書誌事項
- タイトル別名
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- Microgranular-type acute promyelocytic leukemia with weak myeloperoxidase staining: difficulty of morphological diagnosis
- ミエロペルオキシダーゼ センショク ガ ジャク ヨウセイ オ テイシ ケイタイガクテキ シンダン ガ コンナン デ アッタ キュウセイ ゼン コツズイキュウセイ ハッケツビョウ microgranular type
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説明
<p>The 2017 World Health Organization (WHO) classification states that acute promyelocytic leukemia (APL) always presents with strong myeloperoxidase staining. However, we herein report of a 40-year-old woman with the microgranular variant of acute promyelocytic leukemia presenting with weak myeloperoxidase (MPO) staining. The leukemic cells were morphologically similar to monocytic cells, showing distorted-shaped nuclei and weak MPO staining. However, flow cytometry revealed positivity of CD2, CD34, and human leucocyte antigen-DR (HLA-DR) and pointed toward a diagnosis of APL. PML-RARA mRNA detection finally led the patient to a definitive diagnosis. The patient achieved complete remission by induction chemotherapy including tretinoin, cytarabine and idarubicin, and no differentiation syndrome was observed.</p>
収録刊行物
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- 臨床血液
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臨床血液 61 (10), 1511-1513, 2020
一般社団法人 日本血液学会
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詳細情報 詳細情報について
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- CRID
- 1390286426516026752
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- NII論文ID
- 130007937028
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- NII書誌ID
- AN00252940
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- ISSN
- 18820824
- 04851439
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- NDL書誌ID
- 030725746
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- PubMed
- 33162450
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- 本文言語コード
- ja
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- 資料種別
- journal article
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- データソース種別
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- JaLC
- NDLサーチ
- PubMed
- CiNii Articles
- OpenAIRE
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- 抄録ライセンスフラグ
- 使用不可