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Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature

Background: Cyclic Cushing's disease (CD) has been described in about 15% of adult patients with CD. In the pediatric population, diagnosis of CD is rare and cyclic presentations of the disease are not adequately understood or described. Moreover, prepubertal patients usually do not present wit...

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Autores principales: Wȩdrychowicz, Anna, Hull, Barbara, Kalicka-Kasperczyk, Anna, Zieliński, Grzegorz, Starzyk, Jerzy B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813230/
https://www.ncbi.nlm.nih.gov/pubmed/31681172
http://dx.doi.org/10.3389/fendo.2019.00701
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author Wȩdrychowicz, Anna
Hull, Barbara
Kalicka-Kasperczyk, Anna
Zieliński, Grzegorz
Starzyk, Jerzy B.
author_facet Wȩdrychowicz, Anna
Hull, Barbara
Kalicka-Kasperczyk, Anna
Zieliński, Grzegorz
Starzyk, Jerzy B.
author_sort Wȩdrychowicz, Anna
collection PubMed
description Background: Cyclic Cushing's disease (CD) has been described in about 15% of adult patients with CD. In the pediatric population, diagnosis of CD is rare and cyclic presentations of the disease are not adequately understood or described. Moreover, prepubertal patients usually do not present with the typical signs and symptoms of CD, which can obscure or delay diagnosis. In this paper, we report a case of cyclic CD in a prepubertal age girls whose etiology was a pituitary corticotropinoma. Case presentation: A Caucasian 7.8 year old girl was admitted to pediatric endocrinology for the evaluation of short stature and prior obesity. The patient remained overweight despite significant lifestyle modifications, resulting in 6 kg weight loss during the prior 6 months. The physical exam was notable for precocious adrenarche and thelarche, but difficult to differentiate from steatomastia. Hypothalamo-pituitary-adrenal axis diagnostics, including single diurnal excretion of urinary cortisol, morning ACTH, and serum cortisol levels, were all within normal limits, and MRI of the pituitary gland showed no deviations at this time. Because of the clinical suspicion of cyclic hypercortisolemia, she was referred to our outpatient clinic for follow-up. After 6 months, the patient returned with rapid weight gain, accompanied by nocturnal anxiety, exacerbation of depressive behavior, insomnia and excessive sweating, and was readmitted to the ward for testing. Standard diagnostics confirmed CD and repeat MRI at 8.6 years old showed a microadenoma of 3 × 4 mm in the right side of the anterior pituitary gland. Histopathologic examination described an atypical, densely-granulated pituitary corticotroph adenoma with Ki-67 expression above 3%. Conclusion: Cyclic presentations of CD in the prepubescent age group could cause difficulties in diagnosis because of atypical signs and symptoms, which can be absent in the remission phase. Decreases in height percentiles and velocities obtained from the growth chart, as well as fluctuations in weight, and signs of androgenization can allow the clinician to suspect cycling CD in prepubertal patients. Confirmation of cyclic CD diagnosis is only possible during periods of relapse (hypercortisolemic state) and should be investigated according to the current diagnostic standard.
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spelling pubmed-68132302019-11-01 Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature Wȩdrychowicz, Anna Hull, Barbara Kalicka-Kasperczyk, Anna Zieliński, Grzegorz Starzyk, Jerzy B. Front Endocrinol (Lausanne) Endocrinology Background: Cyclic Cushing's disease (CD) has been described in about 15% of adult patients with CD. In the pediatric population, diagnosis of CD is rare and cyclic presentations of the disease are not adequately understood or described. Moreover, prepubertal patients usually do not present with the typical signs and symptoms of CD, which can obscure or delay diagnosis. In this paper, we report a case of cyclic CD in a prepubertal age girls whose etiology was a pituitary corticotropinoma. Case presentation: A Caucasian 7.8 year old girl was admitted to pediatric endocrinology for the evaluation of short stature and prior obesity. The patient remained overweight despite significant lifestyle modifications, resulting in 6 kg weight loss during the prior 6 months. The physical exam was notable for precocious adrenarche and thelarche, but difficult to differentiate from steatomastia. Hypothalamo-pituitary-adrenal axis diagnostics, including single diurnal excretion of urinary cortisol, morning ACTH, and serum cortisol levels, were all within normal limits, and MRI of the pituitary gland showed no deviations at this time. Because of the clinical suspicion of cyclic hypercortisolemia, she was referred to our outpatient clinic for follow-up. After 6 months, the patient returned with rapid weight gain, accompanied by nocturnal anxiety, exacerbation of depressive behavior, insomnia and excessive sweating, and was readmitted to the ward for testing. Standard diagnostics confirmed CD and repeat MRI at 8.6 years old showed a microadenoma of 3 × 4 mm in the right side of the anterior pituitary gland. Histopathologic examination described an atypical, densely-granulated pituitary corticotroph adenoma with Ki-67 expression above 3%. Conclusion: Cyclic presentations of CD in the prepubescent age group could cause difficulties in diagnosis because of atypical signs and symptoms, which can be absent in the remission phase. Decreases in height percentiles and velocities obtained from the growth chart, as well as fluctuations in weight, and signs of androgenization can allow the clinician to suspect cycling CD in prepubertal patients. Confirmation of cyclic CD diagnosis is only possible during periods of relapse (hypercortisolemic state) and should be investigated according to the current diagnostic standard. Frontiers Media S.A. 2019-10-18 /pmc/articles/PMC6813230/ /pubmed/31681172 http://dx.doi.org/10.3389/fendo.2019.00701 Text en Copyright © 2019 Wȩdrychowicz, Hull, Kalicka-Kasperczyk, Zieliński and Starzyk. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Wȩdrychowicz, Anna
Hull, Barbara
Kalicka-Kasperczyk, Anna
Zieliński, Grzegorz
Starzyk, Jerzy B.
Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature
title Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature
title_full Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature
title_fullStr Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature
title_full_unstemmed Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature
title_short Cyclic Cushing's Disease in the Prepubertal Period—A Case Report and Review of Literature
title_sort cyclic cushing's disease in the prepubertal period—a case report and review of literature
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813230/
https://www.ncbi.nlm.nih.gov/pubmed/31681172
http://dx.doi.org/10.3389/fendo.2019.00701
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