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Endocrinology-metabolism
Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2)
Ji-young Lee, Su Yeon Kim, Kwan Hoon Jo, Eun Yeong Mo, Eun Sook Kim, Hye Soo Kim, Je Ho Han, Sung-dae Moon
Korean J Intern Med. 2022;37(2):398-410. Published online December 15, 2021
Background/Aims: Germline mutations of the rearranged during transfection (RET) gene cause multiple endocrine neoplasia type 2 (MEN2). About 85% of RET mutations in MEN2 occur in codon Cys634. The RET D631Y mutation has recently been discovered, and we have studied its molecular expres..
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Cardiology
Clinical profiles of patients with surgically resected pheochromocytoma and paraganglioma
Sun Hwa Lee, Jae-Hyeong Park, Ja-Yeon Lee, Sang-Rok Lee, Kyoung-Suk Rhee, Jei-Keon Chae, Won-Ho Kim, Ji-Young Sul, Jin Kyung Oh, Hee-Jin Kwon, Jae-Hwan Lee, In-Whan Seong
Korean J Intern Med. 2020;35(2):351-359. Published online February 28, 2019
Background/Aims: Pheochromocytoma and paraganglioma (PPGL) are catecholamine-producing tumors that can cause blood pressure (BP) elevation and cardiovascular complications. Clinical presentation of these tumors may be changed through widespread use of imaging studies, which enables detection of PPG..
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A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma
Yoorim Seo, Yeonjeong Jeong, Dong Yoon Kim, Kyueun Choi, Eun Sook Kim, Sung Dae Moon, Je Ho Han
Korean J Intern Med. 2018;33(1):214-217. Published online November 29, 2017
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Endocrinology-metabolism
Clinical characteristics and follow-up of Korean patients with adrenal incidentalomas
Yoon Young Cho, Sunghwan Suh, Ji Young Joung, Hyemin Jeong, Dongmo Je, Hongseok Yoo, Taek Kyu Park, Yong-Ki Min, Kwang-Won Kim, Jae Hyeon Kim
Korean J Intern Med. 2013;28(5):557-564. Published online August 14, 2013
Background/AimsWe investigated the clinical characteristics and follow-up findings of subjects with adrenal incidentalomas in a single, tertiary-care hospital in South Korea. MethodsThe study consisted of a retrospective analysis of 282 adrenal ..
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A Case of a Composite Adrenal Medullary Tumor of Pheochromocytoma and Ganglioneuroma Masquerading as Acute Pancreatitis
Eun-Kyoung Choi, Wan-Ho Kim, Keun-Yong Park
Korean J Intern Med. 2006;21(2):141-145. Published online June 30, 2006
Composite adrenal medullary tumors, composed of both pheochromocytoma and ganglioneuroma, are extremely rare, as are pheochromocytomas masquerading as acute relapsing pancreatitis. We recently experienced a case of a 48-year-old male with both these phenomena. The patient complained of an acute o..
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