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Am J Med Sci ; 355(2): 191-194, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29406048

ABSTRACT

Pheochromocytoma is a neoplasm, which develops from cells of the chromaffin tissues that are derived from the ectodermic neural system and mostly situated within the adrenal medulla. Approximately 15% of pheochromocytoma cases arise from extra-adrenal chromaffin tissue. Pheochromocytoma of the bladder is rare and accounts for less than 0.06% of all bladder neoplasms and less than 1% of all pheochromocytomas. We report a case of a young woman who presented with uncontrolled hypertension, recurrent urinary tract infections and micturition attacks and was found to have a metastatic bladder paraganglioma. In addition, we provide a summary table of the clinical manifestations of paragangliomas based on anatomic locations.


Subject(s)
Adrenal Gland Neoplasms , Hypertension , Urinary Bladder Neoplasms , Urinary Tract Infections , Adrenal Gland Neoplasms/microbiology , Adrenal Gland Neoplasms/pathology , Adrenal Gland Neoplasms/physiopathology , Adult , Female , Humans , Hypertension/microbiology , Hypertension/pathology , Hypertension/physiopathology , Neoplasm Metastasis , Pheochromocytoma/microbiology , Pheochromocytoma/pathology , Pheochromocytoma/physiopathology , Pheochromocytoma/secondary , Urinary Bladder Neoplasms/microbiology , Urinary Bladder Neoplasms/pathology , Urinary Bladder Neoplasms/physiopathology , Urinary Tract Infections/microbiology , Urinary Tract Infections/pathology , Urinary Tract Infections/physiopathology
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