Yonsei Med J.  1969 Dec;10(2):162-169. 10.3349/ymj.1969.10.2.162.

Cushing's Syndrome in Infancy

Affiliations
  • 1Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.

Abstract

Cushing's syndrome is very rare in infancy, especially in Korea. We observed a case of Cushing's syndrome in a one year and 2 month old female baby with the complaints of a 3 months history of obesty and hirsutism and 2 months history of polyphagia. There were retarded bone age, hypertension, increased urinary excretion of 17-hydroxycorticosteroid and 17-ketosteroid and eosinopenia but no thymic shadow in the chest X-ray. There was no response to the dexamethasone test (2mg divided in 4 doses orally for 2 days), which suggested an adrenal tumor. Intravenous pyelography showed that the left kidney was displaced downward as compared to the right kidney and there was a henegg sized radio-opaque shadow at the upper pole of the left kidney suggesting a left adrenal tumor. The tumor, reported as a benign adenoma pathologically, was removed successfully by anterior abdominal approach. Hypertension, eosinopenia and hypokalemia were raturned to normal from 3 days after surgery but 17-hydroxycorticosteroid and 17-ketosteroid were returned to normal from 2 weeks after surgery. We have presented this case and have reviewed the literature.


MeSH Terms

Adenoma/*pathology
Adrenal Gland Neoplasms/*pathology
*Adrenalectomy
Cushing Syndrome/etiology/*surgery
Female
Human
Infant
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