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Clinical features and survival analysis of neuroblastoma with cervical lymph node metastasis in children: su-mmary of 10 years in single center 儿童神经母细胞瘤伴颈部淋巴结转移的临床特点及生存分析:单中心10年总结
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190127-00063
Cheng Huang, Yan Su, Shengcai Wang, M. Jin, Xiufang Chai, Tian-xing Liu, Xiaoman Wang, Lejian He, H. Qin, Huanmin Wang, Xiao-li Ma
Objective To improve the awareness of neuroblastoma (NB) with cervical lymph node metastasis in children patients by summarizing the clinical features of such patients and analyzing their survival situation. Methods The research analyzed the medical records of 225 patients with cervical lymph node metastasis of NB from April 1, 2007 to May 31, 2017 in Beijing Children′s Hospital, Capital Medical University.The treatment were divided into 2 phases according to treatment time (one from April 1, 2007 to December 31, 2011 and the other from January 1, 2012 to May 31, 2017). The survival situation and treatment effect in each phase were analyzed.The following up time ended at Jan 1, 2018. Results (1)Clinical features: total 225 cases admitted in the research with about 37.3% of all the NB patients.One hundred girls(44.4%) and 125 boys(55.6%). The age from 2 months to 147 months, the me-dian age of patients was 37 months.The age under 18 months were 27 cases(12.1%). The majority primary site of tumor was located in retroperitoneal(174 cases, 77.3%) and mediastinum(48 cases, 21.3%). There were 33 cases which metastasic site confined to cervical lymph node(4N stage, 14.7%); 139 cases (62.1%) with bone marrow metastasis, 159 cases (71.0%) with bone metastasis.The number of patients in high-risk group was 208 cases(91.2%), while the low-risk and the medium-risk group was 17 cases(7.5%). (2)Treatment effect and survival analysis: a total of 200 cases received systemic treatment and followed-up in our hospital.The follow up time from 2 months to 123 months, the median follow up time was 23 months.The 3 year overall survival (OS) rate of all the patients was 56.4%, the 3 year event free survival (EFS) rate was 52.0%.While the 5-year OS was 46.5%, and the 5-year EFS was 39.7%.According to the first phase of treatment(April 1, 2007 to December 31, 2011), the 3-year EFS was 49.6%, and the 3-year OS was 54.4%, the 5-year EFS was 39.5%, and the 5-year OS was 44.7%.According to the second phase of treatment(January 1, 2012 to May 31, 2017), the 3-year EFS was 58.1%, and the 3-year OS was 57.3%.The 5-year EFS was 48.7%, and the 5-year OS was 46.8%.About the 4N patients, the 3-year EFS was 71.2%, and the 3-year OS was 82.2%.The 5-year EFS was 61.5%, and the 5-year OS was 76.7%. Conclusions Cervical lymph node is one of the most common distant metastasis of NB.More than half of the patient with bone or bone marrow metastasis.The prognosis of patients′ metastatic disease limited to cervical lymph nodes(4N stage), but still worse than the foreigner haver reported.The probable reason is the proportion of high-risk patients in the center is higher than the foreign research. Key words: Neuroblastoma; Cervical lymph node metastasis; Clinical features; Survival analysis
目的通过总结小儿神经母细胞瘤(NB)伴颈部淋巴结转移的临床特点,分析其生存情况,提高对NB的认识。方法对首都医科大学附属北京儿童医院2007年4月1日至2017年5月31日收治的225例新生儿颈部淋巴结转移患者的病历进行分析。根据治疗时间分为2期(2007年4月1日至2011年12月31日,2012年1月1日至2017年5月31日)。分析各组患者的生存情况及治疗效果。追踪时间截止至2018年1月1日。结果(1)临床特征:本研究共收治225例,约占NB患者总数的37.3%。100名女生(44.4%),125名男生(55.6%)。年龄2 ~ 147个月,中位年龄37个月。18月龄以下27例(12.1%)。肿瘤原发部位以腹膜后(174例,77.3%)和纵隔(48例,21.3%)居多。转移部位局限于颈部淋巴结33例(4N期,14.7%);骨髓转移139例(62.1%),骨转移159例(71.0%)。高危组208例(91.2%),低危、中危组17例(7.5%)。(2)治疗效果及生存分析:我院共200例患者接受了系统治疗及随访。随访时间2 ~ 123个月,中位随访时间23个月。3年总生存率(OS)为56.4%,3年无事件生存率(EFS)为52.0%。5年OS 46.5%, 5年EFS 39.7%。根据第一阶段治疗(2007年4月1日至2011年12月31日),3年EFS为49.6%,3年OS为54.4%,5年EFS为39.5%,5年OS为44.7%。根据第二阶段治疗(2012年1月1日至2017年5月31日),3年EFS为58.1%,3年OS为57.3%。5年EFS为48.7%,5年OS为46.8%。4N例患者中,3年EFS为71.2%,3年OS为82.2%。5年EFS为61.5%,5年OS为76.7%。结论颈淋巴结是NB最常见的远处转移方式之一。半数以上患者有骨或骨髓转移。患者转移性疾病的预后局限于颈部淋巴结(4N期),但仍比国外报道的差。可能的原因是本中心高危患者比例高于国外研究。关键词:神经母细胞瘤;颈部淋巴结转移;临床特征;生存分析
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引用次数: 0
Health-related quality of life among survivors of cancer in children 癌症儿童幸存者与健康相关的生活质量
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20200227-00275
Yongjun Fang, Heng Zhang
Over the past decades, substantial improvements in diagnostics, treatment, techniques and pharmacotherapy have resulted in a steadily increasing population of childhood cancer survivors.Health-related quality of life (HRQoL) of survivors has gradually become the focus of attention.Survivors of cancer in children will face a range of problems, such as physical, psychological and social pressure brought by the disease, growth and development disorders, gonadal dysfunction and late effects (organ dysfunction and secondary cancer). Previous studies have shown that the HRQoL of cancer survivors is significantly lower than that of the normal people, but some studies dedicated that the cancer experience may have a positive impact on the HRQoL of survivors.The quality of life questionnaires is widely used to evaluate HRQoL from the aspects of physical health, mental health and social health.Information from observational, cross-sectional, but particularly longitudinal studies, is needed to further describe HRQoL of cancer survivors in children, as well as provide a foundation for the development of intervention studies.More relevant studies are expected to provide evidence-based basis in making clinical decisions. Key words: Cancer; Survivors; Health-related quality of life; Child
