- Epidemiology and Prognosis of Pheochromocytoma/Paraganglioma in Korea: A Nationwide Study Based on the National Health Insurance Service
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Kim JH, Moon H, Noh J, Lee J, Kim SG
- KMID: 2471732
- Endocrinol Metab.
- 2020 Mar;35(1):157-164.
- doi: 10.3803/EnM.2020.35.1.157
BACKGROUND: Pheochromocytomas and paragangliomas (PPGLs) are rare endocrine tumors originating from chromaffin cells. PPGLs are associated with a high mortality rate and several complications. To date, no epidemiological studies have... -
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- A Brief Overview of the Epidemiology of Pheochromocytoma and Paraganglioma in Korea
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Choi YM
- KMID: 2471724
- Endocrinol Metab.
- 2020 Mar;35(1):95-96.
- doi: 10.3803/EnM.2020.35.1.95
No abstract available. -
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- Incidence of Acute Kidney Injury after Adrenalectomy in Patients with Primary Aldosteronism
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Lee JY, Kim H, Kim HW, Ryu GW, Nam Y, Lee S, Joo YS, Lee S, Park JT, Han SH, Kang SW, Yoo TH, Yun HR
- KMID: 2467960
- Electrolyte Blood Press.
- 2019 Dec;17(2):45-53.
- doi: 10.5049/EBP.2019.17.2.45
BACKGROUND: Aldosterone-induced glomerular hyperfiltration can lead to masked preoperative renal dysfunction in primary aldosteronism(PA) patients. We evaluated whether PA patients had a higher prevalence of acute kidney injury (AKI) after... -
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- Catastrophic catecholamine-induced cardiomyopathy rescued by extracorporeal membrane oxygenation in recurrent malignant pheochromocytoma
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Min D
- KMID: 2460195
- Yeungnam Univ J Med.
- 2019 Sep;36(3):254-259.
- doi: 10.12701/yujm.2019.00213
Pheochromocytoma (PCC) is a rare catecholamine-producing tumor with the incidence in hypertension of 0.1-0.6%. PCC crisis is an endocrine emergency that can lead to hemodynamic disturbance and organ failure such... -
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- Pheochromocytoma with Hypertensive Crisis Caused by Endoscopic Ultrasound-guided Tissue Sampling
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Kim HH, Cho CM, Yeo SJ, Kwon HJ, Cho SH, Seo AN
- KMID: 2455077
- Korean J Pancreas Biliary Tract.
- 2019 Jul;24(3):127-132.
- doi: 10.15279/kpba.2019.24.3.127
Although pheochromocytoma usually presents as a solid tumor, it can also present as a cystic lesion in the adrenal glands. Cystic lesions in the adrenal glands, along with hypertension, need... -
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- Gallbladder Paraganglioma Associated with SDHD Mutation: a Potential Pitfall on ¹â¸F-FDOPA PET Imaging
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Sater ZA, Jha A, Mandl A, Mangelen S, Carrasquillo JA, Ling A, Gonzales M, Lopes Abath Neto O, Miettinen , Adams KT, Nockel P, El Lakis M, Pacak K
- KMID: 2448102
- Nucl Med Mol Imaging.
- 2019 Apr;53(2):144-147.
- doi: 10.1007/s13139-018-0558-1
A 36-year-old male patient initially presented with hypertension, tinnitus, bilateral carotid masses, a right jugular foramen, and a periaortic arch mass with an elevated plasma dopamine level but an otherwise... -
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- A novel RET mutation identified in a patient with pheochromocytoma and renal cell carcinoma
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Kwon JW, Jung ED, Jeon EJ, Park JK, Lee JK, Cho CH
- KMID: 2442558
- Kosin Med J.
- 2018 Dec;33(3):446-453.
- doi: 10.7180/kmj.2018.33.3.446
Pheochromocytomas might be sporadic or genetic. Genetic pheochromocytoma is associated with multiple endocrine neoplasia (MEN) type 2A, MEN type 2B, and von Hippel-Lindau (VHL) disease. RET mutations are identified in... -
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- Adrenal incidentaloma: a case of asymptomatic pheochromocytoma
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Park SY, Rim JC, Cho HC, Lee YC, Kim JA, Choi SR
- KMID: 2430737
- Kosin Med J.
- 2018 Dec;33(2):215-222.
- doi: 10.7180/kmj.2018.33.2.215
An incidentaloma is a tumor found incidentally without clinical symptoms or suspicion; the lesion may be adrenal, pituitary, or thyroidal. We report the case of an asymptomatic individual with preoperatively... -
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- Pheochromocytoma with Brain Metastasis: A Extremely Rare Case in Worldwide
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Cho YS, Ryu HJ, Kim SH, Kang SG
- KMID: 2423983
- Brain Tumor Res Treat.
- 2018 Oct;6(2):101-104.
- doi: 10.14791/btrt.2018.6.e18
Pheochromocytoma (PCC) is a neuroendocrine tumor that mainly arises from the medulla of the adrenal gland. Some PCCs become malignant and metastasize to other organs. For example, it typically involves... -
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- Current Consensus on I-131 MIBG Therapy
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Kayano D, Kinuya S
- KMID: 2418989
- Nucl Med Mol Imaging.
