Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia Associated with Multiple Colon Adenomas/Carcinomas Which Showed a Point Mutation in the APC Gene

37Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

Abstract

We report a male Japanese with corticotropin (ACTH)-independent macronodular adrenocortical hyperplasia (AIMAH) associated with multiple colon adenomas/carcinomas. The plasma cortisol level was elevated with no diurnal rhythm and was not suppressed with dexamethasone. Basal plasma ACTH was immeasurable but subnormally increased after administration of metyrapone or corticotropin releasing hormone. Both adrenals were resected and weighed 90g; the histopathologic findings were similar to those of AIMAH as previously reported. At least 21 colon lesions which were adenomas or carcinomas, were resected endoscopically or surgically. This is the second reported case of the association of AIMAH with multiple colon polyps. An APC gene point mutation was detected in the colon cancer tissue by polymerase chain reaction (PCR)-single strand conformation polymorphism (SSCP)/direct sequencing analysis at the putative splice acceptor site consensus sequence. However, no abnormality of APC gene was detected in the adrenocortical hyperplastic tissue. The possible etiological coexistence of these two diseases is discussed.

Cite

CITATION STYLE

APA

Yamakita, N., Murai, T., Ito, Y., Miura, K., Ikeda, T., Miyamoto, K., … Yoshida, T. (1997). Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia Associated with Multiple Colon Adenomas/Carcinomas Which Showed a Point Mutation in the APC Gene. Internal Medicine, 36(8), 536–542. https://doi.org/10.2169/internalmedicine.36.536

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free