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April 22, 2026JEADV Clinical Practice2 citationsOpen Access

Brentuximab Vedotin‐Induced Rash Sparing CD30‐Positive Mycosis Fungoides Lesions

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IHIsabel HaririAEAlexander H. EnkJHJessica C. Hassel

Key Points

  • This case explores the atypical rash induced by brentuximab vedotin in mycosis fungoides lesions and its implications for treatment.
  • Case report of a 60-year-old male with stage IIB mycosis fungoides experiencing a rash post-treatment with brentuximab vedotin.
  • Histopathological evaluation of affected skin and continued monitoring of mycosis fungoides lesions after rash resolution.
  • Patient developed an erythematous rash after three infusions of brentuximab vedotin, sparing existing mycosis fungoides lesions.
  • Histopathology indicated a lichenoid reaction, while CD30-positive atypical T-cells were present in the unaffected MF lesions.
  • Treatment with systemic corticosteroids resolved the rash and led to complete remission of mycosis fungoides.

Abstract

ABSTRACT Brentuximab vedotin (BV) is an effective treatment for CD30‐positive lymphomas, including mycosis fungoides (MF). However, its use can be associated with various cutaneous adverse effects, including rashes. This case describes a 60‐year‐old male with stage IIB MF who developed a drug‐induced erythematous rash after three infusions of BV. Remarkably, the rash spared pre‐existing MF lesions, which remained demarcated and flattened. Histopathological evaluation confirmed a drug‐induced lichenoid reaction in the affected skin, while the MF lesions exhibited residual disease with CD30‐positive atypical T‐cells. Systemic corticosteroids led to resolution of the rash, and BV therapy was temporarily paused. The patient achieved complete remission of MF with only residual hyperpigmentation at the 10‐month follow‐up. This case highlights a unique interaction between BV and the neoplastic skin environment, warranting further investigation into the underlying mechanisms.

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Cite This Study

Hariri et al. (2026) studied this question.

synapsesocial.com/papers/69e865476e0dea528dde9c6fhttps://doi.org/10.1002/jvc2.70343
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