Adrenocorticotropin-independent macronodular adrenocortical hyperplasia associated with multiple colon adenomas/carcinomas which showed a point mutation in the APC gene

被引:35
作者
Yamakita, N
Murai, T
Ito, Y
Miura, K
Ikeda, T
Miyamoto, K
Onami, S
Yoshida, T
机构
[1] Department of Internal Medicine, Matsunami General Hospital, Gifu
[2] Clin. Res. Ctr. Endocrinol./Metab., Matsunami General Hospital, Gifu
[3] Department of Pathology, Matsunami General Hospital, Gifu
[4] Department of Surgery, Matsunami General Hospital, Gifu
[5] Genetics Division, Natl. Cancer Ctr. Research Institute, Tokyo
[6] Department of Internal Medicine, Matsunami General Hospital, Kasamatsu
关键词
Cushing's syndrome; adrenocortical nodular hyperplasia;
D O I
10.2169/internalmedicine.36.536
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a male Japanese with coritcotropin (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 unmeasurable 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 of 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 in discussed.
引用
收藏
页码:536 / 542
页数:7
相关论文
共 53 条
[11]   REGIONALLY CLUSTERED APC MUTATIONS ARE ASSOCIATED WITH A SEVERE PHENOTYPE AND OCCUR AT A HIGH-FREQUENCY IN NEW MUTATION CASES OF ADENOMATOUS POLYPOSIS COIL [J].
GAYTHER, SA ;
WELLS, D ;
SENGUPTA, SB ;
CHAPMAN, P ;
NEALE, K ;
TSIOUPRA, K ;
DELHANTY, JDA .
HUMAN MOLECULAR GENETICS, 1994, 3 (01) :53-56
[12]   IDENTIFICATION OF A NAVEL GERMLINE MUTATION IN A FAP FAMILY [J].
GEBERT, JF ;
HAHN, M ;
KADMON, M ;
HERFARTH, C ;
SCHACKERT, HK .
HUMAN MOLECULAR GENETICS, 1994, 3 (07) :1167-1168
[13]   IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE [J].
GRODEN, J ;
THLIVERIS, A ;
SAMOWITZ, W ;
CARLSON, M ;
GELBERT, L ;
ALBERTSEN, H ;
JOSLYN, G ;
STEVENS, J ;
SPIRIO, L ;
ROBERTSON, M ;
SARGEANT, L ;
KRAPCHO, K ;
WOLFF, E ;
BURT, R ;
HUGHES, JP ;
WARRINGTON, J ;
MCPHERSON, J ;
WASMUTH, J ;
LEPASLIER, D ;
ABDERRAHIM, H ;
COHEN, D ;
LEPPERT, M ;
WHITE, R .
CELL, 1991, 66 (03) :589-600
[14]  
HAYASHI Y, 1993, NIPPON NAIBUNPI GAKK, V69, P728
[15]   TRANSITION FROM PITUITARY-DEPENDENT TO ADRENAL-DEPENDENT CUSHINGS-SYNDROME [J].
HERMUS, AR ;
PIETERS, GF ;
SMALS, AG ;
PESMAN, GJ ;
LAMBERTS, SW ;
BENRAAD, TJ ;
VANHAELST, UJ ;
KLOPPENBORG, PW .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (15) :966-970
[16]   LYSINE VASOPRESSIN STIMULATION OF CORTISOL SECRETION IN PATIENTS WITH ADRENOCORTICOTROPIN-INDEPENDENT MACRONODULAR ADRENAL-HYPERPLASIA [J].
HORIBA, N ;
SUDA, T ;
AIBA, M ;
NARUSE, M ;
NOMURA, K ;
IMAMURA, M ;
DEMURA, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (08) :2336-2341
[17]  
HORII A, 1992, CANCER RES, V52, P3231
[18]  
ICHII S, 1993, ONCOGENE, V8, P2399
[19]   ACTH-INDEPENDENT MASSIVE BILATERAL ADRENAL DISEASE (AIMBAD) - A SUBTYPE OF CUSHINGS-SYNDROME WITH MAJOR DIAGNOSTIC AND THERAPEUTIC IMPLICATIONS [J].
LIEBERMAN, SA ;
ECCLESHALL, TR ;
FELDMAN, D .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1994, 131 (01) :67-73
[20]   ADRENOCORTICOTROPIN-INDEPENDENT BILATERAL MACRONODULAR ADRENAL-HYPERPLASIA - AN UNUSUAL CAUSE OF CUSHING SYNDROME [J].
MALCHOFF, CD ;
ROSA, J ;
DEBOLD, CR ;
KOZOL, RA ;
RAMSBY, GR ;
PAGE, DL ;
MALCHOFF, DM ;
ORTH, DN .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (04) :855-860