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Difficulties in diagnosis and management of ectopic Cushing syndrome.

Abstract
A 18-year-old man presented to a local hospital with muscle weakness, facial edema, and a 6 kg weight gain over 2 months. After a complete work-up, he was diagnosed with pituitary Cushing syndrome and treated with a bilateral adrenalectomy for Cushing syndrome and pituitary radiotherapy for Nelson syndrome. Twenty-five years later, his ectopic source of adrenocorticotropic hormone was revealed as a pulmonary neuroendocrine tumor, and a pulmonary resection was performed. Subsequently, a biochemical and clinical remission including hyperpigmentation was achieved.
AuthorsSukki Cho, Yong Joon Ra, Choon-Taek Lee, Jin-Haeng Chung, Sook-Whan Sung, Sanghoon Jheon
JournalJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer (J Thorac Oncol) Vol. 3 Issue 4 Pg. 444-6 (Apr 2008) ISSN: 1556-1380 [Electronic] United States
PMID18379368 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Adrenocorticotropic Hormone
Topics
  • ACTH Syndrome, Ectopic (diagnosis, radiotherapy, surgery)
  • Adolescent
  • Adrenalectomy
  • Adrenocorticotropic Hormone (metabolism)
  • Cushing Syndrome (diagnosis, radiotherapy, surgery)
  • Humans
  • Lung Neoplasms (diagnosis, etiology, surgery)
  • Male
  • Nelson Syndrome (diagnosis, radiotherapy, surgery)
  • Neuroendocrine Tumors (diagnosis, etiology, surgery)
  • Positron-Emission Tomography

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