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Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease

Osteoporosis at a young age should prompt clinicians to search for secondary causes, namely endogenous Cushing’s syndrome.We report a case of a 33-year-old male with a history of spontaneous fracture of the 12th thoracic vertebra and florid features of Cushing’s syndrome. The physical exam evidenced...

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Autores principales: Correia, Sara, Ramalho, Diogo, Rocha, Gustavo, Oliveira, Maria J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586192/
https://www.ncbi.nlm.nih.gov/pubmed/36304359
http://dx.doi.org/10.7759/cureus.29401
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author Correia, Sara
Ramalho, Diogo
Rocha, Gustavo
Oliveira, Maria J
author_facet Correia, Sara
Ramalho, Diogo
Rocha, Gustavo
Oliveira, Maria J
author_sort Correia, Sara
collection PubMed
description Osteoporosis at a young age should prompt clinicians to search for secondary causes, namely endogenous Cushing’s syndrome.We report a case of a 33-year-old male with a history of spontaneous fracture of the 12th thoracic vertebra and florid features of Cushing’s syndrome. The physical exam evidenced moon face, facial plethora, muscle atrophy of the upper and lower limbs, and accumulation of abdominal fat. Bone mineral density revealed osteoporosis in the lumbar spine and in the femoral neck. Scintigraphy showed bone fractures in several costal arches, dorsal columns, and sternum. Hypercortisolism was confirmed by blood work. Serum cortisol, adrenocorticotropic hormone and corticotropin (ACTH), and 24-hour urine cortisol values were elevated. Imaging with MRI sellar region was normal and bilateral catheterization of inferior petrosal sinuses was positive. The patient underwent transsphenoidal pituitary surgery (TPS) and a lesion in the right side of the pituitary was identified and resected. Postoperatively, the patient did not meet the remission criteria and we decided to initiate treatment with ketoconazole alongside pituitary radiotherapy. After two years of surgery, the patient presented with recurrent bone fractures, height loss (25 cm), intense fatigue, and difficulty walking without assistance. Due to severe disease, we performed bilateral adrenalectomy, which was essential to control hypercortisolism and improve the patient's quality of life.
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spelling pubmed-95861922022-10-26 Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease Correia, Sara Ramalho, Diogo Rocha, Gustavo Oliveira, Maria J Cureus Endocrinology/Diabetes/Metabolism Osteoporosis at a young age should prompt clinicians to search for secondary causes, namely endogenous Cushing’s syndrome.We report a case of a 33-year-old male with a history of spontaneous fracture of the 12th thoracic vertebra and florid features of Cushing’s syndrome. The physical exam evidenced moon face, facial plethora, muscle atrophy of the upper and lower limbs, and accumulation of abdominal fat. Bone mineral density revealed osteoporosis in the lumbar spine and in the femoral neck. Scintigraphy showed bone fractures in several costal arches, dorsal columns, and sternum. Hypercortisolism was confirmed by blood work. Serum cortisol, adrenocorticotropic hormone and corticotropin (ACTH), and 24-hour urine cortisol values were elevated. Imaging with MRI sellar region was normal and bilateral catheterization of inferior petrosal sinuses was positive. The patient underwent transsphenoidal pituitary surgery (TPS) and a lesion in the right side of the pituitary was identified and resected. Postoperatively, the patient did not meet the remission criteria and we decided to initiate treatment with ketoconazole alongside pituitary radiotherapy. After two years of surgery, the patient presented with recurrent bone fractures, height loss (25 cm), intense fatigue, and difficulty walking without assistance. Due to severe disease, we performed bilateral adrenalectomy, which was essential to control hypercortisolism and improve the patient's quality of life. Cureus 2022-09-21 /pmc/articles/PMC9586192/ /pubmed/36304359 http://dx.doi.org/10.7759/cureus.29401 Text en Copyright © 2022, Correia et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Endocrinology/Diabetes/Metabolism
Correia, Sara
Ramalho, Diogo
Rocha, Gustavo
Oliveira, Maria J
Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease
title Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease
title_full Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease
title_fullStr Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease
title_full_unstemmed Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease
title_short Multiple Bone Fractures in a Patient With Difficult-to-Treat Cushing’s Disease
title_sort multiple bone fractures in a patient with difficult-to-treat cushing’s disease
topic Endocrinology/Diabetes/Metabolism
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586192/
https://www.ncbi.nlm.nih.gov/pubmed/36304359
http://dx.doi.org/10.7759/cureus.29401
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