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小儿口腔平滑肌肉瘤:罕见病例报告。

Pediatric oral leiomyosarcoma: rare case report.

作者信息

Divyambika C V, Sathasivasubramanian S, Krithika C L, Malathi N, Prathiba D

机构信息

Department of Oral Medicine and Radiology, Sri Ramachandra University, Porur, Chennai - 600118, India.

出版信息

J Cancer Res Ther. 2012 Apr-Jun;8(2):282-5. doi: 10.4103/0973-1482.98990.

DOI:10.4103/0973-1482.98990
PMID:22842376
Abstract

Soft tissue sarcomas comprise a group of histologically diverse malignant neoplasms arising from mesenchymal cell lines. Among these, leiomyosarcomas are sarcomas exhibiting smooth muscle differentiation. Occurrence of this neoplasm in the oral cavity is exceedingly rare and its presentation is unusual in children. We present a case report of leiomyosarcoma of the oral cavity in an eight-year old child. Primary oral leiomyosarcoma, being a rare entity in children, this case report emphasizes the prompt recognition of this tumor to institute appropriate multimodality treatment.

摘要

软组织肉瘤是一组起源于间充质细胞系、组织学上多样的恶性肿瘤。其中,平滑肌肉瘤是表现为平滑肌分化的肉瘤。这种肿瘤在口腔中极为罕见,在儿童中的表现也不常见。我们报告一例8岁儿童口腔平滑肌肉瘤的病例。原发性口腔平滑肌肉瘤在儿童中是一种罕见的疾病,本病例报告强调了对这种肿瘤的及时识别,以便进行适当的多模式治疗。

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