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与种系剪接位点突变相关的CBL综合征中的青少年骨髓单核细胞白血病:两例报告及文献综述

Juvenile myelomonocytic leukemia in CBL syndrome associated with germline splice-site mutations: Two case reports and a literature review.

作者信息

Cardoso Leila, Galán-Gómez Víctor, Corral-Sánchez María Dolores, Pérez-Martínez Antonio, Riesco Susana, Isidoro-García María, Escudero Adela

机构信息

Translational Research in Pediatric Oncology, Hematopoietic Transplantation & Cell Therapy Hospital La Paz Institute for Health Research (INGEMM-IdiPAZ) Madrid Spain.

Paediatric Haematology and Oncology Service La Paz University Hospital Madrid Spain.

出版信息

Clin Case Rep. 2021 May 15;9(5):e04260. doi: 10.1002/ccr3.4260. eCollection 2021 May.

Abstract

The clinical and laboratory criteria for hemophagocytic lymphohistiocytosis should be taken into account during the juvenile myelomonocytic leukemia diagnosis, specifically in CBL syndrome, to reveal the presence of primary rather than secondary associated hemophagocytosis.

摘要

在青少年骨髓单核细胞白血病诊断过程中,尤其是在CBL综合征中,应考虑噬血细胞性淋巴组织细胞增生症的临床和实验室标准,以揭示原发性而非继发性相关噬血细胞现象的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82a3/8123759/4c79ffe42ac5/CCR3-9-e04260-g001.jpg

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