Search

Your search keyword '"Neville B Wrignt"' showing total 2 results
Start Over Author "Neville B Wrignt"
2 results on '"Neville B Wrignt"'

1. Successful Curative Therapy With Rituximab and Allogeneic Haematopoietic Stem Cell Transplantation for MALT Lymphoma Associated WithSTK4-Mutated CD4+ Lymphocytopenia

Author

Denise Bonney, Neville B Wrignt, Stephen M. Hughes, Edmund Cheesman, Su Han Lum, and Robert Wynn

Subjects
0301 basic medicine, business.industry, MALT lymphoma, Hematology, medicine.disease, Transplantation, 03 medical and health sciences, Haematopoiesis, 030104 developmental biology, 0302 clinical medicine, Lymphatic system, Oncology, immune system diseases, hemic and lymphatic diseases, 030220 oncology & carcinogenesis, Pediatrics, Perinatology and Child Health, Immunology, medicine, Rituximab, Lymphocytopenia, Stem cell, business, Immunodeficiency, medicine.drug
Abstract

Idiopathic CD4+ lymphocytopenia and extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) are rare diseases in children. We report the first case of a child with STK4-mutated CD4+ lymphocytopenia who developed Epstein-Barr virus associated MALT lymphoma arising in the salivary gland. The child achieved complete remission with rituximab, and her immunodeficiency was cured by haematopoietic stem cell transplantation. The child remained well 24 months post transplantation.

Published
2016

2. Successful Curative Therapy With Rituximab and Allogeneic Haematopoietic Stem Cell Transplantation for MALT Lymphoma Associated With STK4-Mutated CD4+ Lymphocytopenia

Author

Su Han, Lum, Denise, Bonney, Edmund, Cheesman, Neville B, Wrignt, Stephen, Hughes, and Robert, Wynn

Subjects
Child, Preschool, Lymphopenia, Mutation, Hematopoietic Stem Cell Transplantation, Intracellular Signaling Peptides and Proteins, Humans, Transplantation, Homologous, Antineoplastic Agents, Female, Lymphoma, B-Cell, Marginal Zone, Protein Serine-Threonine Kinases, Rituximab
Abstract

Idiopathic CD4+ lymphocytopenia and extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma) are rare diseases in children. We report the first case of a child with STK4-mutated CD4+ lymphocytopenia who developed Epstein-Barr virus associated MALT lymphoma arising in the salivary gland. The child achieved complete remission with rituximab, and her immunodeficiency was cured by haematopoietic stem cell transplantation. The child remained well 24 months post transplantation.

Published
2016

Catalog

Books, media, physical & digital resources
See catalog results