Rodriguez Kenny D, Schneider Kami Wolfe, Suttman Alexandra, Garrington Timothy, Jellins Tennyson, Tholen Kaitlyn, Francom Christian R, Herrmann Brian W
Department of Otolaryngology-Head and Neck Surgery, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
Department of Hematology, Oncology, Bone Marrow Transplantation, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
Ann Otol Rhinol Laryngol. 2022 Feb;131(2):159-163. doi: 10.1177/00034894211014786. Epub 2021 May 10.
Cancer predisposition syndromes are germline pathogenic variants in genes that greatly raise the risk of developing neoplastic diseases. One of the most well-known is Li-Fraumeni syndrome (LFS), which is due to pathogenic variants in the gene. Children with LFS have higher risks for multiple malignancies before adulthood, often with rare and aggressive subtypes.
To examine head and neck manifestations of LFS in children treated at a tertiary children's hospital over a 20-year period.
A retrospective review of LFS children with neoplastic disease presenting in traditional Otolaryngologic head and neck subsites from 2000 to 2019, with patient charts reviewed for relevant clinical, imaging, and operative data.
Of the 40 LFS patients initially identified, 27 neoplastic tumors were identified in 20 children within this cohort (20 primary, 7 second primary). Head and neck subsites aside from the brain or orbit were involved in 22% (6/27) of these tumors, representing 20% (4/20) of primary tumors and 29% (2/7) of second primary tumors. Both second primaries within the head and neck were within the radiation fields of the first primary tumor. The mean ages at primary and second primary diagnosis were 4.6 years (SD 3.5) and 12 years (SD 1.4), respectively. The male/female ratio was 1:6 among all patients with head and neck tumors. All 6 head and neck tumors were sarcomas. Rhabdomyosarcoma ( = 3, 50%) was the most common pathology, and the other 3 demonstrated rare tumor pathological subtypes (synovial cell sarcoma, pleomorphic myxoid liposarcoma, mandibular osteosarcoma). The neck was the most common subsite (75%) within this group for primary tumor presentation.
This study identifies a high potential for head and neck involvement in children with LFS, which has not been previously described in the literature. Otolaryngological care should be included in a multidisciplinary care team surveilling these patients.
癌症易感性综合征是指基因中的种系致病变异,会大幅增加患肿瘤性疾病的风险。其中最著名的一种是李-佛美尼综合征(LFS),它是由该基因的致病变异引起的。患有LFS的儿童在成年前患多种恶性肿瘤的风险更高,且通常是罕见且侵袭性的亚型。
研究一家三级儿童医院在20年期间治疗的LFS患儿的头颈部表现。
回顾性分析2000年至2019年在传统耳鼻喉头颈亚部位出现肿瘤性疾病的LFS患儿,查阅患者病历以获取相关临床、影像学和手术数据。
在最初确定的40例LFS患者中,该队列中的20名儿童共发现27个肿瘤(20个原发性肿瘤,7个第二原发性肿瘤)。除脑或眼眶外,头颈亚部位涉及这些肿瘤的22%(6/27),占原发性肿瘤的20%(4/20)和第二原发性肿瘤的29%(2/7)。头颈部的两个第二原发性肿瘤均在第一个原发性肿瘤的放射野内。原发性和第二原发性诊断时的平均年龄分别为4.6岁(标准差3.5)和12岁(标准差1.4)。所有头颈部肿瘤患者的男女比例为1:6。所有6个头颈部肿瘤均为肉瘤。横纹肌肉瘤(n = 3,50%)是最常见的病理类型,另外3例表现为罕见的肿瘤病理亚型(滑膜细胞肉瘤、多形性黏液样脂肪肉瘤、下颌骨肉瘤)。颈部是该组原发性肿瘤最常见的亚部位(75%)。
本研究发现LFS患儿头颈部受累的可能性很高,这在以前的文献中尚未有描述。耳鼻喉科护理应纳入监测这些患者的多学科护理团队中。