Reséndiz-Colosia Jaime Alonso, Rodriguez-Cuevas Sergio Arturo, Medrano-Ortiz de Zarate María Elena, Flores-Díaz Rutilio, Gallegos-Hernández José Francisco, Gómez-Acosta Fernando
Servicio de Tumores de Cabeza, Cuello y Piel, Hospital de Oncologla, Centro Médico Nacional SigloXXI, Instituto Mexicano del Seguro Social, México D.F., México.
Gac Med Mex. 2009 May-Jun;145(3):207-13.
A growing number of patients with primary hyperparathyroidism (PHPT) are diagnosed in the absence of symptoms following routine biochemical screening. However, in some countries, overt manifestations and osteitis fibrosa cystica (OFC) still dominate the clinical profile of PHPT patients.
We retrospectively studied clinical and biochemical manifestations of 47 consecutive patients with primary hyperparathyroidism who were treated with parathyroidectomy from October 1993 to June 2005.
Mean age was of 51.3 years. Our sample included 40 women (85%) and 7 men (15%). Seventy eight percent of cases had radiological features of OFC, namely subperiosteal bone resorption, cortical cysts and osteopenia. Pathological fracture occurred in nine patients (19.1%). Fifteen (32%) patients had clinically evident bony deformities or brown tumors mostly located in the mandible and maxilla.
Our results indicate that symptomatic osteitis fibrosa cystica and severe decrease of bone mineral density were the primary manifestations of primary hyperparathyroidism. Most patients were referred to an oncology hospital for treatment due to a suspected malignant neoplasm. A comprehensive clinical evaluation with biochemical markers, imaging studies and histological results is needed to establish a possible diagnosis of primary hyperparathyroidism.
越来越多的原发性甲状旁腺功能亢进症(PHPT)患者在常规生化筛查后被诊断为无症状。然而,在一些国家,明显的临床表现和纤维囊性骨炎(OFC)仍然主导着PHPT患者的临床特征。
我们回顾性研究了1993年10月至2005年6月期间接受甲状旁腺切除术的47例连续性原发性甲状旁腺功能亢进症患者的临床和生化表现。
平均年龄为51.3岁。我们的样本包括40名女性(85%)和7名男性(15%)。78%的病例具有OFC的放射学特征,即骨膜下骨质吸收、皮质囊肿和骨质减少。9名患者(19.1%)发生病理性骨折。15名(32%)患者有临床上明显的骨畸形或棕色瘤,主要位于下颌骨和上颌骨。
我们的结果表明,有症状的纤维囊性骨炎和骨矿物质密度严重降低是原发性甲状旁腺功能亢进症的主要表现。大多数患者因疑似恶性肿瘤被转诊至肿瘤医院治疗。需要综合临床评估,结合生化指标、影像学检查和组织学结果来确立原发性甲状旁腺功能亢进症的可能诊断。