在过去的几十年里,诊断、治疗、技术和药物治疗方面的重大改进导致癌症儿童幸存者的数量稳步增加。幸存者的健康相关生活质量(HRQoL)逐渐成为人们关注的焦点。儿童癌症幸存者将面临一系列问题,如疾病带来的身体、心理和社会压力、生长发育障碍、性腺功能障碍和晚期影响(器官功能障碍和继发癌症)。先前的研究表明,癌症幸存者的HRQoL显著低于正常人,但一些研究表明,癌症经历可能会对幸存者的HRQoL产生积极影响。生活质量问卷被广泛用于从身体健康、心理健康和社会健康等方面评价HRQoL。需要来自观察性、横断面、尤其是纵向研究的信息,以进一步描述癌症幸存者在儿童中的HRQoL,并为干预研究的发展提供基础。更多相关研究有望为临床决策提供循证基础。关键词:癌症;幸存者;与健康相关的生活质量;儿童
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引用次数: 0
Application of computer aided design 3D printed navigation template in Salter pelvic osteotomy for dislocation of hip joint in children 计算机辅助设计3D打印导航模板在儿童髋关节脱位Salter骨盆截骨术中的应用
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190327-00253
Ming Yong, Y. Lou, K. Tang, Peng Xu, Pengfei Zheng, Fei Liu
Objective To explore the feasibility of accurate localization for the acetabular direction in Salter pelvic osteotomy for the developmental dislocation of the hip joint in children by using computer aided design and 3D printing technique. Methods The clinical data of 12 patients of unilateral hip dislocation treated with Salter pelvic osteotomy by using 3D printed navigation template in Department of Orthopedics, Children′s Hospital of Nanjing Medical University From October 2016 to April 2017 were retrospectively analyzed.Among the 12 cases, there were 4 males and 8 females, 5 hips on the left and 7 hips on the right, aged 1.5 to 5.0 years old (mean 2.3 years old). According to the CT data, the models of the healthy hip joint were mirrored to the contralateral side by Mimics software.Computer-aided simulations of Salter pelvic osteotomy on models of the affected hip joints were performed.Then, the models of the affec-ted hip joint were rotated to the mirror models of the contralateral hip joint.The navigation templates were designed according to the exposed pelvic surface morphology during the operation.The navigation templates were printed by rapid prototyping technology to guide the operation.Preoperative and postoperative acetabular index (AI) and center edge angle (CEA) of affected side were compared to postoperative AI and CEA of contralateral side respectively. Results A method of making personalized navigation templates for Salter pelvic osteotomy was established in 12 children with developmental dislocation of the hip joint.The operation time ranged from 40.2 to 64.5 min, averaging (50.6±8.5) min.The intraoperative bleeding volume ranged from 35 to 60 mL, averaging 52 mL.No vascular and nerve injury was found in the postoperative examination, and no child had complications such as infection, residual foreign body of the guide plate and so on.There was significant difference in preoperative measurements regarding AI between the affected side [(38.4±2.8)°] and the contralateral side [(21.6±0.8)°](t=-18.77, P 0.05), there was no significant difference in postoperative measurements regarding CEA between the affected side[(21.2±2.6)°] and the contralateral side(t=-0.435, P>0.05). Conclusions The navigation template prepared by computer aided design and 3D printing technology has good accuracy, and is a new approach to accurate acetabular rotation in children with the developmental dislocation of the hip joint for Salter pelvic osteotomy. Key words: Dislocation of hip joint; Osteotomy; 3D printing
目的探讨应用计算机辅助设计和3D打印技术在儿童发育性髋关节脱位的Salter骨盆截骨术中精确定位髋臼方向的可行性。方法回顾性分析2016年10月至2017年4月南京医科大学儿童医院骨科采用3D打印导航模板行Salter骨盆截骨术治疗12例单侧髋关节脱位患者的临床资料。12例患者中男性4例,女性8例,左侧5髋,右侧7髋,年龄1.5 ~ 5.0岁,平均2.3岁。根据CT数据,通过Mimics软件将健康髋关节模型镜像到对侧。计算机辅助模拟Salter骨盆截骨术对受影响髋关节模型的影响。然后,将受累髋关节模型旋转成对侧髋关节的镜像模型。根据术中暴露的骨盆表面形态设计导航模板。采用快速成型技术打印导航模板,指导操作。将患侧髋臼指数(AI)、中心边缘角(CEA)分别与术后髋臼指数(AI)和对侧髋臼角(CEA)进行比较。结果建立了12例儿童发育性髋关节脱位Salter骨盆截骨术的个性化导航模板制作方法。手术时间40.2 ~ 64.5 min,平均(50.6±8.5)min,术中出血量35 ~ 60 mL,平均52 mL,术后检查无血管、神经损伤,患儿无感染、导板异物残留等并发症。术前患侧AI值[(38.4±2.8)°]与对侧AI值[(21.6±0.8)°]差异有统计学意义(t=-18.77, P 0.05),术后患侧CEA值[(21.2±2.6)°]与对侧CEA值差异无统计学意义(t=-0.435, P 0.05)。结论采用计算机辅助设计和3D打印技术制备的导航模板具有良好的精度,是儿童发育性髋关节脱位Salter骨盆截骨术中髋臼精确旋转的新途径。关键词:髋关节脱位;截骨术;3 d打印技术
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引用次数: 0
Study on the clinical characteristics and prognosis for children high-risk group of head and neck rhabdomyosarcoma 儿童头颈部横纹肌肉瘤高危人群的临床特点及预后研究
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190201-00081
Yi Zhang, Weiling Zhang, D. Huang, Yizhuo Wang, Huimin Hu, Song Li, Xue Meng
