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Variations in clinical presentation, frequency of hemophagocytosis and clinical behavior of intravascular lymphoma diagnosed in different geographical regions.
- Source :
-
Haematologica [Haematologica] 2007 Apr; Vol. 92 (4), pp. 486-92. - Publication Year :
- 2007
-
Abstract
- Background and Objectives: This study explored variations in the clinical manifestations of intravascular lymphoma (IVL) on the bases of the association with hemophagocytosis and the country where the diagnosis was made.<br />Design and Methods: The clinical features of 50 Western patients with IVL were compared with those of 123 patients with IVL diagnosed in Eastern countries (87 diagnosed in Japan and 36 in other Asian countries), previously reported in English literature, and collected by an electronic bibliographic search.<br />Results: Hemophagocytosis was absent in Western patients, but reported in 38 (44%) Japanese patients (p=0.00001) and in seven (19%) patients from other Asian countries (p=0.002). No clinical differences were evident between patients with hemophagocytosis-negative IVL diagnosed in Western countries, Japan and other Asian Countries. Conversely, Japanese and non-Japanese patients with hemophagocytosis-related IVL more frequently had stage IV disease, fever, hepato-splenic involvement, marrow infiltration, dyspnea, anemia, and thrombocytopenia, and rarely exhibited cutaneous or central nervous system involvement. Lymph node and peripheral blood involvement was uncommon in all subgroups. In Western patients, anthracycline-based chemotherapy was associated with a 52% remission rate, and a 2-year overall survival of 46%.<br />Interpretation and Conclusions: The clinical features of IVL vary according to the association with hemophagocytosis, regardless of the country in which the diagnosis is made. Western, Japanese and other Asian patients with hemophagocytosis-negative IVL display similar clinical characteristics and should be considered as having classical IVL. Patients with hemophagocytosis-related IVL show significantly different clinical features. Both forms have a poor prognosis. Extensive molecular studies are needed to explore whether these clinical differences might reflect discordant biological entities within IVL.
- Subjects :
- Adolescent
Adult
Aged
Aged, 80 and over
Anthracyclines therapeutic use
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Asia epidemiology
Asian People statistics & numerical data
Brain Neoplasms epidemiology
Brain Neoplasms ethnology
Brain Neoplasms pathology
Disease Progression
Europe epidemiology
Female
Follow-Up Studies
Forecasting
Humans
Japan ethnology
Lymphohistiocytosis, Hemophagocytic diagnosis
Lymphohistiocytosis, Hemophagocytic ethnology
Lymphohistiocytosis, Hemophagocytic etiology
Lymphoma, Large B-Cell, Diffuse classification
Lymphoma, Large B-Cell, Diffuse complications
Lymphoma, Large B-Cell, Diffuse diagnosis
Lymphoma, Large B-Cell, Diffuse drug therapy
Lymphoma, Large B-Cell, Diffuse ethnology
Lymphoma, Large B-Cell, Diffuse pathology
Male
Middle Aged
Organ Specificity
Phenotype
Prognosis
Retrospective Studies
Skin Neoplasms epidemiology
Skin Neoplasms ethnology
Skin Neoplasms pathology
Surveys and Questionnaires
Treatment Outcome
Vascular Neoplasms classification
Vascular Neoplasms complications
Vascular Neoplasms diagnosis
Vascular Neoplasms drug therapy
Vascular Neoplasms ethnology
Vascular Neoplasms pathology
White People statistics & numerical data
Lymphohistiocytosis, Hemophagocytic epidemiology
Lymphoma, Large B-Cell, Diffuse epidemiology
Vascular Neoplasms epidemiology
Subjects
Details
- Language :
- English
- ISSN :
- 1592-8721
- Volume :
- 92
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Haematologica
- Publication Type :
- Academic Journal
- Accession number :
- 17488659
- Full Text :
- https://doi.org/10.3324/haematol.10829