Loading…
Primary Adrenal Insufficiency: a diagnostic challenge
We present a case of a 42-year-old man who was referred to the Department of Endocrinology because of muscle soreness and increased skin pigmentation with suspicion of adrenal insufficiency. No other complaints were present. The patient had a history of arterial hypertension, at the moment well-cont...
Saved in:
Published in: | Acta clinica belgica (English ed. Online) 2016-05, Vol.71 (S3), p.7 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | S3 |
container_start_page | 7 |
container_title | Acta clinica belgica (English ed. Online) |
container_volume | 71 |
creator | Wierckx, K Vandecasteele, S J Van den Bruel, A |
description | We present a case of a 42-year-old man who was referred to the Department of Endocrinology because of muscle soreness and increased skin pigmentation with suspicion of adrenal insufficiency. No other complaints were present. The patient had a history of arterial hypertension, at the moment well-controlled despite of stopping antihypertensive medication and gastroesophageal reflux disease with daily use of a proton pump inhibitor (Esomeprazole 20 mg). There was no relevant family history apart from tuberculosis (TB) of his mother. He denied travel to the tropics or drug use. Physical examination showed a normal blood pressure, increased pulse rate and a marked hyperpigmentation of the skin and mucosa. Laboratory findings showed low morning cortisol of 2 pig/dl (6.2-18 (pg/dL), low DHEAS of 67 pg (88.9-427 pg), high renine of 15187 plU/ml (2.8-39.9 plU/ml) and high ACTH level of > 1250 pg/l (< 46 ng/L). Short corticotrophin test did not evoke a marked increase in serum cortisol. The diagnosis of primary adrenal insufficiency (PAI) was made and the patient was started on hydrocortisone and fludrocortisone therapy. Assessment for anti-adrenal antibodies and catecholamine secretion were negative. 17-OH progesterone levels and very long chain fatty acids were normal. A computed tomography (CT) scan of the abdomen demonstrated bilateral adrenal enlargement with one nodule in each adrenal gland (right: nodule with maximum diameter 44 mm, Hounsfield Units (HU): 40; left: maximum diameter 14 mm, HU: 37). Further assessment with whole-body fluorine-18 fluorodeoxyglucose positron emission tomography-CT (FDG PET-CT) examination showed increased FDG uptake at both adrenals (more pronounced in the right adrenal gland) as well as an increased uptake at some axillary lymph nodes. A tuberculin skin test showed to be positive and may reflect co-existence of TB carriage or TB of the adrenal glands. Due to absence of extra-adrenal TB, further work-up with ultrasonic guided puncture of one adrenal gland is planned 17th of August. PAI is a rare disease with a reported prevalence of about 100-140 cases per million in Western Societies. The most common cause of PAI is auto-immunity (up to 90% in Western countries). Adrenal TB is a relatively infrequent cause of PAI in developed countries, whereas in developing countries, TB remains a major cause of PAI. However, recent increases in human migration have contributed to increased rates of TB in Western Societies. The differential dia |
format | article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_1858231824</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4301045811</sourcerecordid><originalsourceid>FETCH-proquest_journals_18582318243</originalsourceid><addsrcrecordid>eNqNjLEKwjAUAIMoWLT_EHAu2Ly0Td1EFN0c3EtIk5oSU81rhv69HfwAb7nluAVJGKuLDACqJUnySvAMmCjXJEXs9zNQ8xJYQop7sC8ZJnpsg_bS0ZvHaIxVVns1HaikrZWdH3C0iqqndE77Tm_JykiHOv15Q3aX8-N0zd5h-ESNY9MPMcw7bHJRCAa5YBz-q77pXDbi</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1858231824</pqid></control><display><type>article</type><title>Primary Adrenal Insufficiency: a diagnostic challenge</title><source>Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)</source><creator>Wierckx, K ; Vandecasteele, S J ; Van den Bruel, A</creator><creatorcontrib>Wierckx, K ; Vandecasteele, S J ; Van den Bruel, A</creatorcontrib><description>We present a case of a 42-year-old man who was referred to the Department of Endocrinology because of muscle soreness and increased skin pigmentation with suspicion of adrenal insufficiency. No other complaints were present. The patient had a history of arterial hypertension, at the moment well-controlled despite of stopping antihypertensive medication and gastroesophageal reflux disease with daily use of a proton pump inhibitor (Esomeprazole 20 mg). There was no relevant family history apart from tuberculosis (TB) of his mother. He denied travel to the tropics or drug use. Physical examination showed a normal blood pressure, increased pulse rate and a marked hyperpigmentation of the skin and mucosa. Laboratory findings showed low morning cortisol of 2 pig/dl (6.2-18 (pg/dL), low DHEAS of 67 pg (88.9-427 pg), high renine of 15187 plU/ml (2.8-39.9 plU/ml) and high ACTH level of > 1250 pg/l (< 46 ng/L). Short corticotrophin test did not evoke a marked increase in serum cortisol. The diagnosis of primary adrenal insufficiency (PAI) was made and the patient was started on hydrocortisone and fludrocortisone therapy. Assessment for anti-adrenal antibodies and catecholamine secretion were negative. 