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Published on: June 13, 2019
Interdigitating reticulum cell sarcoma with unusual features
S P Hammar1, R H Rudolph, D E Bockus
1Diagnostic Specialties Laboratory, Bremerton, Washington 98310.
Insights
This case report details an interdigitating reticulum cell sarcoma in a patient with prior nodular lymphocytic lymphoma. The patient achieved remission with combined therapy, showing no disease recurrence after two years.
Area of Science:
- Oncology
- Pathology
- Hematology
Background:
- Interdigitating reticulum cell sarcoma (IRCS) is a rare lymphoid neoplasm.
- Co-occurrence of IRCS with other lymphomas presents diagnostic and therapeutic challenges.
- Previous diagnoses of nodular lymphocytic lymphoma can precede IRCS development.
Observation:
- Presents a 67-year-old male patient with a history of nodular lymphocytic lymphoma.
- Describes ultrastructural findings of neoplastic cells with cylindrical confronting cisternae.
- Notes the presence of tubuloreticular structures in associated benign lymphocytes.
Findings:
- Successful treatment of IRCS with a combination of chemotherapy and radiation therapy.
- Patient achieved complete remission with no evidence of disease 2 years post-therapy.
- Demonstrates the potential for favorable outcomes in IRCS with multimodal treatment.
Implications:
- Contributes to understanding the clinical spectrum of interdigitating reticulum cell sarcoma.
- Suggests that IRCS, though rare, can be effectively managed.
- Underscores the importance of detailed ultrastructural analysis in diagnosing rare lymphoid neoplasms.
Abstract:
A case of interdigitating reticulum cell sarcoma is reported in a cervical lymph node of a 67-year-old man who had a previously diagnosed nodular lymphocytic lymphoma in the same anatomic location. Ultrastructurally, the neoplastic cells contained cylindrical confronting cisternae, and associated benign lymphocytes had tubuloreticular structures in their cytoplasm. The patient was treated with combination chemotherapy-radiation therapy and is alive and well with no evidence of disease approximately 2 years after completing therapy. The clinical and pathologic features of previously reported cases of interdigitating reticulum cell sarcomas are compared to those of the reported case.
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