HRA003345
Title:
A Case Report and Literature Review on Nephrogenic Alveolar Soft Part Sarcoma: Clinicopathological Manifestations and Genetic Features
Release date:
2022-10-31
Description:
Alveolar Soft Part Sarcoma (ASPS) is a rare kind of malignant soft tissue tumor with undefined differentiation, of which the incidence rate accounts for only 0.5-1.0% among all kinds of soft tissue tumors. An even rarer ASPS occurs in kidney. Case presentation: Here we reported a case of a 7-year-old girl diagnosed with nephrogenic ASPS, regarding the analyses of the incidence, clinical manifestation, pathology and genetic diagnosis, in order to deepen the recognition of the disease. Conclusions: ASPS is very rare, and tends to occur to young patients. It is very significant to precisely diagnose ASPS at an early stage, which will be the key point for the following treatment choices and prognosis.
Data Accessibility:   
Controlled access Request Data
BioProject:
Study type:
Disease Study
Disease name:
alveolar soft part sarcoma
Data Access Committee

For each controlled access study, there is a corresponding Data Access Committee(DAC) to determine the access permissions. Access to actual data files is not managed by NGDC.


DAC NO.:
DAC name:
DAC for PRJCA012830
Contact person:
Huang Shuaishuai
Email:
ss.huang@aliyun.com
Description:
DAC for PRJCA012830: A Case Report and Literature Review on Nephrogenic Alveolar Soft Part Sarcoma: Clinicopathological Manifestations and Genetic Features
Individuals & samples
Submitter:   Liu Dongyu / dongyu.liu@3dmedcare.com
Organization:   3D Medicines Inc.
Submission date:   2022-10-28
Requests:   -