Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

412 results
Display

Epidemiology and Prognosis of Pheochromocytoma/Paraganglioma in Korea: A Nationwide Study Based on the National Health Insurance Service

Kim JH, Moon H, Noh J, Lee J, Kim SG

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Brief Overview of the Epidemiology of Pheochromocytoma and Paraganglioma in Korea

Choi YM

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Incidence of Acute Kidney Injury after Adrenalectomy in Patients with Primary Aldosteronism

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

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Catastrophic catecholamine-induced cardiomyopathy rescued by extracorporeal membrane oxygenation in recurrent malignant pheochromocytoma

Min D

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pheochromocytoma with Hypertensive Crisis Caused by Endoscopic Ultrasound-guided Tissue Sampling

Kim HH, Cho CM, Yeo SJ, Kwon HJ, Cho SH, Seo AN

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Gallbladder Paraganglioma Associated with SDHD Mutation: a Potential Pitfall on ¹⁸F-FDOPA PET Imaging

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

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A novel RET mutation identified in a patient with pheochromocytoma and renal cell carcinoma

Kwon JW, Jung ED, Jeon EJ, Park JK, Lee JK, Cho CH

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Adrenal incidentaloma: a case of asymptomatic pheochromocytoma

Park SY, Rim JC, Cho HC, Lee YC, Kim JA, Choi SR

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pheochromocytoma with Brain Metastasis: A Extremely Rare Case in Worldwide

Cho YS, Ryu HJ, Kim SH, Kang SG

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Current Consensus on I-131 MIBG Therapy

Kayano D, Kinuya S

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Extra-adrenal paraganglioma masquerading as severe preeclampsia

Kim HJ, Yang SH, Yang SH, Han SS, Kim GJ

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Increased arterial stiffness causing resistant hypertension in an adolescent with Neurofibromatosis type 1

Cho MJ

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Characteristics of Adrenal Incidentalomas in a Large, Prospective Computed Tomography-Based Multicenter Study: The COAR Study in Korea

Ahn SH, Kim JH, Baek SH, Kim H, Cho YY, Suh S, Kim BJ, Hong S, Koh JM, Lee SH, Song KH

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Adrenal Hemangioma: a Rare Incidentaloma

Singh A, Rege S, Surpam S

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bone Health in Adrenal Disorders

Kim BJ, Lee SH, Koh JM

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A novel neurofibromatosis type 1 (NF1) mutation in a patient with NF1 and pheochromocytoma

Seo Y, Jeong Y, Kim DY, Choi K, Kim ES, Moon SD, Han JH

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pheochromocytoma-induced cardiogenic shock successfully treated by extracorporeal circulation

Lee MY, Lee SB, Cha HS, You JH, Choi EY, Park JS

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Huge pheochromocytoma presented with paraaortic lymph node and spine metastases

Park YW, Moon HJ, Han JS, Han JM, Park JW, Ku YH

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Spontaneous ruptured pheochromocytoma: an unusual case report and literature review

Jee YS

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Diabetes and Endocrine Disease

Bae JC, Han JM

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2023 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr