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논문 기본 정보

자료유형
학술저널
저자정보
Jeong, Chaiho (Department of Internal Medicine, College of Medicine, The Catholic University of Korea) Lee, Jinhee (Department of Internal Medicine, College of Medicine, The Catholic University of Korea) Ryu, Seongyul (Department of Internal Medicine, College of Medicine, The Catholic University of Korea) Lee, Hwa Young (Department of Internal Medicine, College of Medicine, The Catholic University of Korea) Shin, Ah Young (Department of Internal Medicine, College of Medicine, The Catholic University of Korea) Kim, Ju Sang (Department of Internal Medicine, College of Medicine, The Catholic University of Korea) Ahn, Joong Hyun (Department of Internal Medicine, College of Medicine, The Catholic University of Korea) Kang, Hye Seon (Department of Internal Medicine, College of Medicine, The Catholic University of Korea)
저널정보
대한결핵 및 호흡기학회 Tuberculosis and Respiratory Diseases 결핵 및 호흡기 질환 제78권 제4호
발행연도
2015.1
수록면
436 - 439 (4page)

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Small cell lung cancer (SCLC), which originated from neuroendocrine tissue, can develop into paraneoplastic endocrine syndromes, such as Cushing syndrome, because of an inappropriate secretion of ectopic adrenocorticotropic hormone (ACTH). This paraneoplastic syndrome is known to be a poor prognostic factor in SCLC. The reason for poor survival may be because of a higher risk of infection associated with hypercortisolemia. Therefore, early detection and appropriate treatment for this syndrome is necessary. But the diagnosis is challenging and the source of ACTH production can be difficult to identify. We report a 69-year-old male patient who had severe hypokalemia, metabolic alkalosis, and hypertension as manifestations of an ACTH-secreting small cell carcinoma of the lung. He was treated with ketoconazole and spironolactone to control the ACTH dependent Cushing syndrome. He survived for 15 months after chemotherapy, which is unusual considering the poor outcome of the ectopic ATH syndrome associated with SCLC.

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