{"title":"原发性甲状旁腺功能亢进:一个病例系列,以患者为中心的诊断和管理方法回顾。","authors":"Adriana Gioia, Clemente Junior Nappi, Martina Socin, Giulia Vallon, Samuele Naviglio, Stella Bernardi, Alessandro Boscarelli, Chiara Dobrinja","doi":"10.62713/aic.3939","DOIUrl":null,"url":null,"abstract":"<p><p>Primary hyperparathyroidism (pHPT) is a prevalent disorder of dysregulated calcium homeostasis, marked by excessive secretion of parathyroid hormone (PTH), which results in alterated calcemia and renal and/or skeletal complications. Most patients are diagnosed before experiencing overt clinical symptoms, often as a result of blood tests performed for other disorders. When symptoms do manifest, they are associated with dysfunction of the parathyroid glands. Surgical treatment is considered the first choice and the only curative treatment for pHPT, offering advantages for both symptomatic and asymptomatic patients. The aim of this study is to report our experience in the management of 6 selected complex cases, which often require a multidisciplinary approach due to the lack of established diagnostic and therapeutic algorithms and the variability of clinical presentation and atypical parathyroid adenoma location. We present a series of cases examining the various treatment approaches in six distinct patients: one patient with parathyroid carcinoma with concomitant parathyroid adenoma, a case involving mediastinal parathyroidectomy, a case with an intrathymic parathyroid adenoma, two cases of recurrent pHPT, and one case of hereditary pHPT in Multiple Endocrine Neoplasia (MEN) 1 syndrome. The combination of parathyroid ultrasound and Tc-99m sestamibi scintigraphy is effective for localizing parathyroid adenomas in most patients. Additional imaging, such as single photon emission computed tomography/computed tomography (SPECT/CT) or 18F-Fluorocholine positron emission tomography/computed tomography (18F-FCH PET/CT), may be necessary in other cases. Intraoperative parathyroid hormone monitoring is valuable for detecting double adenomas in patients affected by hereditary familial hyperparathyroidism from MEN 1. Several studies highlight that the surgeon's expertise is the most critical determinant of a safe and successful surgical outcome.</p>","PeriodicalId":8210,"journal":{"name":"Annali italiani di chirurgia","volume":"96 7","pages":"878-893"},"PeriodicalIF":0.9000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Primary Hyperparathyroidism: A Case Series, Patient-Centered Approach to Diagnosis and Management Review.\",\"authors\":\"Adriana Gioia, Clemente Junior Nappi, Martina Socin, Giulia Vallon, Samuele Naviglio, Stella Bernardi, Alessandro Boscarelli, Chiara Dobrinja\",\"doi\":\"10.62713/aic.3939\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Primary hyperparathyroidism (pHPT) is a prevalent disorder of dysregulated calcium homeostasis, marked by excessive secretion of parathyroid hormone (PTH), which results in alterated calcemia and renal and/or skeletal complications. Most patients are diagnosed before experiencing overt clinical symptoms, often as a result of blood tests performed for other disorders. When symptoms do manifest, they are associated with dysfunction of the parathyroid glands. Surgical treatment is considered the first choice and the only curative treatment for pHPT, offering advantages for both symptomatic and asymptomatic patients. The aim of this study is to report our experience in the management of 6 selected complex cases, which often require a multidisciplinary approach due to the lack of established diagnostic and therapeutic algorithms and the variability of clinical presentation and atypical parathyroid adenoma location. We present a series of cases examining the various treatment approaches in six distinct patients: one patient with parathyroid carcinoma with concomitant parathyroid adenoma, a case involving mediastinal parathyroidectomy, a case with an intrathymic parathyroid adenoma, two cases of recurrent pHPT, and one case of hereditary pHPT in Multiple Endocrine Neoplasia (MEN) 1 syndrome. The combination of parathyroid ultrasound and Tc-99m sestamibi scintigraphy is effective for localizing parathyroid adenomas in most patients. Additional imaging, such as single photon emission computed tomography/computed tomography (SPECT/CT) or 18F-Fluorocholine positron emission tomography/computed tomography (18F-FCH PET/CT), may be necessary in other cases. Intraoperative parathyroid hormone monitoring is valuable for detecting double adenomas in patients affected by hereditary familial hyperparathyroidism from MEN 1. Several studies highlight that the surgeon's expertise is the most critical determinant of a safe and successful surgical outcome.</p>\",\"PeriodicalId\":8210,\"journal\":{\"name\":\"Annali italiani di chirurgia\",\"volume\":\"96 7\",\"pages\":\"878-893\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annali italiani di chirurgia\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.62713/aic.3939\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"SURGERY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annali italiani di chirurgia","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.62713/aic.3939","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"SURGERY","Score":null,"Total":0}
Primary Hyperparathyroidism: A Case Series, Patient-Centered Approach to Diagnosis and Management Review.
Primary hyperparathyroidism (pHPT) is a prevalent disorder of dysregulated calcium homeostasis, marked by excessive secretion of parathyroid hormone (PTH), which results in alterated calcemia and renal and/or skeletal complications. Most patients are diagnosed before experiencing overt clinical symptoms, often as a result of blood tests performed for other disorders. When symptoms do manifest, they are associated with dysfunction of the parathyroid glands. Surgical treatment is considered the first choice and the only curative treatment for pHPT, offering advantages for both symptomatic and asymptomatic patients. The aim of this study is to report our experience in the management of 6 selected complex cases, which often require a multidisciplinary approach due to the lack of established diagnostic and therapeutic algorithms and the variability of clinical presentation and atypical parathyroid adenoma location. We present a series of cases examining the various treatment approaches in six distinct patients: one patient with parathyroid carcinoma with concomitant parathyroid adenoma, a case involving mediastinal parathyroidectomy, a case with an intrathymic parathyroid adenoma, two cases of recurrent pHPT, and one case of hereditary pHPT in Multiple Endocrine Neoplasia (MEN) 1 syndrome. The combination of parathyroid ultrasound and Tc-99m sestamibi scintigraphy is effective for localizing parathyroid adenomas in most patients. Additional imaging, such as single photon emission computed tomography/computed tomography (SPECT/CT) or 18F-Fluorocholine positron emission tomography/computed tomography (18F-FCH PET/CT), may be necessary in other cases. Intraoperative parathyroid hormone monitoring is valuable for detecting double adenomas in patients affected by hereditary familial hyperparathyroidism from MEN 1. Several studies highlight that the surgeon's expertise is the most critical determinant of a safe and successful surgical outcome.
期刊介绍:
Annali Italiani di Chirurgia is a bimonthly journal and covers all aspects of surgery:elective, emergency and experimental surgery, as well as problems involving technology, teaching, organization and forensic medicine. The articles are published in Italian or English, though English is preferred because it facilitates the international diffusion of the journal (v.Guidelines for Authors and Norme per gli Autori). The articles published are divided into three main sections:editorials, original articles, and case reports and innovations.