17-OH progesterone levels and very long chain fatty acids were normal. A computed tomography (CT) scan of the abdomen demonstrated bilateral adrenal enlargement with one nodule in each adrenal gland (right: nodule with maximum diameter 44 mm, Hounsfield Units (HU): 40; left: maximum diameter 14 mm, HU: 37). Further assessment with whole-body fluorine-18 fluorodeoxyglucose positron emission tomography-CT (FDG PET-CT) examination showed increased FDG uptake at both adrenals (more pronounced in the right adrenal gland) as well as an increased uptake at some axillary lymph nodes. A tuberculin skin test showed to be positive and may reflect co-existence of TB carriage or TB of the adrenal glands. Due to absence of extra-adrenal TB, further work-up with ultrasonic guided puncture of one adrenal gland is planned 17th of August. PAI is a rare disease with a reported prevalence of about 100-140 cases per million in Western Societies. The most common cause of PAI is auto-immunity (up to 90% in Western countries). Adrenal TB is a relatively infrequent cause of PAI in developed countries, whereas in developing countries, TB remains a major cause of PAI. However, recent increases in human migration have contributed to increased rates of TB in Western Societies. The differential diagnosis of PAI in our patient includes isolated adrenal TB or other causes of bilateral enlargement of adrenal glands such as primary or secondary neoplastic disease, and infectious diseases (other than TB). In these cases further assessment with adrenal puncture is preferred to provide microbiological examination and histopathology warranting probable long-term tuberculostatic with possible side effects.</description><identifier>ISSN: 1784-3286</identifier><identifier>EISSN: 2295-3337</identifier><language>eng</language><publisher>Ghent: Taylor & Francis Ltd</publisher><subject>Adrenal glands ; Skin ; Tuberculosis</subject><ispartof>Acta clinica belgica (English ed. Online), 2016-05, Vol.71 (S3), p.7</ispartof><rights>Copyright Taylor & Francis Ltd. 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Wierckx, K</creatorcontrib><creatorcontrib>Vandecasteele, S J</creatorcontrib><creatorcontrib>Van den Bruel, A</creatorcontrib><title>Primary Adrenal Insufficiency: a diagnostic challenge</title><title>Acta clinica belgica (English ed. Online)</title><description>We present a case of a 42-year-old man who was referred to the Department of Endocrinology because of muscle soreness and increased skin pigmentation with suspicion of adrenal insufficiency. No other complaints were present. The patient had a history of arterial hypertension, at the moment well-controlled despite of stopping antihypertensive medication and gastroesophageal reflux disease with daily use of a proton pump inhibitor (Esomeprazole 20 mg). There was no relevant family history apart from tuberculosis (TB) of his mother. He denied travel to the tropics or drug use. Physical examination showed a normal blood pressure, increased pulse rate and a marked hyperpigmentation of the skin and mucosa. Laboratory findings showed low morning cortisol of 2 pig/dl (6.2-18 (pg/dL), low DHEAS of 67 pg (88.9-427 pg), high renine of 15187 plU/ml (2.8-39.9 plU/ml) and high ACTH level of > 1250 pg/l (< 46 ng/L). Short corticotrophin test did not evoke a marked increase in serum cortisol. The diagnosis of primary adrenal insufficiency (PAI) was made and the patient was started on hydrocortisone and fludrocortisone therapy. Assessment for anti-adrenal antibodies and catecholamine secretion were negative. 17-OH progesterone levels and very long chain fatty acids were normal. A computed tomography (CT) scan of the abdomen demonstrated bilateral adrenal enlargement with one nodule in each adrenal gland (right: nodule with maximum diameter 44 mm, Hounsfield Units (HU): 40; left: maximum diameter 14 mm, HU: 37). Further assessment with whole-body fluorine-18 fluorodeoxyglucose positron emission tomography-CT (FDG PET-CT) examination showed increased FDG uptake at both adrenals (more pronounced in the right adrenal gland) as well as an increased uptake at some axillary lymph nodes. A tuberculin skin test showed to be positive and may reflect co-existence of TB carriage or TB of the adrenal glands. Due to absence of extra-adrenal TB, further work-up with ultrasonic guided puncture of one adrenal gland is planned 17th of August. PAI is a rare disease with a reported prevalence of about 100-140 cases per million in Western Societies. The most common cause of PAI is auto-immunity (up to 90% in Western countries). Adrenal TB is a relatively infrequent cause of PAI in developed countries, whereas in developing countries, TB remains a major cause of PAI. However, recent increases in human migration have contributed to increased rates of TB in Western Societies. The differential diagnosis of PAI in our patient includes isolated adrenal TB or other causes of bilateral enlargement of adrenal glands such as primary or secondary neoplastic disease, and infectious diseases (other than TB). In these cases further assessment with adrenal puncture is preferred to provide microbiological examination and histopathology warranting probable long-term tuberculostatic with possible side effects.