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一例罕见的原发性心包巨大黏液样脂肪肉瘤。

A rare case of primary giant myxoid liposarcoma of the pericardium.

作者信息

Sinai Khandeparkar Siddhi Gaurish, Kulkarni Maithili Mandar, Mishra Pooja, Mushir Patel Ashmira Zainab

机构信息

Department of Pathology, Smt. Kashibai Navale Medical College and General Hospital, Pune, Maharashtra, India.

出版信息

Indian J Pathol Microbiol. 2023 Apr-Jun;66(2):347-349. doi: 10.4103/ijpm.ijpm_545_21.

Abstract

Primary pericardial neoplasms account for 6.7-12.8% of all primary tumors arising in the cardiac region. Pericardial tumors are most likely to be metastatic and are an extension of the primary tumors from the surrounding structures. Sarcomas of the pericardium are rare. Myxoid liposarcoma (ML) represents about 5% of all the soft-tissue sarcomas in adults. They are usually located in the deep soft tissues of the extremities. There have been less than 20 cases of pericardial liposarcomas reported on PubMed since 1973. Here, we present a rare case of primary giant pericardial myxoid liposarcoma (ML) in a 46-year-old female diagnosed on frozen section and later was confirmed histopathologically.

摘要

原发性心包肿瘤占心脏区域所有原发性肿瘤的6.7% - 12.8%。心包肿瘤最有可能是转移性的,是周围结构原发性肿瘤的延伸。心包肉瘤很罕见。黏液样脂肪肉瘤(ML)约占成人所有软组织肉瘤的5%。它们通常位于四肢深部软组织。自1973年以来,PubMed上报道的心包脂肪肉瘤病例不到20例。在此,我们报告一例罕见的原发性巨大心包黏液样脂肪肉瘤(ML),该病例发生在一名46岁女性身上,术中冰冻切片诊断,随后经组织病理学确诊。

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