T‐cell/histiocyte‐rich large B‐cell lymphoma in a patient with a novel frameshift <i>MSH6</i> mutation-Reference-Cited by-同舟云学术

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T‐cell/histiocyte‐rich large B‐cell lymphoma in a patient with a novel frameshift MSH6 mutation

Published:2022-09-24 Issue:3 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Cekic Sukru¹,Aydin Firdevs²,Karali Yasin¹,Sevinir Betül Berrin¹,Canoz Ozlem³,Boztug Kaan⁴,Unal Ekrem²,Kilic Sara Sebnem¹

Affiliation:

1. Faculty of Medicine Pediatric Immunology Uludag University Bursa Turkey

2. Division of Pediatric Hematology and Oncology Department of Pediatrics Faculty of Medicine Erciyes University Kayseri Turkey

3. Department of Pathology Faculty of Medicine Erciyes University Kayseri Turkey

4. Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences St. Anna Kinderspital und Universitätsklinik für Kinder und Jugendliche Medizinische Universitat Wien St. Anna Children's Cancer Research Institute (CCRI) Vienna Austria

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30008

Reference18 articles.

1. DNA Mismatch Repair

2. A Homozygous Mutation in MSH6 Causes Turcot Syndrome

3. Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

4. Constitutional mismatch repair deficiency and childhood leukemia/lymphoma - report on a novel biallelic MSH6 mutation

5. Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium ‘Care for CMMRD’ (C4CMMRD)

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