Literature DB >> 2214343

A case of a clinically "silent" pheochromocytoma.

K Yoshida1, M Sasaguri, A Kinoshita, M Ideishi, M Ikeda, K Arakawa.   

Abstract

A case of a clinically "silent" pheochromocytoma is presented. The adrenal mass was incidentally discovered by abdominal ultrasonography and computed tomography. In the course of hospitalization, the patient was normotensive and asymptomatic. Plasma catecholamine levels were nearly normal, whereas urinary levels of catecholamine metabolites were slightly elevated. A glucagon provocative test and 131I-metaiodobenzylguanidine scintigram were useful for diagnosing such an atypical pheochromocytoma. A discussion of clinically-unsuspected pheochromocytoma is also presented.

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Year:  1990        PMID: 2214343     DOI: 10.2169/internalmedicine1962.29.27

Source DB:  PubMed          Journal:  Jpn J Med        ISSN: 0021-5120


  3 in total

1.  Encapsulated pheochromocytoma cells secrete potent noncatecholamine factors.

Authors:  Hector R Mobine; George C Engelmayr; Nelson Moussazadeh; Tayyba R Anwar; Lisa E Freed; Elazer R Edelman
Journal:  Tissue Eng Part A       Date:  2009-07       Impact factor: 3.845

2.  Pheochromocytoma-induced cardiomyopathy is modulated by the synergistic effects of cell-secreted factors.

Authors:  Hector R Mobine; Aaron B Baker; Libin Wang; Hiroko Wakimoto; Kurt C Jacobsen; Christine E Seidman; J G Seidman; Elazer R Edelman
Journal:  Circ Heart Fail       Date:  2009-02-10       Impact factor: 8.790

Review 3.  Laparoscopic resection of a large clinically silent paraganglioma at the organ of Zuckerkandl: a rare case report and review of the literature.

Authors:  Xiang Ren; Jiwen Shang; Ruimin Ren; Huajun Zhang; Xue Yao
Journal:  BMC Urol       Date:  2020-10-07       Impact factor: 2.264

  3 in total

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