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Published on: November 4, 2016
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Blastic Plasmacytoid Dendritic Cell Neoplasm: A Rare Entity in Clinical Practice
Bárbara Oliveira1, Carolina Nogueira1, Luís Dias1,2
1Internal Medicine, Hospital de Braga, Braga, PRT.
Cureus
|February 8, 2024
Summary
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare, aggressive cancer. Early detection and collaborative care are crucial for improving patient outcomes in this challenging hematologic malignancy.
Area of Science:
- Hematology
- Oncology
- Immunophenotyping
Background:
- Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematologic malignancy.
- It is classified under histiocytic/dendritic cell neoplasms in the WHO classification.
- BPDCN is known for its aggressive nature and complex clinical presentation.
Observation:
- An 85-year-old female with rheumatoid arthritis presented with constitutional symptoms including low-grade fever, anorexia, and weight loss.
- Symptoms had been present for one month prior to presentation.
- Diagnostic workup included immunophenotyping of a bone marrow aspirate.
Findings:
- Immunophenotyping confirmed the diagnosis of Blastic plasmacytoid dendritic cell neoplasm (BPDCN).
- The case highlights the diagnostic challenges associated with BPDCN.
- The patient's complex medical history potentially influenced the presentation and diagnostic process.
Implications:
- This case underscores the importance of considering rare hematologic malignancies in the differential diagnosis of unexplained constitutional symptoms.
- Early detection and accurate diagnosis are critical for timely and effective treatment of BPDCN.
- Interdisciplinary collaboration among healthcare professionals is essential for optimizing patient care and outcomes in BPDCN.
Keywords:
bpdcncd56+ natural killer (nk) cellshematological malignancynon-cutaneous bpdcnrare cancers
