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Primary Effusion Lymphoma (PEL)-Like Lymphoma in a Child With Congenital Immunodeficiency.
Lam, Grace K S; Abdelhaleem, Mohamed; Somers, Gino R; Roifman, Chaim; Read, Stanley; Abla, Oussama.
Afiliação
  • Lam GK; Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Abdelhaleem M; Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Somers GR; Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Roifman C; Division of Immunology and Allergy, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Read S; Division of Infectious Diseases, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Abla O; Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Pediatr Blood Cancer ; 63(9): 1674-6, 2016 09.
Article em En | MEDLINE | ID: mdl-27186682
Primary effusion lymphoma (PEL) is a rare lymphoma that occurs more frequently in immunocompromised adults and has a poor survival. We report a 9-year-old female with combined immunodeficiency with an Epstein-Barr virus positive/human herpes virus 8 negative PEL-like lymphoma. The treatment with systemic chemotherapy for non-Hodgkin lymphoma, zidovudine, and interferon-α failed to control disease progression. This is the first reported pediatric case of PEL-like lymphoma. Increased diagnostic awareness and more effective treatment strategies are needed for this rare lymphoma.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Efusão Primária / Síndromes de Imunodeficiência Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Efusão Primária / Síndromes de Imunodeficiência Tipo de estudo: Diagnostic_studies Limite: Child / Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article