- 2018 Aug;52(4):254-265.
- doi: 10.1007/s13139-018-0523-z
Metaiodobenzylguanidine (MIBG) is structurally similar to the neurotransmitter norepinephrine and specifically targets neuroendocrine cells including some neuroendocrine tumors. Iodine-131 (I-131)-labeled MIBG (I-131 MIBG) therapy for neuroendocrine tumors has been performed... -
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- Extra-adrenal paraganglioma masquerading as severe preeclampsia
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Kim HJ, Yang SH, Yang SH, Han SS, Kim GJ
- KMID: 2439726
- Obstet Gynecol Sci.
- 2018 Jul;61(4):520-523.
- doi: 10.5468/ogs.2018.61.4.520
Paraganglioma in pregnancy is an extremely rare condition and its diagnosis is often delayed because the clinical symptoms can mimic those of preeclampsia or gestational hypertension. Here, we report the... -
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- Increased arterial stiffness causing resistant hypertension in an adolescent with Neurofibromatosis type 1
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Cho MJ
- KMID: 2415846
- Kosin Med J.
- 2018 Jun;33(1):105-109.
- doi: 10.7180/kmj.2018.33.1.105
Neurofibromatosis type 1 is an autosomal dominant genetic disorder characterized by the presence of café au lait spots, axillary and inguinal freckling, Lisch nodules, and neurofibromas. Hypertension is a relatively... -
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- Characteristics of Adrenal Incidentalomas in a Large, Prospective Computed Tomography-Based Multicenter Study: The COAR Study in Korea
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Ahn SH, Kim JH, Baek SH, Kim H, Cho YY, Suh S, Kim BJ, Hong S, Koh JM, Lee SH, Song KH
- KMID: 2410905
- Yonsei Med J.
- 2018 Jun;59(4):501-510.
- doi: 10.3349/ymj.2018.59.4.501
PURPOSE: Previous studies on adrenal incidentalomas (AIs) are limited by their retrospective design, small numbers of patients, Western populations, or use of an outdated imaging technique. We investigated the characteristics... -
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- Adrenal Hemangioma: a Rare Incidentaloma
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Singh A, Rege S, Surpam S
- KMID: 2414425
- J Endocr Surg.
- 2018 Mar;18(1):84-89.
- doi: 10.16956/jes.2018.18.1.84
Hemangioma of the adrenal gland is a rare benign tumor. The diagnosis is often postoperative on histopathological examination with the presence of blood filled, dilated vascular channels. Approximately 60 surgical... -
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- Bone Health in Adrenal Disorders
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Kim BJ, Lee SH, Koh JM
- KMID: 2407115
- Endocrinol Metab.
- 2018 Mar;33(1):1-8.
- doi: 10.3803/EnM.2018.33.1.1
Secondary osteoporosis resulting from specific clinical disorders may be potentially reversible, and thus continuous efforts to find and adequately treat the secondary causes of skeletal fragility are critical to ameliorate... -
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- A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma
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Seo Y, Jeong Y, Kim DY, Choi K, Kim ES, Moon SD, Han JH
- KMID: 2411527
- Korean J Intern Med.
- 2018 Jan;33(1):214-217.
- doi: 10.3904/kjim.2015.256
No abstract available. -
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- Pheochromocytoma-induced cardiogenic shock successfully treated by extracorporeal circulation
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Lee MY, Lee SB, Cha HS, You JH, Choi EY, Park JS
- KMID: 2400369
- Yeungnam Univ J Med.
- 2017 Dec;34(2):285-289.
- doi: 10.12701/yujm.2017.34.2.285
Pheochromocytoma can present with various symptoms including cardiogenic shock and cardiac arrest. Particularly, in cases of cardiogenic shock of unknown origin, pheochromocytoma should be considered. A 20-year-old woman without any... -
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- Huge pheochromocytoma presented with paraaortic lymph node and spine metastases
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Park YW, Moon HJ, Han JS, Han JM, Park JW, Ku YH
- KMID: 2400362
- Yeungnam Univ J Med.
- 2017 Dec;34(2):247-253.
- doi: 10.12701/yujm.2017.34.2.247
Approximately 10–15% of pheochromocytomas are malignant. There are insufficient histologic criteria for the diagnosis of malignant pheochromocytoma. Thus, the term malignant pheochromocytoma is restricted to tumors with local invasion or... -
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- Spontaneous ruptured pheochromocytoma: an unusual case report and literature review
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Jee YS
- KMID: 2398965
- Ann Surg Treat Res.
- 2017 Sep;93(3):170-172.
- doi: 10.4174/astr.2017.93.3.170
Ruptured pheochromocytoma is a rare disease. Its mortality rate is up to 31%–50%. Proper management of ruptured pheochromocytoma remains unclear. A 44-year-old male patient visited our Emergency Department and presented... -
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- Diabetes and Endocrine Disease
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Bae JC, Han JM
- KMID: 2390868
- J Korean Diabetes.
- 2017 Sep;18(3):155-159.
- doi: 10.4093/jkd.2017.18.3.155
Impaired insulin secretion and insulin resistance are the two main mechanisms leading to type 2 diabetes mellitus. Insulin exerts multiple effects upon target cells, especially skeletal muscle, liver, and adipose... -
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