| Literature DB >> 18458953 |
Detlef Bockenhauer1, Lesley Rees, Hartmut Neumann, Ying Foo.
Abstract
Phaeochromocytoma is a rare cause of hypertension in children, but important to be recognised, as hypertension can be severe and surgery is often curative. Here, we report on a 7-year-old boy with a phaeochromocytoma, who had normal levels of commonly assayed catecholamine metabolites in the urine. Postoperatively, the patient developed renal vein thrombosis. Appropriate screening tests for phaeochromocytomas, peri-operative management, and the high incidence of an underlying genetic basis, even in sporadic cases, are discussed.Entities:
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Year: 2008 PMID: 18458953 DOI: 10.1007/s00467-008-0841-y
Source DB: PubMed Journal: Pediatr Nephrol ISSN: 0931-041X Impact factor: 3.714