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Updated: Dec 31, 2025

Establishment of Epstein-Barr Virus Growth-transformed Lymphoblastoid Cell Lines
Published on: November 8, 2011
Systemic Epstein-Barr virus-positive T-cell lymphoma of childhood
Qiong Wu1, Faliang Ren2, Dirk M Elston3
1Department of Dermatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, China.
Insights
This case study details a rare Epstein-Barr virus (EBV)-positive T-cell lymphoma in a child. The condition initially resolved spontaneously but relapsed, leading to a fatal outcome.
Area of Science:
- Pediatric Oncology
- Virology
- Hematology
Background:
- Epstein-Barr virus (EBV) is a common herpesvirus that can cause various lymphoproliferative disorders.
- T-cell lymphomas are a diverse group of cancers affecting T-lymphocytes, often aggressive.
- Childhood lymphomas require specific diagnostic and therapeutic approaches.
Observation:
- A 7-year-old boy presented with acute fever, oral ulcers, and skin nodules.
- Initial presentation lacked pancytopenia and hemophagocytic syndrome.
- The condition exhibited a period of spontaneous remission.
Findings:
- Systemic Epstein-Barr virus (EBV)-positive T-cell lymphoma of childhood was diagnosed via comprehensive examination.
- Diagnostic methods included laboratory tests, imaging, biopsies, immunohistochemistry, and in situ hybridization for EBER.
- The lymphoma demonstrated an initial spontaneous resolution followed by relapse.
Implications:
- This case highlights the variable clinical course of EBV-positive T-cell lymphoma in children.
- The absence of typical indicators like pancytopenia may complicate early diagnosis.
- Understanding spontaneous remission and relapse patterns is crucial for managing this rare pediatric malignancy.
Abstract:
We report a case of a 7-year-old Chinese boy who presented with acute fever, multiple oral ulcers, and skin nodules. A diagnosis of systemic Epstein-Barr virus (EBV)-positive T-cell lymphoma of childhood was established using systemic laboratory examination, imaging studies, bone marrow and skin biopsy with immunohistochemistry, and in situ hybridization for EBV-encoded RNA (EBER) and gene rearrangements. Notable features of this case include the absence of pancytopenia and hemophagocytic syndrome as well as spontaneous resolution without chemotherapy for several months; however, the condition relapsed, and the patient died.
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