Flagellate erythema secondary to bleomycin: case report with favorable outcome

Authors

  • Ricardo Leal-León Hospital Ángeles Mocel, Servicio de Medicina Interna. Ciudad de México, México https://orcid.org/0009-0007-1066-0300
  • Antonio Tirado-Motel Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Hospital Regional “Dr. Manuel Cárdenas de la Vega”, Servicio de Dermatología. Culiacán, Sinaloa, México https://orcid.org/0000-0001-9177-1465
  • Marian Escribano-Ponce Secretaría de Salud de la Ciudad de México, Centro Dermatológico “Dr. Ladislao de la Pascua”, Servicio de Dermatología. Ciudad de México, México https://orcid.org/0000-0003-0249-5193
  • Vanessa González-Ruiz Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado, Hospital Regional “Licenciado Adolfo López Mateos”, Servicio de Dermatología. Ciudad de México, México https://orcid.org/0000-0002-7074-4959
  • Ma. Teresa de Jesús Vega-González Secretaría de Salud, Instituto Nacional de Cancerología, Servicio de Dermatología. Ciudad de México, México https://orcid.org/0009-0000-6045-8097

DOI:

https://doi.org/10.5281/zenodo.15178515

Keywords:

Erythema, Bleomycin, Hyperpigmentation

Abstract

Background: Flagellate erythema (FE) is a multifactorial dermatosis, frecuently related to the the use of certain drugs. It can occur in up to 20% of patients treated with bleomycin. Drug accumulation in the skin can be due to the lack of the enzyme bleomycin hydrolase. It presents as a widespread dermatosis, predominantly affecting the trunk and upper extremities, characterized by erythematous-hyperpigmented macules of variable size, with a linear arrangement and a "whip-like" appearance, associated with intense pruritus. Management focuses on relieving pruritus with antihistamines and topical steroids, although discontinuation of bleomycin is essential for complete resolution.

Case report: A 19-year-old woman with a history of stage IIIB left ovarian dysgerminoma was undergoing combined chemotherapy (bleomycin, etoposide, and cisplatin). After 3 months of treatment, she developed a widespread dermatosis on the neck and posterior thoracic region, consisting of dark brown hyperpigmented spots with a linear configuration and variable sizes, associated with pruritus, without other symptoms. FE due to bleomycin was diagnosed. High-potency topical corticosteroids were prescribed. After discontinuing bleomycin, there was a progressive disappearance of the dermatosis until complete resolution.

Conclusion: The bleomycin-induced FE must be identified early for appropriate management that allows the continuation of antineoplastic treatment. Discontinuation of the drug should be considered when the patient's quality of life is compromised and balanced with oncological control, which optimizes antineoplastic therapy.

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Author Biography

  • Ricardo Leal-León, Hospital Ángeles Mocel, Servicio de Medicina Interna. Ciudad de México, México

    Hospital Angles Mocel

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Published

2025-05-01

Issue

Section

Clinical Cases