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皮肤受限、甲氨蝶呤相关的 EBV 阳性黏膜溃疡——高度恶性淋巴瘤的一种类似物。4 例报告及文献复习。

Skin-Limited, Methotrexate-Associated Epstein-Barr Virus-Positive Mucocutaneous Ulcer-A Mimicker of High-Grade Lymphoma. A Report of 4 Cases and Review of the Literature.

机构信息

Doctor, Department of Cellular Pathology, Oxford University Hospitals, NHS Foundation Trust, Oxford, Oxfordshire, United Kingdom.

Doctor, Department of Dermatology, Royal Berkshire, NHS Foundation Trust, Reading, Berkshire, United Kingdom; and.

出版信息

Am J Dermatopathol. 2023 Aug 1;45(8):519-531. doi: 10.1097/DAD.0000000000002419.

Abstract

Immunodeficiency-associated lymphoproliferative disorders (IA-LPDs) constitute a diverse range of conditions including posttransplant lymphoproliferative disorders, other iatrogenic IA-LPDs, and lymphoproliferative disorders associated with an underlying primary immune disorder or HIV infection. IA-LPDs are clinically and pathologically heterogeneous, and there is a lack of standardization of diagnostic terminology. They can represent a potential serious diagnostic pitfall because the histological features of clinically indolent proliferations may mimic those of high-grade lymphoma. However, correct identification of these entities is essential given that complete remission may occur upon reversal of the underlying cause of immunosuppression without the need for systemic therapy. IA-LPDs presenting in the skin are rare but well documented. One form of iatrogenic IA-LPD, methotrexate-associated lymphoproliferative disorder (MTX-LPD), can present with cutaneous nodules, plaques, or ulcers. Predominantly, MTX-LPD develops in the context of long-term treatment of autoimmune conditions, such as rheumatoid arthritis, dermatomyositis, and Sjögren syndrome, and may be associated with underlying Epstein-Barr virus (EBV) infection. We present 4 cases of cutaneous EBV-positive B-cell MTX-LPD and describe their clinical and morphological findings. Comparison of our histological findings to the diagnostic criteria for EBV-positive mucocutaneous ulcer (EBVMCU) revealed significant overlap, highlighting the intersection between MTX-LPD and EBVMCU. Withdrawal of methotrexate resulted in healing of all lesions at a mean time of 2 months. In summary, close clinicopathological correlation is vital to identify MTX-LPD presenting as cutaneous EBVMCU given that the initial treatment strategy is that of withdrawal of methotrexate without the need for immediate systemic therapy.

摘要

免疫缺陷相关淋巴组织增生性疾病(IA-LPDs)包括多种疾病,包括移植后淋巴组织增生性疾病、其他医源性 IA-LPDs 以及与潜在原发性免疫疾病或 HIV 感染相关的淋巴组织增生性疾病。IA-LPDs 在临床上和病理学上具有异质性,并且缺乏诊断术语的标准化。它们可能代表潜在的严重诊断陷阱,因为临床上惰性增殖的组织学特征可能与高级别淋巴瘤相似。然而,正确识别这些实体至关重要,因为在逆转免疫抑制的潜在原因后,完全缓解可能发生,而无需全身治疗。皮肤表现的 IA-LPD 罕见但有充分记录。医源性 IA-LPD 的一种形式,即甲氨蝶呤相关淋巴组织增生性疾病(MTX-LPD),可能表现为皮肤结节、斑块或溃疡。主要情况下,MTX-LPD 在长期治疗自身免疫性疾病(如类风湿关节炎、皮肌炎和干燥综合征)的背景下发生,并且可能与潜在的 EBV 感染相关。我们报告了 4 例皮肤 EBV 阳性 B 细胞 MTX-LPD 病例,并描述了它们的临床和形态学发现。将我们的组织学发现与 EBV 阳性黏膜溃疡(EBVMCU)的诊断标准进行比较,发现存在显著重叠,突出了 MTX-LPD 和 EBVMCU 之间的交叉点。停用甲氨蝶呤后,所有病变在平均 2 个月的时间内愈合。总之,密切的临床病理相关性对于识别表现为皮肤 EBVMCU 的 MTX-LPD 至关重要,因为初始治疗策略是停用甲氨蝶呤,而无需立即进行全身治疗。

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