Diagnostic tests for children who are referred for the investigation of Cushing syndrome

被引:114
作者
Batista, Dalia L.
Riar, Jehan
Keil, Meg
Stratakis, Constantine A.
机构
[1] Natl Inst Hlth, Sect Endocrinol & Genet, Dev Endocrinol Branch, Bethesda, MD USA
[2] NICHHD, Pediat Endocrinol Inter Inst Training Program, Natl Inst Hlth, Bethesda, MD 20892 USA
关键词
Cushing syndrome; children; pituitary tumors; adrenal tumors; corticotropin; cortisol;
D O I
10.1542/peds.2006-2402
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVE. Endogenous Cushing syndrome in children is a rare disorder that is most frequently caused by pituitary or adrenocortical tumors. Diagnostic criteria have generally been derived from studies of adult patients despite significant differences in both the physiology of the hypothalamic-pituitary-adrenal axis and the epidemiology of Cushing syndrome in childhood. The purpose of this study was to identify the tests that most reliably and efficiently diagnose pituitary or adrenal tumors in a large cohort of pediatric patients with Cushing syndrome. METHODS. A retrospective review of clinical data of children who were referred to a tertiary care center for evaluation for Cushing syndrome during the years 1997 to 2005 was conducted. A total of 125 consecutive children were studied retrospectively; 105 were found to have Cushing syndrome, which was confirmed histologically; and 20 children who did not have Cushing syndrome or any other endocrinopathy served as the control group. The following tests were performed in all children: midnight and morning cortisol, corticotropin hormone, urinary free cortisol and 17-hydroxycorticosteroid levels, ovine corticotropin-releasing hormone stimulation test, and overnight high-dosage dexamethasone suppression test. Imaging of the pituitary and adrenal glands was also obtained. The main outcome measure was the sensitivity of these parameters for the diagnosis and differential diagnosis of Cushing syndrome at 100% specificity. RESULTS. A midnight cortisol value of >= 1 4.4 mu g/ dL confirmed the diagnosis of Cushing syndrome in almost all children, with a sensitivity of 99% and a specificity of 100%. Suppression of morning cortisol levels > 20% in response to an overnight, high-dosage dexamethasone test excluded all patients with adrenal tumors and identified almost all patients with pituitary tumors ( sensitivity: 97.5%; specificity: 100%). CONCLUSIONS. Our study suggests that among children who were referred for the evaluation of possible Cushing syndrome, a single cortisol value at midnight followed by overnight high-dosage dexamethasone test led to rapid and accurate confirmation and diagnostic differentiation, respectively, of hypercortisolemia caused by pituitary and adrenal tumors.
引用
收藏
页码:E575 / E586
页数:12
相关论文
共 36 条
[1]   Cushing's syndrome caused by corticotropin secretion by pulmonary tumorlets [J].
Arioglu, E ;
Doppman, J ;
Gomes, M ;
Kleiner, D ;
Mauro, D ;
Barlow, C ;
Papanicolaou, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (13) :883-886
[2]   Diagnosis and complications of Cushing's syndrome: A consensus statement [J].
Arnaldi, G ;
Angeli, A ;
Atkinson, AB ;
Bertagna, X ;
Cavagnini, F ;
Chrousos, GP ;
Fava, GA ;
Findling, JW ;
Gaillard, RC ;
Grossman, AB ;
Kola, B ;
Lacroix, A ;
Mancini, T ;
Mantero, F ;
Newell-Price, J ;
Nieman, LK ;
Sonino, N ;
Vance, ML ;
Giustina, A ;
Boscaro, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (12) :5593-5602
[3]   Cushing's syndrome [J].
Boscaro, M ;
Barzon, L ;
Fallo, F ;
Sonino, N .
LANCET, 2001, 357 (9258) :783-791
[4]   A COMPARISON OF THE STANDARD HIGH-DOSE DEXAMETHASONE SUPPRESSION TEST AND THE OVERNIGHT 8-MG DEXAMETHASONE SUPPRESSION TEST FOR THE DIFFERENTIAL-DIAGNOSIS OF ADRENOCORTICOTROPIN-DEPENDENT CUSHINGS-SYNDROME [J].
DICHEK, HL ;
NIEMAN, LK ;
OLDFIELD, EH ;
PASS, HI ;
MALLEY, JD ;
CUTLER, GB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (02) :418-422
[5]   DIURNAL VARIATION OF 17-HYDROXYCORTICOSTEROIDS, SODIUM, POTASSIUM, MAGNESIUM AND CREATININE IN NORMAL SUBJECTS AND IN CASES OF TREATED ADRENAL INSUFFICIENCY AND CUSHINGS SYNDROME [J].
DOE, RP ;
VENNES, JA ;
FLINK, EB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1960, 20 (02) :253-265
[6]   CUSHING SYNDROME DUE TO PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DISEASE - FINDINGS AT CT AND MR IMAGING [J].
DOPPMAN, JL ;
TRAVIS, WD ;
NIEMAN, L ;
MILLER, DL ;
CHROUSOS, GP ;
GOMEZ, MT ;
CUTLER, GB ;
LORIAUX, DL ;
NORTON, JA .
RADIOLOGY, 1989, 172 (02) :415-420
[7]   Differential diagnosis of Cushing's syndrome [J].
Findling, JW .
ENDOCRINOLOGIST, 1997, 7 (01) :S17-S23
[8]   URINE FREE CORTISOL IN THE HIGH-DOSE DEXAMETHASONE SUPPRESSION TEST FOR THE DIFFERENTIAL-DIAGNOSIS OF THE CUSHING SYNDROME [J].
FLACK, MR ;
OLDFIELD, EH ;
CUTLER, GB ;
ZWEIG, MH ;
MALLEY, JD ;
CHROUSOS, GP ;
LORIAUX, DL ;
NIEMAN, LK .
ANNALS OF INTERNAL MEDICINE, 1992, 116 (03) :211-217
[9]   URINARY FREE CORTISOL VALUES IN NORMAL-CHILDREN AND ADOLESCENTS [J].
GOMEZ, MT ;
MALOZOWSKI, S ;
WINTERER, J ;
VAMVAKOPOULOS, NC ;
CHROUSOS, GP .
JOURNAL OF PEDIATRICS, 1991, 118 (02) :256-258
[10]   Cyclical Cushing syndrome presenting in infancy: An early form of primary pigmented nodular adrenocortical disease, or a new entity? [J].
Gunther, DF ;
Bourdeau, I ;
Matyakhina, L ;
Cassarino, D ;
Kleiner, DE ;
Griffin, K ;
Courkoutsakis, N ;
Abu-Asab, M ;
Tsokos, M ;
Keil, M ;
Carney, JA ;
Stratakis, CA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (07) :3173-3182