Shelke Pankaj, Sarode Gargi Sachin, Sarode Sachin Chakradhar, Anand Rahul, Prajapati Ghevaram, Patil Shankargouda
Department of Oral Pathology and Microbiology, Dr. D. Y. Patil Dental College & Hospital, Dr. D. Y. Patil Vidyapeeth, Pune, India.
Department of Preventive Dental Sciences, College of Dentistry, Jazan University, Jazan, Kingdom of Saudi Arabia.
Rare Tumors. 2018 Dec 17;10:2036361318810907. doi: 10.1177/2036361318810907. eCollection 2018.
An alveolar soft-part sarcoma is a malignant neoplasm primarily affecting the soft tissues of head and neck. The aim of the present review is to systematically present the demographic and clinico-pathological data of articles published in the English medical literature. A comprehensive search of the databases (PubMed, Medline, SCOPUS, Web of Science, and Google Scholar) along with cross references to the published articles on alveolar soft-part sarcoma for eligible studies/case reports published since 1957 till date was done to retrieve the data. A total of 74 cases were identified and analyzed from 42 papers published in the English medical literature. All the clinical, radiographic, and prognostic features were analyzed and presented along with the treatment strategies. Alveolar soft-part sarcoma is a rare and aggressive malignancy of uncertain histologic origin with a propensity for vascular invasion and distant metastasis. This neoplasm requires careful clinical, radiographic, and histopathologic evaluation to reach to the correct diagnosis.
肺泡软组织肉瘤是一种主要累及头颈部软组织的恶性肿瘤。本综述的目的是系统地呈现英文医学文献中发表文章的人口统计学和临床病理数据。对数据库（PubMed、Medline、SCOPUS、Web of Science和谷歌学术）进行全面检索，并交叉引用自1957年至今发表的关于肺泡软组织肉瘤的符合条件的研究/病例报告的已发表文章，以检索数据。从英文医学文献中发表的42篇论文中识别并分析了总共74例病例。分析并呈现了所有临床、影像学和预后特征以及治疗策略。肺泡软组织肉瘤是一种罕见且侵袭性强的恶性肿瘤，组织学起源不明，倾向于血管侵犯和远处转移。这种肿瘤需要仔细的临床、影像学和组织病理学评估才能做出正确诊断。
