Shepherd J J, Burgess J R, Greenaway T M, Ware R
Department of Surgery, University of Tasmania and Royal Hobart Hospital, Australia.
Arch Surg. 2000 Jul;135(7):844-8. doi: 10.1001/archsurg.135.7.844.
Preoperative parathyroid radioisotope scanning is of little or no value in patients with multiple endocrine neoplasia type 1 when 4 or more hypertrophied glands are present. Scanning using technetium Tc 99m sestamibi and single photon emission computed tomography will achieve a high level of sensitivity and specificity after 3 or more glands have previously been removed, justifying limited surgical reexploration.
In a prospective study, the preoperative documented report of the predicted site of residual parathyroid was compared with the surgical findings in 13 patients having 19 scans and 17 reoperations.
All patients belonged to one family, previously described as Tasman family 1, and were confirmed by genetic testing as having multiple endocrine neoplasia type 1. In 10 of 13 patients, reexploration was being undertaken more than 10 years after the first operation.
Scanning was regarded as successful when the documented preoperative report correctly predicted the side and quadrant in which a gland was found at surgery. Surgery was regarded as successful when calcium levels decreased to or below normal levels and were maintained.
All 13 scans before first reexploration were successful in identifying the location of a residual parathyroid. From a statistical viewpoint, this equates to 100% sensitivity and 92% specificity. However, despite accurate localization of 1 residual gland in every patient, 7 supernumerary glands in 4 patients and 1 parathyroid remnant in a fifth patient were not localized so that sensitivity in locating all glands in every patient was only 61%. Scans performed for persistent hypercalcemia 48 to 72 hours after reexploration in 2 patients were unsuccessful in demonstrating any residual parathyroid. Scans performed 3 months after surgery in the same 2 patients and a third patient were successful, with sensitivity and specificity of 100%. Apart from patient 11, who awaits reexploration, normocalcemia was eventually achieved in every patient, with 11 of 12 having an initial period of hypocalcemia.
Three months after reexploration and trimming or resection with transplant of half a gland left at first operation, sestamibi scanning achieved sensitivity and specificity of 100% in locating supernumerary parathyroids in patients with multiple endocrine neoplasia type 1 and persistent hypercalcemia. Before first reexploration, however, scans rarely provided new information, predominantly showing only the hypertrophied half-gland remnant.
对于1型多发性内分泌腺瘤病且存在4个或更多增生性腺的患者,术前甲状旁腺放射性同位素扫描几乎没有价值或毫无价值。当先前已切除3个或更多腺体后,使用锝Tc 99m甲氧基异丁基异腈和单光子发射计算机断层扫描将获得较高的敏感性和特异性,这为有限的手术再次探查提供了依据。
在一项前瞻性研究中,将术前记录的残留甲状旁腺预测部位报告与13例患者(进行了19次扫描和17次再次手术)的手术结果进行了比较。
所有患者属于一个家族,先前被描述为塔斯曼家族1,经基因检测确诊为1型多发性内分泌腺瘤病。13例患者中有10例在首次手术后10多年进行了再次探查。
当术前记录报告正确预测手术中发现腺体的一侧和象限,扫描被视为成功。当血钙水平降至或低于正常水平并维持时,手术被视为成功。
首次再次探查前的所有13次扫描均成功识别出残留甲状旁腺的位置。从统计学角度看,这相当于100%的敏感性和92%的特异性。然而,尽管每位患者的1个残留腺体定位准确,但4例患者中的7个多余腺体和第5例患者中的1个甲状旁腺残余未被定位,因此每位患者中所有腺体定位的敏感性仅为61%。2例患者再次探查后48至72小时因持续性高钙血症进行的扫描未能显示任何残留甲状旁腺。在同一2例患者和第3例患者术后3个月进行的扫描成功,敏感性和特异性均为100%。除了等待再次探查的患者11外,每位患者最终均实现了血钙正常,12例中有11例有初期低钙血症阶段。
再次探查并修剪或切除首次手术时留下的半个腺体并移植后3个月,甲氧基异丁基异腈扫描在定位1型多发性内分泌腺瘤病且有持续性高钙血症患者的多余甲状旁腺方面,敏感性和特异性达到100%。然而,在首次再次探查前,扫描很少能提供新信息,主要仅显示增生的半个腺体残余。