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Number of results
2015 | 87 | 7 | 368-370

Article title

Multifocal Extra-Adrenal Paraganglioma – Case Report

Content

Title variants

Languages of publication

EN

Abstracts

EN
Paraganglioma is a rare neoplasm originating from extra-adrenal pheochromocytes of the sympathetic and parasympathetic nervous system. It is usually benign and the treatment method of choice is a complete resection of the tumour. The authors present a case of 66-year-old female patient with a multifocal benign retroperitoneal paraganglioma, which was completely removed during surgery.

Publisher

Year

Volume

87

Issue

7

Pages

368-370

Physical description

Dates

published
1 - 7 - 2015
received
10 - 5 - 2015
online
7 - 9 - 2015

Contributors

  • Department of General Surgery, Copernicus Medical Centre in GdańskKierownik: prof. dr hab.
  • Department of General Surgery, Copernicus Medical Centre in GdańskKierownik: prof. dr hab.
  • Department of General Surgery, Copernicus Medical Centre in GdańskKierownik: prof. dr hab.
  • Department of General Surgery, Copernicus Medical Centre in GdańskKierownik: prof. dr hab.
  • Department of General Surgery, Copernicus Medical Centre in GdańskKierownik: prof. dr hab.
author
  • Department of General Surgery, Copernicus Medical Centre in GdańskKierownik: prof. dr hab.

References

  • 1. Martucci VL, Pacak K: Pheochromocytoma and paraganglioma: Diagnosis, genetics, management, and treatment. Curr Probl Cancer 2014; 38(1): 7-41.
  • 2. Chen H, Sippel RS, O’Dorisio MS et al.: The NANETS Consensus Guideline for the Diagnosis and Management of Neuroendocrine Tumors: Pheochromocytoma, Paraganglioma and Medullary Thyroid Cancer. Pancreas 2010; 39(6): 775-83.
  • 3. Disick GI, Palese MA: Extra-adrenal Pheochromocytoma: Diagnosis and Management. Curr Urol Rep 2007; 8(1): 83-88.
  • 4. Lenders JW, Eisenhofer G, Mannelli M et al.: Phaeochromocytoma. Lancet 2005; 366(9486): 665-75.
  • 5. Guo Q, Li B, Guan J et al.: Intraoperative diagnosis of functional retroperitoneal multiple paraganglioma: A case report. Oncol Lett 2012; 4(4): 829-31.
  • 6. Jafri M, Maher ER : The genetics of phaeochromocytoma: using clinical features to guide genetic testing. Eur J Endocrinol 2012; 166(2): 151-58.
  • 7. Young WF Jr: Paragangliomas: clinical overview. Ann N Y Acad Sci 2006; 1073: 21-29.
  • 8. Sahdev A, Sohaib A, Monson JP et al.: CT and MR imaging of unusual locations of extra-adrenal paragangliomas (pheochromocytomas). Eur Radiol 2005; 15(1): 85-92.
  • 9. Van Slycke S, Caiazzo R, Pigny P et al.: Local-regional recurrence of sporadic or syndromic abdominal extra-adrenal paraganglioma: Incidence, characteristics, and outcome. Surgery 2009; 146(6): 986-92.
  • 10. Yadav S, Singh SK, Sharma SK et al.: Extra-adrenal pheochromocytoma: A cause of ureteral obstruction. J Urol 2000; 163(1): 264.
  • 11. Blecha M, Galanopolous C, Dharkar D et al.: Massive organ of Zuckerkandl inducing small bowel obstruction. J Am Coll Surg 2005; 201(3): 480-81.
  • 12. Stevenson S, Ramani V, Nasim A et al.: Extra-adrenal pheochromocytoma: an unusual cause of thrombosis. J Vasc Surg 2005; 42(3): 570-72.
  • 13. Walz MK, Peitgen K, Neumann HP et al.: Endoscopic treatment of solitary, bilateral, multiple, and recurrent pheochromocytomas and paragangliomas. World J Surg 2002; 26(8): 1005-12.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_1515_pjs-2015-0072
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