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Articles Published Processes
9/15/2014 4:12:00 PM | Browse: 1385 | Download: 2030
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Received |
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2013-10-01 17:52 |
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Peer-Review Started |
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2013-10-01 19:55 |
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First Decision by Editorial Office Director |
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Return for Revision |
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2013-11-05 19:49 |
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Revised |
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2013-11-13 23:04 |
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Publication Fee Transferred |
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Second Decision by Editor |
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2013-12-19 13:00 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2013-12-19 13:22 |
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Articles in Press |
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Edit the Manuscript by Language Editor |
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2013-12-27 16:29 |
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Typeset the Manuscript |
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2014-01-20 09:57 |
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Publish the Manuscript Online |
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2014-02-08 10:32 |
| Category |
Radiology, Nuclear Medicine & Medical Imaging |
| Manuscript Type |
Case Report |
| Article Title |
Renal hilar paraganglioma: A case report
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| Manuscript Source |
Invited Manuscript |
| All Author List |
Zeinab Ali Abou Yehia, Rashid Khalid Sayyid and Ali Ahmad Haydar |
| Funding Agency and Grant Number |
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| Corresponding Author |
Ali Ahmad Haydar, MD, Department of Radiology, AUBMC, PO Box. 11-0236, Riad El Solh, Beirut 1107 2020, Lebanon. ah24@aub.edu.lb |
| Key Words |
Renal; Hilar; Paraganglioma; Pheochromocytoma; Imaging |
| Core Tip |
Chromaffin cell tumors are very rare tumors, the majority of which derive from catecholamine secreting cells in the adrenal glands. Extra-adrenal paragangliomas comprise around 15% of chromaffin cell tumors; they usually arise from sympathetic paraganglia throughout the body. We present a very rare case with the location and presentation of a paraganglioma arising at the renal hilum splaying the renal artery and vein and causing vascular compromise to the left kidney. |
| Publish Date |
2014-02-08 10:32 |
| Citation |
Abou Yehia ZA, Sayyid RK, Haydar AA. Renal hilar paraganglioma: A case report. World J Radiol 2014; 6(1): 15-17
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| URL |
http://www.wjgnet.com/1949-8470/full/v6/i1/15.htm |
| DOI |
http://dx.doi.org/10.4329/wjr.v6.i1.15 |
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