Preemptive NUDT15 Genotyping and Its Impact on Febrile Neutropenia in Pediatric Patients With Acute Lymphoblastic Leukemia in Taiwan [0.03%]
台湾儿童急性淋巴细胞白血病患者中NUDT16L基因分型对发热性中性粒细胞减少症的影响
Chiao-Yu Cheng,Der-Shiun Wang,Chih-Hsiang Yu et al.
Chiao-Yu Cheng et al.
This study investigated whether preemptive NUDT15 genotyping can reduce episodes of febrile neutropenia during the continuation phase of acute lymphoblastic leukemia (ALL) treatment. This retrospective cohort study enrolled 243 children wit...
Parent and Patient Proxies' Preferences on Whole-Body MRI Techniques for Cancer Predisposition Syndromes' Surveillance [0.03%]
遗传性肿瘤综合征筛查中父母及患者委托人对全身磁共振检查的偏好研究
Sayali Joshi,Rahim Moineddin,Paul C Nathan et al.
Sayali Joshi et al.
Purpose: Given trade-offs between whole-body MRI(WBMRI) techniques' attributes for cancer predisposition syndromes (CPS) surveillance, we determined the strength of preferences of adolescents with no cancer history (group...
Pathologic and Molecular Diagnosis of Ewing Sarcoma: A Multicenter Analysis From the Latin American Cooperative Group Trial [0.03%]
拉丁美洲合作组试验：尤因肉瘤病理和分子诊断的多中心分析
André T Brunetto,Lauro J Gregianin,Marialva Sinigaglia et al.
André T Brunetto et al.
Introduction: Ewing Sarcoma (ES) is a small, round, blue cell tumor (SRBCT) characterized by a chromosomal translocation between chromosomes 11 and 22 in ~85% of cases, alongside immunohistochemical (IHC) expression of th...
No Regression With Imatinib Treatment for Craniofacial Fibrous Dysplasia Associated With McCune-Albright Syndrome [0.03%]
与McCune-Albright综合征相关的颅面纤维异常增生症在接受伊马替尼治疗后无病情恶化现象
Özge Yildirim Şalbaş,Özge Besci,Elif Yaşar et al.
Özge Yildirim Şalbaş et al.
Excellent Outcomes of Hematopoietic Stem Cell Transplant for Pediatric High Risk and Relapsed Acute Myeloid Leukemia-A Decade Long Experience From Developing Nation [0.03%]
印度发展中国家儿童高危及复发急性髓系白血病移植的十年经验及其优良预后
Sunisha Arora,Arun S Danewa,Sohini Chakraborty et al.
Sunisha Arora et al.
Aim: Hematopoietic stem cell transplant (HSCT) remains the cornerstone of treatment in patients with high-risk and relapsed acute myeloid leukemia (AML). In the absence of a fully matched donor, haploidentical HSCT is a f...
Efficacy of Stereotactic Body Radiotherapy in Osteosarcoma Bone Metastases [0.03%]
立体定向体放射治疗在骨肉瘤骨转移中的疗效分析
Gustavo A Sosa,David M Gannon,Guozhen Luo et al.
Gustavo A Sosa et al.
Osteosarcoma is the most common primary malignancy of bone in children. Stereotactic body radiotherapy (SBRT) is an ablative technique that can overcome radioresistance. The use of SBRT in treating osteosarcoma bone metastases is understudi...
GNE Mutation-Related Congenital Thrombocytopenia in 2 Siblings: Case Reports and Literature Review [0.03%]
两个同胞中的GNE突变相关先天性血小板减少症：病例报告及文献回顾
Yeter Düzenli Kar,Melike Sezgin Evim,Ugur Cem Mete et al.
Yeter Düzenli Kar et al.
Background: GNE mutations are rare pathologic conditions that can cause severe thrombocytopenia and bleeding tendency from the neonatal period. The clinical presentation of patients with GNE mutations varies from mild ski...
Comparative Analysis of Plasma MicroRNAs in Patients With Kaposiform Hemangioendothelioma and Tufted Angioma Versus Infantile Hemangioma [0.03%]
与婴幼儿血管瘤患者相比,Kaposiform血管内皮瘤和毛细血管扩张性血管瘤患者的血浆microRNA比较分析
Akifumi Nozawa,Michio Ozeki,Mui Sakai et al.
Akifumi Nozawa et al.
Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) can be confused with infantile hemangioma (IH) because of the age of presentation and the presence of a vascular cutaneous lesion. KHE/TA may be complicated by the Kasabach-Merri...
Malignant Transformation of a Pediatric Intracranial Nongerminomatous Germ Cell Tumor to Embryonal Rhabdomyosarcoma: Case Report and Literature Review [0.03%]
儿童颅内非生殖细胞瘤样germinocytoma恶变为胚胎性横纹肌肉瘤的病例报告及文献复习
Elizabeth S Borden,Ben Posorske,Clayton Long et al.
Elizabeth S Borden et al.
Malignant transformation of intracranial nongerminomatous germ cell tumors (NGGCTs) is a rare but clinically relevant phenomenon. We present the case of a 13-year-old boy with a localized, pineal NGGCT. After an initial favorable response, ...
Navigating Management of Spindle Cell/Sclerosing Rhabdomyosarcoma With FUS::TFCP2 Fusion in the Era of Targeted Therapy [0.03%]
靶向治疗时代脊索细胞/硬化性横纹肌肉瘤的诊断和治疗：带有FUS::TFCP2融合的病例报告及文献回顾
Olayinka Okeleji,Reeja Raj,Sherani Farha et al.
Olayinka Okeleji et al.
Spindle cell/sclerosing rhabdomyosarcoma (ssRMS) with FUS-TFCP2 translocation is a rare, aggressive RMS subtype often involving facial and pelvic bones and showing poor response to standard therapy. The FUS-TFCP2 fusion drives ALK gene acti...