Alani Rusul, Awai Andeh, Yetukuri Divya, Patel Vijaykumar
Medical School, Ross University School of Medicine, St. Michael, BRB.
General Surgery, Wellstar Atlanta Medical Center, Atlanta, USA.
Cureus. 2022 Oct 29;14(10):e30854. doi: 10.7759/cureus.30854. eCollection 2022 Oct.
Solitary parathyroid adenoma is the most common cause of primary hyperparathyroidism; however, multiple parathyroid adenomas are an uncommon phenomenon. In this case report, we discuss a patient presenting with two concurrent ipsilateral parathyroid adenomas, and we review the literature. A 61-year-old African American female with a history of hypertension and kidney stones presented for the evaluation of hypercalcemia. Elevated serum calcium of 11 mg/dL was found on routine laboratory tests and low25 hydroxyvitamin-D level. Parathyroid hormone (PTH) was elevated at 172.5 pg/mL and increased to 443 pg/mL after correction of vitamin D deficiency. Renal function tests and thyroid function tests revealed normal findings. Imaging studies with 99mTc-Sestamibi scintigraphy raised concern for the possibility of either a parathyroid adenoma or hyperplasia. Minimally invasive parathyroidectomy with intraoperative PTH monitoring was planned. During surgery, the right superior parathyroid gland was found to be enlarged and was excised. However, intraoperative PTH monitoring showed an initial decrease to 203 pg/mL from a baseline of 443 pg/mL and a subsequent increase to 293 pg/mL suggesting the persistence of hyperparathyroidism. Further exploration of the neck revealed an enlarged right inferior parathyroid gland and two normal left parathyroid glands. Intraoperative PTH monitoring then revealed an appropriate decrease in PTH level to 56 pg/mL 10 minutes after excision of the right inferior parathyroid gland. More than a 50% decrease in PTH was achieved, and further exploration of the opposite side revealed no evidence of four-gland hyperplasia. Pathology reported two concurrent right superior and inferior parathyroid adenomas. Successful and curative parathyroidectomy for primary hyperparathyroidism was achieved. Although rare, multiple parathyroid adenomas occur in a significant minority of cases. Intraoperative PTH monitoring along with preoperative imaging provides guidance for curative parathyroidectomy. Additionally, more sensitive imaging such as four-dimensional computed tomography scans could lead to better localization, visualization, and identification of the second parathyroid adenoma.
孤立性甲状旁腺腺瘤是原发性甲状旁腺功能亢进最常见的病因;然而,多发性甲状旁腺腺瘤是一种罕见现象。在本病例报告中,我们讨论了一名患有两个同侧并发甲状旁腺腺瘤的患者,并对相关文献进行了回顾。一名61岁的非裔美国女性,有高血压和肾结石病史,因高钙血症前来评估。常规实验室检查发现血清钙升高至11mg/dL,25羟维生素D水平降低。甲状旁腺激素(PTH)升高至172.5pg/mL,维生素D缺乏纠正后升至443pg/mL。肾功能检查和甲状腺功能检查结果正常。99mTc-甲氧基异丁基异腈闪烁显像的影像学检查引发了对甲状旁腺腺瘤或增生可能性的担忧。计划进行术中PTH监测的微创甲状旁腺切除术。手术中,发现右上甲状旁腺肿大并予以切除。然而,术中PTH监测显示最初从基线443pg/mL降至203pg/mL,随后又升至293pg/mL,提示甲状旁腺功能亢进持续存在。进一步探查颈部发现右下甲状旁腺肿大,左侧两个甲状旁腺正常。切除右下甲状旁腺10分钟后,术中PTH监测显示PTH水平适当下降至56pg/mL。PTH下降超过50%,对另一侧的进一步探查未发现四腺增生的证据。病理报告为右上和右下甲状旁腺同时并发腺瘤。成功实施了治愈原发性甲状旁腺功能亢进的甲状旁腺切除术。尽管罕见,但多发性甲状旁腺腺瘤在少数病例中出现。术中PTH监测以及术前影像学检查为治愈性甲状旁腺切除术提供了指导。此外,更敏感的影像学检查,如四维计算机断层扫描,可能会更好地定位、可视化并识别第二个甲状旁腺腺瘤。