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. © 2008International Association for the Study of Lung Cancer.
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Cho, S., Ra, Y. J., Lee, C. T., Chung, J. H., Sung, S. W., & Jheon, S. (2008). Difficulties in diagnosis and management of ectopic cushing syndrome. Journal of Thoracic Oncology, 3(4), 444–446. https://doi.org/10.1097/JTO.0b013e318169e316
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