Xanthogranulomatous hypophysitis: A rare presentation in a young female patient

Hypophysitis is a rare inflammatory condition that may present both clinically and radiologically as a neoplastic lesion. Xanthogranulomas are rare intracranial lesions with controversial etiology. Here, we report a clinical case of histologically confirmed xanthogranulomatosis hypophysitis in a you...

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Detalles Bibliográficos
Autores principales: Yaghoubi, Mohammad Ali, Zabihyan, Samira, Saeidinia, Amin, Gharib, Masoumeh, Ghiyasi Moghaddam, Ramin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474903/
https://www.ncbi.nlm.nih.gov/pubmed/36177067
http://dx.doi.org/10.1002/ccr3.6337
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author Yaghoubi, Mohammad Ali
Zabihyan, Samira
Saeidinia, Amin
Gharib, Masoumeh
Ghiyasi Moghaddam, Ramin
author_facet Yaghoubi, Mohammad Ali
Zabihyan, Samira
Saeidinia, Amin
Gharib, Masoumeh
Ghiyasi Moghaddam, Ramin
author_sort Yaghoubi, Mohammad Ali
collection PubMed
description Hypophysitis is a rare inflammatory condition that may present both clinically and radiologically as a neoplastic lesion. Xanthogranulomas are rare intracranial lesions with controversial etiology. Here, we report a clinical case of histologically confirmed xanthogranulomatosis hypophysitis in a young female with type I diabetes mellitus and hypothyroidism.
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spelling pubmed-94749032022-09-28 Xanthogranulomatous hypophysitis: A rare presentation in a young female patient Yaghoubi, Mohammad Ali Zabihyan, Samira Saeidinia, Amin Gharib, Masoumeh Ghiyasi Moghaddam, Ramin Clin Case Rep Case Report Hypophysitis is a rare inflammatory condition that may present both clinically and radiologically as a neoplastic lesion. Xanthogranulomas are rare intracranial lesions with controversial etiology. Here, we report a clinical case of histologically confirmed xanthogranulomatosis hypophysitis in a young female with type I diabetes mellitus and hypothyroidism. John Wiley and Sons Inc. 2022-09-14 /pmc/articles/PMC9474903/ /pubmed/36177067 http://dx.doi.org/10.1002/ccr3.6337 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Yaghoubi, Mohammad Ali
Zabihyan, Samira
Saeidinia, Amin
Gharib, Masoumeh
Ghiyasi Moghaddam, Ramin
Xanthogranulomatous hypophysitis: A rare presentation in a young female patient
title Xanthogranulomatous hypophysitis: A rare presentation in a young female patient
title_full Xanthogranulomatous hypophysitis: A rare presentation in a young female patient
title_fullStr Xanthogranulomatous hypophysitis: A rare presentation in a young female patient
title_full_unstemmed Xanthogranulomatous hypophysitis: A rare presentation in a young female patient
title_short Xanthogranulomatous hypophysitis: A rare presentation in a young female patient
title_sort xanthogranulomatous hypophysitis: a rare presentation in a young female patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474903/
https://www.ncbi.nlm.nih.gov/pubmed/36177067
http://dx.doi.org/10.1002/ccr3.6337
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