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Frequent detection of genetic aberrations reveals novel pathogenesis and treatment modalities in systemic juvenile xanthogranuloma 被引量:1
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作者 Jiaosheng Xu Hongyan Ma +5 位作者 xingfeng yao Xiaofeng Han Yang Wen Siwei Wang Zigang Xu Lin Ma 《Pediatric Investigation》 CAS CSCD 2023年第3期212-215,共4页
Juvenile xanthogranuloma(JXG),the most common form of non-Langerhans cell histiocytosis(non-LCH),is generally confined to the skin during infancy and early childhood.^(1)JXG rarely involves extracutaneous tissues or s... Juvenile xanthogranuloma(JXG),the most common form of non-Langerhans cell histiocytosis(non-LCH),is generally confined to the skin during infancy and early childhood.^(1)JXG rarely involves extracutaneous tissues or systemic organs,resulting in high morbidity and mortality rates.Clonality in JXG has been verified by histopathological and genetic analyses,which have shown it to be tumorous rather than a reactive disorder of JXG.^(2)However,the exact etiopathogenesis of JXG remains unclear. 展开更多
关键词 TREATMENT ORGANS EXACT
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Primary cardiac CIC-rearranged undifferentiated sarcoma in an infant
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作者 Meng Zhang Yeran Yang +3 位作者 Xiaoxing Guan xingfeng yao Yongli Guo Lejian He 《Pediatric Investigation》 CSCD 2021年第4期313-317,共5页
Introduction:Cardiac neoplasms are particularly rare in children,and the majority of these tumors are benign.Approximately 10%of cardiac neoplasms are malignant,including soft tissue sarcomas and lymphomas.Cardiac tum... Introduction:Cardiac neoplasms are particularly rare in children,and the majority of these tumors are benign.Approximately 10%of cardiac neoplasms are malignant,including soft tissue sarcomas and lymphomas.Cardiac tumors could also be metastases.Primitive EWSR1-negative round or spindle cell undifferentiated sarcoma harboring CIC gene translocation is a highly aggressive malignancy mainly occurring in soft tissues.However,it has not yet been described in the heart.Case presentation:We report a sarcoma that arose from the right ventricle in a 1-year-old girl.Histologically,it was composed of closely arranged small round or oval undifferentiated cells with fibrovascular separation,hyaline degeneration,and geographical necrosis.Immunohistochemically,the neoplastic cells exhibited focal membrane positivity for CD99 and diffuse positivity for WT1 and ETV4.Fluorescent in situ hybridization analysis showed EWSR1-negative but CIC-positive split signals.The breakpoint was also confirmed by whole genome sequencing.Conclusion:Based on morphological,immunohistochemical and molecular findings,this cardiac mass was diagnosed as CIC-rearranged sarcoma. 展开更多
关键词 CARDIAC SARCOMA CIC CHILD
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