Suppr超能文献

骨外黏液样软骨肉瘤:基于细针穿刺细胞学检查对一种罕见软组织肿瘤的诊断

Extraskeletal myxoid chondrosarcoma: Diagnosis of a rare soft tissue tumor based on fine needle aspiration cytology.

作者信息

Ananthamurthy Anuradha, Nisheena R, Rao Bhanumati, Correa Marjorie

机构信息

Department of Pathology, St. John's Medical Colege, Bangalore, India.

出版信息

J Cytol. 2009 Jan;26(1):36-8. doi: 10.4103/0970-9371.54867.

Abstract

Extraskeletal myxoid chondrosarcoma (EMC) is a rare soft tissue sarcoma with limited literature available on its cytological features. We report here one such case where a diagnosis of EMC was made based on fine needle aspiration cytology (FNAC). A 51 year-old male presented to our FNAC clinic with a slowly growing mass in the left thigh, which was subjected to fine needle aspiration biopsy. Radiological images showed no involvement of the underlying bone. Magnetic resonance imaging was suggestive of a malignant neoplasm. The FNA smears showed cell fragments and cords of monotonous cells embedded in abundant myxoid stroma. A diagnosis of a myxoid sarcoma favoring an EMC was made in this patient. Subsequent excision of the mass for histopathological examination confirmed this diagnosis. EMC has distinctive cytological features that are helpful in confidently making a diagnosis in the appropriate clinical setting.

摘要

骨外黏液样软骨肉瘤(EMC)是一种罕见的软组织肉瘤,关于其细胞学特征的文献有限。我们在此报告一例通过细针穿刺细胞学检查(FNAC)诊断为EMC的病例。一名51岁男性因左大腿缓慢生长的肿块前来我们的FNAC诊所就诊,该肿块接受了细针穿刺活检。放射影像学检查未显示下方骨骼受累。磁共振成像提示为恶性肿瘤。FNA涂片显示细胞碎片和条索状单一细胞,嵌入丰富的黏液样基质中。该患者诊断为倾向于EMC的黏液样肉瘤。随后对肿块进行切除以进行组织病理学检查,证实了这一诊断。EMC具有独特的细胞学特征,有助于在适当的临床环境中准确做出诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8bd/3167989/ace719ef609b/JCytol-26-36-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验