2019
DOI: 10.1016/j.jdcr.2018.10.013
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EBV+ mucocutaneous ulcers in the setting of pre-existing cutaneous T-cell lymphoproliferative disorders: A report of 2 cases

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Cited by 3 publications
(2 citation statements)
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“…Patients responded well to reduction of immune suppression, with or without rituximab therapy, and no patient had recurrence of the EBV-driven process. More recently two cases of cutaneous MCU were reported in patients who had received therapy for another unrelated primary cutaneous T-cell lymphoproliferative disorder [44]. In this setting correct diagnosis was key to appropriate therapy, as rituximab led to regression in both cases.…”
Section: Mucocutaneous Ulcer (Mcu)mentioning
confidence: 98%
“…Patients responded well to reduction of immune suppression, with or without rituximab therapy, and no patient had recurrence of the EBV-driven process. More recently two cases of cutaneous MCU were reported in patients who had received therapy for another unrelated primary cutaneous T-cell lymphoproliferative disorder [44]. In this setting correct diagnosis was key to appropriate therapy, as rituximab led to regression in both cases.…”
Section: Mucocutaneous Ulcer (Mcu)mentioning
confidence: 98%
“…6,27,[35][36][37][38] Predominantly, they develop in the context of autoimmune conditions treated with methotrexate, although they have also been reported to arise after treatment of T-cell neoplasms, including mycosis fungoides, Sézary syndrome, and T-cell acute lymphoblastic leukemia. 25,[39][40][41][42][43] MTX-LPD can represent a potential serious diagnostic pitfall because their histology may mimic high-grade lymphoma. They demonstrate variable association with EBV infection, with EBV-positive cases displaying surface ulceration, marked tumor cell polymorphism including HRS-like cells, reduced expression of B-cell markers, and/or expression of CD30 and MUM1.…”
Section: Discussionmentioning
confidence: 99%