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LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging

BACKGROUND: Lymphocytic (LH) or autoimmune hypophysitis (AH) is a rare inflammatory disorder of the hypophyseal gland, often miss-diagnosed. LH is predominant in females, occasionally related with other rheumatic disorders (1-20%). The disease can lead to pituitary dysfunction and symptoms of hypopi...

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Autores principales: Gonzalez, Juanita, Monsalve, Claudia, Aguilar, Carolina, Aristizabal, Natalia, Torres, Jose Luis, Pompey, Nestor Alfonso Lopez, Vargas, Laura Valentina Estupiñan, Ramos, Andres Felipe Garcia, Buenaventura, Daisy, Ramirez, Alex, Vargas, Hernando, Herrera, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625532/
http://dx.doi.org/10.1210/jendso/bvac150.990
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author Gonzalez, Juanita
Monsalve, Claudia
Aguilar, Carolina
Aristizabal, Natalia
Torres, Jose Luis
Pompey, Nestor Alfonso Lopez
Vargas, Laura Valentina Estupiñan
Ramos, Andres Felipe Garcia
Buenaventura, Daisy
Ramirez, Alex
Vargas, Hernando
Herrera, Sebastian
author_facet Gonzalez, Juanita
Monsalve, Claudia
Aguilar, Carolina
Aristizabal, Natalia
Torres, Jose Luis
Pompey, Nestor Alfonso Lopez
Vargas, Laura Valentina Estupiñan
Ramos, Andres Felipe Garcia
Buenaventura, Daisy
Ramirez, Alex
Vargas, Hernando
Herrera, Sebastian
author_sort Gonzalez, Juanita
collection PubMed
description BACKGROUND: Lymphocytic (LH) or autoimmune hypophysitis (AH) is a rare inflammatory disorder of the hypophyseal gland, often miss-diagnosed. LH is predominant in females, occasionally related with other rheumatic disorders (1-20%). The disease can lead to pituitary dysfunction and symptoms of hypopituitarism, the most affected axes are the ACTH and TSH. Definitive diagnosis of AH can be based only on pathological examination of a pituitary biopsy sample but such invasive procedure is seldom needed. Different imaging modalities, especially MRI, can be useful but up to 30% can be unremarkable, thus clinical manifestations and biochemical evaluation is of great importance in guiding the diagnosis. Hormonal replacement therapy is the main treatment strategy. Immunosuppressive drugs are indicated by the severity of the symptoms and the underlying autoimmune disease. CLINICAL CASE: A 36 year old patient with active lupus and Sjogren disease presented to the emergency department with syncope and hypotension preceded by a 6 month history of intense fatigue. She did not take any steroids in the 6 months prior. Initial tests were consistent with secondary adrenal insufficiency; low plasma cortisol (<1ug/dl n 5-23 ug/dl) and ACTH-concentrations below detection (< 4 ng/l), central hypothyroidism; abnormal low TSH (0. 04uU/ml n 0.4-4.5 uU/ml) and low free T4 (0.56 ng/dl n 0.8-2 ng/dl), and growth hormone deficiency (IGF1 below age and sex normal values). Craneal CT and pituitary MRI didn't show any anomaly. Based on symptoms, clinical context and test results the pressumtive diagnosis was AH related to her lupus. The patient was treated with hydrocortisone and levothyroxine with excellent response and complete resolution of her symptoms. Clinical Lesson: This case demonstrates that hypophysitis is a clinical entity that can be suspected and treated based on clinical and past medical history even in the context of normal imaging were an invasive procedure such as a biopsy would likely not change the final outcome. Presentation: No date and time listed
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spelling pubmed-96255322022-11-14 LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging Gonzalez, Juanita Monsalve, Claudia Aguilar, Carolina Aristizabal, Natalia Torres, Jose Luis Pompey, Nestor Alfonso Lopez Vargas, Laura Valentina Estupiñan Ramos, Andres Felipe Garcia Buenaventura, Daisy Ramirez, Alex Vargas, Hernando Herrera, Sebastian J Endocr Soc Neuroendocrinology and Pituitary BACKGROUND: Lymphocytic (LH) or autoimmune hypophysitis (AH) is a rare inflammatory disorder of the hypophyseal gland, often miss-diagnosed. LH is predominant in females, occasionally related with other rheumatic disorders (1-20%). The disease can lead to pituitary dysfunction and symptoms of hypopituitarism, the most affected axes are the ACTH and TSH. Definitive diagnosis of AH can be based only on pathological examination of a pituitary biopsy sample but such invasive procedure is seldom needed. Different imaging modalities, especially MRI, can be useful but up to 30% can be unremarkable, thus clinical manifestations and biochemical evaluation is of great importance in guiding the diagnosis. Hormonal replacement therapy is the main treatment strategy. Immunosuppressive drugs are indicated by the severity of the symptoms and the underlying autoimmune disease. CLINICAL CASE: A 36 year old patient with active lupus and Sjogren disease presented to the emergency department with syncope and hypotension preceded by a 6 month history of intense fatigue. She did not take any steroids in the 6 months prior. Initial tests were consistent with secondary adrenal insufficiency; low plasma cortisol (<1ug/dl n 5-23 ug/dl) and ACTH-concentrations below detection (< 4 ng/l), central hypothyroidism; abnormal low TSH (0. 04uU/ml n 0.4-4.5 uU/ml) and low free T4 (0.56 ng/dl n 0.8-2 ng/dl), and growth hormone deficiency (IGF1 below age and sex normal values). Craneal CT and pituitary MRI didn't show any anomaly. Based on symptoms, clinical context and test results the pressumtive diagnosis was AH related to her lupus. The patient was treated with hydrocortisone and levothyroxine with excellent response and complete resolution of her symptoms. Clinical Lesson: This case demonstrates that hypophysitis is a clinical entity that can be suspected and treated based on clinical and past medical history even in the context of normal imaging were an invasive procedure such as a biopsy would likely not change the final outcome. Presentation: No date and time listed Oxford University Press 2022-11-01 /pmc/articles/PMC9625532/ http://dx.doi.org/10.1210/jendso/bvac150.990 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neuroendocrinology and Pituitary
Gonzalez, Juanita
Monsalve, Claudia
Aguilar, Carolina
Aristizabal, Natalia
Torres, Jose Luis
Pompey, Nestor Alfonso Lopez
Vargas, Laura Valentina Estupiñan
Ramos, Andres Felipe Garcia
Buenaventura, Daisy
Ramirez, Alex
Vargas, Hernando
Herrera, Sebastian
LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging
title LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging
title_full LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging
title_fullStr LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging
title_full_unstemmed LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging
title_short LBODP074 Autoimmune Hypophysitis: Diagnosis Beyond Imaging
title_sort lbodp074 autoimmune hypophysitis: diagnosis beyond imaging
topic Neuroendocrinology and Pituitary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625532/
http://dx.doi.org/10.1210/jendso/bvac150.990
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