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Literature DB >> 9735133

Benign and malignant pheochromocytoma: diagnosis, treatment, and follow-Up.

Abstract

The clinical manifestation of pheochromocytoma is presented with specific emphasis on accurate diagnostic approach. The sensitivity, specificity, and indication of localizing studies of pheochromocytomas are reviewed. Management of benign and malignant pheochromocytomas are discussed with follow-up recommendations.

Entities: Disease

Mesh：

Substances：
Catecholamines

Year: 1998 PMID： 9735133

Source DB: PubMed Journal: Surg Oncol Clin N Am ISSN： 1055-3207 Impact factor: 3.495

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Cited

9 in total

1. SAGES guidelines for minimally invasive treatment of adrenal pathology.

Authors: Dimitrios Stefanidis; Melanie Goldfarb; Kent W Kercher; William W Hope; William Richardson; Robert D Fanelli
Journal: Surg Endosc Date: 2013-09-10 Impact factor: 4.584

2. SDHB mutation status and tumor size but not tumor grade are important predictors of clinical outcome in pheochromocytoma and abdominal paraganglioma.

Authors: Yasmine Assadipour; Samira M Sadowski; Meghna Alimchandani; Martha Quezado; Seth M Steinberg; Naris Nilubol; Dhaval Patel; Tamara Prodanov; Karel Pacak; Electron Kebebew
Journal: Surgery Date: 2016-11-10 Impact factor: 3.982

3. MicroCT for high-resolution imaging of ectopic pheochromocytoma tumors in the liver of nude mice.

Authors: Shoichiro Ohta; Edwin W Lai; John C Morris; Douglas A Bakan; Brenda Klaunberg; Susannah Cleary; James F Powers; Arthur S Tischler; Mones Abu-Asab; Daniel Schimel; Karel Pacak
Journal: Int J Cancer Date: 2006-11-01 Impact factor: 7.396

Review 4. Pheochromocytoma.

Authors: M S Eigelberger; Q Y Duh
Journal: Curr Treat Options Oncol Date: 2001-08

Benign and malignant pheochromocytoma: diagnosis, treatment, and follow-Up.

1. SAGES guidelines for minimally invasive treatment of adrenal pathology.

2. SDHB mutation status and tumor size but not tumor grade are important predictors of clinical outcome in pheochromocytoma and abdominal paraganglioma.

3. MicroCT for high-resolution imaging of ectopic pheochromocytoma tumors in the liver of nude mice.

Review 4. Pheochromocytoma.

5. Prospective randomized comparison of laparoscopic versus open adrenalectomy for sporadic pheochromocytoma.

6. Influence of secretory phenotype and preoperative preparation on surgical outcome in pheochromocytoma.

Review 7. Laparoscopic surgery for malignant adrenal tumors.

8. Preliminary experience of the robot-assisted laparoscopic excision of a retroperitoneal mass: A case report.

9. A patient with bilateral pheochromocytoma as part of a Von Hippel-Lindau (VHL) syndrome type 2C.