Results and long-term follow-up after unilateral adrenalectomy for ACTH-independent hypercortisolism in a series of fifty patients

被引:0
作者
M. lacobone
F. Mantero
S. M. Basso
F. Lumachi
G. Favia
机构
[1] University of Padua,Endocrine Surgery Unit, Department of Surgical and Gastroenterological Sciences
[2] University of Padua,Division of Endocrinology, Department of Medical and Surgical Sciences
[3] Sezione di Endocrinochirurgia,Dipartimento di Scienze Chirurgiche e gastroenterologiche
关键词
Cushing’s syndrome; adrenalectomy; follow-up;
D O I
10.1007/BF03347198
中图分类号
学科分类号
摘要
Untreated hypercortisolism is a fatal state, causing functional disability. Even after successful treatment, clinical recovery is slower than the biochemical one, but data about clinical results, well-being and working capacity after surgery are scarce. This retrospective study aimed at evaluating the long-term outcome of patients after adrenalectomy for ACTH-independent hypercortisolism by the analysis of the clinical results, the survival and the subjective well-being status after surgery. Clinical data in 50 patients suffering from ACTH-independent hypercortisolism and treated between 1980 and 2000 by unilateral adrenalectomy were recorded. At a mean follow-up of 134 months, 3 patients were dead. All the surviving patients were asked to self estimate the physical and psychological recovery after surgery. After surgery, 100% of patients were biochemically cured. A clinical recovery was observed in most cases: obesity in 59.6% and hypertension in 57.5%. Bone mass density (BMD) significantly improved (+20%). The long-term mortality rate did not differ from normal population. Subjectively, a full recovery was confirmed by 95.6% of the surviving patients; it was correlated with the subjective feeling of physical recovery (95.6%) and regained working ability (93.3%). Despite of biochemical and clinical cure, no subjective improvement of the psychological conditions was observed in 26.7% of cases. At long-term follow-up, most objective symptoms of Cushing’s syndrome (CS) disappear; subjective health and working ability are often regained, but a psychological impairment could persist in spite of a successful treatment.
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页码:327 / 332
页数:5
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  • [1] Boscaro M(2001)Cushing’s syndrome Lancet 357 783-91
  • [2] Barzon L(1971)The natural history of treated Cushing’s syndrome Br J Surg 58 1-16
  • [3] Fallo F(1985)The clinical response to treatment in adult Cushing’s syndrome following remission of hypercortisolaemia Postgrad Med J 61 205-11
  • [4] Sonino N(1991)Long-term results of treatment of Cushing’s disease by adrenalectomy Eur J Surg 157 461-4
  • [5] Welbourn RB(1994)Cushing’s syndrome from the patient’s perspective Endocrinol Metab Clin North Am 23 607-17
  • [6] Montgomery DA(2001)Incidence and late prognosis of Cushing’s syndrome: a population-based study J Clin Endocrinol Metab 86 117-23
  • [7] Kennedy TL(2003)2003 European Society of Hypertension-European Society of Cardiology guidelines for the management of arterial hypertension J Hypertens 21 1011-53
  • [8] Ross EJ(2001)Osteoporosis prevention, diagnosis, and therapy JAMA 285 785-95
  • [9] Linch DC(1952)Natural history of Cushing’s syndrome Am J Med 13 597-614
  • [10] Grabner P(1982)Cushing’s syndrome-killing disease: discriminatory value of signs and symptoms aiding early diagnosis Lancet 2 646-9