Objective To study the relationship between high-risk factors with the diagnosis, treatment and prognosis of children with high-risk head and neck rhabdomyosarcoma (RMS). Methods Children with high-risk RMS primarily found in head and neck were selected as research objects according to the criteria of RMS risk degree formulated by Children Oncology Group (COG) and Children′s Rhabdomyosarcoma Cooperative Group, Children′s Hematological Oncology Group, China Anti-Cancer Association (CCCG-RMS), and combined treatment including puncture pathology/surgery, chemotherapy and radiotherapy were performed.The relationship with primary site, age, pathology type and metastasis and prognosis were analyzed. Results Twenty-nine patients were collected as research object, 17 cases (58.6%) of male, and 12 cases (41.4%) of female.The primary site: orbit was 7 patients (24.1%), and para-meningeal was 22 patients (75.9%). Clinical stage: 2 cases were stage Ⅲ (6.9%), and 27 cases were stage Ⅳ (93.1%). Followed up to December 31, 2018, 14 patients were dead, 15 patients were survival, and 10 patients were event free survival.The overall survival rate was 48.3%(15/29 cases), and the event free survival rate was 34.5%(10/29 cases). According to Kaplan-Merier survival curve analysis, the average overall survival time was (76.0±12.0) months, 95% confidence interval (95% CI): (53.5-93.2)months.The event free survival time was (62.5±10.6) months, 95% CI: (47.0-83.9)months. Conclusions The prognosis of high-risk head and neck RMS is poor.The center system metastasis is cause of death.Thus, the main task is how to close follow-up and prevention of central nervous system invasion for improving prognosis. Key words: Rhabdomyosarcoma; Head and neck; High-risk group; Prognosis; Child
目的探讨高危因素与儿童高危头颈部横纹肌肉瘤(RMS)的诊断、治疗及预后的关系。方法根据中国抗癌协会儿童肿瘤学组(COG)和儿童横纹肌肉瘤合作学组、儿童血液肿瘤学组(CCCG-RMS)制定的RMS危险程度标准,选择主要发生于头颈部的高危RMS患儿作为研究对象,进行穿刺病理/手术、化疗、放疗联合治疗。分析其与原发部位、年龄、病理类型、转移及预后的关系。结果共收集29例患者作为研究对象,其中男性17例(58.6%),女性12例(41.4%)。眼眶7例(24.1%),脑膜旁22例(75.9%)。临床分期:Ⅲ期2例(6.9%),Ⅳ期27例(93.1%)。随访至2018年12月31日,死亡14例,生存15例,无事件生存10例。总生存率为48.3%(15/29例),无事件生存率为34.5%(10/29例)。Kaplan-Merier生存曲线分析,平均总生存时间为(76.0±12.0)个月,95%可信区间(95% CI)为(53.5 ~ 93.2)个月。无事件生存时间为(62.5±10.6)个月,95% CI:(47.0 ~ 83.9)个月。结论高危头颈部RMS预后较差。中心系统转移是死因。因此,如何密切随访,预防中枢神经系统的侵犯,以改善预后是目前的主要课题。关键词:横纹肌肉瘤;头颈;高危人群;预后;孩子
{"title":"Study on the clinical characteristics and prognosis for children high-risk group of head and neck rhabdomyosarcoma","authors":"Yi Zhang, Weiling Zhang, D. Huang, Yizhuo Wang, Huimin Hu, Song Li, Xue Meng","doi":"10.3760/CMA.J.CN101070-20190201-00081","DOIUrl":"https://doi.org/10.3760/CMA.J.CN101070-20190201-00081","url":null,"abstract":"Objective \u0000To study the relationship between high-risk factors with the diagnosis, treatment and prognosis of children with high-risk head and neck rhabdomyosarcoma (RMS). \u0000 \u0000 \u0000Methods \u0000Children with high-risk RMS primarily found in head and neck were selected as research objects according to the criteria of RMS risk degree formulated by Children Oncology Group (COG) and Children′s Rhabdomyosarcoma Cooperative Group, Children′s Hematological Oncology Group, China Anti-Cancer Association (CCCG-RMS), and combined treatment including puncture pathology/surgery, chemotherapy and radiotherapy were performed.The relationship with primary site, age, pathology type and metastasis and prognosis were analyzed. \u0000 \u0000 \u0000Results \u0000Twenty-nine patients were collected as research object, 17 cases (58.6%) of male, and 12 cases (41.4%) of female.The primary site: orbit was 7 patients (24.1%), and para-meningeal was 22 patients (75.9%). Clinical stage: 2 cases were stage Ⅲ (6.9%), and 27 cases were stage Ⅳ (93.1%). Followed up to December 31, 2018, 14 patients were dead, 15 patients were survival, and 10 patients were event free survival.The overall survival rate was 48.3%(15/29 cases), and the event free survival rate was 34.5%(10/29 cases). According to Kaplan-Merier survival curve analysis, the average overall survival time was (76.0±12.0) months, 95% confidence interval (95% CI): (53.5-93.2)months.The event free survival time was (62.5±10.6) months, 95% CI: (47.0-83.9)months. \u0000 \u0000 \u0000Conclusions \u0000The prognosis of high-risk head and neck RMS is poor.The center system metastasis is cause of death.Thus, the main task is how to close follow-up and prevention of central nervous system invasion for improving prognosis. \u0000 \u0000 \u0000Key words: \u0000Rhabdomyosarcoma; Head and neck; High-risk group; Prognosis; Child","PeriodicalId":9843,"journal":{"name":"中华实用儿科临床杂志","volume":"35 1","pages":"193-196"},"PeriodicalIF":0.0,"publicationDate":"2020-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48192784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of probiotics on apoptosis and proliferation of intestinal epithelial cells in rats with necrotizing enterocolitis 益生菌对坏死性小肠结肠炎大鼠肠上皮细胞凋亡和增殖的影响
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190125-00059
Mengmeng Yuan, Xiao-yun Zhang, Yaping Song, Mingchao Li
