Published online Nov 6, 2020. doi: 10.12998/wjcc.v8.i21.5439
Peer-review started: June 28, 2020
First decision: July 24, 2020
Revised: August 14, 2020
Accepted: September 29, 2020
Article in press: September 29, 2020
Published online: November 6, 2020
Processing time: 130 Days and 23.3 Hours
Anaplastic large cell lymphoma (ALCL) is a rare and heterogeneous malignant tumor, which is classified as anaplastic lymphoma kinase (ALK)positive ALCL and ALK- ALCL. Many patients are diagnosed with ALCL at the stage of bone marrow involvement. However, ALCL patients with clinical manifestations consistent with acute leukemia are relatively rare.
In this report, the patient did not receive appropriate diagnosis and treatment despite a two-year history of lymph node enlargement. Hereafter, she was admitted for B symptoms and was diagnosed as ALK-ALCL by lymph node biopsy. Then, the disease progressed to leukemia without any treatment after 2 mo. The proportion of lymphoma cells in bone marrow was as high as 96%, and the proportion of peripheral blood was 84%. She also had clinical manifestations similar to acute leukemia. After completion of chemotherapy, she developed granulocytopenia and fever and died from septicemia.
ALCL with leukemic presentation is a late manifestation of lymphoma with low chemotherapy tolerance and poor prognosis.
Core Tip: Anaplastic large cell lymphoma (ALCL) is a rare and heterogeneous malignant tumor. Many patients are diagnosed with ALCL at the stage of bone marrow involvement. However, ALCL patients with clinical manifestations consistent with acute leukemia are relatively rare. Here, we reported an anaplastic lymphoma kinase negative ALCL patient with a two-year history of lymph node enlargement who did not receive the appropriate diagnosis and treatment and rapidly progressed to acute leukemia. This suggested that ALCL with leukemic presentation is a late manifestation of lymphoma with low chemotherapy tolerance and poor prognosis.