Arcot Rekha, Moorthy Sujatha Narayana, Rao Shalinee
Department of General Surgery, Sri Ramachandra Medical College and Research Institute, Porur, Chennai, India.
Indian J Endocrinol Metab. 2011 Jul;15(3):194-7. doi: 10.4103/2230-8210.83405.
Hyperparathyroidism (HPT) is a condition that occurs due to exacerbated activity of the parathyroid glands. According to the etiology it may be primary, secondary or tertiary hyperparathyroidism (pHPT, sHPT, tHPT). This is a study done to document and evaluate the presentations of primary and secondary HPT, with the associated complications and the approach to management in these patients, at our hospital.
Twenty-one patients with HPT were encountered at Sri Ramachandra Medical College and Research Institute between January 2000 and January 2010. Operative notes, histopathology files, and medical records were used for the retrospective analysis of the patients with HPT. Parathormone, calcium, and phosphate levels were estimated on all the patients, to determine the primary or secondary etiology of this endocrine abnormality. Furthermore, these patients were subjected to ultrasonography (USG) of the neck and Technetium (99 mTc) scan of the neck to identify the parathyroid gland.
This study revealed that about 76, 19, and 5% of the patients suffered from pHPT, sHPT, and tHPT, respectively, with a female preponderance (62%).The neoplasm in all patients with pHPT was parathyroid adenoma. The patients presented with renal, bony, and menstrual abnormalities. Cases with sHPT had a 15 - 20 year history of chronic kidney disease and they subsequently developed bony abnormalities. Even as all the patients with pHPT were managed with parathyroidectomy, individuals with sHPT were treated conservatively. Postoperative features of hypocalcemia were noted in only one patient.
This study re-emphasizes that pHPT is more common and is often due to an adenoma. Recent advances in parathormone sampling operatively and minimal access surgery, along with accurate and prompt clinical diagnosis, is necessary for the cure of these patients presenting with obscure abdominal, bony, and renal ailments.
甲状旁腺功能亢进症(HPT)是由于甲状旁腺活动加剧而引发的一种病症。根据病因,它可分为原发性、继发性或三发性甲状旁腺功能亢进症(pHPT、sHPT、tHPT)。本研究旨在记录和评估我院原发性和继发性HPT的临床表现、相关并发症以及这些患者的管理方法。
2000年1月至2010年1月期间,在斯里兰卡拉马钱德拉医学院和研究所遇到了21例HPT患者。手术记录、组织病理学档案和病历用于对HPT患者进行回顾性分析。对所有患者进行甲状旁腺激素、钙和磷水平的测定,以确定这种内分泌异常的原发性或继发性病因。此外,这些患者接受了颈部超声检查(USG)和颈部锝(99mTc)扫描,以识别甲状旁腺。
本研究显示,分别约有76%、19%和5%的患者患有pHPT、sHPT和tHPT,女性占优势(62%)。所有pHPT患者的肿瘤均为甲状旁腺腺瘤。患者出现肾脏、骨骼和月经异常。sHPT患者有15 - 20年的慢性肾病病史,随后出现骨骼异常。尽管所有pHPT患者均接受甲状旁腺切除术治疗,但sHPT患者则采用保守治疗。仅1例患者术后出现低钙血症特征。
本研究再次强调,pHPT更为常见,且通常由腺瘤引起。术中甲状旁腺激素采样和微创外科手术的最新进展,以及准确及时的临床诊断,对于治愈这些表现为不明原因腹部、骨骼和肾脏疾病的患者是必要的。