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. 2019 Dec 23;3(24):4238–4251. doi: 10.1182/bloodadvances.2019000647

Table 3.

Clinical and biological presentation of the 4 BPDCN cases expressing a combination of lymphoid markers (B and T) plus myeloid markers

Patients P101 P1506 P1603 P201
Age, y 76 66 69 81
T-cell markers
 CD2 +
 CD5
 CD7 + + +
 CD3
 cCD3
B-cell markers
 CD22 + + +
 CD79a +
 cCD22 ND ND ND
 CD19
Myeloid markers
 CD13
 CD117 +
 CD15
 CD65
 CD33 + + + +
 CD38 + + ND ND
 CD36 + + + +
 MPO
pDC markers
 HLA-DR + + + +
 CD4 + + + +
 CD56 + + + +
 CD123 + + + +
 CD303 ND + ND +
 CD304 ND + ND +
 cTCL1 ND + + ND
Karyotype Failure Normal Normal Normal
Bone marrow aspirate
 Dysplasia No Dysgranulopoiesis Dysgranulopoiesis Trilineage dysplasia
 Blast morphology Large pseudopodia, rare vacuoles, undifferentiated cells Medium size, some vacuoles, immature Typical with vacuoles and pseudopodia Typical with vacuoles and pseudopodia
Cutaneous lesions Extensive petechiae skin purpura, from thighs to neck Multiple brown lesions on the back and trunk Purplish nodular lesions on the forehead and scalp Diffuse ecchymotic lesions on the trunk, face, upper and lower limbs
Immunohistochemistry CD4+ CD56+ MPO CD3 CD20 CD138 immunoglobulin CD4+ CD56+ CD3 CD20 MPO CD123+ CD4+ CD56+ CD45RA+ CD34 MPO TDT CD15 CD3 CD2 CD8 CD20 CD4+ CD56+ CD68+ CD123+ CD303+ TCL1+ CD2AP+

c, intracytoplasmic detection; ND, not done.