Enteropathy-Associated T-Cell Lymphoma Type II Complicated by Autoimmune Hemolytic Anemia
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- Kato Aiko
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Takiuchi Yoko
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Aoki Kazunari
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Ono Yuichiro
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Arima Hiroshi
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Nagano Seiji
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Tabata Sumie
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Yanagita Soshi
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Matsushita Akiko
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Maruoka Hayato
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Wada Masaya
- Gastroenterology, Kobe City Medical Center General Hospital
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- Imai Yukihiro
- Clinical Pathology, Kobe City Medical Center General Hospital
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- Ishikawa Takayuki
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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- Takahashi Takayuki
- Departments of Hematology and Clinical Immunology, Kobe City Medical Center General Hospital
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A 74-year-old man was admitted to hospital because of persistent fever, diarrhea, and abdominal pain. CT scanning showed extensive wall thickening of the colon. He was transferred to our hospital because he further developed ascites and paraaortic lymph node swelling. On presentation, he was extremely emaciated with superficial lymph node swelling, ascitic signs, and leg edema. Histological image of a biopsied mesenteric lymph node demonstrated diffuse infiltration of large abnormal T cells. Surface antigen analysis of abnormal cells in the ascites revealed positivity for CD3, CD8, CD56, and weak positivity for CD103. Polymerase chain reaction analysis showed monoclonal rearrangement of the T cell receptor (TCR) gene. The subtype of TCR was αβ. A diagnosis of enteropathy-associated T cell lymphoma (EATL) type II was made. The lymphoma involved the bone marrow. The patient also had severe hemolytic anemia with a positive Coomb's test result. An additional diagnosis for autoimmune hemolytic anemia (AIHA) was made, which was resistant to methylprednisolone therapy. We first treated him with only vincristine in addition to the steroid to avoid acute tumor lysis syndrome ; however, he died of septic shock that occurred soon after vincristine administration. To the best of our knowledge, this may be the first reported case of EATL complicated by AIHA. [J Clin Exp Hematopathol 51(2) : 119-123, 2011]
収録刊行物
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- Journal of Clinical and Experimental Hematopathology
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Journal of Clinical and Experimental Hematopathology 51 (2), 119-123, 2011
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詳細情報 詳細情報について
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- CRID
- 1390282679679903360
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- NII論文ID
- 10030207669
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- NII書誌ID
- AA11556796
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- COI
- 1:STN:280:DC%2BC38%2FhsVartA%3D%3D
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- ISSN
- 18809952
- 13464280
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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- 使用不可