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dc.contributor.authorYuko-Jowi, C,
dc.contributor.authorMukhwana, R,
dc.contributor.authorOnyango, FE.
dc.date.accessioned2013-04-29T11:26:56Z
dc.date.available2013-04-29T11:26:56Z
dc.date.issued2010
dc.identifier.citationEast Afr Med J. 2010 Jun;87(6):269-72en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/23057270
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/17667
dc.description.abstractA three and a half year old male with multifocal phaeochromocytoma involving the right adrenal gland and an intrathoracic mass is presented. Twenty four hour vanillylmandelic acid (VMA) was negative despite suggestive symptomatology. The diagnosis was made on serial CT scans of the head, thoracic inlet and pelvis. He underwent right adrenalectomy and thoracotomy to remove the abdominal and intrathoracic mass. The diagnosis was confirmed by histology. He remained hypertensive on hefty antihypertensive doses throughout his lifespan and finally succumbed to status epilepticus at the age of ten, six years from the time of diagnosis.en
dc.language.isoenen
dc.titleMultifocal pheochromocytoma in early childhood: case report.en
dc.typeArticleen
local.publisherDepartment of Paediatrics and Child Health, College of Health Sciences, University of Nairobi,en


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