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논문 기본 정보

자료유형
학술저널
저자정보
Justin Byun (Yonsei University College of Medicine) Sung Hyun Kim (Yonsei University College of Medicine) Hyang Sook Jeong (Yonsei University College of Medicine) Yumie Rhee (Yonsei University College of Medicine) Woo Jung Lee (Yonsei University College of Medicine) Chang Moo Kang (Yonsei University College of Medicine)
저널정보
한국간담췌외과학회 Annals of Hepato-Biliary-Pancreatic Surgery 한국간담췌외과학회지 제21권 제1호
발행연도
2017.2
수록면
61 - 65 (5page)

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Tumors that arise from the endocrine pancreas, or the islets of pancreas, are called pancreatic neuroendocrine tumors (NETs). Pancreatic NET have an incidence of <0.1 per one million persons, and can lead to secretion of ectopic adrenocorticotropic hormone (ACTH). Herein, we presented a case of patient with Cushing’s syndrome as a result of ACTH-producing pancreatic NET, who underwent successful laparoscopic distal pancreatosplenectomy. A 40-year-old Korean female patient with ophthalmologic discomfort, osteoporosis, and unexplained hypokalemia was admitted to our hospital. Under the suspicion of ACTH producing pancreatic NET after the diagnostic workup, we decided to perform surgical resection. Laparoscopic distal pancreatosplenectomy was performed; and the pathological examination revealed a 1.5 cm-sized grade 2 neuroendocrine tumor of the pancreas, which was encapsulated within the pancreatic parenchyma. After the operation, the patient no longer displayed cushingoid features. ACTH-producing pancreatic NET is rare, but can be one of the causes of Cushing’s syndrome. Surgical resection is a feasible option in treating ACTH-producing pancreatic NET.

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UCI(KEPA) : I410-ECN-0101-2017-514-002133202