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Updated: Jun 13, 2026

Isolating Human Peripheral Blood Mononuclear Cells and CD4+ T cells from Sézary Syndrome Patients for Transcriptomic Profiling
Published on: October 14, 2021
[Clinicopathological study on the follicular dendritic cell sarcoma]
Shu-hong Zhang1, Xiao-ge Zhou, Yuan-yuan Zheng
1Department of Pathology, Beijing Friendship Hospital, Capital University of Medical Sciences, China.
Follicular dendritic cell sarcoma (FDCS) is a rare, moderately malignant tumor. Clinicopathologic features and immunohistochemistry are crucial for its diagnosis and differentiation from other neoplasms.
Area of Science:
- Oncology
- Pathology
- Immunohistochemistry
Context:
- Follicular dendritic cell sarcoma (FDCS) is an exceptionally rare neoplasm.
- Understanding its clinicopathologic spectrum is vital for accurate diagnosis.
- Differential diagnosis can be challenging due to histological variability.
Purpose:
- To investigate the clinicopathologic features of FDCS.
- To evaluate differential diagnostic methods for FDCS.
- To highlight the role of immunohistochemistry in diagnosing FDCS.
Summary:
- This study examined 5 cases of FDCS, noting diverse locations (lymph node, tonsil, stomach, liver) and growth patterns.
- Neoplastic cells exhibited spindle to ovoid morphology with characteristic immunohistochemical markers (CD21, CD23, CD35, D2-40, CXCL13).
- One case tested positive for Epstein-Barr virus-encoded RNA (EBER).
Impact:
- FDCS should be considered a moderately malignant tumor with potential histological polymorphism.
- Immunohistochemistry is essential for distinguishing FDCS from other tumors.
- Further research into FDCS pathogenesis and treatment is warranted.
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