Subcutaneous panniculitis-like T-cell lymphoma-associated hemophagocytic syndrome with fulminant relapse during corticosteroid treatment and fatal outcome
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology,Hematology
Reference9 articles.
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2. World health organization classification of tumours. Pathology and genetics of tumours of the haematopoietic and lymphoid tissues;Jaffe,2001
3. WHO–EORTC classification of cutaneous lymphomas;Burg,2005
4. Immunophenotypic and molecular features, clinical outcomes, treatments, and prognostic factors associated with subcutaneous panniculitis-like T-cell lymphoma: a systemic analysis of 156 patients reported in the literature;Go;Cancer,2004
5. Subcutaneous panniculitis-like T-cell lymphoma: a clinicopathological, immunophenotypic and molecular analysis of six patients;Hoque;Br J Dermatol,2003
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1. Intrapleural infections in patients with subcutaneous panniculitis‐like T‐cell lymphoma are susceptible to hemophagocytic lymphohistiocytosis;Dermatologic Therapy;2021-07-04
2. Pathology of T-Cell Lymphomas: Diagnosis and Biomarker Discovery;Non-Hodgkin Lymphoma;2015
3. Recurrent diffuse large B-cell lymphoma presenting initially as hemophagocytic syndrome;Acta Haematologica Polonica;2014-01
4. Full Facial Edema: A Novel Presentation of Subcutaneous Panniculitis-Like T-Cell Lymphoma;Journal of Clinical Oncology;2012-09-01
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