Evidence map›Paper›PMID 33469311›Full record

ArticleOncoTargets and therapy2021

Case Report: Myeloid Sarcoma Development During Treatment for B Cell Lymphoblastic Lymphoma in a Boy with KRAS/NRAS Gene Mutations.

Xiuli Yuan, Uet Yu, Senmin Chen, Huanli Xu, Meng Yi, Xianping Jiang, Jianming Song, Xiaowen Chen, Shiyang Chen, Zhenhu Lin and 3 more

Abstract readCase Reports
In one paragraph

Article in OncoTargets and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Xiuli Yuan *Department of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Uet Yu *Department of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.ORCID 0000-0003-4391-3398
Senmin ChenDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Huanli XuDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Meng YiDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Xianping JiangDepartment of Pathology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Jianming SongDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Xiaowen ChenInstitute for Medical Research, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Shiyang ChenInstitute for Medical Research, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Zhenhu LinInstitute for Medical Research, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Changgang LiDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Feiqiu WenDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.
Sixi LiuDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we report a rare case of a 12-year-old boy who was initially diagnosed with B cell lymphoblastic lymphoma (BLBL) and developed myeloid sarcoma (MS) eight months after chemotherapy. Next-generation sequencing (NGS) showed mutations of KRAS and NRAS genes in both the bone marrow and lymph node. He presented an abnormal karyotype of 46, XY, -9, der (16) t (9; 16) (q13; q12), +mar. He received chemotherapy according to the South China Children's Leukemia Group 2016 protocol. Complete remission was achieved by the 15th day post-treatment. Eight months later and immediately prior to the start of maintenance therapy, the patient developed fever, skin nodules in both upper arms, and enlargement of bilateral testes. Pathological analysis of skin and testicular biopsies suggested the diagnosis of myeloid sarcoma (MS). Again, NGS examination showed mutations of KRAS and NRAS genes. The patient underwent haploidentical hematopoietic stem cell transplantation but unfortunately did not survive. The interval of eight-month interval between the initial disease onset and MS brings into question whether MS developed as part of the initial onset of disease or as a secondary tumor in association with chemotherapy. Thus, understanding the pathogenesis of MS involving abnormalities of lymphoid progenitors may assist in the prediction of prognosis and development of novel target therapies.

Indexed as

B cell lymphoblastic lymphomacase reportKRASmyeloid sarcomaNRAS

Identifiers

PMID33469311
PMCPMC7812042

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