下颌下腺滑膜肉瘤伴P63异常表达一例罕见病例报告

Q4 Medicine
Afnan Elsayed , Haneen Al-Maghrabi , Hosam Alardati , Ameen Alherabi , Abdelrazak Meliti
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引用次数: 1

摘要

滑膜肉瘤是一种通常累及四肢和关节周围软组织的肿瘤。10%的病例累及头颈部,组织学上多为双相。摘要颌下腺是原发性滑膜肉瘤不常见的解剖部位。在此,我们提出一个独特的病例原发性颌下腺滑膜肉瘤形态模仿孤立的纤维性肿瘤。此外,肿瘤细胞显示异常的p63核表达。免疫图谱和分子研究分别证实了TLE1的表达和SYT(18-11.2)的重排。据我们所知,本病例是英文文献中第一例p63表达的病例,也是第二例原发性颌下腺滑膜肉瘤的报道病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synovial sarcoma of submandibular gland with aberrant P63 expression a case report of rare event

Synovial sarcoma is a tumor commonly involves extremities and periarticular soft tissue of young adults. Head and neck region is involved in 10% of cases, mostly biphasic in histology. Submandibular gland is an uncommon anatomic location for primary synovial sarcoma. Herein, we present a unique case of primary submandibular gland synovial sarcoma morphologically mimicking a solitary fibrous tumor. Moreover, the neoplastic cells reveal an aberrant p63 nuclear expression. The immunoprofile and the molecular studies confirmed TLE1 expression and SYT (18-11.2) rearrangement, respectively. To the best of our knowledge, the present case is the first with a p63 expression and the second reported case of primary submandibular gland synovial sarcoma in English literature.

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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
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审稿时长
16 weeks
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