Objective To study the effect of compound Lactobacillus acidophilus on the apoptosis of intestinal epithelial cells and expression of proliferating cell nuclear antigen (PCNA) in rats with necrotizing enterocolitis, so as to provide some theoretical reference for the application of compound Lactobacillus acidophilus in the prevention and treatment of necrotizing enterocolitis(NEC) for newborn infants. Methods Thirty-six 48-hour old newborn SD rats were randomly divided into normal group, model group and intervention group, with 12 rats in each group.The NEC model was established by hypoxia and cold stimulation for 3 days, and the intervention group was given the compound Lactobacillus acidophilus at the same time; after the model was established, all the rats were sacrificed after 12 hours of fasting and their intestinal tissues were excised by terminal-deoxynucleoitidyl transferase mediated nick end labeling (TUNEL) method to determine the condition of apoptosis and to detect expression of the PCNA gene in the intestinal tissues by fluorescent quantitative PCR. Results (1) The apoptosis rates of the intestinal tissues: in the model group, the normal group and the intervention group were (88.33±2.77)%, (4.75±0.75)% and (44.41±4.81)%, respectively, and the differences had statistical significance(all P<0.05). (2) The PCNA expression in the intestinal tissue by real-time PCR in the model group, normal group and intervention group were (9.28±3.26)×10-4, (15.35±1.91)×10-4 and (12.09±3.06)×10-4, respectively, and the differences had statistical significance(all P<0.05). Conclusions The apoptosis rate of intestinal epithelial cells increases and PCNA expression decreases when NEC occurs.Compound Lactobacillus acidophilus can reduce apoptosis, promote intestinal epithelial cell proliferation, and thus help to reduce the risk and severity of NEC in neonatal rats. Key words: Neonatal necrotizing enterocolitis; Apoptosis; Proliferating cell nuclear antigen; Compound Lactobacillus acidophilus
目的研究复方嗜酸乳杆菌对坏死性小肠结肠炎大鼠肠上皮细胞凋亡及增殖细胞核抗原(PCNA)表达的影响,为复方嗜酸乳杆菌在新生儿坏死性小肠结肠炎防治中的应用提供一定的理论参考。方法36只48小时新生SD大鼠随机分为正常组、模型组和干预组,每组12只。通过缺氧和冷刺激建立NEC模型3天,干预组同时给予复方嗜酸乳杆菌;模型建立后,禁食12小时处死所有大鼠,用末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)切除肠组织,以确定细胞凋亡情况,并用荧光定量PCR检测肠组织中PCNA基因的表达。结果(1)肠组织凋亡率:模型组、正常组和干预组分别为(88.33±2.77)%、(4.75±0.75)%和(44.41±4.81)%,差异有统计学意义(均P<0.05),×10-4和(12.09±3.06)×10-4,差异有统计学意义(均P<0.05)。复方嗜酸乳杆菌可以减少细胞凋亡,促进肠上皮细胞增殖,从而有助于降低新生大鼠NEC的风险和严重程度。关键词:新生儿坏死性小肠结肠炎;细胞凋亡;增殖细胞核抗原;复方嗜酸乳杆菌
{"title":"Effects of probiotics on apoptosis and proliferation of intestinal epithelial cells in rats with necrotizing enterocolitis","authors":"Mengmeng Yuan, Xiao-yun Zhang, Yaping Song, Mingchao Li","doi":"10.3760/CMA.J.CN101070-20190125-00059","DOIUrl":"https://doi.org/10.3760/CMA.J.CN101070-20190125-00059","url":null,"abstract":"Objective \u0000To study the effect of compound Lactobacillus acidophilus on the apoptosis of intestinal epithelial cells and expression of proliferating cell nuclear antigen (PCNA) in rats with necrotizing enterocolitis, so as to provide some theoretical reference for the application of compound Lactobacillus acidophilus in the prevention and treatment of necrotizing enterocolitis(NEC) for newborn infants. \u0000 \u0000 \u0000Methods \u0000Thirty-six 48-hour old newborn SD rats were randomly divided into normal group, model group and intervention group, with 12 rats in each group.The NEC model was established by hypoxia and cold stimulation for 3 days, and the intervention group was given the compound Lactobacillus acidophilus at the same time; after the model was established, all the rats were sacrificed after 12 hours of fasting and their intestinal tissues were excised by terminal-deoxynucleoitidyl transferase mediated nick end labeling (TUNEL) method to determine the condition of apoptosis and to detect expression of the PCNA gene in the intestinal tissues by fluorescent quantitative PCR. \u0000 \u0000 \u0000Results \u0000(1) The apoptosis rates of the intestinal tissues: in the model group, the normal group and the intervention group were (88.33±2.77)%, (4.75±0.75)% and (44.41±4.81)%, respectively, and the differences had statistical significance(all P<0.05). (2) The PCNA expression in the intestinal tissue by real-time PCR in the model group, normal group and intervention group were (9.28±3.26)×10-4, (15.35±1.91)×10-4 and (12.09±3.06)×10-4, respectively, and the differences had statistical significance(all P<0.05). \u0000 \u0000 \u0000Conclusions \u0000The apoptosis rate of intestinal epithelial cells increases and PCNA expression decreases when NEC occurs.Compound Lactobacillus acidophilus can reduce apoptosis, promote intestinal epithelial cell proliferation, and thus help to reduce the risk and severity of NEC in neonatal rats. \u0000 \u0000 \u0000Key words: \u0000Neonatal necrotizing enterocolitis; Apoptosis; Proliferating cell nuclear antigen; Compound Lactobacillus acidophilus","PeriodicalId":9843,"journal":{"name":"中华实用儿科临床杂志","volume":"35 1","pages":"227-230"},"PeriodicalIF":0.0,"publicationDate":"2020-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47382247","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Arsenic trioxide upregulates UL16 binding protein 1 expression in KG1a cells through ataxia telangiectasia mutated and RAD3-related kinase pathway 三氧化二砷通过共济失调毛细血管扩张突变和rad3相关激酶途径上调KG1a细胞UL16结合蛋白1的表达
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190301-00146
M. Ji, Jiaxing Dong, S. Cui, Xiaohui Si, Yahui Li, Xinqing Niu
