The long-term outcome after adrenalectomy and prophylactic pituitary radiotherapy in adrenocorticotropin-dependent Cushing's syndrome. 1995

P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
Department of Endocrinology, St. Bartholomew's Hospital, West Smithfield, London, United Kingdom.

We have reviewed our experience of adrenalectomy performed as part of the management of 56 patients with ACTH-dependent Cushing's syndrome between 1946 and 1993. Forty-three patients were operated on at our institution. Surgery-related mortality did not occur, but complications developed in 14 (33%); these were minor in 12. Eleven patients (29%) of the 38 for whom long-term follow-up data were available and who did not have a proven ectopic source of ACTH subsequently developed Nelson's syndrome, diagnosed on the basis of clinical pigmentation and markedly elevated ACTH levels that were not normally suppressible with glucocorticoids. The effects of prophylactic pituitary radiotherapy were assessed in 38 patients who underwent adrenalectomy at our institution and 18 who underwent surgery elsewhere. Patients who had received prophylactic radiotherapy were less likely to develop Nelson's syndrome (5 of 20, 25%) compared to those who did not (18 of 36, 50%; P > 0.07), and there was a low incidence of radiotherapy-induced hypopituitarism. We conclude that total adrenalectomy has proved to be a safe and effective operation and still may be indicated in selected patients with ACTH-dependent Cushing's syndrome; because prophylactic pituitary radiotherapy reduces the incidence of subsequent Nelson's syndrome by 50%, it should always be considered in the management of these patients.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009347 Nelson Syndrome A syndrome characterized by HYPERPIGMENTATION, enlarging pituitary mass, visual defects secondary to compression of the OPTIC CHIASM, and elevated serum ACTH. It is caused by the expansion of an underlying ACTH-SECRETING PITUITARY ADENOMA that grows in the absence of feedback inhibition by adrenal CORTICOSTEROIDS, usually after ADRENALECTOMY.
D010902 Pituitary Gland A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM. Hypophysis,Hypothalamus, Infundibular,Infundibular Stalk,Infundibular Stem,Infundibulum (Hypophysis),Infundibulum, Hypophyseal,Pituitary Stalk,Hypophyseal Infundibulum,Hypophyseal Stalk,Hypophysis Cerebri,Infundibulum,Cerebri, Hypophysis,Cerebrus, Hypophysis,Gland, Pituitary,Glands, Pituitary,Hypophyseal Stalks,Hypophyses,Hypophysis Cerebrus,Infundibular Hypothalamus,Infundibular Stalks,Infundibulums,Pituitary Glands,Pituitary Stalks,Stalk, Hypophyseal,Stalk, Infundibular,Stalks, Hypophyseal,Stalks, Infundibular
D011183 Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. Complication, Postoperative,Complications, Postoperative,Postoperative Complication
D003480 Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. Cushing's Syndrome,Hypercortisolism,Syndrome, Cushing,Syndrome, Cushing's
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000315 Adrenalectomy Excision of one or both adrenal glands. (From Dorland, 28th ed) Adrenalectomies

Related Publications

P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
April 2001, The Journal of clinical endocrinology and metabolism,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
November 1977, Acta endocrinologica,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
December 1994, Surgery,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
January 2019, Archives of endocrinology and metabolism,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
January 2004, Digestive surgery,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
November 1992, The Journal of clinical endocrinology and metabolism,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
July 1996, The Journal of clinical endocrinology and metabolism,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
June 1984, World journal of surgery,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
March 1979, Endocrinology,
P J Jenkins, and P J Trainer, and P N Plowman, and W S Shand, and A B Grossman, and J A Wass, and G M Besser
October 1959, Lancet (London, England),
Copied contents to your clipboard!