Bal Simrun K, Sorensen Meredith J, Crawford Andrew Robert
Department of Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Section of Endocrine Surgery, Department of Surgery, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
AACE Clin Case Rep. 2021 Aug 3;8(1):37-40. doi: 10.1016/j.aace.2021.07.004. eCollection 2022 Jan-Feb.
We report a case of normocalcemic primary hyperparathyroidism, a diagnosis prompted by radiographic "salt and pepper" calvarial lesions, typically described in hypercalcemic primary hyperparathyroidism or secondary hyperparathyroidism.
A 60-year-old woman noticed indentations of her scalp and presented to her primary care provider. Radiography of the calvarium demonstrated granular "salt and pepper" lesions, prompting investigation. The patient was found to have an elevated parathyroid hormone (PTH) level of 79 pg/mL (reference range, 14-54 pg/mL) and a normal albumin-corrected calcium level of 9.8 mg/dL (reference range, 8.6-10.4 mg/dL). She was referred to our endocrine clinic and described having bone aches, fevers, leg cramps, and a remote history of nephrolithiasis. Her physical examination revealed hypertension. Repeat laboratory evaluation confirmed elevated PTH and normal albumin-corrected calcium. Secondary causes of hyperparathyroidism were ruled out. Her 25-hydroxyvitamin D level was 35 ng/mL (reference range, 30-100 ng/mL), with a normal creatinine level (0.73 mg/dL; reference range, 0.5-0.99 mg/dL). The patient underwent ultrasound and sestamibi scintigraphy, with uptake in the right inferior thyroid pole. She was found to have a 6-mm parathyroid adenoma and underwent a targeted parathyroidectomy, with normalization of serum PTH.
Many cases of normocalcemic primary hyperparathyroidism are diagnosed in asymptomatic patients presenting with low bone mass; however, imaging prompted this patient's evaluation. Ultimately, the calvarial lesions were thought secondary to bone resorption from increased osteoclast activity.
This case highlights an atypical presentation of normocalcemic primary hyperparathyroidism in that the evaluation was precipitated by unexpected radiographic evidence of metabolic bone disease, rather than by symptoms or biochemical studies.
我们报告一例血钙正常的原发性甲状旁腺功能亢进症,其诊断是由颅骨X线片上的“椒盐样”病变引发的,这种病变通常见于高钙血症性原发性甲状旁腺功能亢进症或继发性甲状旁腺功能亢进症。
一名60岁女性注意到头皮有凹陷,遂就诊于其初级保健医生。颅骨X线片显示有颗粒状“椒盐样”病变,促使进一步检查。该患者甲状旁腺激素(PTH)水平升高至79 pg/mL(参考范围为14 - 54 pg/mL),白蛋白校正钙水平正常,为9.8 mg/dL(参考范围为8.6 - 10.4 mg/dL)。她被转诊至我们的内分泌门诊,并自述有骨痛、发热、腿部痉挛,以及既往有肾结石病史。体格检查发现她有高血压。再次实验室检查证实PTH升高而白蛋白校正钙正常。继发性甲状旁腺功能亢进的病因被排除。她的25 - 羟维生素D水平为35 ng/mL(参考范围为30 - 100 ng/mL),肌酐水平正常(0.73 mg/dL;参考范围为0.5 - 0.99 mg/dL)。患者接受了超声和锝 - 甲氧基异丁基异腈闪烁扫描,发现甲状腺右下极有摄取。她被发现有一个6毫米的甲状旁腺腺瘤,并接受了靶向甲状旁腺切除术,血清PTH恢复正常。
许多血钙正常的原发性甲状旁腺功能亢进症病例是在无症状但骨量低的患者中诊断出来的;然而,影像学检查促使了对该患者的评估。最终,颅骨病变被认为是破骨细胞活性增加导致骨吸收继发的。
本病例突出了血钙正常的原发性甲状旁腺功能亢进症的非典型表现,即评估是由代谢性骨病意外的影像学证据引发的,而非症状或生化检查。