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Primary adrenal insufficiency in case of antiphospholipid syndrome

Addison's disease or primary adrenal insufficiency (PAI) is a rare manifestation of antiphospholipid syndrome (APS). PAI is the most common among the endocrinologic manifestations and can also rarely be the presenting symptom of APS. Venous thrombosis and/or adrenal hemorrhage are the leading c...

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Autores principales: Sanyal, Debmalya, Raychaudhuri, Moutusi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830323/
https://www.ncbi.nlm.nih.gov/pubmed/24251177
http://dx.doi.org/10.4103/2230-8210.119590
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author Sanyal, Debmalya
Raychaudhuri, Moutusi
author_facet Sanyal, Debmalya
Raychaudhuri, Moutusi
author_sort Sanyal, Debmalya
collection PubMed
description Addison's disease or primary adrenal insufficiency (PAI) is a rare manifestation of antiphospholipid syndrome (APS). PAI is the most common among the endocrinologic manifestations and can also rarely be the presenting symptom of APS. Venous thrombosis and/or adrenal hemorrhage are the leading cause of PAI in APS. Autoimmune adrenal failure is postulated to be another possible mechanism. We report a case of PAI in a 44-year-old lady preceding primary APS, probably autoimmune, without any evidence of adrenal hemorrhage or infarction. High index of clinical suspicion for PAI in APS is needed; conversely APS should be considered as a possible pathogenetic process in patients presenting with Addison's disease where the etiology is not obvious.
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spelling pubmed-38303232013-11-18 Primary adrenal insufficiency in case of antiphospholipid syndrome Sanyal, Debmalya Raychaudhuri, Moutusi Indian J Endocrinol Metab Brief Communication Addison's disease or primary adrenal insufficiency (PAI) is a rare manifestation of antiphospholipid syndrome (APS). PAI is the most common among the endocrinologic manifestations and can also rarely be the presenting symptom of APS. Venous thrombosis and/or adrenal hemorrhage are the leading cause of PAI in APS. Autoimmune adrenal failure is postulated to be another possible mechanism. We report a case of PAI in a 44-year-old lady preceding primary APS, probably autoimmune, without any evidence of adrenal hemorrhage or infarction. High index of clinical suspicion for PAI in APS is needed; conversely APS should be considered as a possible pathogenetic process in patients presenting with Addison's disease where the etiology is not obvious. Medknow Publications & Media Pvt Ltd 2013-10 /pmc/articles/PMC3830323/ /pubmed/24251177 http://dx.doi.org/10.4103/2230-8210.119590 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Sanyal, Debmalya
Raychaudhuri, Moutusi
Primary adrenal insufficiency in case of antiphospholipid syndrome
title Primary adrenal insufficiency in case of antiphospholipid syndrome
title_full Primary adrenal insufficiency in case of antiphospholipid syndrome
title_fullStr Primary adrenal insufficiency in case of antiphospholipid syndrome
title_full_unstemmed Primary adrenal insufficiency in case of antiphospholipid syndrome
title_short Primary adrenal insufficiency in case of antiphospholipid syndrome
title_sort primary adrenal insufficiency in case of antiphospholipid syndrome
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830323/
https://www.ncbi.nlm.nih.gov/pubmed/24251177
http://dx.doi.org/10.4103/2230-8210.119590
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