National Hospital of Sri Lanka, Colombo, Sri Lanka.
Provincial Directorate of Health Services-Western Province, Colombo, Sri Lanka.
BMC Endocr Disord. 2022 Oct 25;22(1):259. doi: 10.1186/s12902-022-01169-2.
Parathyroid carcinoma is an uncommon cause of PTH-dependent hypercalcemia. Only a handful of cases have been reported of parathyroid carcinoma during pregnancy.
Twenty-four - Year - old female presented with proximal myopathy was found to have hypercalcemia. Her serum corrected total calcium was - 15 mg/dl (8.5 - 10.3), serum phosphate - 2.3 mg/dl (2.5 - 4.5), intact PTH - 118 pg/ml (20 - 80), Vitamin D - 15 ng/ml and Urine Ca/Cr ratio - 2.1 (0.1 - 0.2). Her CECT-neck revealed a well-defined mass lesion posterior to the right lobe of the thyroid - 2.6 cm × 2.5 cm × 2.9 cm in size. She was started on vitamin D supplementation, and she underwent right lower focal parathyroidectomy. Her PTH levels normalized following surgery. Her histology revealed an atypical parathyroid adenoma. She was treated with calcium and vitamin D. Her follow up was uneventful. One year following initial surgery the patient became pregnant and at 16 weeks of POA, the patient presented with a rapidly enhancing neck mass for one week duration. Her biochemical investigations were suggestive of a recurrence of primary hyperparathyroidism. Her ultrasound scan of the neck revealed a well-defined discreate hypoechoic nodule, superior to the thyroid isthmus which was confirmed by a non-contrast MRI scan of the neck. She underwent an uncomplicated second trimester parathyroid tumour excision with normalization of post op PTH. Her histology revealed a parathyroid carcinoma with vascular and capsular invasion. Her genetic studies revealed a novel frameshift mutation of the CDC73 gene. She was treated with calcium and vitamin D supplementation and closely followed up with ionized calcium and PTH levels which were normal throughout the pregnancy. She had an uncomplicated caesarean section at a POA of 37 weeks. Currently she is twelve weeks post-partum, in remission of disease.
This case shows the importance of stringent follow up of atypical parathyroid adenoma patients, the benefit of second trimester surgery in management of hypercalcemia due to parathyroid carcinoma during pregnancy and the importance of identifying the novel CDC73 gene mutation.
甲状旁腺癌是引起甲状旁腺激素依赖性高钙血症的罕见原因。只有少数几例甲状旁腺癌在怀孕期间的报道。
一名 24 岁女性因近端肌无力就诊,发现血钙升高。她的血清校正总钙为 15mg/dl(8.5-10.3),血清磷为 2.3mg/dl(2.5-4.5),完整的甲状旁腺激素为 118pg/ml(20-80),维生素 D 为 15ng/ml,尿钙/肌酐比值为 2.1(0.1-0.2)。她的颈部 CECT 显示甲状腺右侧叶后有一个界限清楚的肿块病变,大小为 2.6cm×2.5cm×2.9cm。她开始接受维生素 D 补充治疗,并接受了右下叶局灶性甲状旁腺切除术。手术后她的甲状旁腺激素水平恢复正常。她的组织学显示为非典型甲状旁腺腺瘤。她接受了钙和维生素 D 的治疗。她的随访结果无异常。初次手术后一年,患者怀孕,在妊娠 16 周时,患者出现了为期一周的快速增强颈部肿块。她的生化检查提示原发性甲状旁腺功能亢进症复发。她的颈部超声检查显示甲状腺峡部上方有一个界限清楚的离散低回声结节,经颈部非增强 MRI 扫描证实。她接受了一次无并发症的妊娠中期甲状旁腺肿瘤切除术,术后甲状旁腺激素恢复正常。她的组织学显示甲状旁腺癌伴血管和包膜侵犯。她的基因研究显示 CDC73 基因的一个新的移码突变。她接受了钙和维生素 D 的补充治疗,并密切监测离子钙和甲状旁腺激素水平,整个孕期均正常。她在妊娠 37 周时进行了无并发症的剖宫产。目前,她产后 12 周,疾病处于缓解期。
本病例表明,对非典型甲状旁腺腺瘤患者进行严格随访的重要性,在怀孕期间因甲状旁腺癌引起高钙血症时,妊娠中期手术的益处,以及识别新型 CDC73 基因突变的重要性。