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Clinical and biologic features of CD4+CD56+ malignancies

Feuillard, Jean ; Jacob, Marie-Christine ; Valensi, Françoise ; Maynadié, Marc ; Gressin, Rémy ; Chaperot, Laurence ; Arnoulet, Christine ; Brignole-Baudouin, Françoise ; Drénou, Bernard ; Duchayne, Eliane ; Falkenrodt, Annie ; Garand, Richard ; Homolle, Emanuelle ; Husson, Bernard ; Kuhlein, Emilienne ; Le Calvez, Geneviève ; Sainty, Danielle ; Sotto, Marie-France ; Trimoreau, Franck ; Béné, Marie-Christine

Blood, 2002-03, Vol.99 (5), p.1556-1563 [Periódico revisado por pares]

Washington, DC: Elsevier Inc

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Título:
Clinical and biologic features of CD4+CD56+ malignancies
Autor: Feuillard, Jean ; Jacob, Marie-Christine ; Valensi, Françoise ; Maynadié, Marc ; Gressin, Rémy ; Chaperot, Laurence ; Arnoulet, Christine ; Brignole-Baudouin, Françoise ; Drénou, Bernard ; Duchayne, Eliane ; Falkenrodt, Annie ; Garand, Richard ; Homolle, Emanuelle ; Husson, Bernard ; Kuhlein, Emilienne ; Le Calvez, Geneviève ; Sainty, Danielle ; Sotto, Marie-France ; Trimoreau, Franck ; Béné, Marie-Christine
Assuntos: Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antigens, Neoplasm - analysis ; Antigens, Neoplasm - immunology ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; CD4 Antigens - analysis ; CD4 Antigens - immunology ; CD56 Antigen - analysis ; CD56 Antigen - immunology ; Child ; Child, Preschool ; Dendritic Cells - immunology ; Dendritic Cells - pathology ; Female ; Follow-Up Studies ; Hematologic and hematopoietic diseases ; Hematologic Neoplasms - classification ; Hematologic Neoplasms - immunology ; Hematologic Neoplasms - pathology ; Humans ; Immunodeficiencies. Immunoglobulinopathies ; Immunoglobulinopathies ; Immunopathology ; Immunophenotyping ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness - immunology ; Neoplastic Cells, Circulating - immunology ; Skin Neoplasms - classification ; Skin Neoplasms - immunology ; Skin Neoplasms - pathology ; Treatment Outcome
É parte de: Blood, 2002-03, Vol.99 (5), p.1556-1563
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Descrição: CD4+CD56+ malignancies are rare hematologic neoplasms, which were recently shown to correspond to the so-called type 2 dendritic cell (DC2) or plasmacytoid dendritic cells. This study presents the biologic and clinical features of a series of 23 such cases, selected on the minimal immunophenotypic criteria defining the DC2 leukemic counterpart, that is, coexpression of CD4 and CD56 in the absence of B, T, and myeloid lineage markers. Clinical presentation typically corresponded to cutaneous nodules associated with lymphadenopathy or spleen enlargement or both. Cytopenia was frequent. Circulating malignant cells were often detected. Massive bone marrow infiltration was seen in 20 of 23 (87%) patients. Most tumor cells exhibited nuclei with a lacy chromatin, a blastic aspect, large cytoplasm-containing vacuoles or microvacuoles beside the plasma membrane, and cytoplasmic expansions resembling pseudopodia. Other immunophenotypic characteristics included both negative (CD16, CD57, CD116, and CD117) and positive (CD36, CD38, CD45 at low levels, CD45RA, CD68, CD123, and HLA DR) markers. The prognosis was rapidly fatal in the absence of chemotherapy. Complete remission was obtained in 18 of 23 (78%) patients after polychemotherapy. Most patients had a relapse in less than 2 years, mainly in the bone marrow, skin, or central nervous system. Considering these clinical and biologic features, the conclusion is made that CD4+CD56+malignancies constitute a genuine homogeneous entity. Furthermore, some therapeutic options were clearly identified. Finally, relationships between the pure cutaneous indolent form of the disease and acute leukemia as well as with the lymphoid/myeloid origin of the CD4+CD56+ malignant cell are discussed.
Editor: Washington, DC: Elsevier Inc
Idioma: Inglês

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Clinical and biologic features of CD4+CD56+ malignancies

Washington, DC: Elsevier Inc

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