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在常见口腔癌的时代,软腭平滑肌肉瘤的诊断会被漏诊吗?——罕见病例报告及文献综述

Can a diagnosis of Leiomyosarcoma soft palate be missed in the era of commoner oral carcinomas? - Rare case report and review of literature.

作者信息

Kumar Naina, Gothwal Ravindra Singh, Lakhera Kamal Kishore, Chatterjee Aishwarya, Singh Suresh, Sharma Raj Govind, Patel Pinakin

机构信息

Department of Surgical Oncology, SMS Medical College, Jaipur, Rajasthan, India.

Department of Radiation Oncology, SMS Medical College, Jaipur, Rajasthan, India.

出版信息

J Cancer Res Ther. 2023 Apr-Jun;19(3):835-838. doi: 10.4103/jcrt.jcrt_1024_21.

Abstract

Leiomyosarcomas (LMSs) of the head and neck are an extremely rare entity. Of all smooth muscle tumors, 4%-10% occur in the head and neck and only 0.06% in the oral cavity. Because of its infrequency, it has been associated with both delayed diagnosis and misdiagnosis. Here, we report the clinicopathological findings of a case of primary LMS of the soft palate in a 42-year-old male patient with an emphasis on the judicious use of ancillary diagnostic modalities to arrive at a definitive diagnosis. Intraorally, LMSs present as painless, lobulated, fixed masses of the submucosal tissues in middle-aged or older individuals. The treatment modalities and lymph nodal dissection criteria are dissimilar to more common oral carcinomas. Hence, definitive diagnosis is necessary.

摘要

头颈部平滑肌肉瘤(LMS)是一种极为罕见的疾病。在所有平滑肌肿瘤中,4%-10%发生于头颈部,而仅0.06%发生于口腔。由于其罕见性,它常与诊断延迟和误诊相关。在此,我们报告一例42岁男性患者软腭原发性LMS的临床病理表现,重点在于合理使用辅助诊断方法以得出明确诊断。在口腔内,LMS表现为中年或老年个体黏膜下组织无痛、分叶状、固定的肿块。其治疗方式和淋巴结清扫标准与更常见的口腔癌不同。因此,明确诊断是必要的。

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