Angioimmunoblastic T-Cell Lymphoma Initially Presenting with Replacement of Bone Marrow and Peripheral Plasmacytosis
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- Sakai Hisashi
- Department of Internal Medicine, Takeda General Hospital
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- Tanaka Hideaki
- Department of Internal Medicine, Takeda General Hospital
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- Katsurada Tatsuya
- Department of Hematology, Takeda General Hospital
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- Yoshida Yataro
- Department of Hematology, Takeda General Hospital
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- Okamoto Eiichi
- Department of Pathology, Takeda General Hospital
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- Ohno Hitoshi
- Department of Internal Medicine, Takeda General Hospital
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A 73-year-old man presented with lymphadenopathy, hepatosplenomegaly, and a variety of hematological and immunological abnormalities. The bone marrow was replaced by polymorphic cellular infiltrates containing aggregates of CD10+ T-cells. Circulating lymphoplasmacytic/immunoblastic cells showed an early plasma cell immunophenotype on flow cytometric analysis. Combination of these observations indicated that the underlying disorder of this patient was angioimmunoblastic T-cell lymphoma (AITL); postmortem pathology was consistent with progression of peripheral T-cell lymphoma. Even in the absence of definitive lymph node biopsy, the appearance of the bone marrow and the peripheral blood can lead to the diagnosis of AITL.<br>
収録刊行物
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- Internal Medicine
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Internal Medicine 46 (7), 419-424, 2007
一般社団法人 日本内科学会
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詳細情報 詳細情報について
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- CRID
- 1390001204871623040
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- NII論文ID
- 130000078774
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- ISSN
- 13497235
- 09182918
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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