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遗传检测在急性白血病的诊断和生物学中的应用。

Genetic Testing in the Diagnosis and Biology of Acute Leukemia.

机构信息

Department of Pathology, Boston Children's Hospital, Boston, MA.

Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque.

出版信息

Am J Clin Pathol. 2019 Aug 1;152(3):322-346. doi: 10.1093/ajcp/aqz093.

Abstract

OBJECTIVES

The 2017 Workshop of the Society for Hematopathology/European Association for Haematopathology examined the role of molecular genetics in the diagnosis and biology of acute leukemia.

METHODS

Acute leukemias were reviewed in two sessions: "Genetic Testing in Diagnosis of Acute Leukemias" (53 cases) and "Genetics Revealing the Biology of Acute Leukemias" (41 cases).

RESULTS

Cases included acute lymphoblastic leukemia, acute myeloid leukemia, and acute leukemia of ambiguous lineage. Many cases demonstrated genetic alterations of known diagnostic, prognostic, and/or therapeutic significance, while others exhibited alterations that illuminated disease biology. The workshop highlighted the complexity of acute leukemia diagnosis and follow-up, while illustrating advantages and pitfalls of molecular genetic testing.

CONCLUSIONS

Our understanding of the molecular genetics of acute leukemias continues to grow rapidly. Awareness of the potential complexity of genetic architecture and environment is critical and emphasizes the importance of integrating clinical information with morphologic, immunophenotypic, and molecular genetic evaluation.

摘要

目的

血液病理学协会/欧洲血液病理学协会 2017 年研讨会探讨了分子遗传学在急性白血病的诊断和生物学中的作用。

方法

在两个会议上对急性白血病进行了回顾:“急性白血病的基因检测”(53 例)和“遗传学揭示急性白血病的生物学”(41 例)。

结果

病例包括急性淋巴细胞白血病、急性髓细胞白血病和急性混合谱系白血病。许多病例显示了具有已知诊断、预后和/或治疗意义的基因改变,而其他病例则表现出改变了疾病生物学的改变。该研讨会强调了急性白血病诊断和随访的复杂性,同时说明了分子遗传学检测的优势和陷阱。

结论

我们对急性白血病分子遗传学的理解仍在迅速发展。认识到遗传结构和环境的潜在复杂性至关重要,这强调了将临床信息与形态学、免疫表型和分子遗传学评估相结合的重要性。

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