Background. Agranular CD4+CD56+hematodermic neoplasm (blastic NK-cell lymphoma) has been recently described. The skin is often the first organ involved. Observations. Two old men of respectively 70 and 77 years consulted for infiltrated cutaneous lesions. Preliminary histological examination of cutaneous biopsy taken in both patients showed a malignant proliferation suggesting a cutaneous lymphoma, and the patients were referred. Histological examination of new biopsies showed a very similar proliferation in the 2 cases of monotonous medium-sized mononuclear cells without expression of the common antigens CD3 and CD20 and the expression of receptor gene or the immunoglobulin heavy chain gene were evidenced. No extracutanous involvement was initially detected in the first patient. Thrombocytopenia associated with the abnormal presence of 15 p. 100 of circulating CD4+CD56+cells was initially found in the second patient. The first patient was treated with chemotherapy, with complete remission. A cutaneous relapse promptly occurred,followed by bone and cerebral localizations. The patient died one year after the diagnosis of the disease, in spite of intensification of the treatment. Treatment is still ongoing in the second patient. Comments. The histological presentation of these two patients was very similar withanunusalphenotypeoftumorcellsexpressingCD4,CD56, CD123, but not expressing CD3 and CD20. Some cases have beenpublishedunderthe“termofblasticNKlymphoma”which is the actual term for the disease in the WHO classification. However, the tumor cells derive from the dendritic plasmacytoid cells, also called type 2 dendritic cells, and perhaps from a common precursor to lymphocyte T and dendritic plasmacytoid cells. In spite of complete cutaneous response in the 2 cases presented, as in other reports, extra-cutaneous involvement occurs quickly. Overall survival is usually poor since nearly all the patients died in less than 3 years. This justifies attempting agressive protocols, with bone marrow allograft in the younger patients. Background. Agranular CD4 + CD56 + hematodermic neoplasm (blastic NK-cell lymphoma) has been recently described. The histories are often the first organ involved. Observations. Two old men of respectively 70 and 77 years consulted for infiltrated cutaneous lesions. of cutaneous biopsy taken in both patients showed a malignant proliferation suggestive of a cutaneous lymphoma, and the patients were referred. Histological examination of new biopsies showed a very similar proliferation in the 2 cases of monotonous medium-sized mononuclear cells without expression of the common antigens CD3 and CD20 and the expression of receptor gene or the immunoglobulin heavy chain gene were evidenced. No extracutanous involvement was initially detected in the first patient. Thrombocytopenia associated with the abnormal presence of 15 p. 100 of circulating CD4 + CD56 + cells was initially found in the second patient. The first patient was treated with chemotherapy, with complete remis sion. A cutaneous relapse promptly occurred, followed by bone and cerebral localizations. The patient died one year after the diagnosis of the disease, in spite of intensification of the treatment. Treatment is still ongoing in the second patient. Comments. The histological presentation of these two patients was very similar withanunusal phenotypeoftumorcellsexpressingCD4, CD56, CD123, but not expressing CD3 and CD20. Some cases have beenbuildupunderthe “termofblasticNKlymphoma ” which is the actual term for the disease in the WHO classification. However, the tumor cells derive from the dendritic plasmacytoid cells, also called type 2 dendritic cells, and perhaps from a common precursor to lymphocyte T and dendritic plasmacytoid cells. In spite of complete cutaneous response in the 2 cases presented, as in other reports, extra-cutaneous involvement quite quickly. Overall survival is usually poor from nearly all the patients died in less than 3 years. This justifies attempting agressiveprotocols, with bone marrow allograft in the younger patients.