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

IF 1 4区 医学 Q4 DERMATOLOGY American Journal of Dermatopathology Pub Date : 2025-02-01 DOI:10.1097/DAD.0000000000002905
Sarah Nocco, Cynthia Magro
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Abstract

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.

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自身免疫性疾病背景下原发性皮肤甲氨蝶呤相关t细胞淋巴增生性疾病:病例系列和文献综述
摘要:甲氨蝶呤(MTX)是一种针对某些自身免疫性疾病和多种血液系统恶性肿瘤的抗代谢药物,与主要为b细胞谱系的医源性淋巴细胞增生性疾病(LPD)有关。不太常见的是t细胞肿瘤,其原发性皮肤受累被认为是罕见的。其中一名提交人在行医时遇到了三起案件。患者年龄从38岁到99岁不等(2女1男),其中2例患有类风湿关节炎,1例患有强直性脊柱炎。3例患者均接受甲氨蝶呤治疗。这些病例包括皮下外周t细胞淋巴瘤(NOS)(1例),蕈样真菌病(1例)和原发性侵袭性表皮细胞毒性t细胞淋巴瘤(1例),经证实是致命的。1例甲氨蝶呤停药后症状自发消退;后来在停用甲氨蝶呤期间复发。2名患者死亡,1名死于无关原因,1名死于淋巴瘤。先前报道的7例包括皮下泛膜炎样t细胞淋巴瘤(2例)、原发性皮肤CD4+ LPD(2例)、外周t细胞淋巴瘤(NOS)(1例)、间变性大细胞淋巴瘤(1例)和局限于脂肪的外周t细胞淋巴瘤(1例)。7例MTX停药患者中有6例出现无复发的消退。患者使用MTX的平均时间为4年,平均年龄为61岁,男性略多于女性。7例患者中3例eb编码区阳性,3例阴性。MTX相关t细胞LPD涉及长期MTX治疗的老年患者,其中EBER阳性比皮外MTX相关t细胞LPD更常见。典型的CTCL表现为皮下受累,占病例的很大比例。甲氨蝶呤停药后会出现退行性反应,但并非所有病例都如此。
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来源期刊
CiteScore
1.80
自引率
9.10%
发文量
453
审稿时长
3 months
期刊介绍: The American Journal of Dermatopathology offers outstanding coverage of the latest diagnostic approaches and laboratory techniques, as well as insights into contemporary social, legal, and ethical concerns. Each issue features review articles on clinical, technical, and basic science advances and illuminating, detailed case reports. With the The American Journal of Dermatopathology you''ll be able to: -Incorporate step-by-step coverage of new or difficult-to-diagnose conditions from their earliest histopathologic signs to confirmatory immunohistochemical and molecular studies. -Apply the latest basic science findings and clinical approaches to your work right away. -Tap into the skills and expertise of your peers and colleagues the world over peer-reviewed original articles, "Extraordinary cases reports", coverage of practical guidelines, and graphic presentations. -Expand your horizons through the Journal''s idea-generating forum for debating controversial issues and learning from preeminent researchers and clinicians
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