Human T-cell Lymphotropic Virus Type-1-associated Bronchioloalveolar Disorder with Non-necrotizing Granulomas: A Case Report and Literature Review
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- Kimura Satomi
- Division of Respiratory Medicine, University of Fukui Hospital, Japan
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- Umeda Yukihiro
- Division of Respiratory Medicine, University of Fukui Hospital, Japan
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- Egashira Ryoko
- Department of Radiology, Faculty of Medicine, Saga University, Japan
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- Tabata Kazuhiro
- Department of Pathology, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan
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- Muramoto Akifumi
- Division of Diagnostic Pathology/Surgical Pathology, University of Fukui Hospital, Japan
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- Morita Mihoko
- Department of Hematology and Oncology, University of Fukui Hospital, Japan
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- Yamaguchi Makiko
- Division of Respiratory Medicine, University of Fukui Hospital, Japan
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- Waseda Yuko
- Division of Respiratory Medicine, University of Fukui Hospital, Japan
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- Imamura Yoshiaki
- Division of Diagnostic Pathology/Surgical Pathology, University of Fukui Hospital, Japan
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- Yamauchi Takahiro
- Department of Hematology and Oncology, University of Fukui Hospital, Japan
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- Ishizuka Tamotsu
- Division of Respiratory Medicine, University of Fukui Hospital, Japan
抄録
<p>Human T-cell lymphotropic virus type-1 (HTLV-1)-associated bronchioloalveolar disorder (HABA) is a pulmonary disorder characterized by lymphocytic infiltration of the peribronchiolar space and interstitium in HTLV-1 carriers and in adult T-cell leukemia/lymphoma (ATLL). We herein report an 85-year-old woman carrying HTLV-1 with HABA who presented with a miliary pattern of micronodules in both lungs on high-resolution computed tomography and a lymphocytic infiltrate with non-necrotizing granulomas on pathology. This rare case of HABA should be differentiated from sarcoidosis, hypersensitivity pneumonitis, or miliary tuberculosis. </p>
収録刊行物
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- Internal Medicine
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Internal Medicine 63 (8), 1149-1155, 2024-04-15
一般社団法人 日本内科学会