An unusual presentation of a case of T cell angiotropic (intravascular) lymphoma
暂无分享,去创建一个
S. Songia | A. Biondi | G. Isimbaldi | S. Bianchi | L. Corral | M. Valente
[1] L. Tucker,et al. Malignancies in children who initially present with rheumatic complaints. , 1999, The Journal of pediatrics.
[2] R. Winkelmann,et al. Malignant Angioendotheliomatosis Is an Angiotropic Intravascular Lymphoma: Immunohistochemical, Ultrastructural, and Molecular Genetics Studies , 1995, The American Journal of dermatopathology.
[3] E. Berti,et al. Heteroduplex analysis of T-cell receptor gamma gene rearrangements for diagnosis and monitoring of cutaneous T-cell lymphomas. , 1994, Blood.
[4] L. Cavazzini,et al. Immunoblastic malignant lymphoma in adult onset Still's disease. , 1993, The Journal of rheumatology.
[5] O. Sangueza,et al. Intravascular lymphomatosis: report of an unusual case with T cell phenotype occurring in an adolescent male , 1992, Journal of cutaneous pathology.
[6] T. Tada,et al. Congenital angiotropic lymphoma (intravascular lymphomatosis) of the T‐cell type , 1991, Cancer.
[7] C. Lombard,et al. Immunohistochemical and cytogenetic studies indicate that malignant angioendotheliomatosis is a primary intravascular (angiotropic) lymphoma , 1990, Cancer.
[8] J. Tappeiner,et al. [On the recognition of systematized endotheliomatosis of the cutaneous blood vessels (reticuloendotheliosis?]. , 1959, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.