ADRENALECTOMY IN CUSHING'S DISEASE

Author:

Ernest Ingrid,Ekman Hans

Abstract

SUMMARY Forty-four patients with Cushing's disease underwent bilateral adrenalectomy and 39 survivors were followed for, on an average, eight years and a half. There were three postoperative deaths and two other patients died within one year after operation. Thirty patients are now working but six remain invalidized. In four subjects cortisol secretion persisted in spite of "total" adrenalectomy but a clinical remission ultimately occurred. Five patients, who presented with an atypical clinical picture, failed to show any obvious changes in the distribution of fat or in the complexion. Body weight did not decrease after surgery in several patients and in many others body weight increased again after an initial loss of weight. Menstruations reappeared in all premenopausal women except two. Manifest diabetes, which was found in seven subjects, disappeared and in several other cases glucose tolerance improved. The blood pressure, which was high in most patients, normalized or decreased in all hypertensive patients but the blood pressure still remains elevated in 22 subjects. ECG-abnormalities disappeared in 11 of 17 subjects, who presented with ST-T changes and/or high amplitude R waves. The size of the heart decreased in most patients with cardiomegaly. A remarkable improvement in the radiological appearance of the vertebrae occurred in a 16-year-old boy but in the other patients there were no such changes. Mental disturbances, which were a main cause of preoperative disability, disappeared in most cases. Two patients, however, continue to be invalidized from mental disease, which developed during the course of the hypercorticism. One patient presented with a grossly evident pituitary tumour and in four other subjects a large pituitary tumour developed after adrenalectomy together with hyperpigmentation. Pituitary apoplexy occurred in one of these patients and another was operated upon because of visual field losses. It is concluded that the remission obtained after adrenalectomy for Cushing's disease increases the survival rate and makes a normal life possible in most patients. However, persistent hypertension and cardiovascular disease as well as the possibility of the development of a pituitary tumour make the late prognosis somewhat uncertain.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Cushing's Disease and Pregnancy;Pituitary;2004-12

2. Thyrotropin-producing pituitary adenomas;Journal of Neurosurgery;1993-10

3. ACTH-Producing Pituitary Tumors;Endocrinology and Metabolism Clinics of North America;1991-06

4. LONG-TERM FOLLOW-UP OF LOW-DOSE EXTERNAL PITUITARY IRRADIATION FOR CUSHING'S DISEASE;Clinical Endocrinology;1990-10

5. Trans-sphenoidal microsurgical treatment of Nelson's syndrome;Neurosurgical Review;1985-09

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