Log in to save to my catalogue

Malignant Intrarenal/Renal Pelvis Paraganglioma with Co-Occurring SDHB and ATRX Mutations

Malignant Intrarenal/Renal Pelvis Paraganglioma with Co-Occurring SDHB and ATRX Mutations

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2313380025

Malignant Intrarenal/Renal Pelvis Paraganglioma with Co-Occurring SDHB and ATRX Mutations

About this item

Full title

Malignant Intrarenal/Renal Pelvis Paraganglioma with Co-Occurring SDHB and ATRX Mutations

Publisher

New York: Springer US

Journal title

Endocrine pathology, 2019-12, Vol.30 (4), p.270-275

Language

English

Formats

Publication information

Publisher

New York: Springer US

More information

Scope and Contents

Contents

Paragangliomas are rare neuroendocrine tumors which originate from embryonic neural crest cells. These tumors may arise from parasympathetic or sympathetic paraganglia, may secrete catecholamines, and can occur in varied anatomic locations, with some locations being less common than others. Hereditary paraganglioma-pheochromocytoma (PGL/PCC) syndro...

Alternative Titles

Full title

Malignant Intrarenal/Renal Pelvis Paraganglioma with Co-Occurring SDHB and ATRX Mutations

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2313380025

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2313380025

Other Identifiers

ISSN

1046-3976

E-ISSN

1559-0097

DOI

10.1007/s12022-019-09594-1

How to access this item