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[儿童严重慢性贫血与内分泌紊乱]

[Severe chronic anemia and endocrine disorders in children].

作者信息

Hauschild Michael, Theintz Gérald

机构信息

Unité d'endocrinologie-diabétologie pédiatrique, Département médico-chirurgical de pédiatrie, CHUV, 1011 Lausanne.

出版信息

Rev Med Suisse. 2007 Apr 18;3(107):988-91.

PMID:17526372
Abstract

Hemolytic anemias can induce various anomalies of the endocrine glands which can already be observed in children. Endocrine dysfunction is also found in the course of therapy for aplastic anemias, usually as undesirable side effects. In Europe, 2-9% of the population belongs to ethnic minorities at risk for developing hemolytic anemia. Pituitary affinity to iron deposition explains the high incidence of hypogonadism, puberty delay and growth retardation although other factors have to be considered. Growth hormone deficiency has to be ruled out as it can occur in a minority of subjects with thalassemia and sickle-cell disease (drepanocytosis). Diabetes mellitus, hypothyroidism and hypoparathyroidism may also develop. Follow-up includes close monitoring of growth and pubertal development in order to guide therapeutic interventions.

摘要

溶血性贫血可诱发内分泌腺的各种异常,这在儿童中已可观察到。再生障碍性贫血治疗过程中也会出现内分泌功能障碍,通常是不良副作用。在欧洲,2%至9%的人口属于有患溶血性贫血风险的少数民族。垂体对铁沉积的亲和性解释了性腺功能减退、青春期延迟和生长发育迟缓的高发生率,不过还需考虑其他因素。必须排除生长激素缺乏症,因为少数地中海贫血和镰状细胞病(镰状细胞血症)患者可能会出现这种情况。糖尿病、甲状腺功能减退和甲状旁腺功能减退也可能发生。随访包括密切监测生长和青春期发育,以指导治疗干预。

相似文献

1
[Severe chronic anemia and endocrine disorders in children].[儿童严重慢性贫血与内分泌紊乱]
Rev Med Suisse. 2007 Apr 18;3(107):988-91.
2
Endocrine complications in patients with Thalassaemia Major.重型地中海贫血患者的内分泌并发症
Pediatr Endocrinol Rev. 2007 Dec;5(2):642-8.
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Advances in the recognition and treatment of endocrine complications in children with chronic illness.慢性病患儿内分泌并发症的识别与治疗进展。
Adv Pediatr. 1999;46:101-49.
4
Prevalence of endocrine complications and short stature in patients with thalassaemia major: a multicenter study by the Thalassaemia International Federation (TIF).重型地中海贫血患者内分泌并发症及身材矮小的患病率:地中海贫血国际联合会(TIF)的一项多中心研究
Pediatr Endocrinol Rev. 2004 Dec;2 Suppl 2:249-55.
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Endocrine complications in thalassaemia major.重型地中海贫血的内分泌并发症
Prog Clin Biol Res. 1989;309:77-83.
6
Hypogonadism, diabetes mellitus, hypothyroidism, hypoparathyroidism: incidence and prevalence related to iron overload and chelation therapy in patients with thalassaemia major followed from 1980 to 2007 in the Ferrara Centre.性腺功能减退、糖尿病、甲状腺功能减退、甲状旁腺功能减退:1980年至2007年在费拉拉中心随访的重型地中海贫血患者中与铁过载及螯合疗法相关的发病率和患病率
Pediatr Endocrinol Rev. 2008 Oct;6 Suppl 1:158-69.
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[Endocrine syndromes in hemochromatosis].[血色素沉着症中的内分泌综合征]
Ann Med Interne (Paris). 1971 Dec;122(12):1225-34.
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Increased prevalence of iron-overload associated endocrinopathy in thalassaemia versus sickle-cell disease.地中海贫血与镰状细胞病相比,铁过载相关内分泌病的患病率增加。
Br J Haematol. 2006 Nov;135(4):574-82. doi: 10.1111/j.1365-2141.2006.06332.x. Epub 2006 Oct 10.
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Small pituitary size in children with Fanconi anemia.范可尼贫血患儿垂体体积小。
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Iron loading and endocrine functions in nontransfused patients with beta-thalassemia intermedia or sickle-cell thalassemia.中间型β地中海贫血或镰状细胞性地中海贫血非输血患者的铁负荷与内分泌功能
Isr J Med Sci. 1981 Jan;17(1):22-7.

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