Increased 18F-FDG Avidity on PET/CT During Treatment for Rhabdomyosarcoma Confirmed to Be Mature Rhabdomyoblasts [0.03%]
成熟横纹肌瘤细胞的氟脱氧葡萄糖正电子发射断层扫描摄取增加
Nicole Baca,Fataneh Majlessipour,Christopher T Watterson et al.
Nicole Baca et al.
Background: Fluorine-18 fluorodeoxyglucose positron emission tomography (18F-FDG-PET) is useful for staging rhabdomyosarcoma. Using this modality as a predictor of outcome and for disease surveillance in rhabdomyosarcoma ...
Assessment of Immunization Status Following Non-HSCT Chemotherapy-treated Pediatric Leukemia Survivors [0.03%]
非造血干细胞移植化疗治疗的儿童急性白血病长期生存者的免疫状态评估
Hussien Ahmed H Abdelgawad,Kathleen Hinkle,Briana Fodor et al.
Hussien Ahmed H Abdelgawad et al.
Background: Chemotherapy for pediatric leukemia induces profound immunosuppression, resulting in waning protection against vaccine-preventable diseases. Despite high survival rates, standardized revaccination protocols fo...
Frequent Use of Hematologic Testing in Children Admitted for Nonaccidental Trauma [0.03%]
儿童意外伤害住院患者的血液检测使用情况
Meghan McCormick,Ramasubramanian Kalpatthi
Meghan McCormick
Nonaccidental trauma (NAT) can present with bleeding symptoms. Judicious use of hematologic testing is recommended to evaluate for medical causes of bleeding, while acknowledging inherited bleeding disorders and NAT may be present concurren...
Unresponsive Systemic Mastocytosis in a Young AML With RUNX1::RUNX1T1 Fusion With Rare KIT c.1255_1257delGAC Mutation: A Clinical Deadlock [0.03%]
一种年轻的AML伴RUNX1::RUNX1T1融合和罕见的KIT c.1255_1257delGAC突变的系统性非组绝症：一个临床困境
Vinu Balraam Kv,Amiya R Nayak,Jasmita Dass et al.
Vinu Balraam Kv et al.
Background: Systemic mastocytosis (SM) with associated acute myeloid leukemia (AML) is a rare malignancy usually linked to KIT p.D816V mutations. Observat...
Local Control and Survival Outcomes in Pediatric Nonrhabdomyosarcoma Soft Tissue Sarcoma: The Mayo Clinic Experience [0.03%]
儿童非横纹肌肉瘤软组织肉瘤的局部控制和生存结果：梅奥诊所的经验
Elizabeth L McKone,Kristofer W Roberts,William S Harmsen et al.
Elizabeth L McKone et al.
Objective: This single institutional analysis explored outcomes and factors associated with local control and survival in pediatric patients with nonrhabdomyosarcoma soft tissue sarcoma (NRSTS). ...
Diagnostic Pitfalls in Pediatric Acute Promyelocytic Leukemia: All-trans Retinoic Acid-Associated Hypercalcemia Mimicking Fungal Meningitis and the Risks of Azole Coadministration [0.03%]
儿童急性早幼粒细胞白血病的诊断陷阱：全反式维甲酸相关性高钙血症模仿真菌性脑膜炎及合并使用唑类药物的风险
Chengying Yuan,Zhi Wan,Ju Gao et al.
Chengying Yuan et al.
Objective: To alert clinicians to the risk of severe hypercalcemia arising from the ATRA-azole interaction and to highlight a rare diagnostic pitfall involving a false-positive cerebrospinal fluid (CSF) (1,3)-β-D-glucan ...
Unmanipulated Haploidentical Stem Cell Transplantation Outcome in a Pediatric Patient With CD27 Deficiency and EBV-Induced Diffuse Large B-Cell Lymphoma With Primary CNS Involvement [0.03%]
CD27缺陷并EB病毒诱导的原发性中枢神经系统弥漫性大B细胞淋巴瘤患儿单倍体相合外周血干细胞移植后预处理效果分析
Mohammad Jahanpanah,Maryam Behfar,Saeed Yousefian et al.
Mohammad Jahanpanah et al.
Background: CD27 deficiency is a rare primary immunodeficiency associated with severe Epstein-Barr virus (EBV)-related complications, including lymphoma. ...
Immunoglobulin Supplementation Practices and Effects During Pediatric B-Cell Acute Lymphoblastic Leukemia Therapy [0.03%]
儿童B细胞急性淋巴细胞白血病治疗期间的免疫球蛋白补充实践和影响
Holly J Edington,Nicholas P DeGroote,Jason Stevenson et al.
Holly J Edington et al.
Although some children with B-cell acute lymphoblastic leukemia (B-ALL) receive intravenous immunoglobulin (IVIG) during conventional therapy, supplementation practices vary, and data describing the indications and their impact are lacking....
Pritam Singha Roy,Jaydip Bhaumik,Anand Bardia et al.
Pritam Singha Roy et al.
Immunotherapy in Pediatric Constitutional Mismatch Repair Deficiency (CMMRD)-Associated Colorectal Cancer: Report of a Rare Variant and Recommendations for Screening [0.03%]
儿童遗传性错配修复缺陷（CMMRD）相关结直肠癌免疫治疗：罕见病例报告及筛查建议
Leigh Selesner,Cortnie R Vaughn,Saad Jazrawi et al.
Leigh Selesner et al.
Background: Constitutional mismatch repair deficiency is a rare pediatric cancer predisposition syndrome caused by mutations in mismatch repair genes. Obs...