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Updated: Feb 15, 2026

Isolation of Primary Murine Skeletal Muscle Microvascular Endothelial Cells
Published on: March 6, 2019
Primary skeletal muscle lymphoma: A case report.
Dogan Nasi R Binici1, Ali Karaman2, Ozge Timur1
1Department of Internal Medicine, Erzurum Regional Training and Research Hospital, Erzurum 25040, Turkey.
This study reports a rare case of primary muscle non-Hodgkin lymphoma in a 41-year-old female. The patient achieved a complete radiological response after chemotherapy using the cyclophosphamide, hydroxydaunomycin, oncovin, and prednisone regimen.
Area of Science:
- Oncology
- Pathology
Background:
- Primary lymphomas of bone or skeletal muscle are exceptionally rare.
- Lymphomatous involvement of muscle typically occurs via direct invasion, metastasis, or rarely, as a primary tumor.
- This case focuses on primary muscle lymphoma, a less common presentation.
Purpose of the Study:
- To present a rare case of primary muscle non-Hodgkin lymphoma.
- To describe the associated clinicopathological findings.
- To review the relevant literature on primary muscle lymphomas.
Main Methods:
- A case study of a 41-year-old female patient with a painful mass in the right lower extremity.
- Surgical resection of the mass.
- Histopathological examination for diagnosis.
- Review of existing medical literature.
Main Results:
- Diagnosis of diffuse large B-cell lymphoma originating from the muscle with cutaneous and subcutaneous infiltration.
- Patient received six cycles of cyclophosphamide, hydroxydaunomycin, oncovin, and prednisone (CHOP) chemotherapy.
- Complete radiological response achieved post-treatment.
Conclusions:
- Primary muscle lymphoma is a rare entity requiring accurate diagnosis and tailored treatment.
- The CHOP regimen demonstrated efficacy in treating this case of primary muscle diffuse large B-cell lymphoma.
- Further research into primary muscle lymphomas is warranted.
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