Abstract |
Patients with rheumatoid arthritis, whether treated or not with immunosuppressive agents including methotrexate, have an increased risk of lymphoproliferative disorders. Termed "iatrogenic immunodeficiency-associated lymphoproliferative disorders" in the 2008 World Health Organization classification of lymphoid neoplasms, they include Hodgkin and non-Hodgkin lymphomas. Composite lymphomas are rare, particularly in skin, with none reported in immunodeficiency states. We report the case of a 67 year-old woman with a long history of rheumatoid arthritis, on methotrexate treatment, who developed multiple skin lesions exhibiting a malignant infiltrate displaying both B- and T-cell phenotypes and dual clonal gene rearrangement by polymerase chain reaction, consistent with a cutaneous composite lymphoma. The patient received chemotherapy including rituximab with partial response, but the T-cell component recurred. To the best of our knowledge, this is the first case report of a cutaneous composite lymphoma in a patient with an iatrogenic immunodeficiency representing a dual challenge, diagnostic for the pathologist and therapeutic for the hematologist.
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Authors | Hassan Huwait, Beatrice Wang, Chaim Shustik, René P Michel |
Journal | The American Journal of dermatopathology
(Am J Dermatopathol)
Vol. 32
Issue 1
Pg. 65-70
(Feb 2010)
ISSN: 1533-0311 [Electronic] United States |
PMID | 20098085
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Antirheumatic Agents
- DNA, Neoplasm
- Methotrexate
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Topics |
- Aged
- Antirheumatic Agents
(adverse effects)
- Arthritis, Rheumatoid
(complications, drug therapy, pathology)
- DNA, Neoplasm
(analysis)
- Female
- Gene Rearrangement, B-Lymphocyte
(genetics)
- Gene Rearrangement, T-Lymphocyte
(genetics)
- Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor
(genetics)
- Humans
- Lymphoma, B-Cell
(chemically induced, genetics, pathology)
- Lymphoma, T-Cell, Cutaneous
(chemically induced, genetics, pathology)
- Methotrexate
(adverse effects)
- Neoplasms, Multiple Primary
(chemically induced, genetics, pathology)
- Skin Neoplasms
(chemically induced, genetics, pathology)
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