Adrenal myelolipoma associated with congenital adrenal 21-hydroxylase deficiency.

Abstract

The occurrence of adrenal myelolipomas is reported in an untreated patient with congenital adrenal 21-hydroxylase deficiency. Laparotomy demonstrated the presence of two lesions, a large tumor which arose from an ectopic adrenal cortex and a smaller tumor in the left adrenal gland. Six cases of adrenal myelolipomas and congenital adrenal hyperplasia have been reported in the literature. All patients were associated with excessive ACTH secretion for a long period of time. The relative frequency of this association, coupled with the observation by Selye and Stone (Am J Pathol 26:211, 1950) that anterior pituitary extracts cause myelolipomatous changes in rats, may indicate a possible role for ACTH in the development of myelolipomas.

• Authors: C Murakami, M Ishibashi, M Kondo, S Ohshiro, M Fujita, S Sato, M Kako, H Furue, K Mizuguchi, T Yamaji
• Journal: Internal medicine (Tokyo, Japan) (Intern Med) Vol. 31 Issue 6 Pg. 803-6 (Jun 1992) ISSN: 0918-2918 [Print] Japan
• PMID: 1327310 (Publication Type: Case Reports, Journal Article)

Chemical References

• Adrenocorticotropic Hormone

Topics

• Adrenal Gland Neoplasms (complications, etiology, pathology)
• Adrenal Hyperplasia, Congenital (complications, enzymology)
• Adrenocorticotropic Hormone (physiology)
• Adult
• Humans
• Lipoma (complications, etiology, pathology)
• Male