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Immunohistological analysis of pathogenic infiltrates in the epidermis and liver of a patient with toxic epidermal necrolysis accompanied by vanishing bile duct syndrome.
Toyoda, Tomohiro; Hashimoto, Koji; Ogawa, Youichi; Tohyama, Mikiko; Muto, Yoshinori; Murashima, Takayuki; Akao, Kei; Honma, Koichi; Tanaka, Atsushi.
Afiliação
  • Toyoda T; Department of Dermatology, Kameda Medical Center, Chiba, Japan.
  • Hashimoto K; Department of Dermatology, Kameda Medical Center, Chiba, Japan.
  • Ogawa Y; Department of Dermatology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
  • Tohyama M; Department of Dermatology, Shikoku Cancer Center, Ehime, Japan.
  • Muto Y; Department of Dermatology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
  • Murashima T; Department of Dermatology, Kameda Medical Center, Chiba, Japan.
  • Akao K; Department of Dermatology, Kameda Medical Center, Chiba, Japan.
  • Honma K; Department of Pathology, Kameda Medical Center, Chiba, Japan.
  • Tanaka A; Department of Dermatology, Kameda Medical Center, Chiba, Japan.
J Dermatol ; 49(12): 1343-1347, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36176039
ABSTRACT
Toxic epidermal necrolysis (TEN) is a severe cutaneous adverse drug reaction characterized by extensive epidermal detachment, which is reportedly mediated by drug-specific cytotoxic CD8+ T cells, inflammatory monocytes, and neutrophils. Besides the skin, TEN often damages other organs, and it remains unknown whether they are mediated by similar pathogenic cells that cause epidermal damage. We experienced a case who developed TEN complicated with vanishing bile duct syndrome. Immunohistological analysis revealed the infiltration of CD8+ T cells, inflammatory monocytes, and neutrophil extracellular trap-forming neutrophils in the lesions of both the skin and liver with different degree of infiltration of these cells. These data suggest a difference of dominant pathogenic cells between skin and liver of patients with TEN.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Stevens-Johnson Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Stevens-Johnson Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article