Malignant melanotic Xp11 neoplasms exhibit a clinicopathologic spectrum and gene expression profiling akin to alveolar soft part sarcoma: a proposal for reclassification-Reference-Cited by-同舟云学术

Malignant melanotic Xp11 neoplasms exhibit a clinicopathologic spectrum and gene expression profiling akin to alveolar soft part sarcoma: a proposal for reclassification

Published:2020-07-02 Issue:4 Volume:251 Page:365-377
ISSN:0022-3417
Container-title:The Journal of Pathology
language:en
Short-container-title:J. Pathol.

Author:

Wang Xiao‐tong¹,Fang Ru¹,Zhang Ru‐song¹,Ye Sheng‐bing¹,Li Rui¹,Wang Xuan¹,Pan Rui¹,Liu Chong²,Chen Jie‐yu³,Zhao Ming⁴,Teng Xiao‐dong⁵,Yu Wen‐juan⁶,Li Yu‐jun⁶,Wang Feng‐hua⁷,Zhang Jian‐guo⁸,Yang Qi‐chang⁹,Zhang Yong‐sheng¹⁰,Lu Zhen‐feng¹,Ma Heng‐hui¹,Zhou Xiao‐jun¹,Xia Qiu‐yuan¹,Rao Qiu¹^ORCID

Affiliation:

1. Department of Pathology, Jinling Hospital Nanjing University School of Medicine Nanjing PR China

2. Department of Pathology, The First Affiliated Hospital Nanjing Medical University Nanjing PR China

3. Department of Pathology, The Affiliated Drum Tower Hospital Nanjing University Medical School Nanjing PR China

4. Department of Pathology, Zhejiang Provincial People's Hospital People's Hospital of Hangzhou Medical College Hangzhou PR China

5. Department of Pathology, The First Affiliated Hospital, College of Medicine Zhejiang University Hangzhou PR China

6. Department of Pathology The Affiliated Hospital of Qingdao University Qingdao PR China

7. Department of Pathology Guangzhou Women and Children's Medical Center Guangzhou PR China

8. Department of Pathology The Affiliated Hospital of Nantong University Nantong PR China

9. Department of Pathology The Second Affiliated Hospital of Nantong University Nantong PR China

10. Department of Pathology The Second Affiliated Hospital of Soochow University Suzhou PR China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Publisher

Wiley

Subject

Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/path.5470

Reference52 articles.

1. Renal cell carcinoma with TFE3 translocation and succinate dehydrogenase B mutation

2. TFE3 Break-apart FISH Has a Higher Sensitivity for Xp11.2 Translocation–associated Renal Cell Carcinoma Compared With TFE3 or Cathepsin K Immunohistochemical Staining Alone

3. Malignant Perivascular Epithelioid Cell Neoplasm (PEComa) of the Urinary Bladder With TFE3 Gene Rearrangement

4. Melanotic Xp11.2 Neoplasm of the Ovary

5. PSF/SFPQ Is a Very Common Gene Fusion Partner in TFE3 Rearrangement–associated Perivascular Epithelioid Cell Tumors (PEComas) and Melanotic Xp11 Translocation Renal Cancers

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Perivascular epithelioid cell neoplasm (PEComa) harboring TFE3 gene rearrangements in a patient with Lynch syndrome;Gastroenterología y Hepatología;2024-06

2. ASPSCR1::TFE3 Drives Alveolar Soft Part Sarcoma by Inducing Targetable Transcriptional Programs;Cancer Research;2024-04-24

3. An unusual case of primary splenic soft part alveolar sarcoma: case report and review of the literature with emphasis on the spectrum of TFE3-associated neoplasms;Diagnostic Pathology;2024-04-20

4. Clinicopathologic and Molecular Characterization of Xanthomatous Giant Cell Renal Cell Carcinomas;American Journal of Surgical Pathology;2024-04-09

5. Recurrent Tuberous Sclerosis Complex/Mammalian Target of Rapamycin Mutations Define Primary Renal Hemangioblastoma as a Unique Entity Distinct From Its Central Nervous System Counterpart;American Journal of Surgical Pathology;2024-03-19