Objective To observe the effect of arsenic trioxide (ATO) on the expression of NKG2D ligand UL16 binding protein 1(ULBP1) in acute myeloid leukemia KG1a cells, and explore the molecular mechanism for its regulation of ULBP1 expression. Methods KG1a cells were cultured in vitro.Then, the inhibition of KG1a cell proli-feration by different concentrations of ATO was detected by cell counting kit-8(CCK8) assay, and the expression of ULBP1 mRNA and surface protein in KG1a cells were examined by real-time RT-PCR and flow cytometry, respectively.After that, the blocking effects of ataxia telangiectasia mutated and RAD3-related kinase (ATM/ATR) inhibitor caffeine on ATO-upregulated expression of ULBP1 mRNA and surface protein expressions were investigated, and the effects of ATO on the expression of CHK1 and CHK2 proteins and their phosphorylation in KG1a cells were observed by Western blot method. Results Different concentrations (1, 2, 3, 4, 5 μmol/L) of ATO could inhibit the proliferation of KG1a cells, which was concentration dependent, and the half inhibitory (IC50) concentration to KG1a cells was 2.7 μmol/L.The expression of ULBP1 mRNA on KG1a cells were increased when incubated with ATO at concentration 1, 2, 3, 4, 5 μmol/L, compared without ATO group, ULBP1 mRNA expression level relatively increased respectively to (1.86±0.30) times, (3.02±0.71) times, (3.16±0.75) times, (4.80±0.70) times and (3.70±0.89) times, and the differences were statistically significant (all P<0.05). Furthermore, ATO (1, 2, 3, 4 and 5 μmol/L) upregulated ULBP1 protein expression on KG1a cells compared with that in the group without caffeine, and the differences were statistically significant (all P<0.05). After caffeine pretreat KG1a cell 2 h and ATO incubate KG1a cell 24 h, ULBP1 mRNA and protein expression levels were significantly reduced.When caffeine concentration was 8 mmol/L, ULBP1 mRNA expression level relatively reduces from (9.55±0.38) times to (6.36±0.93) times compared with that in the group without caffeine, and the difference was statistically significant (P<0.05). When caffeine concentration was 2, 4 and 8 mmol/L respectively, the expression of ULBP1 protein was reduced from that in the group without caffein treatment (3.50±0.08) times to (2.17±0.07) times, (2.02±0.06) times and (1.75±0.06) times, respectively, and the differences were statistically significant (all P<0.05). The expression of CHK1 and CHK2 proteins decreased with the increase of ATO concentration, while p-CHK1 and p-CHK2 are increased as ATO. Conclusions ATO upregulate the expression of ULBP1 mRNA and protein in KG1a cells, and the ATM/ATR-CHK1/CHK2 pathway may be involved in it. Key words: Arsenic trioxide; KG1a cells; Natural killer cell; UL16 binding protein 1; Ataxia telangiectasia mutated and RAD3-related kinase pathway
目的观察三氧化二砷(ATO)对急性髓系白血病KG1a细胞NKG2D配体UL16结合蛋白1(ULBP1)表达的影响,探讨其调控ULBP1表达的分子机制。方法体外培养KG1a细胞。然后,通过细胞计数试剂盒-8(CCK8)法检测不同浓度ATO对KG1a细胞增殖的抑制作用,并分别通过实时RT-PCR和流式细胞术检测ULBP1mRNA和表面蛋白在KG1a细胞中的表达。之后,研究了共济失调毛细血管扩张突变和RAD3相关激酶(ATM/ATR)抑制剂咖啡因对ATO上调ULBP1mRNA和表面蛋白表达的阻断作用,并通过Western印迹法观察了ATO对KG1a细胞中CHK1和CHK2蛋白表达及其磷酸化的影响。结果不同浓度(1、2、3、4、5μmol/L)的ATO均能抑制KG1a细胞增殖,且呈浓度依赖性,对KG1a细胞的半数抑制浓度(IC50)为2.7μmol/L,ULBP1mRNA表达水平相对升高,分别为(1.86±0.30)倍、(3.02±0.71)倍、、(3.16±0.75)倍,(4.80±0.70)倍和(3.70±0.89)倍,差异有统计学意义(均P<0.05),咖啡因预处理KG1a细胞2 h和ATO孵育KG1a细胞24 h后,ULBP1mRNA和蛋白表达水平显著降低。当咖啡因浓度为8mmol/L时,ULBP1mRNA的表达水平与不含咖啡因组相比从(9.55±0.38)倍相对降低到(6.36±0.93)倍,差异有统计学意义(P<0.05),ULBP1蛋白的表达从未经咖啡因处理组的(3.50±0.08)倍减少到(2.17±0.07)倍、(2.02±0.06)倍和(1.75±0.06。结论ATO上调KG1a细胞ULBP1mRNA和蛋白的表达,ATM/ATR-CHK1/CHK2通路可能参与其中;KG1a细胞;自然杀伤细胞;UL16结合蛋白1;共济失调毛细血管扩张突变与RAD3相关激酶途径
{"title":"Arsenic trioxide upregulates UL16 binding protein 1 expression in KG1a cells through ataxia telangiectasia mutated and RAD3-related kinase pathway","authors":"M. Ji, Jiaxing Dong, S. Cui, Xiaohui Si, Yahui Li, Xinqing Niu","doi":"10.3760/CMA.J.CN101070-20190301-00146","DOIUrl":"https://doi.org/10.3760/CMA.J.CN101070-20190301-00146","url":null,"abstract":"Objective \u0000To observe the effect of arsenic trioxide (ATO) on the expression of NKG2D ligand UL16 binding protein 1(ULBP1) in acute myeloid leukemia KG1a cells, and explore the molecular mechanism for its regulation of ULBP1 expression. \u0000 \u0000 \u0000Methods \u0000KG1a cells were cultured in vitro.Then, the inhibition of KG1a cell proli-feration by different concentrations of ATO was detected by cell counting kit-8(CCK8) assay, and the expression of ULBP1 mRNA and surface protein in KG1a cells were examined by real-time RT-PCR and flow cytometry, respectively.After that, the blocking effects of ataxia telangiectasia mutated and RAD3-related kinase (ATM/ATR) inhibitor caffeine on ATO-upregulated expression of ULBP1 mRNA and surface protein expressions were investigated, and the effects of ATO on the expression of CHK1 and CHK2 proteins and their phosphorylation in KG1a cells were observed by Western blot method. \u0000 \u0000 \u0000Results \u0000Different concentrations (1, 2, 3, 4, 5 μmol/L) of ATO could inhibit the proliferation of KG1a cells, which was concentration dependent, and the half inhibitory (IC50) concentration to KG1a cells