Khandwala Hasnain M, Boctor Markham A
Department of Medicine and the Division of Endocrinology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Endocr Pract. 2004 Jul-Aug;10(4):345-7. doi: 10.4158/EP.10.4.345.
To report a case of primary hyperparathyroidism (PHPT) that presented with recurrent hypercalcemia due to multiple myeloma after successful parathyroidectomy.
The initial manifestations, investigations, and postoperative follow-up of a case of hypercalcemia due to PHPT are described. The studies performed for evaluation for recurrent hypercalcemia and the subsequent diagnosis of multiple myeloma are discussed. The association between these disorders and reports of similar cases in the literature are reviewed.
A 72-year-old woman was referred for incidentally discovered hypercalcemia. She had no history of kidney stones or fractures. Further investigations revealed a high parathyroid hormone (PTH) level, hypercalciuria, and low bone mass, particularly at the cortical sites. Parathyroidectomy was performed, and a right inferior parathyroid adenoma was removed. Postoperatively, both the calcium and PTH levels normalized. She presented 9 months later with a 3-week history of pain in her left hip, polyuria, nausea, and vomiting. The patient had severe hypercalcemia and a suppressed PTH level. Further investigations revealed multiple bony lytic lesions, abnormalities on serum protein electrophoresis, and features consistent with multiple myeloma on a bone marrow biopsy specimen.
Hypercalcemia can occur in patients with PHPT and multiple myeloma; however, the occurrence of both disorders in the same patient is rare. Review of the literature revealed only a few cases similar to ours. Evidence in the literature suggests that monoclonal gammopathies occur more often in patients with PHPT than in the general population; therefore, screening for monoclonal gammopathy may be warranted in patients with PHPT.
报告一例原发性甲状旁腺功能亢进症(PHPT)患者,在甲状旁腺切除术后因多发性骨髓瘤出现复发性高钙血症。
描述一例因PHPT导致高钙血症患者的初始表现、检查及术后随访情况。讨论为评估复发性高钙血症所进行的研究以及随后多发性骨髓瘤的诊断。回顾这些疾病之间的关联以及文献中类似病例的报告。
一名72岁女性因偶然发现高钙血症前来就诊。她无肾结石或骨折病史。进一步检查发现甲状旁腺激素(PTH)水平升高、高钙尿症及低骨量,尤其是皮质部位。行甲状旁腺切除术,切除一枚右下甲状旁腺腺瘤。术后钙和PTH水平均恢复正常。9个月后,她出现左髋部疼痛3周、多尿、恶心和呕吐症状。患者有严重高钙血症且PTH水平受抑制。进一步检查发现多处骨质溶解性病变、血清蛋白电泳异常以及骨髓活检标本具有与多发性骨髓瘤相符的特征。
PHPT和多发性骨髓瘤患者均可出现高钙血症;然而,同一患者同时发生这两种疾病较为罕见。文献回顾显示仅有少数与我们病例类似的情况。文献证据表明,单克隆丙种球蛋白病在PHPT患者中比在普通人群中更常见;因此,对PHPT患者进行单克隆丙种球蛋白病筛查可能是必要的。