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18F-FDG-PET/CT is effective in distinguishing myelofibrosis due to bone marrow infiltration of diffuse large B-cell lymphoma from triple-negative primary myelofibrosis.
Kumagai, Takuma; Satoh, Yoko; Koshiishi, Megumi; Ooishi, Saori; Sueki, Yuki; Nakajima, Kei; Mitsumori, Toru; Kirito, Keita.
Afiliação
  • Kumagai T; Department of Hematology/Oncology, University of Yamanashi.
Rinsho Ketsueki ; 58(3): 228-232, 2017.
Article em Ja | MEDLINE | ID: mdl-28381690
ABSTRACT
Although myelofibrosis is mainly associated with myeloproliferative neoplasms (MPN), especially primary myelofibrosis (PMF), a variety of hematological malignancies, including acute myeloid leukemia, multiple myeloma and malignant lymphoma, also cause myelofibrosis with markedly varying degrees of severity. Thus, it is extremely important to accurately diagnose the underlying diseases that cause fibrosis in bone marrow. Analyses of JAK2, MPL and calreticulin gene mutations are useful for distinguishing MPN from other diseases, since 90% of MPN patients have a mutation in one of these genes. However, 10% of PMF patients do not have mutations in any of these genes, and these patients have a disease known as triple negative PMF. It is sometimes difficult to accurately distinguish triple negative PMF from secondary myelofibrosis caused by other diseases. Herein, we present a case of diffuse large B cell lymphoma (DLBCL) with bone marrow involvement, mimicking triple negative primary myelofibrosis. 18F-FDG-PET was useful for correctly diagnosing DLBCL.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medula Óssea / Linfoma Difuso de Grandes Células B / Mielofibrose Primária Tipo de estudo: Diagnostic_studies Limite: Aged / Humans / Male Idioma: Ja Revista: Rinsho Ketsueki Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medula Óssea / Linfoma Difuso de Grandes Células B / Mielofibrose Primária Tipo de estudo: Diagnostic_studies Limite: Aged / Humans / Male Idioma: Ja Revista: Rinsho Ketsueki Ano de publicação: 2017 Tipo de documento: Article