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Intravenous Immunoglobulin Monotherapy for Granulomatous Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency.
Hasegawa, Mizue; Sakai, Fumikazu; Okabayashi, Asako; Sato, Akitoshi; Yokohori, Naoko; Katsura, Hideki; Asano, Chihiro; Kamata, Toshiko; Koh, Eitetsu; Sekine, Yasuo; Hiroshima, Kenzo; Ogura, Takashi; Takemura, Tamiko.
Afiliación
  • Hasegawa M; Division of Respiratory Medicine, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Sakai F; Department of Diagnostic Radiology, Saitama Medical University International Medical Center, Japan.
  • Okabayashi A; Department of Diagnostic Radiology, Saitama Medical University International Medical Center, Japan.
  • Sato A; Division of Respiratory Medicine, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Yokohori N; Division of Respiratory Medicine, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Katsura H; Division of Respiratory Medicine, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Asano C; Division of Respiratory Medicine, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Kamata T; Division of Hematology, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Koh E; Division of Thoracic Surgery, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Sekine Y; Division of Thoracic Surgery, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Hiroshima K; Division of Thoracic Surgery, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Ogura T; Division of Pathology, Tokyo Women's Medical University Yachiyo Medical Center, Japan.
  • Takemura T; Department of Respiratory Medicine, Kanagawa Cardiovascular and Respiratory Center, Japan.
Intern Med ; 56(21): 2899-2902, 2017 Nov 01.
Article en En | MEDLINE | ID: mdl-28924106
ABSTRACT
Common variable immunodeficiency (CVID) is a heterogeneous subset of immunodeficiency disorders. Recurrent bacterial infection is the main feature of CVID, but various non-infectious complications can occur. A 42-year-old woman presented with cough and abnormal chest X-ray shadows. Laboratory tests showed remarkable hypogammaglobulinemia. Computed tomography revealed multiple consolidation and nodules on the bilateral lung fields, systemic lymphadenopathy, and splenomegaly. A surgical lung biopsy specimen provided the final diagnosis of lymphoproliferative disease in CVID, which was grouped under the term granulomatous lymphocytic interstitial lung disease. Interestingly, the lung lesions of this case resolved immediately after the initiation of intravenous immunoglobulin monotherapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunoglobulinas Intravenosas / Inmunodeficiencia Variable Común / Enfermedades Pulmonares Intersticiales Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Intern Med Asunto de la revista: MEDICINA INTERNA Año: 2017 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunoglobulinas Intravenosas / Inmunodeficiencia Variable Común / Enfermedades Pulmonares Intersticiales Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Intern Med Asunto de la revista: MEDICINA INTERNA Año: 2017 Tipo del documento: Article País de afiliación: Japón
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