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Hyponatremic-Hypertensive Syndrome in Ovarian Paraganglioma
Indian Pediatr ; 2019 Jan; 56(1): 69-71
Article | IMSEAR | ID: sea-199248
ABSTRACT

Background:

Hyponatremic-hypertensive syndrome (HHS) is characterized bycombination of polyuria, polydipsia, hypertension, hyponatremia and hypokalemia inassociation with unilateral renal artery stenosis. Case characteristics A 10-year- old girlpresented with polyuria, polydipsia, hypertension, hyponatremia, hypokalemia andproteinuria. Ultrasonography with doppler study revealed bilateral normal renal arteries.Completed tomography of abdomen detected a left adnexal mass, which was laterconfirmed as ovarian paraganglioma on histopathology.

Outcome:

After tumor excision,polyuria subsided and blood pressure normalized. Message Hyponatremic-HypertensiveSyndrome does not always result from unilateral renal artery stenosis. High index of clinicalsuspicion with appropriate imaging technique may clinch rare endocrine causes ofhypertension, like paraganglioma.
Full text: Available Index: IMSEAR (South-East Asia) Journal: Indian Pediatr Year: 2019 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Journal: Indian Pediatr Year: 2019 Type: Article