An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing Syndrome

ABSTRACT: Objective: To describe a unique case of a 61-year-old patient presenting with ectopic Cushing syndrome as a paraneoplastic phenomenon due to adrenocorticotropic hormone (ACTH)-secreting bone metastasis of an olfactory neuroblastoma (ON).Methods: We report a detailed case, with clinical, bi...

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Main Authors: Katrien Clotman, MD, Marcel Twickler, MD, PhD, Eveline Dirinck, MD, PhD, Jan Van Den Brande, MD, Martin Lammens, MD, PhD, Ann Verhaegen, MD, Christophe De Block, MD, PhD, Luc Van Gaal, MD, PhD
Format: Article
Language:English
Published: Elsevier 2017-01-01
Series:AACE Clinical Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2376060520301930
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spelling doaj-563ee452f7304bed9b7b53b63b5192102021-04-30T07:23:54ZengElsevierAACE Clinical Case Reports2376-06052017-01-0133e278e283An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing SyndromeKatrien Clotman, MD0Marcel Twickler, MD, PhD1Eveline Dirinck, MD, PhD2Jan Van Den Brande, MD3Martin Lammens, MD, PhD4Ann Verhaegen, MD5Christophe De Block, MD, PhD6Luc Van Gaal, MD, PhD7From the 1Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, Edegem, Belgium.; Address correspondence to Dr. Katrien Clotman, Antwerp University Hospital, Wilrijkstraat 10, 2650 Edegem, Belgium.From the 1Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, Edegem, Belgium.From the 1Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, Edegem, Belgium.Department of Oncology, Antwerp University Hospital, Edegem, Belgium.Department of Pathology, Antwerp University Hospital, Edegem, Belgium.From the 1Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, Edegem, Belgium.From the 1Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, Edegem, Belgium.From the 1Department of Endocrinology, Diabetology and Metabolism, Antwerp University Hospital, Edegem, Belgium.ABSTRACT: Objective: To describe a unique case of a 61-year-old patient presenting with ectopic Cushing syndrome as a paraneoplastic phenomenon due to adrenocorticotropic hormone (ACTH)-secreting bone metastasis of an olfactory neuroblastoma (ON).Methods: We report a detailed case, with clinical, biochemical, and imaging findings and compare it with existing literature.Results: A patient with an ON, with subsequent 10-year stable disease after initial craniofacial surgery, presented with paraparesis due to progressively metastasized ON disease located in the thoracic spine. During palliative chemotherapy, severe hypokalemia and muscle weakness developed, being part of paraneoplastic Cushing syndrome. Examination showed that metastatic bone lesions were mostly responsible for the ectopic secretion of ACTH, with just a few ACTH-secreting tumor cells located in the primary tumor. She was treated with a combination of ketoconazole and metyrapone that controlled cortisol levels. However, low potassium levels persisted. Finally, she underwent a bilateral adrenal resection, after which most cushingoid symptoms disappeared. She died 1 month later.Conclusion: Our case shows a growing ON with several bone metastases, which is a rare clinical condition. Moreover, this is the first report that ON is associated with bone metastases that express excessive ACTH secretion (and suggesting dedifferentiation of the primary tumor during chemotherapy treatment). Ectopic Cushing syndrome (with ACTH secreted by ON bone metastasis) can present late in the clinical trajectory. Finally, a bilateral adrenalectomy was needed to correct the life-threatening hypokalemia as part of the ectopic Cushing syndrome.Abbreviations: ACTH adrenocorticotropic hormone; CRH corticotropin-releasing hormone; IPSS inferior petrosal sinus smapling; ON olfactory neuroblastomahttp://www.sciencedirect.com/science/article/pii/S2376060520301930
collection DOAJ
language English
format Article
sources DOAJ
author Katrien Clotman, MD
Marcel Twickler, MD, PhD
Eveline Dirinck, MD, PhD
Jan Van Den Brande, MD
Martin Lammens, MD, PhD
Ann Verhaegen, MD
Christophe De Block, MD, PhD
Luc Van Gaal, MD, PhD
spellingShingle Katrien Clotman, MD
Marcel Twickler, MD, PhD
Eveline Dirinck, MD, PhD
Jan Van Den Brande, MD
Martin Lammens, MD, PhD
Ann Verhaegen, MD
Christophe De Block, MD, PhD
Luc Van Gaal, MD, PhD
An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing Syndrome
AACE Clinical Case Reports
author_facet Katrien Clotman, MD
Marcel Twickler, MD, PhD
Eveline Dirinck, MD, PhD
Jan Van Den Brande, MD
Martin Lammens, MD, PhD
Ann Verhaegen, MD
Christophe De Block, MD, PhD
Luc Van Gaal, MD, PhD
author_sort Katrien Clotman, MD
title An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing Syndrome
title_short An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing Syndrome
title_full An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing Syndrome
title_fullStr An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing Syndrome
title_full_unstemmed An Endocrine Picture In Disguise: A Progressive Olfactory Neuroblastoma Complicated With Ectopic Cushing Syndrome
title_sort endocrine picture in disguise: a progressive olfactory neuroblastoma complicated with ectopic cushing syndrome
publisher Elsevier
series AACE Clinical Case Reports
issn 2376-0605
publishDate 2017-01-01
description ABSTRACT: Objective: To describe a unique case of a 61-year-old patient presenting with ectopic Cushing syndrome as a paraneoplastic phenomenon due to adrenocorticotropic hormone (ACTH)-secreting bone metastasis of an olfactory neuroblastoma (ON).Methods: We report a detailed case, with clinical, biochemical, and imaging findings and compare it with existing literature.Results: A patient with an ON, with subsequent 10-year stable disease after initial craniofacial surgery, presented with paraparesis due to progressively metastasized ON disease located in the thoracic spine. During palliative chemotherapy, severe hypokalemia and muscle weakness developed, being part of paraneoplastic Cushing syndrome. Examination showed that metastatic bone lesions were mostly responsible for the ectopic secretion of ACTH, with just a few ACTH-secreting tumor cells located in the primary tumor. She was treated with a combination of ketoconazole and metyrapone that controlled cortisol levels. However, low potassium levels persisted. Finally, she underwent a bilateral adrenal resection, after which most cushingoid symptoms disappeared. She died 1 month later.Conclusion: Our case shows a growing ON with several bone metastases, which is a rare clinical condition. Moreover, this is the first report that ON is associated with bone metastases that express excessive ACTH secretion (and suggesting dedifferentiation of the primary tumor during chemotherapy treatment). Ectopic Cushing syndrome (with ACTH secreted by ON bone metastasis) can present late in the clinical trajectory. Finally, a bilateral adrenalectomy was needed to correct the life-threatening hypokalemia as part of the ectopic Cushing syndrome.Abbreviations: ACTH adrenocorticotropic hormone; CRH corticotropin-releasing hormone; IPSS inferior petrosal sinus smapling; ON olfactory neuroblastoma
url http://www.sciencedirect.com/science/article/pii/S2376060520301930
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