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Rare non-Hodgkin lymphoma of childhood and adolescence: A consensus diagnostic and therapeutic approach to pediatric-type follicular lymphoma, marginal zone lymphoma, and nonanaplastic peripheral T-cell lymphoma
A. Attarbaschi, O. Abla, L. Arias Padilla, A. Beishuizen, GAA. Burke, L. Brugières, J. Bruneau, B. Burkhardt, ESG. d'Amore, W. Klapper, U. Kontny, M. Pillon, M. Taj, SD. Turner, A. Uyttebroeck, W. Woessmann, K. Mellgren,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, přehledy
PubMed
32452165
DOI
10.1002/pbc.28416
Knihovny.cz E-zdroje
- MeSH
- alografty MeSH
- dítě MeSH
- folikulární lymfom * diagnóza terapie MeSH
- kojenec MeSH
- lidé MeSH
- lymfom z B-buněk marginální zóny * diagnóza terapie MeSH
- mladiství MeSH
- periferní T-buněčný lymfom * diagnóza terapie MeSH
- předškolní dítě MeSH
- transplantace hematopoetických kmenových buněk * MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Pediatric-type follicular (PTFL), marginal zone (MZL), and peripheral T-cell lymphoma (PTCL) account each for <2% of childhood non-Hodgkin lymphoma. We present clinical and histopathological features of PTFL, MZL, and few subtypes of PTCL and provide treatment recommendations. For localized PTFL and MZL, watchful waiting after complete resection is the therapy of choice. For PTCL, therapy is subtype-dependent and ranges from a block-like anaplastic large cell lymphoma (ALCL)-derived and, alternatively, leukemia-derived therapy in PTCL not otherwise specified and subcutaneous panniculitis-like T-cell lymphoma to a block-like mature B-NHL-derived or, preferentially, ALCL-derived treatment followed by hematopoietic stem cell transplantation in first remission in hepatosplenic and angioimmunoblastic T-cell lymphoma.
Department of Pathology Necker Enfants Maladies Hospital Paris France
Department of Pathology University of Padova Padova Italy
Department of Pediatric Hematology and Oncology University Hospital Leuven Leuven Belgium
Department of Pediatric Hematology and Oncology University of Münster Münster Germany
Department of Pediatric Hematology and Oncology University of Padova Padova Italy
Princess Máxima Center for Pediatric Oncology Utrecht The Netherlands
Citace poskytuje Crossref.org
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- $a Attarbaschi, Andishe $u Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.
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- $a Pediatric-type follicular (PTFL), marginal zone (MZL), and peripheral T-cell lymphoma (PTCL) account each for <2% of childhood non-Hodgkin lymphoma. We present clinical and histopathological features of PTFL, MZL, and few subtypes of PTCL and provide treatment recommendations. For localized PTFL and MZL, watchful waiting after complete resection is the therapy of choice. For PTCL, therapy is subtype-dependent and ranges from a block-like anaplastic large cell lymphoma (ALCL)-derived and, alternatively, leukemia-derived therapy in PTCL not otherwise specified and subcutaneous panniculitis-like T-cell lymphoma to a block-like mature B-NHL-derived or, preferentially, ALCL-derived treatment followed by hematopoietic stem cell transplantation in first remission in hepatosplenic and angioimmunoblastic T-cell lymphoma.
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