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Published on: March 30, 2018
Primary cerebral diffuse large B-cell lymphoma relapsed solely in the skin with the same clonal origin
Shih-Sung Chuang1, Hongxiang Liu, Yuanxue Huang
1Department of Pathology, Chi-Mei Medical Center, 901 Chung-Hwa Road, Yung-Kang City, Tainan County 710, Taiwan. cmh5301@mail.chimei.org.tw
Applied Immunohistochemistry & Molecular Morphology : AIMM
|December 31, 2008
Summary
This case study details an 82-year-old man with primary central nervous system lymphoma (PCNSL) who experienced two isolated skin relapses. The findings confirm a shared clonal origin between the brain and skin tumors, a rare presentation of PCNSL.
Area of Science:
- Oncology
- Neurology
- Dermatology
Background:
- Diffuse large B-cell lymphoma is the most common primary central nervous system lymphoma (PCNSL), often associated with a poor prognosis.
- Relapses typically occur early and within the central nervous system; isolated systemic relapse, particularly in the skin, is exceptionally rare.
Observation:
- An 82-year-old male patient presented with a unique case of PCNSL.
- The patient experienced two consecutive relapses exclusively in the skin, with no concurrent local failure or other systemic involvement.
- Histological and immunophenotypic analysis of all specimens revealed identical lymphoma cells (CD20+, IgM+, bcl-2+, bcl-6+, MUM1+).
Findings:
- B-cell clonality studies confirmed that the brain and subsequent skin tumors originated from the same clone.
- This represents the first documented case of PCNSL relapsing solely in the skin with confirmed clonal identity.
Implications:
- This case expands the known spectrum of PCNSL relapse patterns.
- Highlights the importance of considering cutaneous involvement in PCNSL follow-up, even in the absence of other systemic disease.
- Further research into the mechanisms driving isolated skin relapse in PCNSL may be warranted.
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