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Multiple neurofibromas plus fibrosarcoma with familial NF1 pathogenicity:A case report
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作者 Yang Wang Xiao-Fan Lu +2 位作者 Lu-Lu Chen Ying-Wei Zhang Bing Zhang 《World Journal of Clinical Cases》 SCIE 2020年第7期1306-1310,共5页
BACKGROUND Neurofibromatosis(NF)is a genetic disease consisting of seven types,of which types 1 to 4 are caused by a dominant autosomal gene mutation;such disease sometimes arises in patients with NF type 1.However,it... BACKGROUND Neurofibromatosis(NF)is a genetic disease consisting of seven types,of which types 1 to 4 are caused by a dominant autosomal gene mutation;such disease sometimes arises in patients with NF type 1.However,it remains unclear whether the origin of neurofibrosarcoma is directly linked to the incidence of NF type 1,as no reports have been published on this issue.Here,we report a case of NF1-positive multiple neurofibromas with malignant fibrosarcomatous transformation in the pleural cavity.CASE SUMMARY A 51-year-old male was admitted to our hospital due to fever accompanied by coughing,chest tightness and asthma for more than one month.The preliminary diagnosis was NF type 1,which was pathologically confirmed by a subsequent thoracoabdominal subcutaneous biopsy.The definitive diagnosis was neurofibrosarcoma with a pathogenic NF1 gene.The patient refused surgery and chemoradiotherapy,and died two months later.NF is a genetic disease consisting of seven types,of which types 1 to 4 are caused by a dominant autosomal gene mutation.The case reported belongs to the class of NF1-positive dominant inheritance.Neurofibrosarcoma is a malignant tumor derived from cells surrounding the peripheral nerves.However,due to the lack of previous reports,it remains unclear whether the origin of neurofibrosarcoma is directly linked to the incidence of NF type 1.CONCLUSION We report the first case of NF1-positive multiple neurofibromas with malignant fibrosarcomatous transformation in the pleural cavity. 展开更多
关键词 MULTIPLE NEUROFIBROMAS FIBROSARCOMA NEUROFIBROMATOSIS type 1 PATHOGENICITY pseudochylothorax PLEURAL cavity Case report
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肺癌术后真假乳糜胸的鉴别诊断和治疗 被引量:1
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作者 杨劼 吴卓鹏 +8 位作者 古卫权 叶俊 杨胜利 王飞 肖叶 张小文 赵宁 吴玲玲 刘冬生 《中华胸心血管外科杂志》 CSCD 北大核心 2022年第8期481-486,共6页
目的:探讨肺癌术后真性乳糜胸和假乳糜胸的鉴别诊断和不同的治疗方法。方法:分析2016年1月至2021年12月1584例非小细胞肺癌的手术患者的临床资料,发现21例真性乳糜胸和8例假性乳糜胸,分析比较其胸腔积液常规生化、乳糜试验、总胆固醇、... 目的:探讨肺癌术后真性乳糜胸和假乳糜胸的鉴别诊断和不同的治疗方法。方法:分析2016年1月至2021年12月1584例非小细胞肺癌的手术患者的临床资料,发现21例真性乳糜胸和8例假性乳糜胸,分析比较其胸腔积液常规生化、乳糜试验、总胆固醇、甘油三酯、总胆固醇/甘油三酯比值,白细胞计数、细菌培养和治疗方法的不同。结果:肺癌术后真性乳糜胸发病率为1.3%,假性乳糜胸发病率为0.5%;右侧真性乳糜胸占80.9%%,明显高于左侧真性乳糜胸19.1%,差异有统计学意义(P<0.05)。假性乳糜胸均发生在右侧(100%)。真性乳糜胸和假性乳糜胸胸腔积液胆固醇、甘油三酯水平差异有统计学意义(P<0.05),假性乳糜胸的白细胞计数明显高于真性乳糜胸,差异有统计学意义(P<0.05)。两组治疗前胸腔引流量,术后引流时间以及术后住院时间差异有统计学意义(P<0.05)。真性乳糜胸保守治疗13例,成功率为61.9%,胸导管夹闭术8例,手术率为38.1%;假性乳糜胸全部进行保守治疗,成功率为100%。结论:遇到肺癌术后乳糜胸除了胸腔积液乳糜试验、常规生化检查,还需检测胸腔积液中的总胆固醇、甘油三酯、总胆固醇与甘油三酯比值,以鉴别真性乳糜胸和假性乳糜胸,胸腔积液中甘油三酯含量高的诊断为真性乳糜胸;胸腔积液中胆固醇/甘油三酯比值>1的诊断为假性乳糜胸,假性乳糜胸一般采用保守治疗。真性乳糜胸根据不同情况采用保守和手术治疗,如连续3天胸腔引流量>800 ml/天或者造成严重水电解质紊乱的,建议行经右胸腔镜胸导管夹闭术。 展开更多
关键词 非小细胞肺癌 真性乳糜胸 假性乳糜胸 鉴别诊断 治疗
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