Ananthamurthy Anuradha, Nisheena R, Rao Bhanumati, Correa Marjorie
Department of Pathology, St. John's Medical Colege, Bangalore, India.
J Cytol. 2009 Jan;26(1):36-8. doi: 10.4103/0970-9371.54867.
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.
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。