hypophysitis. There are multiple histological subtypes, the most common being lymphocytic, and the pathogenesis is variable and diverse. Hypophysitis can be primary and idiopathic or autoimmune related, or secondary to local lesions, systemic disease, medications, and more. Although hypophysitis was previously accepted as an exceedingly rare diagnosis, a greater understanding of the disease process and new insights into possible etiologic sources have contributed to an increased frequency of recognition. This review provides an overview of hypophysitis, its causes, and detection strategies and management.
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spelling pubmed-100578212023-03-30 Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities Rawanduzy, Cameron A. Winkler-Schwartz, Alexander Couldwell, William T. Int J Mol Sci Review Inflammatory disease of the pituitary gland is known as hypophysitis. There are multiple histological subtypes, the most common being lymphocytic, and the pathogenesis is variable and diverse. Hypophysitis can be primary and idiopathic or autoimmune related, or secondary to local lesions, systemic disease, medications, and more. Although hypophysitis was previously accepted as an exceedingly rare diagnosis, a greater understanding of the disease process and new insights into possible etiologic sources have contributed to an increased frequency of recognition. This review provides an overview of hypophysitis, its causes, and detection strategies and management. MDPI 2023-03-21 /pmc/articles/PMC10057821/ /pubmed/36982990 http://dx.doi.org/10.3390/ijms24065917 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rawanduzy, Cameron A.
Winkler-Schwartz, Alexander
Couldwell, William T.
Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities
title Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities
title_full Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities
title_fullStr Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities
title_full_unstemmed Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities
title_short Hypophysitis: Defining Histopathologic Variants and a Review of Emerging Clinical Causative Entities
title_sort hypophysitis: defining histopathologic variants and a review of emerging clinical causative entities
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057821/
https://www.ncbi.nlm.nih.gov/pubmed/36982990
http://dx.doi.org/10.3390/ijms24065917
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