Mengyuan Zhou, Yudi He, Yanwen Luo, Ou Wang, Quan Liao, Yuxin Jiang, He Liu, Qingli Zhu
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Histopathologic examinations were conducted for all lesions removed during neck surgery, and the results were considered as the reference standard.</p><p><strong>Results: </strong>A total of 19 pregnant patients with PHPT who had undergone parathyroidectomy were retrospectively included in the study. The median age was 30 years. Sixteen (16/19, 84.2%) patients had single-gland disease and three (15.8%) had two lesions. Three patients were confirmed as multiple endocrine neoplasia type 1. The median size of all lesions was 1.8 cm (0.6-7.5 cm). All patients had undergone US examination, and eight patients had <sup>99m</sup>Tc-MIBI scintigraphy. A total of 21 lesions were found on US. The diagnostic sensitivity of the US was 95.45% per lesion and 100% per patient. One lesion, with a maximum diameter of 0.6 cm, was missed preoperatively by either US or <sup>99m</sup>Tc-MIBI scintigraphy. Nine patients had surgery in the second trimester and 88.89% of them had a full-term pregnancy after surgery. There were no complications in the newborns.</p><p><strong>Conclusions: </strong>In pregnant PHPT patients, US achieved high sensitivity for preoperative lesion localization. Surgery during the second trimester after accurately localizing the lesion(s) by US improved the patients' pregnancy outcomes.</p>","PeriodicalId":19651,"journal":{"name":"Orphanet Journal of Rare Diseases","volume":"20 1","pages":"148"},"PeriodicalIF":3.4000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11960009/pdf/","citationCount":"0","resultStr":"{\"title\":\"Primary hyperparathyroidism during pregnancy: ultrasound as an accurate preoperative localization imaging modality.\",\"authors\":\"Mengyuan Zhou, Yudi He, Yanwen Luo, Ou Wang, Quan Liao, Yuxin Jiang, He Liu, Qingli Zhu\",\"doi\":\"10.1186/s13023-024-03519-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Accurate identification of parathyroid lesions in primary hyperparathyroidism (PHPT) patients is essential for minimally invasive surgery during pregnancy.</p><p><strong>Materials and methods: </strong>Patients who were diagnosed with PHPT during pregnancy and who had undergone surgical treatment between January 2005 and September 2023 were retrospectively included. Demographic and clinical characteristics and preoperative parathyroid ultrasound (US) and technetium-99m sestamibi (<sup>99m</sup>Tc-MIBI) scintigraphy results were collected. Histopathologic examinations were conducted for all lesions removed during neck surgery, and the results were considered as the reference standard.</p><p><strong>Results: </strong>A total of 19 pregnant patients with PHPT who had undergone parathyroidectomy were retrospectively included in the study. The median age was 30 years. Sixteen (16/19, 84.2%) patients had single-gland disease and three (15.8%) had two lesions. Three patients were confirmed as multiple endocrine neoplasia type 1. The median size of all lesions was 1.8 cm (0.6-7.5 cm). All patients had undergone US examination, and eight patients had <sup>99m</sup>Tc-MIBI scintigraphy. A total of 21 lesions were found on US. The diagnostic sensitivity of the US was 95.45% per lesion and 100% per patient. One lesion, with a maximum diameter of 0.6 cm, was missed preoperatively by either US or <sup>99m</sup>Tc-MIBI scintigraphy. Nine patients had surgery in the second trimester and 88.89% of them had a full-term pregnancy after surgery. There were no complications in the newborns.</p><p><strong>Conclusions: </strong>In pregnant PHPT patients, US achieved high sensitivity for preoperative lesion localization. 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引用次数: 0
摘要
背景:准确识别原发性甲状旁腺功能亢进(PHPT)患者的甲状旁腺病变对妊娠期微创手术至关重要。材料和方法:回顾性纳入2005年1月至2023年9月期间诊断为妊娠期PHPT并接受手术治疗的患者。收集患者的人口学、临床特征及术前甲状旁腺超声(US)和锝- 99mTc-MIBI显像结果。颈部手术切除病灶均行组织病理学检查,并将检查结果作为参考标准。结果:回顾性分析了19例行甲状旁腺切除术的妊娠PHPT患者。中位年龄为30岁。单腺体病变16例(16/19,84.2%),双腺体病变3例(15.8%)。3例确诊为1型多发性内分泌瘤。所有病变的中位大小为1.8 cm (0.6-7.5 cm)。所有患者均行US检查,8例患者行99mTc-MIBI显像检查。在US上共发现21个病变。US的诊断敏感性为每个病变95.45%,每个患者100%。术前US或99mTc-MIBI显像均未发现1例最大直径0.6 cm的病变。9例患者在妊娠中期手术,88.89%的患者术后足月妊娠。新生儿无并发症发生。结论:在妊娠期PHPT患者中,US对术前病变定位具有较高的敏感性。在超声准确定位病变后的妊娠中期手术改善了患者的妊娠结局。
Primary hyperparathyroidism during pregnancy: ultrasound as an accurate preoperative localization imaging modality.
Background: Accurate identification of parathyroid lesions in primary hyperparathyroidism (PHPT) patients is essential for minimally invasive surgery during pregnancy.
Materials and methods: Patients who were diagnosed with PHPT during pregnancy and who had undergone surgical treatment between January 2005 and September 2023 were retrospectively included. Demographic and clinical characteristics and preoperative parathyroid ultrasound (US) and technetium-99m sestamibi (99mTc-MIBI) scintigraphy results were collected. Histopathologic examinations were conducted for all lesions removed during neck surgery, and the results were considered as the reference standard.
Results: A total of 19 pregnant patients with PHPT who had undergone parathyroidectomy were retrospectively included in the study. The median age was 30 years. Sixteen (16/19, 84.2%) patients had single-gland disease and three (15.8%) had two lesions. Three patients were confirmed as multiple endocrine neoplasia type 1. The median size of all lesions was 1.8 cm (0.6-7.5 cm). All patients had undergone US examination, and eight patients had 99mTc-MIBI scintigraphy. A total of 21 lesions were found on US. The diagnostic sensitivity of the US was 95.45% per lesion and 100% per patient. One lesion, with a maximum diameter of 0.6 cm, was missed preoperatively by either US or 99mTc-MIBI scintigraphy. Nine patients had surgery in the second trimester and 88.89% of them had a full-term pregnancy after surgery. There were no complications in the newborns.
Conclusions: In pregnant PHPT patients, US achieved high sensitivity for preoperative lesion localization. Surgery during the second trimester after accurately localizing the lesion(s) by US improved the patients' pregnancy outcomes.
期刊介绍:
Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.