hyperaldosteronism/peavalu

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Adrenalectomy in primary aldosteronism: a long-term follow-up study in 52 patients.

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Logi sisse

From 1975 to 1989, 52 patients with primary aldosteronism underwent adrenalectomy. There were 16 men and 36 women. The average age was 42.5 years, ranging from 28 years to 70 years. They were all hypertensive, with average pre-operative diastolic pressures varying from 105 to 140 mm Hg (median 117

A case report of idiopathic hyperaldosteronism characterized by bilateral adrenal adenoma.

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Logi sisse

Primary aldosteronism (PA) comprises 2 main subtypes: unilateral aldosterone-producing adenoma (APA) and idiopathic hyperaldosteronism or named as bilateral adrenal hyperplasia (BAH). An accurate discrimination between APA and BAH is crucial because the former is treated with

Idiopathic intracranial hypertension associated with either primary or secondary aldosteronism.

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BACKGROUND Idiopathic intracranial hypertension (IIH) is a syndrome consisting of headache, visual field defects and papilledema of uncertain etiology. The prospect was raised previously as to an association between aldosteronism and increased intracranial pressure in 2 middle-aged women with IIH

Hyperaldosteronism and pheochromocytoma: new tricks and tests.

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Logi sisse

Hyperaldosteronism, previously thought to represent only 1% to 2% of cases of hypertension, may cause as much as 25% of hypertension in a primary care setting. The renin/aldosterone ratio is the best test for initial screening, followed by localization if possible. Aldosterone antagonists, such as

Adrenal adenoma with primary aldosteronism in a child: a case report.

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Logi sisse

Primary aldosteronism caused by an aldosterone-producing adrenal adenoma was documented in an 11-year-old girl who presented with persistent hypertension, headache, tinnitus and hypokalemia. Elevated plasma aldosterone concentration (PAC) (45.5 ng/dl) and suppressed plasma renin activity (PRA) (<

Safety of medical adjustment and confirmatory testing in the diagnostic workup of primary aldosteronism.

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Logi sisse

Saline infusion (SIT) and captopril challenge tests (CCT) are standard confirmatory procedures routinely used in the diagnostic workup of primary aldosteronism (PA). However, side effects and complications during testing have not been systematically

Primary hyperaldosteronism: a case of unilateral adrenal hyperplasia with contralateral incidentaloma.

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Logi sisse

Primary hyperaldosteronism is one of the most common causes of secondary hypertension but clear differentiation between its various subtypes can be a clinical challenge. We report the case of a 37-year-old African-American woman with refractory hypertension who was admitted to our hospital for

Hypertension Accompanied by Hyperaldosteronism, Hyperkalemia, and Hyperchloremic Acidosis: A Case Report and Literature Review

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This study reported on a 24-year-old woman who complained of a paroxysmal headache for six months and elevated blood pressure for four months. Laboratory examination revealed increased serum potassium and chloride levels, metabolic acidosis, suppressed renin activity, and increased plasma

A pediatric Conn syndrome case.

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Logi sisse

Conn syndrome, which is rarely encountered in children, is characterized by increased aldosterone, low renin level, and arterial hypertension. Severe complications, such as impaired vascular smooth muscle function secondary to increased aldosterone, endothelial dysfunction, deterioration of left

Diagnostic challenges and good treatment outcomes in pediatric paraganglioma of the abdomen: A case report.

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Logi sisse

BACKGROUND Paraganglioma is a catecholamine-producing neuroendocrine tumor. Management of paraganglioma including its diagnosis is difficult, because it has no characteristic symptoms and many diseases can manifest as headache and high blood pressure. Herein, we report a rare case of paraganglioma

Enflurane anaesthesia for removal of aldosterone producing adenoma.

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Logi sisse

In a 31-year old woman with a six year history of headache and hypertension a diagnosis of primary aldosteronism was made on the basis of urine samples containing 45 mug/day of aldosterone. The preoperative systemic blood pressure was 240 mm Hg systolic and 120 mm Hg diastolic. The serum potassium

A Novel Case of Somatic KCNJ5 Mutation in Pediatric-Onset Aldosterone-Producing Adenoma.

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Logi sisse

Aldosterone-producing adenoma (APA), a subtype of primary aldosteronism, is a common cause of secondary hypertension in adults. Somatic KCNJ5 mutations have been identified in about 12%-80% of adult-onset APA. In contrast, there has been no previous reported case of pediatric-onset APA in whom a

[The Conn syndrome. The clinical and surgical aspects of 18 cases of adrenal adenoma].

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OBJECTIVE Presentation of a series of 18 patients who underwent surgery of aldosterone-producing adrenal adenoma (Conn's syndrome) over the last 10 years. Assessment of the most significant clinical and pathological aspects from a surgical point of view. METHODS Retrospective study evaluating a

[Retroperitoneal masses: two case reports--Case 11/2009].

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METHODS A 35-year old patient (male, headaches, visual impairment, 170/100 mmHg, case 1) and a 61-year old patient (female, headaches, epistaxis, 230/110 mmHg, case 2) were investigated in our hospital. METHODS Laboratory findings in case 1 verified acute renal failure (serum creatinine 23 mg/dl,

[Kidney full of stones, and an adrenal gland not quite normal].

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A 31-year-old patient was followed for cystinuria, justifying CT scans. In 2006, a tissue mass of 3cm of the right adrenal gland, homogeneous, measured at 3.5cm in 2007 was noted. Blood pressure was 90/61mmHg, without orthostatic hypotension. During the clinical interview, no discomfort, sweat

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