T‐cell lymphoblastic lymphoma with subsequent acute nonlymphocytic leukemia. A case report

A case of T‐cell lymphoblastic lymphoma is described in which the patient presented with a characteristic mediastinal mass and lack of bone marrow involvement. Immunologic studies of the surface phenotype of the malignant cells in a pleural effusion with monoclonal antibodies revealed the cells to b...

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Veröffentlicht in:Cancer 1982-07, Vol.50 (1), p.118-124
Hauptverfasser: Posner, Marshall R., Said, Jonathan, Pinkus, Geraldine S., Nadler, Lee M., Hardy, Russell, Flatow, Frederick, Skarin, Arthur T.
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container_end_page 124
container_issue 1
container_start_page 118
container_title Cancer
container_volume 50
creator Posner, Marshall R.
Said, Jonathan
Pinkus, Geraldine S.
Nadler, Lee M.
Hardy, Russell
Flatow, Frederick
Skarin, Arthur T.
description A case of T‐cell lymphoblastic lymphoma is described in which the patient presented with a characteristic mediastinal mass and lack of bone marrow involvement. Immunologic studies of the surface phenotype of the malignant cells in a pleural effusion with monoclonal antibodies revealed the cells to be of thymic origin and distinguished them from the surface phenotypes seen in T‐cell acute lymphoblastic leukemia. Twenty‐five months after presentation with lymphoma, the patient developed an acute nonlymphocytic leukemia. With the improved prognosis seen in lymphoblastic lymphoma with intensive combination chemotherapy, it is expected that more cases of subsequent acute nonlymphocytic leukemia will be seen. In view of the natural history of lymphoblastic lymphoma to develop into lymphoblastic leukemia, it is important to be alert to a complicating nonlymphocytic leukemia.
doi_str_mv 10.1002/1097-0142(19820701)50:1<118::AID-CNCR2820500122>3.0.CO;2-8
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subjects Adult
Humans
Leukemia, Myeloid, Acute - diagnosis
Lymphoma, Non-Hodgkin - diagnosis
Male
Mediastinal Neoplasms - diagnosis
Mediastinal Neoplasms - pathology
Neoplasms, Multiple Primary
T-Lymphocytes
title T‐cell lymphoblastic lymphoma with subsequent acute nonlymphocytic leukemia. A case report
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