正常血钙水平原发性甲状旁腺功能亢进:与多发腺瘤相关的长期随访。

Larissa Pimentel, Sirley Portela, Alyne Loureiro, Francisco Bandeira
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引用次数: 4

摘要

正常血钙缺乏性原发性甲状旁腺功能亢进(NPHPT)是一种以甲状旁腺激素(PTH)升高为特征的疾病,而血清钙正常且没有继发原因。该病例描述说明了长期随访的绝经后妇女NPHPT患者进展多发性腺瘤。本病例报告一位77岁女性,患有慢性全身疼痛和骨质疏松症。患者初始血清PTH为105 pg/mL,血清总钙9.6 mg/dL,白蛋白4.79 g/dL,磷2.8 mg/dL,补充后25OHD为34.6 ng/mL。骨密度测定(BMD)结果如下:腰椎:t评分-3.0,股骨颈:t评分-2.6,桡骨远端:-4.2。排除其他继发性甲状旁腺功能亢进的原因,宫颈超声和Tc-99-Sestamibi扫描均为阴性。她使用口服阿仑膦酸和三次注射唑来膦酸治疗骨质疏松症。在第10年的随访中,在连续的宫颈造影阴性后,超声显示一个结节,提示右侧下甲状旁腺肿大。细针抽吸(FNA)获得的液体中PTH水平超过5,000 pg/mL, Sestamibi扫描为阴性。患者行甲状旁腺切除术,组织学检查证实甲状旁腺瘤。术后血清甲状旁腺激素在正常血钙水平下仍升高。随后的宫颈超声显示一个新的实性结节,提示右上甲状旁腺肿大。吸入液中甲状旁腺激素的水平非常高。第二次甲状旁腺切除术,切除组织学证实的甲状旁腺瘤。总之,这是一种不寻常的NPHPT表现,并突出了其长期并发症。
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Normocalcemic primary hyperparathyroidism: long-term follow-up associated with multiple adenomas.

Normocalcemic primary hyperparathyroidism (NPHPT) is a condition characterized by elevation of the parathyroid hormone (PTH) in the presence of normal serum calcium and the absence of secondary causes. The case described illustrates the long-term follow-up of a postmenopausal woman with NPHPT patient who progressed with multiple adenomas. This case reports a 77-year-old female who has chronic generalized pain and osteoporosis. Her initial serum PTH was 105 pg/mL, with total serum calcium of 9.6 mg/dL, albumin 4.79 g/dL, phosphorus 2.8 mg/dL, and 25OHD after supplementation was 34.6 ng/mL. The bone densitometry (BMD) results were as follows: lumbar spine: T-score -3.0, femoral neck: T-score -2.6 and distal radius: -4.2. Other causes of secondary hyperparathyroidism were ruled out and cervical ultrasound and Tc-99-Sestamibi scan were negative. She used oral alendronate and three infusions of zoledronic acid for treatment of osteoporosis. In the 10th year of follow-up, after successive negative cervical imaging, ultrasound showed a nodule suggestive of an enlarged right inferior parathyroid gland. PTH levels in fluid which was obtained during fine-needle aspiration (FNA) were over 5,000 pg/mL and a Sestamibi scan was negative. The patient underwent parathyroidectomy, and a histological examination confirmed parathyroid adenoma. Post-operatively serum PTH remained elevated in the presence of normal serum calcium levels. A follow-up cervical ultrasound showed a new solid nodule suggestive of an enlarged right superior parathyroid gland. PTH levels in the aspiration fluid were remarkably high. A second parathyroidectomy was performed, with the excision of a histologically confirmed parathyroid adenoma. In conclusion, this is an unusual presentation of NPHPT and highlights the long-term complications.

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[Multiple endocrine neoplasia type 2]. [Thyroid hormone resistance syndrome]. A case of thyroid hormone resistance: a rare mutation. [Giant metastasis of thyroid papillar carcinoma]. Angiotensin-II induced insulin resistance.
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