An unusual case of ectopic corticotrophin-releasing hormone syndrome caused by an adrenal noncatecholamine-secreting pheochromocytoma: a case report
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DIPHALLUS: A REPORT OF AN UNUSUAL CASE
We report an unusual case of diphaIlus in a five year old boy. The two organs appeared separately, one orthotopically in the pubic area and the other in the perineum with no urinary meatus. A perineal hypospadias with meatus in the anterior anal verge was also present. The right testis was undescended and the scrotum was mildly bifid. The patient was continent for both voiding and defeca...
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INTRODUCTION Although the syndrome of inappropriate antidiuretic hormone has connection with various malignant tumors, there are few reports associated with advanced gastric cancer. CASE PRESENTATION We describe the case of a 63-year-old Korean male with inappropriate antidiuretic hormone syndrome due to an ectopic antidiuretic hormone-producing advanced gastric adenocarcinoma manifested with...
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Adrenocortical tumors (ACTs) are extremely rare in infants. Pediatric ACTs are therapeutic and diagnostic challenge because histological criteria for distinguishing benign from malignant tumors seen in adults are not always reliable in children .The aim of this report was to present clinical features, hormonal profile, and histopathological characteristics of an infant with Adrenal tumors. A...
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ژورنال
عنوان ژورنال: BMC Endocrine Disorders
سال: 2018
ISSN: 1472-6823
DOI: 10.1186/s12902-018-0269-8