Department of Paediatric Oncology and Haematology, GPOH-MET registry, Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
Pediatr Blood Cancer. 2020 Feb;67(2):e28056. doi: 10.1002/pbc.28056. Epub 2019 Nov 13.
Multiple endocrine neoplasia (MEN) 2B is characterized by early development of aggressive medullary thyroid carcinoma (MTC), visible physical stigmata, and associated symptoms. In most cases, de novo mutations are revealed. There are premonitory symptoms and stigmata that enable early diagnosis, before an inoperable MTC develops. The German Society for Paediatric Oncology and Haematology (GPOH)-Malignant Endocrine Tumours (MET) registry maintains records of children with MTC in Germany since 1997.
Children with a diagnosis of MTC in MEN 2B recorded in the GPOH-MET study were analyzed retrospectively. Stigmata and symptoms associated with MEN 2B were examined.
From inception through 2017, 24 patients aged 0.2-17.3 years were included. Symptoms affecting the oral/dental (88.0%), musculoskeletal (79.2%), and gastrointestinal (70.8%) systems were recognized most frequently. Gastrointestinal and musculoskeletal symptoms preceded symptoms of MTC. Twelve patients had short stature. Regarding the prevalence of single symptoms, neuromas of the lips and the oral cavity were mentioned most frequently. Five patients died from MTC. Patients diagnosed by tumor symptoms showed more advanced disease than those with disease detected by other means. Children diagnosed via associated stigmata and symptoms or positive family history had significantly improved overall survival (OS) compared to children diagnosed via symptoms of MTC (OS 100% vs 53.3%).
In children with MEN 2B, oral/dental, musculoskeletal, and gastrointestinal symptoms are most common. If children are diagnosed via associated symptoms and stigmata, OS is improved. Most of the children were diagnosed with growth disturbances; this finding requires verification and ranging in other patient cohorts.
多发性内分泌肿瘤 2B 型(MEN2B)的特征是早期发生侵袭性甲状腺髓样癌(MTC)、可见的躯体特征和相关症状。在大多数情况下,发现的是新生突变。存在预示性症状和体征,可在无法手术的 MTC 发生之前进行早期诊断。自 1997 年以来,德国儿科肿瘤学和血液学学会(GPOH)-恶性内分泌肿瘤(MET)登记处一直记录德国儿童的 MTC 病例。
对 GPOH-MET 研究中记录的 MEN2B 型中的 MTC 患儿进行回顾性分析。检查与 MEN2B 相关的体征和症状。
从开始到 2017 年,共纳入 24 例 0.2-17.3 岁的患者。最常识别到影响口腔/牙科(88.0%)、肌肉骨骼(79.2%)和胃肠道(70.8%)系统的症状。胃肠道和肌肉骨骼症状先于 MTC 症状出现。12 例患者身材矮小。就单一症状的患病率而言,唇部和口腔神经瘤被提及最多。5 例患者死于 MTC。因肿瘤症状而诊断的患者与因其他方式诊断的患者相比,疾病处于更晚期。通过相关体征和症状或阳性家族史诊断的患儿与通过 MTC 症状诊断的患儿相比,总体生存率(OS)显著提高(OS 100%vs53.3%)。
在 MEN2B 型患儿中,口腔/牙科、肌肉骨骼和胃肠道症状最为常见。如果患儿通过相关症状和体征诊断,则 OS 得到改善。大多数患儿因生长障碍而确诊;这一发现需要在其他患者队列中得到验证和分类。