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Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature

BACKGROUND: Autoimmune hypophysitis very rarely spreads to nearby organs outside the pituitary tissue, for unknown reasons, with only 5 reported cases of hypophysitis spreading over the cavernous sinus. CASE PRESENTATION: Three patients presented with cases of non-infectious hypophysitis spreading o...

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Autores principales: Kanoke, Atsushi, Ogawa, Yoshikazu, Watanabe, Mika, Kumabe, Toshihiro, Tominaga, Teiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877864/
https://www.ncbi.nlm.nih.gov/pubmed/24373428
http://dx.doi.org/10.1186/1756-0500-6-560
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author Kanoke, Atsushi
Ogawa, Yoshikazu
Watanabe, Mika
Kumabe, Toshihiro
Tominaga, Teiji
author_facet Kanoke, Atsushi
Ogawa, Yoshikazu
Watanabe, Mika
Kumabe, Toshihiro
Tominaga, Teiji
author_sort Kanoke, Atsushi
collection PubMed
description BACKGROUND: Autoimmune hypophysitis very rarely spreads to nearby organs outside the pituitary tissue, for unknown reasons, with only 5 reported cases of hypophysitis spreading over the cavernous sinus. CASE PRESENTATION: Three patients presented with cases of non-infectious hypophysitis spreading outside the pituitary tissue over the cavernous sinus. All three cases were diagnosed with histological confirmation by transsphenoidal surgery, and the patients showed remarkable improvement with postoperative pulse dose steroid therapy, including disappearance of abnormal signal intensities in the bilateral hypothalami on magnetic resonance imaging, resolution of severe stenosis of the internal carotid artery, and normalization of swollen pituitary tissues. Two of 3 cases fulfilled the histological criteria of immunoglobulin G4-related disease, although none of the patients had high serum immunoglobulin G4 level. CONCLUSION: The true implications of such unusual spreading of hypophysitis to nearby organs are not fully understood, but the mechanism of occurrence might vary according to the timing of inflammation in this unusual mode of spreading. Pulse dose steroid therapy achieved remarkably good outcomes even in the patient with progressive severe stenosis of the internal carotid artery and rapid visual deterioration.
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spelling pubmed-38778642014-01-03 Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature Kanoke, Atsushi Ogawa, Yoshikazu Watanabe, Mika Kumabe, Toshihiro Tominaga, Teiji BMC Res Notes Case Report BACKGROUND: Autoimmune hypophysitis very rarely spreads to nearby organs outside the pituitary tissue, for unknown reasons, with only 5 reported cases of hypophysitis spreading over the cavernous sinus. CASE PRESENTATION: Three patients presented with cases of non-infectious hypophysitis spreading outside the pituitary tissue over the cavernous sinus. All three cases were diagnosed with histological confirmation by transsphenoidal surgery, and the patients showed remarkable improvement with postoperative pulse dose steroid therapy, including disappearance of abnormal signal intensities in the bilateral hypothalami on magnetic resonance imaging, resolution of severe stenosis of the internal carotid artery, and normalization of swollen pituitary tissues. Two of 3 cases fulfilled the histological criteria of immunoglobulin G4-related disease, although none of the patients had high serum immunoglobulin G4 level. CONCLUSION: The true implications of such unusual spreading of hypophysitis to nearby organs are not fully understood, but the mechanism of occurrence might vary according to the timing of inflammation in this unusual mode of spreading. Pulse dose steroid therapy achieved remarkably good outcomes even in the patient with progressive severe stenosis of the internal carotid artery and rapid visual deterioration. BioMed Central 2013-12-28 /pmc/articles/PMC3877864/ /pubmed/24373428 http://dx.doi.org/10.1186/1756-0500-6-560 Text en Copyright © 2013 Kanoke et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Kanoke, Atsushi
Ogawa, Yoshikazu
Watanabe, Mika
Kumabe, Toshihiro
Tominaga, Teiji
Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature
title Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature
title_full Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature
title_fullStr Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature
title_full_unstemmed Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature
title_short Autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature
title_sort autoimmune hypophysitis presenting with intracranial multi-organ involvement: three case reports and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877864/
https://www.ncbi.nlm.nih.gov/pubmed/24373428
http://dx.doi.org/10.1186/1756-0500-6-560
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