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Halogenoderma: A Case Report and Review of the Literature.
Ghazzawi, Raghad A; Alqurashi, Mohammed G; Almalki, Nada A; Alosaimi, Ashwaq K; Al Hawsawi, Khalid.
Afiliação
  • Ghazzawi RA; Medicine and Surgery, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU.
  • Alqurashi MG; Internal Medicine, King Saud Bin Abdulaziz University for Health Sciences College of Medicine, Jeddah, SAU.
  • Almalki NA; Medicine and Surgery, Taif University, Taif, SAU.
  • Alosaimi AK; Dermatology, Umm Al-Qura University, Makkah, SAU.
  • Al Hawsawi K; Dermatology, King Abdulaziz Hospital, Makkah, SAU.
Cureus ; 14(11): e31846, 2022 Nov.
Article em En | MEDLINE | ID: mdl-36579296
ABSTRACT
Halogenoderma (HD) is an uncommon dermatosis that develops following exposure to halogens such as iodide and bromide, referred to as iododerma and bromoderma, respectively. Here, we report the case of a 40-year-old male who presented with a three-week history of slightly itchy progressive skin lesions associated with low-grade fever and malaise. The patient had a history of using food supplements containing iodide and bromide for four months prior to the appearance of skin rashes. Skin examination revealed multiple crusted papules and nodules scattered on his face, neck, and trunk. A skin biopsy was taken from the lesions. The epidermis showed crustation, exocytosis of neutrophils, and multiple intraepidermal abscesses. The dermis showed heavy cellular infiltrates composed mainly of neutrophils. The skin lesions disappeared completely after the cessation of food supplements, along with the use of topical corticosteroids for a few weeks.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article