Your browser doesn't support javascript.
loading
[Coexistence of IgG4-related autoimmune hepatitis and inflammatory pseudotumors of the liver:a case report].
Adachi, Yasuyo; Iwata, Norikazu; Adachi, Yasushi; Nakamura, Hiroko; Kikuchi, Takefumi; Nakamura, Masahiro; Mita, Hiroaki; Yoshida, Yukinari; Kinoshita, Ichiro; Ishii, Yoshifumi; Endo, Takao.
Afiliación
  • Adachi Y; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Iwata N; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Adachi Y; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Nakamura H; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Kikuchi T; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Nakamura M; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Mita H; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Yoshida Y; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
  • Kinoshita I; Department of Respiratory Medicine, Keiyukai Sapporo Hospital.
  • Ishii Y; Department of Pathology, Sapporo Shirakaba-dai Hospital.
  • Endo T; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Sapporo Shirakaba-dai Hospital.
Nihon Shokakibyo Gakkai Zasshi ; 117(6): 532-541, 2020.
Article en Ja | MEDLINE | ID: mdl-32565511
IgG4-related autoimmune hepatitis (IgG4-AIH) is characterized by hepatic inflammation and is considered an IgG4-related disease. Several inflammatory pseudotumors (IPTs) are also considered as IgG4-related diseases;however, there have been no reports of cases wherein both diseases occurred concurrently. An older adult with liver dysfunction was admitted to the hospital and was diagnosed with IgG4-AIH following a liver biopsy;IgG4-positive plasma cell infiltration in the portal tract and high serum IgG4 concentration were detected. A few months following biopsy, imaging studies revealed two IPTs in the liver. The patient was diagnosed with cryptogenic organized pneumonia several months after imaging and was treated with steroids in a different hospital. Her liver dysfunction improved, and one of the two IPTs disappeared in response to steroid treatment. The following is an account of a rare case of IgG4-AIH with IPTs of the liver.
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Hepatitis Autoinmune / Granuloma de Células Plasmáticas / Hepatopatías Límite: Aged / Female / Humans Idioma: Ja Revista: Nihon Shokakibyo Gakkai Zasshi Año: 2020 Tipo del documento: Article Pais de publicación: Japón
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Autoinmunes / Hepatitis Autoinmune / Granuloma de Células Plasmáticas / Hepatopatías Límite: Aged / Female / Humans Idioma: Ja Revista: Nihon Shokakibyo Gakkai Zasshi Año: 2020 Tipo del documento: Article Pais de publicación: Japón