Literature DB >> 10197697

Cardiac pheochromocytoma: resection after diagnosis by 111-indium octreotide scan.

J C Lin1, B A Palafox, H A Jackson, A J Cohen, A B Gazzaniga.   

Abstract

Cardiac pheochromocytoma is an exceedingly rare and unusual clinical entity. Only 37 previous surgically treated adult patients were found in review of the surgical literature. We report the case of a 13-year-old boy who had a cardiac pheochromocytoma that was localized by the 111-indium diethylenetriamine pentaacetic acid octreotide scintigraphy scan and confirmed by magnetic resonance imaging after computed tomographic and B1-iodine-metaiodobenzylguanidine scans had failed. At operation, a 6-cm pheochromocytoma of the left atrium was found and successfully resected with reconstruction of the left atrium using autologous pericardium.

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Year:  1999        PMID: 10197697     DOI: 10.1016/s0003-4975(98)01291-0

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  2 in total

Review 1.  Primary cardiac pheochromocytoma with multiple endocrine neoplasia.

Authors:  Chaoji Zhang; Guotao Ma; Xingrong Liu; Heng Zhang; Haibo Deng; Justin Nowell; Qi Miao
Journal:  J Cancer Res Clin Oncol       Date:  2011-06-26       Impact factor: 4.553

2.  A primary right atrium paraganglioma in a 15-year-old patient.

Authors:  Wen-Qi Yuan; Wei-Qinq Wang; Ting-Wei Su; Hai-Tao Chen; Zhong-Wei Shi; Wen-Qiang Fang; Biao Li; Xiao-Long Jin; Wang-Fu Zang; Guang Ning
Journal:  Endocrine       Date:  2007-11-28       Impact factor: 3.633

  2 in total

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