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[弥漫性甲状腺肿伴甲状腺功能亢进症中甲状腺自身免疫的生物学和组织学标准研究]

[A study of biological and histological criteria of thyroid autoimmunity in diffuse goiters with hyperthyroidism].

作者信息

Leprat F, Felicie-Dellan E, Trouette H, Latapie M J, Masson B, De Mascarel A, Latapie J L, Roger P

机构信息

Service d'Endocrinologie et Maladies Métaboliques, Hôpital Haut-Lévèque, CHU Bordeaux, Pessac.

出版信息

Ann Endocrinol (Paris). 1997;58(5):393-8.

PMID:9685997
Abstract

Hyperthyroidism is usually classified as follows: with diffuse or with toxic plurinodular goiter, respectively considered as autoimmune and non-autoimmune thyroid disorders. This classification seems partially inadequate as signs of thyroid immunity may be found in some plurinodular toxic goiter and alternatively may by lacking in some cases of Graves' disease. These observations led us to study the intensity of intrathyroidal autoimmune process (IAP) and the levels of TBIAb, TPO- and Thyroglobulin-antibodies in 105 cases with diffuse goiter, hyperthyroidism and elevated RAIU (92 women and 13 men, age 34 +/- 11, mean +/- SD). The intensity of intrathyroidal autoimmune process (IAP) was determined by one pathologist (HT) by semi quantitative method applicable to routine clinical use. Subtotal thyroidectomy was performed because of a large goiter (n = 29), a concomitant cold nodule (n = 20), a recurrent disease (n = 18), intolerance to antithyroid drugs (n = 5) or because patients chose surgical treatment (n = 33). All cases were rendered euthyroid at the time of surgery using antithyroid drugs or iodine. The results show a lack of IAP and undetectable levels of TBIAb, TPO- and Thyroglobulin-antibodies in 10%, 11%, 25% and 47% respectively. The intensity of IAP was not different in case of first episode or recurrence of hyperthyroidism and was not related to type or duration of medical treatment. Comparison of patients with or without IAP show higher levels of TPO- and thyroglobulin-antibodies but not of TBIAb in the former group (P < 0.005). TBIAb were higher when ophthalmopathy and/or dermopathy were present vs absent (p < 0.05) and were correlated with FT4 levels (p < 0.05). The negative predictive value of TBIAb, TPO- and thyroglobulin-antibodies to predict the lack of significant IAP was 42%, 65% and 64%. The total absence of clinical, biological and histological signs of thyroid autoimmunity was found in only one case (female aged 35 with first episode of hyperthyroidism and no family history of thyroid disease) (0.9%). These results suggest that routine available criteria of thyroid immunity (including IAP) have a low specificity. It follows that they are probably inadequate to screen cases of hereditary toxic familial hyperplasia, a rare entity of still unknown prevalence.

摘要

甲状腺功能亢进症通常分类如下

分别为伴有弥漫性或毒性多结节性甲状腺肿,分别被视为自身免疫性和非自身免疫性甲状腺疾病。这种分类似乎部分不充分,因为在一些多结节性毒性甲状腺肿中可能发现甲状腺免疫迹象,而在某些格雷夫斯病病例中可能缺乏这些迹象。这些观察结果促使我们研究105例弥漫性甲状腺肿、甲状腺功能亢进症且放射性碘摄取率升高患者(92名女性和13名男性,年龄34±11岁,均值±标准差)的甲状腺内自身免疫过程(IAP)强度以及TBIAb、TPO和甲状腺球蛋白抗体水平。甲状腺内自身免疫过程(IAP)强度由一名病理学家(HT)采用适用于常规临床应用的半定量方法确定。由于甲状腺肿大(n = 29)、伴有冷结节(n = 20)、复发性疾病(n = 18)、对抗甲状腺药物不耐受(n = 5)或患者选择手术治疗(n = 33)而进行了甲状腺次全切除术。所有病例在手术时使用抗甲状腺药物或碘使甲状腺功能恢复正常。结果显示,分别有10%、11%、25%和47%的病例缺乏IAP且未检测到TBIAb、TPO和甲状腺球蛋白抗体水平。甲状腺功能亢进症首次发作或复发时IAP强度无差异,且与治疗类型或持续时间无关。有或无IAP的患者比较显示,前一组中TPO和甲状腺球蛋白抗体水平较高,但TBIAb水平无差异(P < 0.005)。存在眼病和/或皮肤病时TBIAb水平高于不存在时(p < 0.05),且与FT4水平相关(p < 0.05)。TBIAb、TPO和甲状腺球蛋白抗体预测无明显IAP的阴性预测值分别为42%、65%和64%。仅在1例患者(35岁女性,首次发作甲状腺功能亢进症,无甲状腺疾病家族史)中发现完全没有甲状腺自身免疫的临床、生物学和组织学迹象(0.9%)。这些结果表明,常规可用的甲状腺免疫标准(包括IAP)特异性较低。因此,它们可能不足以筛查遗传性毒性家族性增生病例,这是一种患病率仍未知的罕见疾病。

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