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[Adrenocortical carcinoma with Cushing syndrome: report of a case].

作者信息

Kunimi K, Oshinoya Y, Naito K, Hisazumi H, Niki T, Matsuda T, Mizukami Y, Matsubara F

机构信息

Department of Urology, School of Medicine, Kanazawa University.

出版信息

Hinyokika Kiyo. 1989 Jun;35(6):1015-9.

PMID:2801388
Abstract

We report a 45-year-old female with left adrenocortical carcinoma resulting in Cushing syndrome. She visited the 3rd Department of Internal Medicine, Kanazawa University Hospital with complaints of moon face, amenorrhea and hypertension. A diagnosis of left adrenal tumor with Cushing syndrome was made and she was transferred to our clinic. Left thoracoabdominal adrenalectomy was performed. The histologic report was compatible with adrenocortical carcinoma with no invasion into adjunctive tissues. She is now on endocrinologic study and is being administered 1,1-dichloro-2-[o-chlorophenyl]-2[p-chlorophenyl] ethane. There is no evidence of local recurrence or remote metastasis.

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