Clinically Silent Pheochromocytoma in Adrenal Incidentaloma:A Case Report and Review of the Literature

نویسندگان

  • Sjen-Jung Shen
  • Hon-Mei Cheng
  • Allen W. Chiu
  • Chien-Wen Chou
  • Chwen-Yi Yang
  • Su-Yu Chen
چکیده

Improvements in imaging studies have resulted in an increase in incidentally discovered adrenal tumors. The adrenal incidentaloma was found in at least 2% on abdominal CT imaging, and pheochromocytoma was reported to be about 5.1 to 6.5% among these patients. Here we report a case of silent pheochromocytoma presented as an incidentally discovered adrenal mass on abdominal sonogram. Clinically no apparent symptom and sign of pheochromocytoma was noted. Urine normetanephrine was 1072.2μg/day, 2.4 fold above the upper reference limits, metanephrine and 3-methoxytyramine were still within normal range. Surgical excision of the tumor in the right adrenal gland was performed with pathological report as a benign pheochromocytoma. Although transient hypertension was noted during the procedure of laparoscopic adrenalectomy, there was no complication occurred through the course. Majority of incidentally discovered adrenal masses are nonhypersecretory benign adenomas; but a hormone screening evaluation is necessary to reveal cases with clinically unsuspected hypersecretory nature. For prevention of possible lethal outcome, patients with silent pheochromocytoma scheduled to undergo surgery should be treated according to the hemodynamic parameters. ( J Intern Med Taiwan 2003;14:248-254 )

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Adrenocortical Carcinoma Mimicking Pheochromocytoma: A case Report and Review of Literature

Adrenocortical carcinoma (ACC) is an uncommon malignancy originating from cortex of adrenal gland. The most common pitfall in diagnosis of ACC is to distinguish it from pheochromocytoma. Here we report a 62-year-old hypertensive man with presentation of dyspnea. The laboratory data showed an increase in urine cortisol and renin with a mild increase in aldosterone, but decrease in adrenocorticot...

متن کامل

PHEOCHROMOCYTOMA OF URINARY BLADDER: REPORT OF A CASE AND BRIEF REVIEW OF THE LITERATURE

A case of pheochromocytoma of the bladder is presented with a r eview of the literature. We discuss general management principles of bladder pheochromocytoma. Successful diagnosis and treatment of this lesion requires a high index of suspicion based upon the patient's symptom complex, allowing preoperative preparation prior to surgical treatment.

متن کامل

Congenital Adrenal Hyperplasia and Schmid Metaphyseal Chondrodysplasia in a Child

Congenital adrenal hyperplasia (CAH) is a group of hereditary diseases, which are autosomal recessive. CAH occurs due to defect in one of the cortisol coding genes and often clinically presents itself with signs of androgen overproduction. In this article, we report a case of CAH and Schmid metaphyseal dysplasia. Our literature review indicated that this report is the first attempt on CYP11B1 a...

متن کامل

INSULIN REQUIRING DIABETES MELLITUS AS A FEATURE Of PHEOCHROMOCYTOMA: REPORT OF A CASE

We report the case of a 65 year old man with recent onset of insulin requiring diabetes mellitus, frequent attacks of anginal chest pain, paroxysmal hypertension poorly controlled with three medications, hyperlipidemia, and mild renal insufficiency. The patient was found to have pheochromocytoma of the left adrenal gland, resection of which resulted in total resolution of diabetes, hyperte...

متن کامل

Seventeen Alpha-Hydroxylase Deficiency Associated with Absent Gonads and Myelolipoma: A Case Report and Review of Literature

Congenital adrenal hyperplasia comprises a group of disorders resulting from defects in enzymes required for the synthesis of cortisol. The clinical presentation depends on the specific enzyme defect. We report a rare case of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency. A 26-year-old female patient referred with hypertension and hypokalemia. She also had primary amenor...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2004