Kandil Emad, Alabbas Haytham H, Lum Ying W, Tufaro Anthony P
Division of Endocrine and Oncological Surgery, Department of Surgery, Tulane University School of Medicine, and Tulane University Hospital, New Orleans, LA, USA.
South Med J. 2010 Mar;103(3):236-8. doi: 10.1097/SMJ.0b013e3181d0fe11.
Familial hyperparathyroidism includes the diagnoses of multiple endocrine neoplasia type 1, type 2A, and familial isolated primary hyperparathyroidism. Familial isolated primary hyperparathyroidism is a rare, distinct form of familial primary hyperparathyroidism, mainly due to four-gland hyperplasia or single-gland adenoma. We describe our success in treating a 24-year-old woman with familial isolated primary hyperparathyroidism with resection of double adenoma, using the guide of intraoperative parathyroid hormone (PTH) monitoring. Familial isolated primary hyperparathyroidism usually presents with four-gland hyperplasia or single-gland adenoma. However, double adenoma should be considered in the differential diagnosis. Using intraoperative parathyroid hormone levels and minimal-access surgery in familial isolated primary hyperparathyroidism may be promising.
家族性甲状旁腺功能亢进症包括1型、2A型多发性内分泌腺瘤病以及家族性孤立性原发性甲状旁腺功能亢进症的诊断。家族性孤立性原发性甲状旁腺功能亢进症是一种罕见的、独特的家族性原发性甲状旁腺功能亢进症形式,主要由四腺增生或单腺腺瘤引起。我们描述了在术中甲状旁腺激素(PTH)监测的引导下,成功为一名患有家族性孤立性原发性甲状旁腺功能亢进症的24岁女性切除双腺瘤的治疗过程。家族性孤立性原发性甲状旁腺功能亢进症通常表现为四腺增生或单腺腺瘤。然而,在鉴别诊断中应考虑双腺瘤。在家族性孤立性原发性甲状旁腺功能亢进症中使用术中甲状旁腺激素水平和微创手术可能前景广阔。