was 2.7 μmol/L.The expression of ULBP1 mRNA on KG1a cells were increased when incubated with ATO at concentration 1, 2, 3, 4, 5 μmol/L, compared without ATO group, ULBP1 mRNA expression level relatively increased respectively to (1.86±0.30) times, (3.02±0.71) times, (3.16±0.75) times, (4.80±0.70) times and (3.70±0.89) times, and the differences were statistically significant (all P<0.05). Furthermore, ATO (1, 2, 3, 4 and 5 μmol/L) upregulated ULBP1 protein expression on KG1a cells compared with that in the group without caffeine, and the differences were statistically significant (all P<0.05). After caffeine pretreat KG1a cell 2 h and ATO incubate KG1a cell 24 h, ULBP1 mRNA and protein expression levels were significantly reduced.When caffeine concentration was 8 mmol/L, ULBP1 mRNA expression level relatively reduces from (9.55±0.38) times to (6.36±0.93) times compared with that in the group without caffeine, and the difference was statistically significant (P<0.05). When caffeine concentration was 2, 4 and 8 mmol/L respectively, the expression of ULBP1 protein was reduced from that in the group without caffein treatment (3.50±0.08) times to (2.17±0.07) times, (2.02±0.06) times and (1.75±0.06) times, respectively, and the differences were statistically significant (all P<0.05). The expression of CHK1 and CHK2 proteins decreased with the increase of ATO concentration, while p-CHK1 and p-CHK2 are increased as ATO. \u0000 \u0000 \u0000Conclusions \u0000ATO upregulate the expression of ULBP1 mRNA and protein in KG1a cells, and the ATM/ATR-CHK1/CHK2 pathway may be involved in it. \u0000 \u0000 \u0000Key words: \u0000Arsenic trioxide; KG1a cells; Natural killer cell; UL16 binding protein 1; Ataxia telangiectasia mutated and RAD3-related kinase pathway","PeriodicalId":9843,"journal":{"name":"中华实用儿科临床杂志","volume":"35 1","pages":"231-235"},"PeriodicalIF":0.0,"publicationDate":"2020-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47564808","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epidemiology and prognostic factors of infantile malignant solid tumor 婴幼儿恶性实体瘤的流行病学及预后因素
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20200301-00298
X. Yuan
As an important part of childhood tumors, infantile malignant solid tumor is relatively rare, which has some common characteristics of childhood cancer as well as its own particularity.Most infantile tumors are embryo-derived tumors, whose pathogenesis is related to developmental biology, genetics and environmental factors.The distribution of constituent ratio of infantile malignant tumors is different from that of older children, and the epidemiological data statistics can be influenced by the imperfect children tumor registration system, population migration, birth defects and perinatal factors, environmental exposure, gender, race and other factors.Heterogeneity is one of the prominent features of malignant solid tumor in infants. The experience gained from treatment of older children cannot be directly extrapolated to infants.The principle of treating infantile malignant solid tumors should take into account both the effectiveness and the long-term impact on infant growth.Early diagnosis and appropriate treatment mean that the prognosis of most infants with malignant solid tumor to be better than that of older children.Therefore, it is necessary to manage these tumors as a separate entity.The advance of epidemiology and prognostic factors of infantile malignant solid tumors at home and abroad was reviewed in this paper. Key words: Infant; Malignant; Solid tumor; Incidence rate; Constituent ratio; Prognosis
婴幼儿恶性实体瘤作为儿童肿瘤的重要组成部分,相对罕见,既有儿童癌症的一些共同特点,也有其自身的特殊性。大多数婴儿肿瘤是胚胎源性肿瘤,其发病机制与发育生物学、遗传学和环境因素有关。婴儿恶性肿瘤的构成比分布与年龄较大的儿童不同,流行病学数据统计可能受到儿童肿瘤登记制度不完善、人口迁移、出生缺陷和围产期因素、环境暴露、性别、种族等因素的影响。异质性是婴儿恶性实体瘤的突出特征之一。从治疗年龄较大儿童中获得的经验不能直接外推到婴儿身上。治疗婴儿恶性实体瘤的原则应考虑其有效性和对婴儿生长的长期影响。早期诊断和适当治疗意味着大多数患有恶性实体瘤的婴儿的预后要好于年龄较大的儿童。因此,有必要将这些肿瘤作为一个单独的实体进行管理。本文综述了国内外婴幼儿恶性实体瘤流行病学及预后因素的研究进展。关键词:婴儿;恶性;实体瘤;发病率;成分比例;预后
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引用次数: 0
Case report of successful treatment of severe aluminum phosphide poisoning through veno-arterial extracorporeal membrane oxygenation 静脉-动脉体外膜氧合治疗重度磷化铝中毒成功一例
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190108-00006
Boliang Fang, Zheng Li, S. Qian, Heng-miao Gao, J. Zeng
首都医科大学附属北京儿童医院重症医学科收治磷化铝中毒并急性心力衰竭患儿1例,女,12岁,吸入磷化铝48 h出现进行性加重的心力衰竭及心源性休克,经静-动脉体外膜肺氧合支持治疗后痊愈,且未遗留后遗症。重症磷化铝中毒者常规治疗下病死率高,静-动脉体外膜肺氧合成功用于治疗此类患者在国内尚属首次报道。
A 12-year-old female patient with aluminum phosphide poisoning and acute heart failure was admitted to the Intensive Care Department of Beijing Children's Hospital Affiliated to Capital Medical University. She developed progressive heart failure and cardiogenic shock after inhaling aluminum phosphide for 48 hours. After receiving intravenous extracorporeal membrane oxygenation support treatment, she recovered without any sequelae. The mortality rate of severe aluminum phosphide poisoning patients under routine treatment is high, and the successful use of extracorporeal membrane oxygenation in the treatment of such patients is still the first report in China.
