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Share your interactive ePaper on all platforms and on your website with our embed function. Volume 7 - No. AbstractParagangliomas of urinary bladder are rareneoplasms coming from the chromaffin tissue.
Moreover, bladder paragangliomaduring pregnancy is intriguing but extremely rare. Here, we report a year-old woman with a bladderparaganglioma at 24 weeks gestation duringher second pregnancy. Her symptoms were characterizedby repeated painless gross hematuriaand acute urine retention with normal blood pressureand unelevated plasma catecholamine level.
Ultrasound and CT computer tomography scanboth detected the tumor, cystoscopy and pathologicresults of biopsy finally confirmed the diagnosisof bladder paraganglioma. The tumor wassuccessfully removed by partial cystectomy afterpregnant termination.
Additionally, a brief reviewof eight other cases was studied. Furthermore,bladder paraganglioma combined with pregnancyis extremely rare. The authors searched the litera-Table 1. Giving the searching results from PubMed, Embaseand the Cochrane library, only 8 cases reportedin English are available and no new report has beenadded to the database for this recent decade[].