Sandbox: T cell: Difference between revisions

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Adult T‐cell leukaemia/lymphoma (ATLL) is a mature T‐cell neoplasm of post‐thymic lymphocytes  
Adult T‐cell leukaemia/lymphoma (ATLL) is a mature T‐cell neoplasm of post‐thymic lymphocytes  
Etiologically linked to the human T‐cell lymphotropic virus, HTLV‐I, HTLV‐I serology is a mandatory investigation
Etiologically linked to the human T‐cell lymphotropic virus, HTLV‐I, HTLV‐I serology is a mandatory investigation
Transmission of HTLV-1 is believed to occur from mother to child; by sexual contact; and through exposure to contaminated blood, either through blood transfusion or sharing of contaminated needles
The disease manifests in 75% of cases with leukaemia and in the remaining as a pure lymphomatous form
The disease manifests in 75% of cases with leukaemia and in the remaining as a pure lymphomatous form


anaemia and thrombocytopenia is variable
anaemia and thrombocytopenia is variable
Neutrophilia and eosinophilia Present
Neutrophilia and eosinophilia Present
hypercalcaemia
lytic bone lesions
tumor-induced osteolysis hypercalcaemia
elevated serum levels of IL-1, TGFβ, PTHrP, macrophage inflammatory protein (MIP-1α), and receptor activator of nuclear factor-κB ligand (RANKL) have been associated with hypercalcemia


Diffuse infiltration of the lymph node leading expansion of the paracortical area
Diffuse infiltration of the lymph node leading expansion of the paracortical area

Revision as of 12:53, 3 November 2015

Adult T‐cell leukaemia/lymphoma (ATLL) is a mature T‐cell neoplasm of post‐thymic lymphocytes Etiologically linked to the human T‐cell lymphotropic virus, HTLV‐I, HTLV‐I serology is a mandatory investigation

Transmission of HTLV-1 is believed to occur from mother to child; by sexual contact; and through exposure to contaminated blood, either through blood transfusion or sharing of contaminated needles


The disease manifests in 75% of cases with leukaemia and in the remaining as a pure lymphomatous form

anaemia and thrombocytopenia is variable Neutrophilia and eosinophilia Present lytic bone lesions tumor-induced osteolysis hypercalcaemia elevated serum levels of IL-1, TGFβ, PTHrP, macrophage inflammatory protein (MIP-1α), and receptor activator of nuclear factor-κB ligand (RANKL) have been associated with hypercalcemia

Diffuse infiltration of the lymph node leading expansion of the paracortical area Infiltration of the dermis skin infiltration, epidermotropism present and Pautrier's microabcesses

antibodies to HTLV‐I are demonstrable

+3, +7, +21, monosomy X,deletion of chromosome Y anf chromosomes 6 and 14q; 14q11 and break points e TCR‐alpha and ‐delta chain genes TCRA and TCRD 14q32 of TCL1 mutations of tumour‐suppressor genes CDKN2A (p16), CDKN2B (p15) and TP53 (p53)


pleomorphic, a medium size lymphocyte conndensed chromatin convoluted or polylobated nucleus nucleoli are not visibl cytoplasm agranular “flower cell”

CD4 positive CD8 positive CD2 and CD5 positive CD7 negativ CD3 and T‐cell receptor (TCR)‐β may be down‐regulated