{"title":"Case report of successful treatment of severe aluminum phosphide poisoning through veno-arterial extracorporeal membrane oxygenation","authors":"Boliang Fang, Zheng Li, S. Qian, Heng-miao Gao, J. Zeng","doi":"10.3760/CMA.J.CN101070-20190108-00006","DOIUrl":"https://doi.org/10.3760/CMA.J.CN101070-20190108-00006","url":null,"abstract":"首都医科大学附属北京儿童医院重症医学科收治磷化铝中毒并急性心力衰竭患儿1例,女,12岁,吸入磷化铝48 h出现进行性加重的心力衰竭及心源性休克,经静-动脉体外膜肺氧合支持治疗后痊愈,且未遗留后遗症。重症磷化铝中毒者常规治疗下病死率高,静-动脉体外膜肺氧合成功用于治疗此类患者在国内尚属首次报道。","PeriodicalId":9843,"journal":{"name":"中华实用儿科临床杂志","volume":"35 1","pages":"239-240"},"PeriodicalIF":0.0,"publicationDate":"2020-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42014128","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Relationship between joints bleeding and joint assessment in children with severe haemophilia A 重度A型血友病患儿关节出血与关节评估的关系
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190213-00097
W. Yao, Qing Zhang, Min Zhou, L. Tang, Xiaobo Luo, Ningning Zhang, Sheng Yang, Yan Wang, P. Ding, S. Cai, Zhenping Chen, Xiaojing Li, R. Wu
Objective To understand the relationship between joint bleeding and joint disease in hemophilia children, and to provide a theoretical basis for clinical treatment and prognosis. Methods The patients with severe hemophilia A between 1 and 7 years old and with relevant nodal bleeding records were selected.All the patients admitted in Beijing Children′s Hospital, Capital Medical University, and Chengdu New Century Women′s and Children′s Hospital since June 2016 to January 2017.All the joint bleeding of each child was taken as the study joint, and the joint bleeding was collected during the last 3 months.The joints were assessed by using ultrasound, X-ray, magnetic resonance imaging(MRI) and Hemophilia Joint Health Score (HJHS) scoring systems.The correlation analysis was conducted between the joint bleeding, ultrasound, X-ray, MRI and HJHS scores.The correlation analysis was conducted for baseline ultrasound, X-ray, MRI and HJHS scores. Results (1) There were 18 patients enrolled.The mean age was (5.6±1.8) years old.There were 30 joints bleeding in the observation period in total, with the annul median joint bleeding times of 4 (4-16 times), and the annul median target joint bleeding times of 8 (4-16 times). (2) Joint bleeding times of was correlated with ultrasound and X-ray evaluation (r=0.390, P=0.033; r=0.517, P=0.008), and not correlated with HJHS or MRI(all P>0.05). (3) There was significantly positive correlation among ultrasound, X-ray, HJHS and MRI [r=0.815(ultrasound vs.X-ray), r=0.510(ultrasound vs.HJHS), r=0.812(ultrasound vs.MRI), r=0.666(X-ray vs.HJHS), r=0.911(X-ray vs.MRI), r=0.781(HJHS vs.MRI), all P 0.05). Conclusions The results of joint bleeding and joint evaluation are inconsistent.Joint bleeding can not truly reflect the situation of joint diseases.The assessment of hemophilia should include comprehensive evaluation of joint structure, function, activity ability and other aspects to guide the treatment of haemophi-lia children. Key words: Haemophilia A; Child; Bleeding joints; Joint assessment
目的了解血友病患儿关节出血与关节疾病的关系,为临床治疗及预后提供理论依据。方法选取年龄在1 ~ 7岁,有相关淋巴结出血记录的重症A型血友病患者。2016年6月至2017年1月在北京儿童医院、首都医科大学和成都新世纪妇幼医院住院的所有患者。所有患儿的关节出血作为研究关节,收集近3个月的关节出血情况。采用超声、x线、磁共振成像(MRI)和血友病关节健康评分(HJHS)评分系统对关节进行评估。对关节出血、超声、x线、MRI与HJHS评分进行相关性分析。对基线超声、x线、MRI与HJHS评分进行相关性分析。结果(1)共入组18例患者。平均年龄(5.6±1.8)岁。观察期内共发生关节出血30例,全年关节出血中位数4次(4 ~ 16次),全年目标关节出血中位数8次(4 ~ 16次)。(2)关节出血次数与超声、x线评价相关(r=0.390, P=0.033;r=0.517, P=0.008),与HJHS、MRI无关(P均为0.05)。(3)超声、x线、HJHS、MRI呈显著正相关[r=0.815(超声vs. x线),r=0.510(超声vs.HJHS), r=0.812(超声vs.MRI), r=0.666(x线vs.HJHS), r=0.911(x线vs.MRI), r=0.781(HJHS vs.MRI), P均为0.05)。结论关节出血与关节评估结果不一致。关节出血不能真实反映关节疾病的情况。血友病的评估应包括关节结构、功能、活动能力等方面的综合评价,以指导血友病患儿的治疗。关键词:A型血友病;孩子;关节出血;联合评估
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引用次数: 0
Molecular response and prognosis of pediatric patients with Ph-positive acute lymphoblastic leukemia treated by tyrosine kinase inhibitors with chemotherapy 酪氨酸激酶抑制剂联合化疗治疗Ph阳性急性淋巴细胞白血病患儿的分子反应及预后
