Rock Kathy, Fattah Nariman, O'Malley Diarmuid, McDermott Enda
Surgical Professorial Unit, Saint Vincent's University Hospital, Dublin 4, Ireland.
J Med Case Rep. 2010 Jan 29;4:28. doi: 10.1186/1752-1947-4-28.
Hypercalcaemic hyperparathyroid crisis is a rare but life-threatening complication of primary hyperparathyroidism. Parathyroid carcinoma is a rare malignancy with an incidence of 0.5% to 4% of all reported cases of primary hyperparathyroidism.
We report the case of a 60-year-old Caucasian man with hypercalcaemic hyperparathyroid crisis associated with parathyroid carcinoma. He presented with a classic hypercalcaemic syndrome and his serum calcium and parathyroid hormone levels were at 4.65 mmol/L and 1743 ng/L, respectively. He initially presented with a two-week history of weakness and lethargy and a one-week history of vomiting, polyuria and polydipsia. An emergency left thyroid lobectomy and left lower parathyroidectomy were performed. There was a prompt decrease in his parathyroid hormone level immediately after surgery. Histology revealed that our patient had a 4-cm parathyroid carcinoma.
In patients with parathyroid carcinoma, the optimal surgical treatment is en bloc resection with ipsilateral thyroid lobectomy and removal of any enlarged or abnormal lymph nodes. Surgery is the only curative treatment. In our patient, prompt surgical intervention proved successful. At six months the patient is well with no evidence of disease recurrence. This case highlights the importance of considering a hyperparathyroid storm in the context of a parathyroid carcinoma. Parathyroid carcinoma is a rare entity and our knowledge is mainly derived from case reports and retrospective studies. This case report increases awareness of this serious and life-threatening complication. This report also illustrates how prompt and appropriate management provides the best outcome for the patient.
高钙血症性甲状旁腺危象是原发性甲状旁腺功能亢进症一种罕见但危及生命的并发症。甲状旁腺癌是一种罕见的恶性肿瘤,在所有报道的原发性甲状旁腺功能亢进症病例中发病率为0.5%至4%。
我们报告一例60岁白种男性,患有与甲状旁腺癌相关的高钙血症性甲状旁腺危象。他表现出典型的高钙血症综合征,其血清钙和甲状旁腺激素水平分别为4.65 mmol/L和1743 ng/L。他最初出现两周的虚弱和嗜睡病史以及一周的呕吐、多尿和烦渴病史。急诊行左侧甲状腺叶切除术和左下甲状旁腺切除术。术后甲状旁腺激素水平立即迅速下降。组织学检查显示我们的患者患有一个4厘米的甲状旁腺癌。
对于甲状旁腺癌患者,最佳手术治疗是整块切除同侧甲状腺叶并切除任何肿大或异常的淋巴结。手术是唯一的治愈性治疗方法。在我们的患者中,及时的手术干预证明是成功的。六个月时患者情况良好,无疾病复发迹象。该病例突出了在甲状旁腺癌背景下考虑甲状旁腺危象的重要性。甲状旁腺癌是一种罕见疾病,我们的知识主要来源于病例报告和回顾性研究。本病例报告提高了对这种严重且危及生命的并发症的认识。本报告还说明了及时且恰当的治疗为患者带来最佳预后的情况。