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一例罕见的起源于骨组织的肱骨滑膜肉瘤:病例报告

A Rare Case of Humerus Synovial Sarcoma Originated from Bone Tissue: Case Report.

作者信息

Heidari Mohsen, Izadi Mehdi, Hatami Saeed

机构信息

Department of Orthopedic Surgery, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Adv Biomed Res. 2023 Jan 30;12:21. doi: 10.4103/abr.abr_385_21. eCollection 2023.

Abstract

Synovial sarcoma (SS) is a malignant mesenchymal neoplasm that is relatively common in the distal extremities. Primary SS of bone is an extremely rare finding. Here in this report, we present a 44-year-old male patient referred with bone and later bone fracture that was finally diagnosed with primary SS of thumerus. So far, 13 documented cases of primary SS of the bone have been reported. The current case is the second known case of primary SS of humerus. Our case was treated with both neoadjuvant and adjuvant chemotherapies associated with surgical tumor removal and prosthesis implantation. Follow-up of the case demonstrated significant remission but with late metastasis and subsequent advanced chemotherapy regimens.

摘要

滑膜肉瘤(SS)是一种恶性间叶性肿瘤,在四肢远端相对常见。原发性骨滑膜肉瘤是一种极为罕见的病例。在本报告中,我们介绍了一名44岁男性患者,该患者最初因骨问题就诊,后来发生骨折,最终被诊断为原发性肱骨滑膜肉瘤。迄今为止,已报告了13例有记录的原发性骨滑膜肉瘤病例。本病例是已知的第二例原发性肱骨滑膜肉瘤。我们的病例接受了新辅助化疗和辅助化疗,并结合手术切除肿瘤和假体植入。对该病例的随访显示病情显著缓解,但出现了晚期转移,随后采用了晚期化疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/10012016/afa3e52deeb0/ABR-12-21-g001.jpg

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