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儿童口腔颌面区域的肺泡软组织肉瘤:两例病例的免疫组织化学和超微结构诊断。

Alveolar Soft Part Sarcoma of the Oro-Maxillofacial Region in the Pediatric Age Group: Immunohistochemical and Ultrastructural Diagnosis of Two Cases.

机构信息

Department of Pathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India.

Departments of Otorhinolaryngology and Head & Neck Surgery, All India Institute of Medical Sciences, New Delhi, 110029, India.

出版信息

Head Neck Pathol. 2021 Dec;15(4):1303-1307. doi: 10.1007/s12105-020-01263-8. Epub 2021 Jan 4.

Abstract

Alveolar soft part sarcoma (ASPS) is infrequent in children. While head and neck locations, including the orbit and tongue, are described, only six cases of sinonasal ASPS are reported in the literature. We report two cases of pediatric oro-maxillofacial ASPS. The first case presented as a sinonasal mass in a 13-year-old girl, while the second was a tongue lesion in a 4-year-old female. Histologic examination, TFE3 immunopositivity, and ultrastructural findings of rhomboid crystalline inclusions helped confirm the diagnosis. The diagnosis of ASPS is challenging in children and in uncommon sites like the head and neck. Patients should be routinely followed up for detection of residual or recurrent disease, particularly in cases with positive resection margins.

摘要

肺泡软组织肉瘤(ASPS)在儿童中较为罕见。虽然已有文献报道头颈部包括眼眶和舌部的发病部位,但仅报道了 6 例鼻腔鼻窦 ASPS。我们报告了两例儿童口腔颌面 ASPS。第一例为 13 岁女孩的鼻腔鼻窦肿块,第二例为 4 岁女孩的舌部病变。组织学检查、TFE3 免疫阳性和菱形结晶包涵体的超微结构发现有助于确诊。儿童和头颈部等不常见部位的 ASPS 诊断具有挑战性。应常规对患者进行随访以检测残留或复发疾病,尤其是在切缘阳性的病例中。

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本文引用的文献

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Alveolar soft-part sarcoma of the oral cavity: A review of literature.口腔肺泡软部肉瘤:文献综述
Rare Tumors. 2018 Dec 17;10:2036361318810907. doi: 10.1177/2036361318810907. eCollection 2018.
6
Alveolar soft part sarcoma of the oral and maxillofacial region: clinical analysis in a series of 18 patients.口腔颌面部肺泡软部肉瘤:18例临床分析
Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 Apr;119(4):396-401. doi: 10.1016/j.oooo.2014.12.013. Epub 2014 Dec 24.

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