Addison's disease and ACTH-producing pituitary microadenoma

A 28-year-old man diagnosed with primary adrenal insufficiency (Addison's disease) in 2002. Following diagnosis, replacement therapy with hydrocortisone and fludrocortisone was indicated. Hydrocortisone replacement therapy was unsuccessful, and increased ACTH levels as high as 996 pg/dl were ob...

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Main Authors: S.S. Ortega, Y.H. Aguiar, P.P. Marrero, S.M. Casas
Format: Article
Language:English
Published: Permanyer 2015-10-01
Series:Revista Médica del Hospital General de México
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0185106315000529
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spelling doaj-486995968b4d4bc1b84384b32b083f6e2020-11-25T03:21:25ZengPermanyerRevista Médica del Hospital General de México0185-10632015-10-0178417717910.1016/j.hgmx.2015.08.007Addison's disease and ACTH-producing pituitary microadenomaS.S. OrtegaY.H. AguiarP.P. MarreroS.M. CasasA 28-year-old man diagnosed with primary adrenal insufficiency (Addison's disease) in 2002. Following diagnosis, replacement therapy with hydrocortisone and fludrocortisone was indicated. Hydrocortisone replacement therapy was unsuccessful, and increased ACTH levels as high as 996 pg/dl were observed on outpatient follow-up. A pituitary MRI revealed a pituitary microadenoma. These findings raised three possibilities: (1) treatment is insufficient; (2) there is no relationship between Addison's disease and pituitary microadenoma; and (3) the microadenoma is similar to Nelson's syndrome. This latter is the most satisfactory explanation of this patient's clinical picture.http://www.sciencedirect.com/science/article/pii/S0185106315000529Nelson's syndromeACTHAddison's diseaseAutoimmune adrenalitis
collection DOAJ
language English
format Article
sources DOAJ
author S.S. Ortega
Y.H. Aguiar
P.P. Marrero
S.M. Casas
spellingShingle S.S. Ortega
Y.H. Aguiar
P.P. Marrero
S.M. Casas
Addison's disease and ACTH-producing pituitary microadenoma
Revista Médica del Hospital General de México
Nelson's syndrome
ACTH
Addison's disease
Autoimmune adrenalitis
author_facet S.S. Ortega
Y.H. Aguiar
P.P. Marrero
S.M. Casas
author_sort S.S. Ortega
title Addison's disease and ACTH-producing pituitary microadenoma
title_short Addison's disease and ACTH-producing pituitary microadenoma
title_full Addison's disease and ACTH-producing pituitary microadenoma
title_fullStr Addison's disease and ACTH-producing pituitary microadenoma
title_full_unstemmed Addison's disease and ACTH-producing pituitary microadenoma
title_sort addison's disease and acth-producing pituitary microadenoma
publisher Permanyer
series Revista Médica del Hospital General de México
issn 0185-1063
publishDate 2015-10-01
description A 28-year-old man diagnosed with primary adrenal insufficiency (Addison's disease) in 2002. Following diagnosis, replacement therapy with hydrocortisone and fludrocortisone was indicated. Hydrocortisone replacement therapy was unsuccessful, and increased ACTH levels as high as 996 pg/dl were observed on outpatient follow-up. A pituitary MRI revealed a pituitary microadenoma. These findings raised three possibilities: (1) treatment is insufficient; (2) there is no relationship between Addison's disease and pituitary microadenoma; and (3) the microadenoma is similar to Nelson's syndrome. This latter is the most satisfactory explanation of this patient's clinical picture.
topic Nelson's syndrome
ACTH
Addison's disease
Autoimmune adrenalitis
url http://www.sciencedirect.com/science/article/pii/S0185106315000529
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