Revista de la Facultad de Medicina

Chilblain lupus: A case report

DOI: https://doi.org/10.37345/23045329.v2i2.120

Case reports | Publicado: 2024-11-30

Autores:

  • Paulo Marroquin Mijangos
    Hospital General San Juan de Dios
  • Rita Pineda Sic
    Hospital General San Juan de Dios
  • Joselyn Alvarez Meza
    Hospital General San Juan de Dios
  • María García González
    Hospital General San Juan de Dios

Chilblain lupus is a rare form of cutaneous lupus erythematosus. This is characterized by the presence of erythematous-violaceous papules that appear as a consequence of changes in temperature. Case description: A 23-year-old male patient with a history of itchy violaceous papules on the face, hands, and feet after an episode of vomiting. ANA: 2; Anti-Smith: 3.8 U/mL, Anti-RO: 25 U/mL. Histology revealed interface dermatitis, predominantly lymphocytic perivascular infiltrate, and foci of diffuse septal lobular panniculitis. Conclusion: Early detection of chilblain lupus allows local and pharmacological treatment to be provided to avoid long-term complications such as necrosis or infections.

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Facultad de Medicina de la Universidad Francisco Marroquín

Email: revistamedicina@ufm.edu

ISSN online 2304-5353 / ISSN printed 2304-5329

 

Cómo citar

Chilblain lupus: A case report. (2024). Revista De La Facultad De Medicina, 2(2), 42-49. https://doi.org/10.37345/23045329.v2i2.120