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纤维结构不良/McCune-Albright 综合征(FD/MAS)中恶性肿瘤患病率增加:来自国家转诊中心和荷兰全国病理登记处(PALGA)的数据。

Increased Prevalence of Malignancies in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS): Data from a National Referral Center and the Dutch National Pathology Registry (PALGA).

机构信息

Department of Medicine, Division Endocrinology, Center for Bone Quality, Leiden University Medical Center, Leiden, The Netherlands.

Department of Orthopaedic Surgery, Center for Bone Quality, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Calcif Tissue Int. 2021 Mar;108(3):346-353. doi: 10.1007/s00223-020-00780-6. Epub 2020 Nov 23.

Abstract

Malignant transformation of fibrous dysplasia lesions has been reported in patients with fibrous dysplasia/McCune-Albright syndrome (FD/MAS). Recently, we have observed an increased risk for breast cancer. In this study, the prevalence of skeletal and extraskeletal malignancies in patients with FD/MAS in the Netherlands was assessed by analyzing data from our cohort of FD/MAS patients, the Dutch Pathology Registry (PALGA), and the Netherlands Cancer Registry (NCR). We extracted data on sex, age at diagnosis of FD/MAS, type of FD/MAS, type of malignancy, and age at diagnosis of malignancy and histology of bone and malignant tissue when available, including GNAS-mutation analysis from patients' medical records. Standardized Morbidity Ratios (SMRs) with 95% confidence intervals were calculated. Twelve malignancies were identified in the LUMC FD/MAS cohort and 100 in the PALGA cohort. In this cohort, SMR was increased for osteosarcoma (19.7, 95% CI 3.5-48.9), cervical cancer (4.93, 95%CI 1.7-8.2), thyroid cancer (3.71, 95% CI 1.1-7.8), prostate cancer (3.08, 95% CI 1.8-4.6), and melanoma (2.01, 95%CI 1.2-3.1). SMRs for pancreatic cancer or hepatocellular carcinoma could not be calculated due to low numbers. The small number of malignancies identified in our FD/MAS cohort precluded the calculation of SMRs for our cohort specifically. Our findings show that patients with FD/MAS appear to have an increased risk for osteosarcoma, cervical, thyroid, and prostate cancer and melanoma. However, these data should be interpreted with caution, as true incidence rates of the identified malignancies may be influenced by the inclusion of only patients with histologically confirmed FD/MAS. The etiology of this increased risk for malignancies still needs to be elucidated.

摘要

纤维发育不良病变的恶性转化已在纤维发育不良/麦卡恩-阿尔布赖特综合征(FD/MAS)患者中报道。最近,我们观察到乳腺癌风险增加。在这项研究中,通过分析我们的 FD/MAS 患者队列、荷兰病理学登记处(PALGA)和荷兰癌症登记处(NCR)的数据,评估了荷兰 FD/MAS 患者中骨骼和骨骼外恶性肿瘤的患病率。我们从患者的病历中提取了关于性别、FD/MAS 诊断年龄、FD/MAS 类型、恶性肿瘤类型以及恶性肿瘤和骨组织的诊断年龄和组织学的数据,包括 GNAS 突变分析。计算了标准化发病比(SMR)和 95%置信区间。在 LUMC FD/MAS 队列中发现了 12 种恶性肿瘤,在 PALGA 队列中发现了 100 种恶性肿瘤。在该队列中,骨肉瘤(19.7,95%CI 3.5-48.9)、宫颈癌(4.93,95%CI 1.7-8.2)、甲状腺癌(3.71,95%CI 1.1-7.8)、前列腺癌(3.08,95%CI 1.8-4.6)和黑色素瘤(2.01,95%CI 1.2-3.1)的 SMR 增加。由于数量较少,无法计算胰腺癌或肝细胞癌的 SMR。由于我们的 FD/MAS 队列中发现的恶性肿瘤数量较少,因此无法专门计算我们队列的 SMR。我们的研究结果表明,FD/MAS 患者似乎患有骨肉瘤、宫颈癌、甲状腺癌和前列腺癌以及黑色素瘤的风险增加。然而,由于仅包括组织学证实的 FD/MAS 患者,因此这些数据的解释应谨慎进行。这种恶性肿瘤风险增加的确切发病率可能受到影响。这种恶性肿瘤风险增加的病因仍需要阐明。

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