Ovarian germ cell tumor/mastocytosis with KIT mutation: A unique clinicopathological entity-Reference-Cited by-同舟云学术

Ovarian germ cell tumor/mastocytosis with KIT mutation: A unique clinicopathological entity

Published:2021-10-04 Issue:1 Volume:61 Page:50-54
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Xiao Peifang¹,Chen Ping²,Lang Xingping²,An Qi³,Yang Chunxiao²,Chen Si²,Wang Kai²,Chen Nan²,Hao Yang²,Ding Jingwen²,Li Zhiheng¹⁴,Hu Shaoyan¹^ORCID,Xiao Sheng⁴^ORCID

Affiliation:

1. Department of Hematology Children's Hospital of Soochow University Suzhou China

2. Suzhou Sano Precision Medicine Ltd China

3. Xuzhou Children's Hospital, Xuzhou Medical University Xuzhou China

4. Department of Pathology Brigham and Women's Hospital, Harvard Medical School Boston Massachusetts USA

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.23000

Reference21 articles.

1. Gata2, Fli1, and Scl form a recursively wired gene-regulatory circuit during early hematopoietic development

2. Distinct Origins of Adult and Embryonic Blood in Xenopus

3. Aggressive Systemic Mastocytosis After Germ Cell Tumor of the Ovary

4. N822K c-kit mutation in CD30-positive cutaneous pleomorphic mastocytosis after germ cell tumour of the ovary

5. A variant c-KITmutation, D816H, fundamental to the sequential development of an ovarian mixed germ cell tumor and systemic mastocytosis with chronic myelomonocytic leukemia

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