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A Brief Overview of the Epidemiology of Pheochromocytoma and Paraganglioma in Korea

Choi YM

No abstract available.
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Malignant Gastric Paraganglioma with Liver Metastasis: Imaging Findings and Literature Review

Kim YR, Lee YH, Yun KJ

Paraganglioma is a neuroendocrine tumor that grows in organs other than the adrenal gland and typically originates in the chromaffin cells, which are distributed along the regions of the sympathetic...
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A Case of Concurrent Ampullary Adenoma and Gangliocytic Paraganglioma at the Minor Papilla Treated with Endoscopic Resection

Ko JK, Park DH, Hwang HS

A gangliocytic paraganglioma is a benign tumor of the digestive system with a very low incidence. The tumor is histopathologically characterized by a triphasic pattern consisting of epithelioid, ganglion, and...
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A Incidentally Diagnosed Duodenal Subepithelial Mass: Gangliocytic Paraganglioma Treated by Endoscopic Mucosal Resection

Yeo GE, Kwon HJ, Kim JH, Chang HK, Park JG

Gangliocytic paraganglioma is a very rare tumor that is usually located in the duodenum. It is characterized by benign behavior and favorable outcomes; however, it sometimes shows regional lymph node...
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Vagal Paraganglioma: Surgical Removal with Superior Laryngeal Nerve Preservation

Kotsis T, Christoforou P

Vagal paragangliomas (VPGLs) represent 70% of humans, providing motor fibers to the larynx. The patient recovered uneventfully and was discharged on the 3rd postoperative day. These tumors are therapeutically challenging...
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Eruption of Metastatic Paraganglioma After Successful Therapy with ¹⁷⁷Lu/⁹⁰Y-DOTATOC and ¹⁷⁷Lu-DOTATATE

Wolf KI, Jha A, van Berkel A, Wild D, Janssen I, Millo CM, Janssen M, Gonzales M, Timmers HJ, Pacak K

Metastatic paraganglioma treatment options are limited. Peptide receptor radionuclide therapy (PRRT) has been introduced as a novel management option for metastatic neuroendocrine tumors demonstrating safety, efficacy, and increased quality of...
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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...
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Carotid Artery Occlusion Caused by Invasion of Paraganglioma

Noh SM, Kang HG

No abstract available.
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Trauma-Induced Retroperitoneal Paraganglioma Rupture Which Was Misunderstood as a Massive Retroperitoneal Hemorrhage

Shim H, Jang JY, Kim YJ, Lim JS, Bae KS

No abstract available.
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Incidental Mesenteric Paraganglioma: A Case Report and Literature Review

Granger J, Mahapatra , Hamid B, Gillespie , Fok M, Vimalachandran D

Mesenteric paragangliomas are a rare entity; consequently, only 12 cases have been reported to date. Although considered benign and often found incidentally, they have the potential to metastasize and are...
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Malignant Paraganglioma in the Common Hepatic Duct

Lee HS, Jeong CU, Lee ES, Kwon YJ, Kim YS, Kim JD, Lee YJ

Paragangliomas are rare extra-adrenal neoplasms of neural crest origin. The neoplasms may develop at various sites, but most are located in the para-aortic space along the sympathetic chain. A paraganglioma...
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Perioperative anesthetic management of a patient with catecholamine-secreting paraganglioma: A case report

Park SL, Rhyu CJ, Kim KI, Chon SW, Kim TW, Koh JW

Paraganglioma is an uncommon neuroendocrine tumor of cells that originate in the autonomic nervous system. Some paragangliomas have the ability to secrete catecholamines, similar to secretions in pheochromocytoma. For this...
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Extra-Adrenal Malignant Paragangliomas Presenting as Mesenteric and Pararectal Masses: A Case Report

Lee S, Lee J, Kim BH, Kim KA, Park CM

Extra-adrenal paraganglioma is a rare tumor arising from the neural crest cells. Most tumors that develop in the abdomen arise from paraganglia along the paravertebral and para-aortic areas, in particular...
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Update on Modern Management of Pheochromocytoma and Paraganglioma

Lenders JW, Eisenhofer G

Despite all technical progress in modern diagnostic methods and treatment modalities of pheochromocytoma/paraganglioma, early consideration of the presence of these tumors remains the pivotal link towards the best possible outcome...
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Right Atrial Paraganglioma: An Extremely Rare Primary Cardiac Neoplasm Mimicking Myxoma

Garg A, Mishra D, Bansal M, Maharia HR, Goyal V

In this report, we present a case of 35-year-old lady who had presented with atypical chest pain and exertional breathlessness for past six months. Transthoracic and transesophageal echocardiograms showed a...
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Imaging Findings of a Primary Paraganglioma of the Liver: A Case Report

Ji SW, Kang UR, Park JB

Primary hepatic paraganglioma is an extremely rare type of tumor originating from extra-adrenal chromaffin cells. We report a case of primary intrahepatic paraganglioma in a 52-year-old man, with pathologic confirmation...
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Simultaneous Manifestation of Gangliocytic Paraganglioma and Heterotopic Pancreas of Ampulla of Vater Treated by Endoscopic Resection

Kang GE, Kim H, Lee JK, Kim DH, Jeong BN, Jang JH, Yeo SM, Sohn KR

Gangliocytic paraganglioma is an uncommon tumor of digestive system that is usually found in the second portion of duodenum. It is generally considered benign tumor, although few reports of local...
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A Gangliocytic Paraganglioma of the Ampulla of Vater Removed by Endoscopic Resection

Jung JH, Yoo BM, Um YJ, Cho H, Ahn YH, Yang MJ, Hwang JC, Kim JH

Gangliocytic paraganglioma (GP) is an extremely rare tumor that mostly occurs in the periampullary area of the duodenum. It is characterized by benign behavior and favorable outcomes, but sometimes shows...
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Paraganglioma Presenting as Dilated Cardiomyopathy with Cardiogenic Shock and Sepsis

Lee CW, Hong SP, Lee JH, Kim JW, Lee HC, Kwon HH

Rarely, a paraganglioma can lead to disastrous cardiac complications such as heart failure, cardiomyopathy, or myocardial infarction and inflammatory complications such as sepsis. We describe a 41-year-old man who developed...
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A Rare Case of Thymic Gangliocytic Paraganglioma

Yang JW, Han J, Lee HW, Cho SY, Kim HK

No abstract available.
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