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Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia-A Case Report and Literature Overview.

[congenital adrenal hyperplasia]

Objective: In this paper, the etiology, differential diagnosis and therapy of testicular adrenal rest tumors was presented based on a patient presentation and an overview of the most recent literature concerning this subject.Methods: Retrospective analysis of the clinical and biochemical data of an 18-year old male patient diagnosed at the age of 2 weeks with the classic salt-wasting form of congenital adrenal hyperplasia that has been monitored in the Pediatric and Adolescent Out-Patient Department since the age of 4 years.Results: The results of adrenal hormone concentrations (17- OHP, 17 KS, pregnans) had been unsatisfactory, especially in last 5 years. Scrotal US detected TARTs bilaterally. After increasing the dose of hydrocortisone and introducing dexamethasone considerable regression of the tumors was noted.Conclusion: Lack of complete regression of the lesions is caused by fibrosis and is probably due to decreased sensitivity of ACTH and angiotensin II receptors in this tissue.

Diseases presenting "is probably due to decreased sensitivity of acth and angiotensin ii receptors in this tissue" symptom

  • congenital adrenal hyperplasia

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