Desai M P
Edocrinology Division, Bai Jerbai Wadia Hospital for Children and Research Centre, Parel, Mumbai.
Indian J Pediatr. 1997 Jan-Feb;64(1):11-20. doi: 10.1007/BF02795771.
The profile of thyroid disorders encountered in pediatric and adolescent age groups in India is similar to that seen in most parts of the world except for the prevalence of iodine deficiency disorders in certain endemic regions of this country. Clinical presentation is most commonly for hypothyroidism and goiters and infrequently for hyperthyroidism. Of nearly 800 children referred for thyroid problems, 79% had hypothyroidism (goitrous as well as nongoitrous), 19% had euthyroid goiters and 2% had hyperthyroidism. Hypothyroidism was due to thyroid dysgenesis in 75% (aplasia/hypoplasia--50% and ectopic thyroid gland 25%), thyroiditis in nearly 5% and dyshormonogenes is in 20%. The incidence of congenital hypothyroidism in our experience of screening nearly 40,000 newborns is about 1 in 2,640, which is much higher than the worldwide average of 1 in 3,800. Diagnostic delay in hypothyroidism is common and is related to lack of awareness amongst primary healthy care practitioners and family physicians as well as the cost and availability of laboratory investigations. This delay, compounded with inadequate therapeutic surveillance is responsible for the poor outcome in affected children. High incidence of dyshormonogenesis, inherited as autosomal recessive trait also calls for genetic counselling and routine sibling examination. Our results of family studies on first degree relatives of children with thyroiditis revealed presence of antimicrosomal antibodies in 43% and thyroid disease in 26%. Many etiologic factors cause goiters which may be functionally euthyroid or hypothyroid with almost equal frequency in our series. In nearly 200 schools children surveyed for goiter prevalence, 8% in high socioeconomic groups and about 21% in the low income group, had goiters. Female predominance was marked. However, iodine deficiency was not the sole cause as revealed by dietary survey and urinary iodine estimations. Hyperthyroidism is infrequent, less severe and in our experience responded well to long-term administration of antithyroid drugs. A high index of clinical awareness and education of primary health workers will help a great deal in improving the ultimate outcome in children with thyroid disorders/hypothyroidism.
除了该国某些地方性甲状腺肿流行地区碘缺乏病的患病率外,印度儿童和青少年年龄组中甲状腺疾病的情况与世界上大多数地区相似。临床表现最常见的是甲状腺功能减退和甲状腺肿,甲状腺功能亢进则较少见。在近800名因甲状腺问题转诊的儿童中,79%患有甲状腺功能减退(包括甲状腺肿性和非甲状腺肿性),19%患有甲状腺功能正常的甲状腺肿,2%患有甲状腺功能亢进。甲状腺功能减退的病因中,75%是甲状腺发育异常(甲状腺缺如/发育不全占50%,异位甲状腺占25%),近5%是甲状腺炎,20%是激素合成障碍。在我们对近40000名新生儿进行筛查的经验中,先天性甲状腺功能减退的发病率约为2640分之一,远高于全球平均的3800分之一。甲状腺功能减退的诊断延迟很常见,这与基层医疗保健从业者和家庭医生缺乏认识以及实验室检查的费用和可及性有关。这种延迟,再加上治疗监测不足,是导致患病儿童预后不良的原因。激素合成障碍的高发病率,作为常染色体隐性遗传特征,也需要进行遗传咨询和对同胞进行常规检查。我们对甲状腺炎患儿一级亲属的家族研究结果显示,43%存在抗微粒体抗体,26%患有甲状腺疾病。许多病因可导致甲状腺肿,在我们的系列研究中,甲状腺功能正常或甲状腺功能减退的频率几乎相等。在对近200名在校儿童进行甲状腺肿患病率调查时,高社会经济群体中有8%,低收入群体中有约21%患有甲状腺肿。女性占主导地位。然而,饮食调查和尿碘测定显示,碘缺乏并非唯一原因。甲状腺功能亢进较少见,病情较轻,根据我们的经验,长期服用抗甲状腺药物效果良好。基层卫生工作者的高临床意识和教育将极大地有助于改善甲状腺疾病/甲状腺功能减退患儿的最终结局。