To assess the results of bilateral adrenalectomy and further assess the relevance of Nelson's syndrome as a complication of bilateral adrenalectomy.
33 patients treated by bilateral adrenalectomy at the Hammersmith Hospital were identified (earliest operation performed in 1958). Although all bilateral adrenalectomies in recent years were included, it was not possible to confirm that all bilateral adrenalectomies were identified between 1958 and 1990 due to deficient theatre records.
Retrospective analysis of outcome measures.
Patients were divided into 4 groups depending on their initial diagnosis;
1.Pituitary-dependent Cushing's disease
2.Ectopic ACTH syndrome
3.Bilateral adrenal hyperplasia
Main outcome measures
Indications for bilateral adrenalectomy; survival following bilateral adrenalectomy; and the occurrence of Nelson's syndrome.
-Indications for bilateral adrenalectomy in patients with Cushing's disease were as follows: 50% after failed previous transsphenoidal surgery (only treatment); 31% as a primary treatment modality; 13% after failed previous radiotherapy (only treatment); and 6% after failed previous transsphenoidal surgery and radiotherapy.
Indications for bilateral adrenalectomy in patients with ectopic ACTH syndrome were as follows: 70% as a primary treatment after failure to locate a tumour; 20% as a primary treatment as a result of an unresectable tumour source; and 10% after failed previous surgery and radiotherapy.
-Ninety-one percent of patients were alive at time of data collection; follow-up ranged from 0.5 to 43 years following bilateral adrenalectomy.
-Nine percent of patients have developed Nelson's syndrome (and this only occurred in patients with pituitary dependent Cushing's).
In the set of patients studied, Nelson's syndrome was not a common complication, and only occurred in the patients with pituitary-dependent Cushing's treated with bilateral adrenalectomy.
22 - 24 Mar 2004
British Endocrine Societies