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Primary Breast Natural Killer/T-cell lymphoma with Cutaneous Involvement: A Case Report
Alternative Therapies in Health and Medicine
|August 13, 2023
Summary
Extranodal natural killer/T-cell lymphoma is a rare cancer, particularly when originating in the breast. Early pathological diagnosis is crucial for this aggressive lymphoma, as ultrasound findings can be misleading.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Extranodal natural killer/T-cell lymphoma (ENKTL) is a rare non-Hodgkin lymphoma, accounting for less than 1% of cases.
- ENKTL is geographically prevalent in East Asia and Central/South America, contrasting with its rarity in Western countries.
- Key pathological hallmarks of ENKTL include angiocentricity/angioinvasion and significant tissue necrosis.
Observation:
- A rare case of primary breast extranodal natural killer/T-cell lymphoma is presented in a 72-year-old woman.
- The patient exhibited a painless right breast tumor with specific ultrasonographic features (uneven internal echo, strip blood flow signal).
- Despite surgical resection and CHOP chemotherapy, the patient succumbed to lymphoma and multiple organ dysfunction syndrome 27 months post-diagnosis.
Findings:
- Primary breast ENKTL represents an exceptionally rare clinical presentation.
- Ultrasonographic diagnosis of breast ENKTL poses challenges, increasing the risk of misdiagnosis or missed diagnosis.
- Post-biopsy pathological examination is paramount for accurate diagnosis of this rare lymphoma.
Implications:
- This case underscores the rarity and diagnostic challenges associated with primary breast ENKTL.
- Emphasizes the critical role of histopathological confirmation in diagnosing extranodal lymphomas, especially in unusual primary sites.
- Highlights the aggressive nature of ENKTL and the need for vigilant diagnostic approaches.