Q4 Medicine Pub Date : 2020-03-19 DOI: 10.3760/CMA.J.CN101070-20190222-00125
Yu-Juan Xue, A. Lu, Jun Wu, Y. Zuo, Y. Jia, Le-ping Zhang
Objective To explore the molecular response and prognostic factors of pediatric patients with Ph-positive acute lymphoblastic leukemia (Ph+ ALL) treated by tyrosine kinase inhibitors (TKI) with chemotherapy in TKI era. Methods The clinical data of children newly diagnosed with Ph+ ALL admitted at Department of Pediatrics, Peking University People′s Hospital from August 2006 to February 2017 were retrospectively reviewed.The molecular biological characteristics and survival prognosis of the 30 patients who received continuous TKI with chemotherapy from early induction combined and no subsequent transplantation were analyzed. Results The 30 patients with Ph+ ALL had 19 males and 11 females with a median age of 8-year-old (ranging from 2 to 16 years). The complete remission (CR) rate after the first cycle of induction chemotherapy was 96.7% (29/30 cases), with overall CR rate of 100.0%; Before treatment, the mean level of BCR/ABL mRNA in the 30 patients was 73.2% (0.12%-160.60%) and the level declined significantly with the progression of chemotherapy courses, reaching the plateau stage at the 6th month of chemotherapy (Z=-1.922, P>0.05); nine patients had recurrence, with a median recurrence time of 7 months (3.7-58.8 months). Univariate analysis showed that age (P<0.05), the lever of minimal residual disease (MRD) after induction chemotherapy (P<0.01) and the MRD level at the 3th month of induction chemotherapy (P<0.01) affected the recurrence rate.The median follow-up time of 30 patients was 42.6 months (6.4-96.5 months), and the 3-year overall survival (OS) rate and event-free survival (EFS) rate were (78.6±7.8)% and (72.4±8.4)%, respectively; Cox multivariate analysis showed that the initial white blood cell count ≥34.0×109/L (OR=11.955, 95% CI: 1.075-132.899, P<0.05) and BCR/ABL mRNA reduction less than 3 log from baseline [major molecular response (MMR)] at the 3th month of induction chemotherapy (OR=8.563, 95% CI: 1.254-58.478, P<0.05) were independent risk factors affecting the 3-year EFS rate.In addition, the initial white blood cell count ≥34.0×109/L (OR=14.327, 95% CI: 1.843-243.592, P<0.05) was also an independent risk factor affecting the 3-year OS rate. Conclusions The application of TKI can significantly deepen the molecular response of Ph+ ALL in children.In the TKI era, the initial white blood cell count ≥ 34.0×109/L and BCR/ABL mRNA reduction less than 3 log from baseline (MMR) at the 3th month of induction chemotherapy are independent risk factors for the long-term survival of pediatric Ph+ ALL. Key words: Philadelphia chromosome; Acute lymphoblastic leukemia; Child; Tyrosine kinase inhibitor; Mole-cular response
目的探讨酪氨酸激酶抑制剂(TKI)联合化疗治疗Ph阳性急性淋巴细胞白血病(Ph+ALL)患儿的分子反应及预后因素。方法回顾性分析2006年8月至2017年2月北京大学人民医院儿科收治的Ph+ALL患儿的临床资料。分析了30例从早期诱导联合化疗到无后续移植的连续TKI患者的分子生物学特征和生存预后。结果30例Ph+ALL患者,男19例,女11例,中位年龄8岁(2~16岁)。诱导化疗第一周期后完全缓解率为96.7%(29/30例),总CR率为100.0%;30例患者治疗前BCR/ABL mRNA平均水平为73.2%(0.12%-160.60%),随着化疗进程的进行,BCR/ABLmRNA水平明显下降,化疗6个月达到平稳期(Z=-1.922,P>0.05);9例复发,中位复发时间为7个月(3.7-58.8个月)。单因素分析显示,年龄(P<0.05)、诱导化疗后最小残留病变(MRD)水平(P<0.01)和诱导化疗第3个月MRD水平(P>0.01)影响复发率。30例患者的中位随访时间为42.6个月(6.4-96.5个月),3年总生存率(OS)和无事件生存率(EFS)分别为(78.6±7.8)%和(72.4±8.4)%;Cox多变量分析显示,诱导化疗第3个月时,初始白细胞计数≥34.0×109/L(OR=11.955,95%CI:1.075-132.899,P<0.05)和BCR/ABL mRNA自基线[主要分子反应(MMR)]减少小于3 log(OR=8.563,95%CI:1.254-58.478,P<0.05)是影响3年EFS发生率的独立危险因素。此外,初始白细胞计数≥34.0×109/L(OR=14.327,95%CI:1.843-243.592,P<0.05)也是影响3年OS发生率的独立危险因素。结论TKI的应用可显著加深儿童Ph+ALL的分子应答。在TKI时代,诱导化疗第3个月时,初始白细胞计数≥34.0×109/L和BCR/ABL mRNA自基线减少小于3 log(MMR)是儿童Ph+ALL长期生存的独立风险因素。关键词:费城染色体;急性淋巴细胞白血病;儿童;酪氨酸激酶抑制剂;鼹鼠反应
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引用次数: 1
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中华实用儿科临床杂志
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