首页> 外文期刊>Thyroid: official journal of the American Thyroid Association >Late primary autoimmune hypothyroidism in a patient with postdelivery autoimmune hypopituitarism associated with antibodies to growth hormone and prolactin-secreting cells
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Late primary autoimmune hypothyroidism in a patient with postdelivery autoimmune hypopituitarism associated with antibodies to growth hormone and prolactin-secreting cells

机译:分娩后自身免疫性垂体功能低下的晚期原发性自身免疫性甲状腺功能减退症与生长激素和催乳素分泌细胞抗体相关

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Background: Pituitary and thyroid autoimmunity can be triggered by pregnancy. We report the first association of combined growth hormone (GH) and prolactin secretion deficiency due to autoimmune damage to GH- and prolactin-secreting cells in a patient with postdelivery lactation failure, presenting subsequently with primary autoimmune hypothyroidism. Patient Findings: A 34-year-old woman presented with lactation failure following the delivery of her first child. She had a family history of hypothyroidism without a history of pituitary dysfunction. Physical examination did not show any abnormal findings. Laboratory investigations showed normal gonadotropin levels after the restoration of normal menstrual cycles following pregnancy, normal basal and stimulated cortisol levels, but an impaired GH response to insulin-induced hypoglycemia, and low basal prolactin and insulin-like growth factor-1 concentrations. Thyroid function was normal when initially investigated three months after delivery, but five months later, marked primary hypothyroidism (thyrotropin levels >100 mIU/L) occurred. Immunological investigation revealed the presence of antipituitary antibodies, identified by double immunofluorescence and targeting GH- and prolactin-secreting cells. Antithyroid antibodies, in the normal range three months postpartum, became significantly elevated when the hypothyroidism appeared. Autoimmune hypophysitis is responsible for selective or multiple pituitary-hormone deficiencies, sometimes involving thyrotropin secretion and causing secondary hypothyroidism, but usually associated with hyperprolactinemia. To our knowledge, this is the first observation of autoimmune hypopituitarism involving deficient growth hormone and prolactin secretion in a patient with lactation failure after delivery, subsequently followed by severe primary autoimmune hypothyroidism, thus falling into an unusual constellation of autoimmune polyendocrine syndrome type 3. Conclusions: Considering the well-known relationship between pregnancy and autoimmunity, an early postdelivery immunological and functional investigation in women presenting with disorders of lactation may be useful to detect potential pituitary and thyroid dysfunction even at a subclinical stage.
机译:背景:垂体和甲状腺自身免疫可由妊娠触发。我们报道了由于分娩后泌乳衰竭的患者对GH和泌乳素分泌细胞的自身免疫损害而导致的联合生长激素(GH)与催乳素分泌不足的首次关联,随后表现为原发性自身免疫性甲状腺功能减退症。患者发现:一名34岁妇女在分娩第一个孩子后出现泌乳失败。她有甲状腺功能减退的家族史,无垂体功能减退史。体格检查未发现任何异常发现。实验室研究显示,怀孕后恢复正常的月经周期后,促性腺激素水平正常,基础和刺激皮质醇水平正常,但对胰岛素诱导的低血糖的GH反应减弱,基础催乳素和胰岛素样生长因子-1浓度低。最初在分娩后三个月检查甲状腺功能是正常的,但是五个月后,出现了明显的原发性甲状腺功能减退症(促甲状腺激素水平> 100 mIU / L)。免疫学调查显示存在抗垂体抗体,可通过双重免疫荧光法鉴定,并靶向分泌GH和催乳激素的细胞。出现甲状腺功能减退症时,在产后三个月的正常范围内,抗甲状腺抗体显着升高。自身免疫性垂体炎是导致选择性或多种垂体激素缺乏的原因,有时涉及促甲状腺激素分泌并引起继发性甲状腺功能减退,但通常与高泌乳素血症相关。据我们所知,这是在分娩后泌尿衰竭的患者中首次发现自身免疫性垂体功能低下,包括生长激素和催乳激素分泌不足,随后是严重的原发性自身免疫性甲状腺功能减退症,从而陷入了异常的自身免疫性多内分泌综合征3型。 :考虑到妊娠与自身免疫之间的众所周知的关系,即使是在亚临床阶段,对出现泌乳障碍的女性进行早期产后免疫学和功能研究也可能有助于发现潜在的垂体和甲状腺功能障碍。

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