Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-1107, USA.
J Urol. 2011 Jun;185(6):2050-5. doi: 10.1016/j.juro.2011.02.051. Epub 2011 Apr 15.
Managing oncocytoma in the setting of bilateral renal masses is a challenging scenario. Nevertheless, to our knowledge the pathological concordance of an oncocytic neoplasm in 1 kidney with tumors in the contralateral kidney is not known. We evaluated the influence of germline Birt-Hogg-Dubé mutation on concordance rates to assist in managing these cases.
We reviewed the records of patients at the National Institutes of Health between 1983 and 2009 who had bilateral renal masses, known pathology bilaterally and oncocytoma or an oncocytic neoplasm in at least 1 kidney. Oncocytoma or an oncocytic neoplasm in 2 renal units was considered concordant. Demographic, pathological and clinical data were collected.
The population consisted of 40 patients, including 23 with and 17 without a diagnosis of Birt-Hogg-Dubé syndrome. Patients with the syndrome were younger (p <0.01) but there were no other differences between the 2 groups. However, patients with the syndrome had statistically lower histological concordance between bilateral masses than patients without the diagnosis (Fisher's exact test p <0.01). Also, the 8 patients without Birt-Hogg-Dubé syndrome who had multifocal renal masses showed 100% oncocytoma concordance between renal units.
Of patients with bilateral renal masses those with Birt-Hogg-Dubé syndrome have significantly lower histological concordance than those without the syndrome. Patients with Birt-Hogg-Dubé syndrome should be monitored and treated differently than those without detected genetic mutations, especially patients with multifocal oncocytomas. Genetic testing for Birt-Hogg-Dubé should be considered in the treatment algorithm of patients with bilateral renal masses and known oncocytoma.
在双侧肾脏肿块的情况下管理嗜酸细胞瘤是一个具有挑战性的情况。然而,据我们所知,单侧肾脏的嗜酸细胞瘤与对侧肾脏肿瘤的病理一致性尚不清楚。我们评估了种系 Birt-Hogg-Dubé 突变对一致性率的影响,以协助处理这些病例。
我们回顾了 1983 年至 2009 年期间在国立卫生研究院就诊的患者的记录,这些患者双侧肾脏均有肿块,双侧均有已知的病理学和至少单侧有嗜酸细胞瘤或嗜酸细胞瘤。双侧肾脏单位均有嗜酸细胞瘤或嗜酸细胞瘤被认为是一致的。收集了人口统计学、病理学和临床数据。
该人群包括 40 例患者,其中 23 例患有 Birt-Hogg-Dubé 综合征,17 例未患有该综合征。患有该综合征的患者年龄较小(p<0.01),但两组之间无其他差异。然而,患有该综合征的患者双侧肿块之间的组织学一致性明显低于未诊断出该综合征的患者(Fisher 精确检验,p<0.01)。此外,8 例未患有 Birt-Hogg-Dubé 综合征且有多发性肾肿块的患者,其肾脏单位的嗜酸细胞瘤一致性为 100%。
在双侧肾脏肿块患者中,患有 Birt-Hogg-Dubé 综合征的患者的组织学一致性明显低于未患有该综合征的患者。患有 Birt-Hogg-Dubé 综合征的患者应与未检测到遗传突变的患者进行不同的监测和治疗,尤其是患有多发性嗜酸细胞瘤的患者。在双侧肾脏肿块和已知嗜酸细胞瘤患者的治疗算法中,应考虑进行 Birt-Hogg-Dubé 基因检测。