» Articles » PMID: 39851907

Primary Cutaneous Methotrexate-Associated T-Cell Lymphoproliferative Disorder in the Setting of Autoimmune Disease: A Case Series and Review of the Literature

Overview
Date 2025 Jan 24
PMID 39851907
Authors
Affiliations
Soon will be listed here.
Abstract

Methotrexate (MTX), an antimetabolite targeting certain autoimmune conditions and various hematologic malignancies, has been associated with iatrogenic lymphoproliferative disease (LPD) primarily of B-cell lineage. Less commonly are T-cell neoplasms where primary skin involvement is considered rare. Three cases were encountered in the medical practice of one of the authors. The patients ranged in age from 38 years to 99 years (2 women and 1 man) with 2 having rheumatoid arthritis and 1 having ankylosing spondylitis. All 3 patients received MTX. The cases included subcutaneous peripheral T-cell lymphoma not otherwise specified (NOS) (1 patient), mycosis fungoides (1 patient), and a primary aggressive epidermotropic cytotoxic T-cell lymphoma (1 patient) that proved to be fatal. One patient had spontaneous regression following MTX withdrawal; she later developed a recurrence while off MTX. Two patients died, 1 of unrelated causes and 1 of lymphoma. Seven previously reported cases included subcutaneous panniculitis-like T-cell lymphoma (2 cases), primary cutaneous CD4+ LPD (2 cases), peripheral T-cell lymphoma (NOS) (1 case), anaplastic large cell lymphoma (1 case), and peripheral T-cell lymphoma localized to fat (1 case). Regression without recurrence occurred in 6 of the 7 patients with MTX withdrawal. The patients were on the MTX for an average of 4 years and had a median age of 61 years with a slight dominance of men over women. Three of the 7 cases showed Epstein-Barr encoding region (EBER) positivity while the 3 cases reported in this series were negative. MTX-associated T-cell LPD involves older patients on long-term MTX where EBER positivity is more frequent than extracutaneous MTX-associated T-cell LPD. A spectrum of classic forms of CTCL is seen with subcutaneous involvement representing a significant percentage of cases. Regression with MTX withdrawal occurs although not in every case.

References
1.
Cipriani P, Ruscitti P, Carubbi F, Liakouli V, Giacomelli R . Methotrexate: an old new drug in autoimmune disease. Expert Rev Clin Immunol. 2014; 10(11):1519-30. DOI: 10.1586/1744666X.2014.962996. View

2.
Satou A, Nakamura S . EBV-positive B-cell lymphomas and lymphoproliferative disorders: Review from the perspective of immune escape and immunodeficiency. Cancer Med. 2021; 10(19):6777-6785. PMC: 8495296. DOI: 10.1002/cam4.4198. View

3.
Omori I, Kawanabe R, Hashimoto Y, Mitsui A, Kodama K, Nogi S . Cutaneous methotrexate-related T-cell lymphoproliferative disorder with CD4, CD30, CD56, EBV-positive tumor cell infiltration: a case illustration and a brief review. Am J Blood Res. 2021; 11(2):163-167. PMC: 8165712. View

4.
Satou A, Banno S, Kohno K, Takahara T, Takahashi E, Nobata H . Primary cutaneous methotrexate-associated B-cell lymphoproliferative disorders other than EBV-positive mucocutaneous ulcer: clinical, pathological, and immunophenotypic features. Pathology. 2021; 53(5):595-601. DOI: 10.1016/j.pathol.2020.10.019. View

5.
Satou A, Tsuzuki T, Nakamura S . Other Iatrogenic Immunodeficiency-Associated Lymphoproliferative Disorders with a T- or NK-cell phenotype. J Clin Exp Hematop. 2019; 59(2):56-63. PMC: 6661958. DOI: 10.3960/jslrt.19013. View