Donati L, Antonelli A, Bertoni F, Moscogiuri D, Andreani M, Venturi S, Filippi T, Gasperini L, Neri S, Baschieri L
Ospedale Figlie di S. Camillo, Roma, Italy.
Thyroid. 1992 Winter;2(4):283-90. doi: 10.1089/thy.1992.2.283.
Endemic cretinism is still present in an endemic goiter area of the central Apennines (Montefeltro) (goiter prevalence 55%; mean urinary iodine level 39 micrograms/g creatinine). Clinical and biochemical features of patients with myxedematous, neurologic, and mixed cretinism were studied. Also, in this area, as in most other, neurologic cretinism is more prevalent than myxedematous and mixed forms. The hormonal profiles of the three types of cretinism were clearly different. Nevertheless, all myxedematous cretins had some neurologic disorders (hyperreflexia, increased muscle tone, disorder of gait, Babinski sign, hypoacusia) that were similar to those present in neurologic cretins. These findings suggest that neurologic damage is very similar in all forms of endemic cretinism, reflecting a diffuse insult to the developing fetal nervous system. Furthermore, these data support the hypothesis that the primary pathophysiologic event in the different types of endemic cretinism is represented by maternal and fetal hypothyroidism, while differences may be explained by the extent and duration of postnatal hypothyroidism. All the cretins were over 35 of age, suggesting a severe iodine deficiency in the past decades, and a progressive improvement of nutritional status resulted in "silent iodine prophylaxis." However, recent studies have revealed the persistence of a moderate iodine deficiency, a high prevalence of neurologic hypoacusia, and reduction of mental performance in normal schoolchildren of this area. These findings constitute strong evidence in favor of adequate iodine prophylaxis.
亚平宁山脉中部(蒙特费尔特罗)的一个地方性甲状腺肿病区仍存在地方性克汀病(甲状腺肿患病率55%;尿碘平均水平为39微克/克肌酐)。对黏液水肿型、神经型和混合型克汀病患者的临床和生化特征进行了研究。此外,在该地区,与大多数其他地区一样,神经型克汀病比黏液水肿型和混合型更为普遍。三种类型克汀病的激素谱明显不同。然而,所有黏液水肿型克汀病患者都有一些神经功能障碍(反射亢进、肌张力增加、步态障碍、巴宾斯基征、听力减退),这些与神经型克汀病患者的症状相似。这些发现表明,在所有形式的地方性克汀病中,神经损伤非常相似,这反映了发育中的胎儿神经系统受到弥漫性损害。此外,这些数据支持以下假设:不同类型地方性克汀病的主要病理生理事件是母体和胎儿甲状腺功能减退,而差异可能由出生后甲状腺功能减退的程度和持续时间来解释。所有克汀病患者年龄均超过35岁,这表明过去几十年碘严重缺乏,而营养状况的逐步改善导致了“隐性碘预防”。然而,最近的研究显示该地区仍存在中度碘缺乏、神经型听力减退的高患病率以及正常学龄儿童智力表现下降。这些发现构成了支持充分碘预防的有力证据。