Central Diabetes Insipidus in Children and Young Adults: Etiological Diagnosis and Long-Term Outcome of Idiopathic Cases

被引:71
作者
Di Iorgi, Natascia [1 ]
Allegri, Anna Elsa Maria [2 ]
Napoli, Flavia [2 ]
Calcagno, Annalisa [1 ]
Calandra, Erika [1 ]
Fratangeli, Nadia [1 ]
Vannati, Marianna [1 ]
Rossi, Andrea [3 ]
Bagnasco, Francesca [4 ]
Haupt, Riccardo [4 ]
Maghnie, Mohamad [1 ]
机构
[1] Univ Genoa, Ist Giannina Gaslini, Dept Pediat, I-16147 Genoa, Italy
[2] Ist Giannina Gaslini, Dept Pediat, I-16147 Genoa, Italy
[3] Ist Giannina Gaslini, I-16147 Genoa, Italy
[4] Ist Giannina Gaslini, Epidemiol Biostat & Comm Unit, I-16147 Genoa, Italy
关键词
LANGERHANS CELL HISTIOCYTOSIS; LYMPHOCYTIC INFUNDIBULONEUROHYPOPHYSITIS; PITUITARY-STALK; NATURAL-HISTORY; EXPERIENCE; TUMORS; ADOLESCENTS; DEFICIENCY; SOCIETY;
D O I
10.1210/jc.2013-3724
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Central diabetes insipidus (CDI) is considered idiopathic in 20% to 50% of affected subjects. Objective: The purpose of this study was to determine whether a systematic diagnostic workup could achieve better etiologic diagnosis in children and adolescents presenting with polyuria and polydipsia. Design and Setting: This is a prospective study conducted at a tertiary referral center. Patients underwent clinical and endocrine evaluations every 6 months and neuroimaging every 6 months for 2 years and yearly for 3 years. Endocrine function and neuroimaging were also reassessed after adult height achievement. Participants: A total of 85 consecutive patients with CDI were enrolled at a median age of 7.5 years; those with idiopathic CDI were stratified based on pituitary stalk thickness. Main Outcome Measures: To establish the etiology of CDI, we determined the time lag between its onset and the specific diagnosis, the long-term impact on pituitary function, and the overall long-term outcomes. Results: Of the subjects, 24 (28.2%) received an etiologic diagnosis at presentation and 11 (13%) within 2.5 years (n = 7 germinomas and n = 4 Langerhans cell histiocytosis), 7 (8.2%) were lost to follow-up, and 43 (50.6%) were considered to have idiopathic disease and were followed until the median age of 17.3 years. Neuroimaging identified 40 of 43 patients with self-limited inflammatory/autoimmune pituitary stalk thickness within the first 6 months, the severity of which was significantly correlated to pituitary dysfunction. The probability of >10-year-survival without an anterior pituitary defect was related to the severity of pituitary stalk thickness, and 53% showed permanent anterior pituitary defects. Three patients developed Langerhans cell histiocytosis and 1 developed Hodgkin lymphoma after a median of 9 and 13 years, respectively. Conclusions: A diagnostic etiology was achieved in 96% of patients with CDI. Risk stratification based on the degree of pituitary stalk thickness is of prognostic value for long-term outcomes including permanent pituitary dysfunction. New guidance is provided for the management of these patients.
引用
收藏
页码:1264 / 1272
页数:9
相关论文
共 30 条
[1]   Autosomal recessive familial neurohypophyseal diabetes insipidus: onset in early infancy [J].
Abu Libdeh, Abdulsalam ;
Levy-Khademi, Floris ;
Abdulhadi-Atwan, Maha ;
Bosin, Emily ;
Korner, Mira ;
White, Perrin C. ;
Zangen, David H. .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2010, 162 (02) :221-226
[2]   Acquired central diabetes insipidus in children: A 12-year Brisbane experience [J].
Al-Agha, AE ;
Thomsett, MJ ;
Ratcliffe, JF ;
Cotterill, AM ;
Batch, JA .
JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2001, 37 (02) :172-175
[3]   Familial forms of diabetes insipidus: clinical and molecular characteristics [J].
Babey, Muriel ;
Kopp, Peter ;
Robertson, Gary L. .
NATURE REVIEWS ENDOCRINOLOGY, 2011, 7 (12) :701-714
[4]   20 years of experience in idiopathic central diabetes insipidus [J].
Charmandari, E ;
Brook, CGD .
LANCET, 1999, 353 (9171) :2212-2213
[5]   Diabetes Insipidus - Diagnosis and Management [J].
Di Iorgi, Natascia ;
Napoli, Flavia ;
Allegri, Anna Elsa Maria ;
Olivieri, Irene ;
Bertelli, Enrica ;
Gallizia, Annalisa ;
Rossi, Andrea ;
Maghnie, Mohamad .
HORMONE RESEARCH IN PAEDIATRICS, 2012, 77 (02) :69-84
[6]   The relation of Langerhans cell histiocytosis to acute leukemia, lymphomas, and other solid tumors -: The LCH-Malignancy Study Group of the Histiocyte Society [J].
Egeler, RM ;
Neglia, JP ;
Aricò, M ;
Favara, BE ;
Heitger, A ;
Nesbit, ME ;
Nicholson, HS .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1998, 12 (02) :369-+
[7]  
Ghirardello S, 2007, J PEDIATR ENDOCR MET, V20, P359
[8]   CENTRAL DIABETES-INSIPIDUS - 22 YEARS EXPERIENCE [J].
GREGER, NG ;
KIRKLAND, RT ;
CLAYTON, GW ;
KIRKLAND, JL .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1986, 140 (06) :551-554
[9]   Permanent consequences in Langerhans cell histiocytosis patients: A pilot study from the Histiocyte Society - Late effects study group [J].
Haupt, R ;
Nanduri, V ;
Calevo, MG ;
Bernstrand, C ;
Braier, JL ;
Broadbent, V ;
Rey, G ;
McClain, KL ;
Janka-Schaub, G ;
Egeler, RM .
PEDIATRIC BLOOD & CANCER, 2004, 42 (05) :438-444
[10]  
Haupt R, 2005, HISTIOCYTIC DISORDERS OF CHILDREN AND ADULTS, P272