A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features

被引：0
作者：
Wang, Xue [1 ]
Yu, Jingjing [2 ]
Fan, Xiaodong [3 ]
Ma, Suya [1 ]
Xie, Xiaohong [1 ]
Gao, Ning [4 ]
Huang, Shuaishuai [3 ]
Lu, Aimei [1 ]
机构：
[1] Ningbo Yinzhou Second Hosp, Dept Ultrasound, Ningbo 315000, Zhejiang, Peoples R China
[2] Ningbo Yinzhou Second Hosp, Dept Pathol, Ningbo 315000, Zhejiang, Peoples R China
[3] Ningbo Yinzhou Second Hosp, Dept Urol Surg, Ningbo 315000, Zhejiang, Peoples R China
[4] 3D Med Inc, Tumor Compan Diag Broad Market Business Unit, Shanghai, Peoples R China
来源：
BMC UROLOGY | 2023年 / 23卷 / 01期
关键词：
Nephrogenic; Alveolar soft part sarcoma; Clinical manifestation; Genetic; TFE3; GRANULAR-CELL TUMOR; BREAST;
D O I：
10.1186/s12894-023-01182-0
中图分类号：
R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];
学科分类号：
1002 ; 100201 ;
摘要：
BackgroundAlveolar 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 presentationHere 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.ConclusionsASPS 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.
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