Two patients with bladder pheochromocytoma are presented and 22 previously published cases are reviewed. From the analysis of these 24 patients the following conclusions are made: bladder pheochromocytoma may appear at any age but is more common in the second and fourth decades. Females are more oft
Ultrasound demonstration of a pheochromocytoma of the bladder
β Scribed by A. Goodman; J. K. Lipinski
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 185 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0091-2751
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β¦ Synopsis
CASE HISTORY
A 19-year-old black female with paroxysmal headaches, palpitations and sweating without an obvious precipitating cause was admitted to our hospital for evaluation. The BP was 290/180 and there was bilateral papiloedema. Her past history included a pregnancy at age 15 when she was treated for pre-eclamptic toxemia. She delivered a normal infant but was lost to follow-up. There were no hematuria or symptoms of catechalomine excess on micturition. The clinical suspicion of a phaeochromocytoma was confirmed biochemically with markedly elevated urinary vanillyl mandelic acid, total metanephrines and total catecholamines. Preoperative localization included CAT scanning of the abdomen and thorax and abdominal angiography. These initial investigations failed to demonstrate a tumor but subsequent selective venous sampling localized high Norepinephrine concentrations from the area drained by the left common iliac vein. The ultrasound demonstrated a 4.6 x 4.4 cm mass in the dome of the bladder [Fig. )]. The CAT scan confirmed this localization.
At laparotomy a 5-cm benign pheochromocytoma was found arising from the dome of the bladder and was removed by partial cystectomy. Postoperatively the patient became normotensive and continues well.
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