Nigam Sonu, Dhingra Kajal Kiran, Gulati Achal
Department of Pathology, Maulana Azad Medical College, Bahadur Shah Zafar Marg, New Delhi, India.
J Oral Pathol Med. 2006 Feb;35(2):126-8. doi: 10.1111/j.1600-0714.2006.00368.x.
Ectomesenchymal chondromyxoid tumor (ECMT) is a rare tumor. Only 26 cases of ECMT have been reported, all occurred in the anterior tongue. We present a case of a 30-year-old male with a nodule in the hard palate, which was reported as ECMT on histopathology. The differential diagnosis considered included are extraskeletal myxoid chondroma, ECMT, pleomorphic adenoma, oral focal mucinosis, chondroid choristoma, and ossifying fibromyxoid tumor. After serial sections no other component was observed and a diagnosis of ECMT was made by exclusion. The patient is asymptomatic on follow up. A review of existing literature is also presented here.
外胚间叶性软骨黏液样瘤(ECMT)是一种罕见肿瘤。仅报道过26例ECMT,均发生于舌前部。我们报告1例30岁男性,硬腭有一结节,组织病理学报告为ECMT。考虑的鉴别诊断包括骨外黏液样软骨瘤、ECMT、多形性腺瘤、口腔局灶性黏液变性、软骨样迷离瘤和骨化性纤维黏液样肿瘤。经连续切片未观察到其他成分,通过排除法诊断为ECMT。患者随访时无症状。本文还对现有文献进行了综述。