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Alveolar soft part sarcoma in childhood and adolescence: Report of three cases and review of literature.儿童及青少年肺泡软组织肉瘤:三例报告并文献复习
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Lingual Alveolar Soft Part Sarcoma in a 78-Year-Old Woman: A Case Report and Comprehensive Review of the Literature from 1952 to 2022.78 岁女性舌侧牙槽部软组织肉瘤:病例报告及 1952 年至 2022 年文献复习
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本文引用的文献

1
Genetic diversity in alveolar soft part sarcoma: A subset contain variant fusion genes, highlighting broader molecular kinship with other MiT family tumors.肺泡软组织肉瘤的遗传多样性:一个亚组包含变异融合基因,凸显了与其他MiT家族肿瘤更广泛的分子亲缘关系。
Genes Chromosomes Cancer. 2020 Jan;59(1):23-29. doi: 10.1002/gcc.22803. Epub 2019 Aug 31.
2
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.
3
Diagnosis, Prognosis, and Treatment of Alveolar Soft-Part Sarcoma: A Review.《腺泡状软组织肉瘤的诊断、预后和治疗:综述》。
JAMA Oncol. 2019 Feb 1;5(2):254-260. doi: 10.1001/jamaoncol.2018.4490.
4
Positive Tumor Response to Combined Checkpoint Inhibitors in a Patient With Refractory Alveolar Soft Part Sarcoma: A Case Report.一名难治性肺泡软组织肉瘤患者对联合检查点抑制剂产生阳性肿瘤反应:病例报告
J Glob Oncol. 2018 Sep;4:1-6. doi: 10.1200/JGO.2017.009993. Epub 2017 Jul 6.
5
Alveolar soft part sarcoma in children and young adults: A report of 69 cases.儿童和青年成人生殖器透明细胞汗腺瘤临床病理观察
Pediatr Blood Cancer. 2018 May;65(5):e26953. doi: 10.1002/pbc.26953. Epub 2018 Jan 19.
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.
7
Alveolar soft part sarcoma and granular cell tumor: an immunohistochemical comparison study.肺泡软组织肉瘤和颗粒细胞瘤:一项免疫组织化学比较研究。
Hum Pathol. 2014 May;45(5):1039-44. doi: 10.1016/j.humpath.2013.12.021. Epub 2014 Jan 21.
8
Paediatric and adolescent alveolar soft part sarcoma: A joint series from European cooperative groups.儿科和青少年肺泡软组织肉瘤:来自欧洲合作组的联合系列。
Pediatr Blood Cancer. 2013 Nov;60(11):1826-32. doi: 10.1002/pbc.24683. Epub 2013 Jul 16.
9
Oral alveolar soft part sarcoma in childhood and adolescence: report of two cases and review of literature.儿童和青少年口腔牙槽软组织肉瘤:两例报告并文献复习
Head Neck Pathol. 2013 Mar;7(1):40-9. doi: 10.1007/s12105-012-0395-y. Epub 2012 Sep 8.
10
Alveolar soft part sarcoma of the paranasal sinuses masquerading as a giant invasive pituitary adenoma.鼻窦肺泡软组织肉瘤伪装成巨大侵袭性垂体腺瘤。
Ann Diagn Pathol. 2013 Jun;17(3):276-80. doi: 10.1016/j.anndiagpath.2012.07.004. Epub 2012 Aug 24.

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.

DOI:10.1007/s12105-020-01263-8
PMID:33398684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8633254/
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。