</description><subject>Adrenal glands</subject><subject>Skin</subject><subject>Tuberculosis</subject><issn>1784-3286</issn><issn>2295-3337</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNjLEKwjAUAIMoWLT_EHAu2Ly0Td1EFN0c3EtIk5oSU81rhv69HfwAb7nluAVJGKuLDACqJUnySvAMmCjXJEXs9zNQ8xJYQop7sC8ZJnpsg_bS0ZvHaIxVVns1HaikrZWdH3C0iqqndE77Tm_JykiHOv15Q3aX8-N0zd5h-ESNY9MPMcw7bHJRCAa5YBz-q77pXDbi</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Wierckx, K</creator><creator>Vandecasteele, S J</creator><creator>Van den Bruel, A</creator><general>Taylor & Francis Ltd</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>20160501</creationdate><title>Primary Adrenal Insufficiency: a diagnostic challenge</title><author>Wierckx, K ; Vandecasteele, S J ; Van den Bruel, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_18582318243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adrenal glands</topic><topic>Skin</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wierckx, K</creatorcontrib><creatorcontrib>Vandecasteele, S J</creatorcontrib><creatorcontrib>Van den Bruel, A</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Acta clinica belgica (English ed. Online)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wierckx, K</au><au>Vandecasteele, S J</au><au>Van den Bruel, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary Adrenal Insufficiency: a diagnostic challenge</atitle><jtitle>Acta clinica belgica (English ed. Online)</jtitle><date>2016-05-01</date><risdate>2016</risdate><volume>71</volume><issue>S3</issue><spage>7</spage><pages>7-</pages><issn>1784-3286</issn><eissn>2295-3337</eissn><abstract>We present a case of a 42-year-old man who was referred to the Department of Endocrinology because of muscle soreness and increased skin pigmentation with suspicion of adrenal insufficiency. No other complaints were present. The patient had a history of arterial hypertension, at the moment well-controlled despite of stopping antihypertensive medication and gastroesophageal reflux disease with daily use of a proton pump inhibitor (Esomeprazole 20 mg). There was no relevant family history apart from tuberculosis (TB) of his mother. He denied travel to the tropics or drug use. Physical examination showed a normal blood pressure, increased pulse rate and a marked hyperpigmentation of the skin and mucosa. Laboratory findings showed low morning cortisol of 2 pig/dl (6.2-18 (pg/dL), low DHEAS of 67 pg (88.9-427 pg), high renine of 15187 plU/ml (2.8-39.9 plU/ml) and high ACTH level of > 1250 pg/l (< 46 ng/L). Short corticotrophin test did not evoke a marked increase in serum cortisol. The diagnosis of primary adrenal insufficiency (PAI) was made and the patient was started on hydrocortisone and fludrocortisone therapy. Assessment for anti-adrenal antibodies and catecholamine secretion were negative. 17-OH progesterone levels and very long chain fatty acids were normal. A computed tomography (CT) scan of the abdomen demonstrated bilateral adrenal enlargement with one nodule in each adrenal gland (right: nodule with maximum diameter 44 mm, Hounsfield Units (HU): 40; left: maximum diameter 14 mm, HU: 37). Further assessment with whole-body fluorine-18 fluorodeoxyglucose positron emission tomography-CT (FDG PET-CT) examination showed increased FDG uptake at both adrenals (more pronounced in the right adrenal gland) as well as an increased uptake at some axillary lymph nodes. A tuberculin skin test showed to be positive and may reflect co-existence of TB carriage or TB of the adrenal glands. Due to absence of extra-adrenal TB, further work-up with ultrasonic guided puncture of one adrenal gland is planned 17th of August. PAI is a rare disease with a reported prevalence of about 100-140 cases per million in Western Societies. The most common cause of PAI is auto-immunity (up to 90% in Western countries). Adrenal TB is a relatively infrequent cause of PAI in developed countries, whereas in developing countries, TB remains a major cause of PAI. However, recent increases in human migration have contributed to increased rates of TB in Western Societies. The differential diagnosis of PAI in our patient includes isolated adrenal TB or other causes of bilateral enlargement of adrenal glands such as primary or secondary neoplastic disease, and infectious diseases (other than TB). In these cases further assessment with adrenal puncture is preferred to provide microbiological examination and histopathology warranting probable long-term tuberculostatic with possible side effects.</abstract><cop>Ghent</cop><pub>Taylor & Francis Ltd</pub></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1784-3286 |
ispartof | Acta clinica belgica (English ed. Online), 2016-05, Vol.71 (S3), p.7 |
issn | 1784-3286 2295-3337 |
language | eng |
recordid | cdi_proquest_journals_1858231824 |
source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list) |
subjects | Adrenal glands Skin Tuberculosis |
title | Primary Adrenal Insufficiency: a diagnostic challenge |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T01%3A15%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Primary%20Adrenal%20Insufficiency:%20a%20diagnostic%20challenge&rft.jtitle=Acta%20clinica%20belgica%20(English%20ed.%20Online)&rft.au=Wierckx,%20K&rft.date=2016-05-01&rft.volume=71&rft.issue=S3&rft.spage=7&rft.pages=7-&rft.issn=1784-3286&rft.eissn=2295-3337&rft_id=info:doi/&rft_dat=%3Cproquest%3E4301045811%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_journals_18582318243%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1858231824&rft_id=info:pmid/&rfr_iscdi=true |