adrenocortical adenoma/maumivu ya kichwa

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7 matokeo

Pheochromocytoma associated with adrenocortical adenoma: case report and literature review.

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala

Ingia / Ingia

The case of a 60-year-old woman with pheochromocytoma and concomitant adrenocortical adenoma in the same gland is presented. She complained of episodic headache, palpitation, nausea, vomiting and sweating. Physical examination revealed that the patient has generalized obesity, wet skin and

Unique association of pheochromocytoma with contralateral nonfunctioning adrenal cortical adenoma.

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Ingia / Ingia

A 57-year-old woman complaining of hypertensive attacks associated with headache and palpitation was admitted to our hospital for examination of bilateral adrenal tumors in 1985. After right pheochromocytoma was diagnosed, right adrenalectomy was performed. The left adrenal tumor was small; thus,

Pregnancy during the course of Cushing's syndrome: a case report and literature review

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Ingia / Ingia

Summary: Cushing's syndrome is an endocrine disorder that causes anovulatory infertility secondary to hypercortisolism; therefore, pregnancy rarely occurs during its course. We present the case of a 24-year-old, 16-week pregnant female

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

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Ingia / Ingia

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

A Case of Malignant Pheochromocytoma Presenting 7 Years After the Initial Surgery.

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Ingia / Ingia

BACKGROUND Pheochromocytoma (PHEO) is a rare tumor of the adrenal medulla and sympathetic ganglion that produces the catecholamines norepinephrine and epinephrine. Traditionally, approximately 10% of PHEOs were thought to be malignant, but recent developments in PHEO research have noted that

Clinicopathological Features of Adrenal Tumors: a Ten-year Study in Yazd, Iran.

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Ingia / Ingia

BACKGROUND Adrenal tumors are relatively uncommon, and have different presentations, so we decided to evaluate the clinico-pathological characteristics of benign and malignant tumors in a ten-year period. METHODS This cross sectional-analytical study was conducted on adrenal resection samples taken

[Association of pheochromocytoma with contralateral nonfunctioning adrenal adenoma].

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala

Ingia / Ingia

A 52-year-old woman complaining of abdominal pain, headaches and palpitations was admitted to our hospital for investigation of a bilateral adrenal tumor. Bilateral adrenalectomy was subsequently performed. The definitive diagnosis was right pheochromocytoma and left adrenocortical adenoma. Only

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