Image de couverture de livre

Aggressive Systemic Mastocytosis Related to Germline p.D816V KIT Mutation

Fuente: Wiley Open Access

Enregistré dans:

Détails bibliographiques
Auteurs principaux:	Antonia Kiwit, Julian Trah, Amelie T. van der Ven, Ilske Oschlies, Nikolas von Bubnoff, Carsten Müller, Ingo Müller, Martin Blohm, Philipp Deindl, Sofia Apostolidou, Dominique Singer, Kai Lehmberg
Format:	Artículo Open Access
Publié:	Wiley 2025
Sujets:	Pediatric Blood & Cancer
Accès en ligne:	Acceder al recurso
Tags:	Ajouter un tag Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires

A Rare Case of Recurrent Infant Mediastinal Malignant Rhabdoid Tumor With MSH2 Germline Mutation
par: Qizi Wu, et autres
Publié: (2025)

Face validity of the Kids’ ITP Tools (KIT) in the era of thrombopoietin receptor agonists
par: Catherine McGuire, et autres
Publié: (2024)

Two Faces of NOTCH1 in Childhood Lymphoblastic T‐Cell Neoplasia: Prognostic Divergence of Mutational and Structural Aberrations
par: Marie C. Heider, et autres
Publié: (2026)

Pathogenic Germline PALB2 and RAD50 Variants in Patients With Relapsed Ewing Sarcoma
par: Molly Mack, et autres
Publié: (2026)

Comment on: Novel Findings in Pediatric and Adolescent Patients With Cancer and a Germline SMARCA4 Variant. First Familial Case of Neuroblastoma in a Mother–Daughter Pair With a Shared Germline SMARCA4 Variant
par: Dildar Bahar Genc, et autres
Publié: (2025)

KIT ‐mutated pediatric core‐binding factor systemic mastocytosis‐acute myeloid leukemia treated with avapritinib and decitabine
par: Irtiza N. Sheikh, et autres
Publié: (2024)

Case of Refractory Classic Hodgkin Lymphoma With a Germline Pathogenic Monoallelic Variant in the TNFRSF13B Gene
par: Mónica Camacho‐Arias, et autres
Publié: (2024)

Evaluating the Utility of Paired Tumor and Germline Targeted DNA Sequencing for Pediatric Oncology Patients: A Single Institution Report
par: Natalie Waligorski, et autres
Publié: (2026)

A Unique Case of a Pediatric Patient with Six Childhood Cancers in Association with a Germline TP53 Gene Pathogenic Variant
par: Shaelene Standing, et autres
Publié: (2024)

Osteosarcoma in an Adolescent With Germline DYNC1H1 ‐Related Disorder: A Novel Association With Whole Genome and Transcriptome Tumour Analysis
par: Cameron J. Grisdale, et autres
Publié: (2025)

Congenital Myelodysplastic Syndrome in a Newborn With Germline JAK2 Variant Treated With Liposomal Cytarabine–Daunorubicin and Allogeneic Hematopoietic Stem Cell Transplant
par: Kristin E. Zorn, et autres
Publié: (2025)

A Unique Presentation of Early‐Onset Colon Cancer in the Setting of Helicobacter pylori Positivity, IgA Deficiency, and a Germline 18p Deletion
par: Kelsey Gay, et autres
Publié: (2025)

Novel Pediatric Aggressive Adipose Tumor With Pathogenic TERT Promoter Variant and an Initial Durable Response to Vincristine and Dactinomycin
par: Lucy Hare, et autres
Publié: (2026)

Aggressive Pediatric Primitive Round Cell Tumors with MN1::ZNF341 Fusion: A Mimic of Neuroblastoma
par: Serena Y. Tan, et autres
Publié: (2024)

RAS Pathway Mutations and Therapeutics in Vascular Anomalies
par: Sara Alharbi, et autres
Publié: (2025)

Severe Precapillary Pulmonary Hypertension and Right Ventricular Failure After Hematopoietic Stem Cell Transplantation: Successful Outcomes With Aggressive Upfront Triple Therapy
par: Stine Andersen, et autres
Publié: (2025)

Reply to: Comment on: Increased Plasma ST2 Levels Precede the Development of Severe Acute GvHD and Chronic GvHD After Pediatric Hematopoietic Stem Cell Transplantation
par: Nakisa Kamari‐Kany, et autres
Publié: (2025)

Successful Use of Targeted HIF‐2α Inhibition in EPAS1‐Mutated Congenital Erythrocytosis
par: Elliot Ensink, et autres
Publié: (2025)

Concurrent Somatic Mutations of the SETBP1 and KRAS Genes in Pediatric AML: A Case Report
par: Ryo Okuse, et autres
Publié: (2026)

