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妊娠合并原发性甲状旁腺功能亢进症 8 例临床分析。

PRIMARY HYPERPARATHYROIDISM DURING PREGNANCY: A CASE SERIES OF 8 PATIENTS.

出版信息

Endocr Pract. 2019 Nov;25(11):1127-1136. doi: 10.4158/EP-2019-0035. Epub 2019 Aug 15.

Abstract

Due to a lack of typical clinical manifestations and physiologic changes in calcium metabolism during pregnancy, primary hyperparathyroidism (PHPT) during pregnancy is commonly underdiagnosed, and treatment during this unique period presents a clinical challenge. Hence, the aim of the present study was to summarize the cases of 8 pregnant patients with PHPT who were treated at our center to provide better clinical insight into this condition. Our study comprised a retrospective analysis of 8 pregnant PHPT patients and a control group of 22 age-matched, nonpregnant PHPT patients during the same period. Clinical manifestations, biochemical indices, pathologic types, therapeutic strategies, and pregnancy outcomes were compiled, and 25 patients were screened for germline mutations in the , , and genes. The most-common symptoms in the pregnancy group involved the gastrointestinal tract (GIT) in 7/8 cases (87.5%), followed by urinary system involvement (50%) and joint pain (50%). In contrast, GIT symptoms in the control group were significantly less common (31.82%; = .012). There was a trend of more-severe elevation of serum parathyroid hormone levels in the control group compared to that in the pregnancy group ( = .053). No differences were found in blood-ionized calcium, phosphate, or alkaline phosphatase levels between the two groups. In the pregnancy group, the serum albumin-corrected calcium level was reduced from 3.42 ± 0.66 mmol/L to 2.89 ± 0.46 mmol/L ( = .025) after hydration and medical treatment. Six patients, three of whom were in the second trimester of pregnancy, underwent parathyroidectomy, and 3 patients were after childbirth or had induced labor. Postoperative serum calcium levels were reduced to within the normal range. Fetal/neonatal complications were observed in 4 of 5 patients who had not received surgical treatment during pregnancy. In addition, 2 of 5 pregnant PHPT patients were found to carry mutations, whereas no mutations were detected in any of the 20 nonpregnant patients. In this case series of PHPT during pregnancy, the most-common complaint of GIT symptoms may be easily confused with pregnancy reactions, which might contribute to the under- or misdiagnosis of this clinical entity. Patients who did not receive surgical treatment during pregnancy had high incidences of fetal/neonatal complications and worse pregnancy outcomes. = calcium-sensing receptor; = cell division cycle 73; = gastrointestinal tract; = multiple endocrine neoplasia; = primary hyperparathyroidism; = parathyroid hormone; = serum calcium.

摘要

由于孕妇钙代谢的典型临床表现和生理变化缺失,妊娠期间甲状旁腺功能亢进症(PHPT)常被漏诊,而在这一特殊时期的治疗也极具挑战性。因此,本研究旨在总结我院治疗的 8 例妊娠合并 PHPT 患者的病例,为该病的临床诊治提供更好的认识。

本研究回顾性分析了 8 例妊娠合并 PHPT 患者和同期 22 例非妊娠 PHPT 患者的病例。汇总了临床表现、生化指标、病理类型、治疗策略和妊娠结局,并对 25 例患者的 、 、 基因进行了种系突变筛查。

妊娠组最常见的症状是胃肠道(GIT)受累 7/8 例(87.5%),其次是泌尿系统受累(50%)和关节痛(50%)。相比之下,对照组的 GIT 症状明显较少(31.82%; =.012)。与对照组相比,妊娠组甲状旁腺激素水平升高更为严重(趋势性; =.053)。两组血钙、血磷或碱性磷酸酶水平无差异。妊娠组患者经水化和药物治疗后,血清白蛋白校正钙水平从 3.42±0.66 mmol/L 降至 2.89±0.46 mmol/L( =.025)。6 例患者中,有 3 例在妊娠中期接受甲状旁腺切除术,3 例在产后或行引产术。术后血清钙水平降至正常范围。在未接受妊娠期间手术治疗的 4 例患者中观察到胎儿/新生儿并发症。此外,5 例妊娠 PHPT 患者中有 2 例发现携带 突变,而 20 例非妊娠患者中均未发现突变。

在本妊娠 PHPT 病例系列中,最常见的胃肠道症状可能与妊娠反应容易混淆,这可能导致对该临床实体的漏诊或误诊。未在妊娠期间接受手术治疗的患者胎儿/新生儿并发症发生率高,妊娠结局较差。 = 钙敏感受体; = 细胞分裂周期蛋白 73; = 胃肠道; = 多发性内分泌肿瘤; = 甲状旁腺功能亢进症; = 甲状旁腺激素; = 血清钙。

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