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软骨黏液样纤维瘤的细胞诊断

Cytodiagnosis of chondromyxoid fibroma.

作者信息

Walke Vaishali A, Nayak Suprita P, Munshi Maitreyee M, Bobhate Sudhakar K

机构信息

Department of Pathology, Government Medical College, Nagpur, Maharashtra, India.

出版信息

J Cytol. 2010 Jul;27(3):96-8. doi: 10.4103/0970-9371.71873.

DOI:10.4103/0970-9371.71873
PMID:21187884
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2983082/
Abstract

Chondromyxoid fibroma (CMF) is an unusual tumor that predominantly affects long bones of young adults. We present two cases of CMF that were diagnosed on cytology. The specific cytological features included varying combinations of chondroid, myxoid and fibroid elements. These features when correlated with clinico-radiological findings helped to arrive at a correct diagnosis. Thus a definitive diagnosis of CMF can be made on cytology based on which further line of treatment can be planned.

摘要

软骨黏液样纤维瘤(CMF)是一种少见的肿瘤,主要累及年轻成年人的长骨。我们报告两例经细胞学诊断的CMF病例。其特异性细胞学特征包括软骨样、黏液样和纤维样成分的不同组合。这些特征与临床放射学检查结果相结合有助于作出正确诊断。因此,基于细胞学检查可对CMF作出明确诊断,并据此制定进一步的治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7d/2983082/a5afaf128105/JCytol-27-96-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7d/2983082/4a3d91110638/JCytol-27-96-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7d/2983082/6f8319a2ce72/JCytol-27-96-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7d/2983082/a5afaf128105/JCytol-27-96-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7d/2983082/4a3d91110638/JCytol-27-96-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7d/2983082/6f8319a2ce72/JCytol-27-96-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7d/2983082/a5afaf128105/JCytol-27-96-g003.jpg

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本文引用的文献

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Myxoid chondrosarcoma of the sphenoid sinus and chondromyxoid fibroma of the iliac bone: cytomorphologic findings of two distinct and uncommon myxoid lesions.蝶窦黏液样软骨肉瘤及髂骨软骨黏液样纤维瘤:两种不同且罕见黏液样病变的细胞形态学表现
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