Mantzoros Ioannis, Kyriakidou Despoina, Galanos-Demiris Konstantinos, Chatzakis Christos, Parpoudi Styliani, Sapidis Nikolaos, Loutzidou Lydia, Ioannidis Orestis, Angelopoulos Stamatis, Tsalis Konstantinos G
Fourth Surgical Department, Aristotle University of Thessaloniki, General Hospital "G. Papanikolaou", Thessaloniki, Greece.
Surgical Department, General Hospital of Edessa, Edessa, Greece.
Am J Case Rep. 2018 Nov 8;19:1334-1337. doi: 10.12659/AJCR.911452.
BACKGROUND Solitary parathyroid adenomas are the leading cause of primary hyperparathyroidism in 0% to 85% of cases. Diagnosis of parathyroid adenoma is based on typical clinical presentation of hypercalcemia, biochemical profile, and modern imaging studies. The purpose of this article is to present the diagnostic and therapeutic approach used for a 73-year-old female patient with a giant parathyroid adenoma measuring 5×2.5×2.5 cm and weighing 30 grams. CASE REPORT A 73-year-old female was referred to the outpatient clinic of our Surgical Department with the diagnosis of primary hyperparathyroidism. The patient suffered from typical symptoms of hypercalcemia such as weakness, bone disease, and recurrent nephrolithiasis; she had a painless cervical mass for 5 months. Primary hyperparathyroidism was confirmed based on the patient's biochemical profile, which showed increased levels of serum calcium and parathyroid hormone. SestaMIBI scintigraphy with 99mTechnetium and cervical ultrasonography revealed a large nodule at the inferior pole of the right lobe of the thyroid gland. Intraoperatively, a giant parathyroid adenoma was found and excised. Additionally, levels of intact parathyroid hormone (IOiPTH) were determined intraoperatively and a 95% reduction was found, 20 minutes after the removal of the adenoma. CONCLUSIONS This is an extremely rare case of a giant solitary parathyroid adenoma. Diagnosis of a giant hyperfunctioning solitary parathyroid adenomas was based on clinical presentation, biochemical profile, and imaging studies. Selective treatment was based on surgical excision combined with IOiPTH levels measurement.
在0%至85%的病例中,孤立性甲状旁腺腺瘤是原发性甲状旁腺功能亢进的主要原因。甲状旁腺腺瘤的诊断基于高钙血症的典型临床表现、生化指标以及现代影像学检查。本文旨在介绍对一名73岁女性患者的诊断和治疗方法,该患者患有一个大小为5×2.5×2.5厘米、重30克的巨大甲状旁腺腺瘤。
一名73岁女性因原发性甲状旁腺功能亢进被转诊至我们外科门诊。患者出现高钙血症的典型症状,如乏力、骨病和复发性肾结石;她有一个无痛性颈部肿块已5个月。根据患者的生化指标确诊为原发性甲状旁腺功能亢进,其血清钙和甲状旁腺激素水平升高。99m锝标记的甲氧基异丁基异腈闪烁扫描和颈部超声检查显示甲状腺右叶下极有一个大结节。术中发现并切除了一个巨大的甲状旁腺腺瘤。此外,术中测定了完整甲状旁腺激素(iPTH)水平,腺瘤切除后20分钟发现其降低了95%。
这是一例极其罕见的巨大孤立性甲状旁腺腺瘤病例。巨大功能性孤立性甲状旁腺腺瘤的诊断基于临床表现、生化指标和影像学检查。选择性治疗基于手术切除并结合iPTH水平测定。