Coagulation Dysfunction Caused by a De Novo Mutation of Gene SLC37A4
par: Mauro Guariento, et autres
Publié: (2024)

A Novel Mutation in the Adenosine Deaminase‐2 Gene Presenting as Severe Chronic Neutropenia With Myeloid Hypoplasia
par: Pronamee Borah, et autres
Publié: (2025)

Cooley's Legacy Endures—Elliptocytes in X‐Linked Sideroblastic Anemia Due to Aminolevulinate Synthase 2 Mutations
par: Alex Ciurej, et autres
Publié: (2026)

Cytopenia, Hypocellular Bone Marrow, and Shortened Telomere Length Beyond Biallelic Telomere Biology Gene Mutations
par: Giovanni Franco, et autres
Publié: (2026)

A Rare Case of FANCC ‐Mutated Fanconi Anaemia Presenting With a Negative Chromosome Breakage Test
par: Mohsin Badat, et autres
Publié: (2026)

Reduced‐Intensity Chemotherapy With Immunotherapy for Children With Down Syndrome and B‐Cell Acute Lymphoblastic Leukemia
par: Ashley C. Holland, et autres
Publié: (2025)

Diagnosing Acute Graft‐Versus‐Host Disease in Children Undergoing Hematopoietic Stem Cell Transplantation—Comparison of the Modified Glucksberg Criteria Versus the MAGIC Criteria
par: Sarah Weischendorff, et autres
Publié: (2025)

Unraveling Juvenile Hyaline Fibromatosis: A Case of Novel ANTXR2 Mutations Associated with Subcutaneous Masses and Hydronephrosis
par: Shu‐Di Zhang, et autres
Publié: (2024)

Increasing Paternal Age Associated With Elevated Risk of De Novo Mutations in Offspring Diagnosed With Sporadic Bilateral Retinoblastoma
par: Maral Adel Fahmideh, et autres
Publié: (2025)

Emergence and Implications of DNMT3A Mutations in Pediatric AML Post‐HSCT: A Case Report and Literature Review
par: Aarushi Madan, et autres
Publié: (2025)

A Rare Case of Pediatric Hepatocellular Carcinoma Secondary to Mitochondrial DNA Depletion Syndrome Type 3 ( DGUOK Mutation)
par: Tejasvi R, et autres
Publié: (2026)

Life‐Threatening Infantile Fibrosarcoma in an Infant
par: Katharina Daugs, et autres
Publié: (2025)

Access Program for Unapproved and Off‐Label Drug Use in Pediatric BRAF V600E‐Mutated Brain Tumors in Japan
par: Maya Suzuki, et autres
Publié: (2025)

X‐Linked Sideroblastic Anemia Caused by ALAS2 Intron 1 Mutation Successfully Treated by Allogenic Hematopoietic Stem Cell Transplant
par: Shurui Du, et autres
Publié: (2026)

Oncogenic NRAS Mutation in Incipient Sarcomatous Transformation of Cystic Nephroma From a Patient With DICER1 ‐Related Tumor Predisposition Syndrome
par: Nahir Cortes‐Santiago, et autres
Publié: (2025)

MEK Inhibition With Trametinib for the treatment of MAP2K1‐Mutated Rosai–Dorfman–Destombes Disease Arising from the Nasopharynx in a Paediatric Patient
par: Claire Cuerden, et autres
Publié: (2025)

Cerebrospinal Fluid Liquid Biopsy Enables Targeted Therapy Without Tissue Diagnosis in Pediatric Low‐Grade Gliomas With BRAF V600E Mutation
par: Hannah Sultan, et autres
Publié: (2026)

Rare EWSR1::PBX1 Fusion‐Positive Infant B‐ALL With Coexisting KRAS Mutation: Sustained Molecular Remission Achieved With Standard Chemotherapy
par: Xiaoyong Chen, et autres
Publié: (2025)

Soluble Thrombomodulin Is Associated With Endothelial Dysfunction Syndromes After Pediatric Hematopoietic Stem Cell Transplantation
par: Denise Elbæk Horan, et autres
Publié: (2025)

A Novel TAL2::TCRB Fusion With PI3K/AKT Pathway Mutations in Pediatric T‐Cell Acute Lymphoblastic Leukemia: Diagnostic and Therapeutic Implications
par: Qiang Yao, et autres
Publié: (2025)

Increased Plasma ST2 Levels Precede the Development of Severe Acute GvHD and Chronic GvHD After Pediatric Hematopoietic Stem Cell Transplantation
par: Nakisa Kamari‐Kany, et autres
Publié: (2025)