AI Article Synopsis

  • Aggressive natural killer cell leukemia (ANKL) is a rare and fast-progressing disease that can be challenging to diagnose and treat.
  • A study tracked nine patients over ten years who exhibited severe symptoms, leading to thorough bone marrow (BM) examinations to confirm ANKL and rule out other conditions like lymphoma and hemophagocytic lymphohistiocytosis (HLH).
  • Key findings included high levels of specific markers (like CD2 and CD56) in neoplastic cells and indications of HLH in several patients, suggesting that strong clinical signs and certain tests (like NK cell activity) can aid ANKL diagnosis.

Article Abstract

Aggressive natural killer cell leukemia (ANKL) is a rare disease with an aggressive clinical course. We aimed to assess the clinicopathological characteristics of the difficult to diagnose ANKL. During ten years, nine patients with ANKL were diagnosed. All the patients exhibited aggressive clinical course and underwent the BM study to rule out lymphoma and hemophagocytic lymphohistiocytosis (HLH). BM examination showed varying degrees of infiltration of neoplastic cells, which were mainly positive for CD2, CD56, cytoplasmic CD3 and EBV in situ hybridization. Five BM aspirates showed histiocytic proliferation with active heomphagocytosis. Normal or increased NK cell activity test results were obtained from 3 patients who were available for testing. Four had multiple BM studies until diagnosis. An aggressive clinical course and positive EBV in situ hybridization, often with associated secondary HLH, should raise the suspicion of an ANKL. Conducting additional supplementary tests such as NK cell activity and NK cell proportion would be helpful for the diagnosis of ANKL.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925985PMC
http://dx.doi.org/10.7150/ijms.77583DOI Listing

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