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翼腭窝血管周上皮样细胞肿瘤(PEComa)

Perivascular epithelioid cell tumor (PEComa) of the pterygopalatine fossa.

作者信息

Dougherty Michael I, Payne Spencer C, Gupta Akriti, Mattos Jose L

机构信息

Department of Otolaryngology- Head and Neck Surgery University of Virginia School of Medicine Charlottesville Virginia.

Department of Pathology University of Virginia School of Medicine Charlottesville Virginia.

出版信息

Clin Case Rep. 2020 Feb 5;8(3):553-558. doi: 10.1002/ccr3.2676. eCollection 2020 Mar.

Abstract

Perivascular epithelioid cell tumors (PEComas) are a rare group of mesenchymal tumors associated with tuberous sclerosis. These tumors are typically treated with resection and rarely recur or exhibit malignant behavior. A 78-year-old woman presented with an incidentally discovered pterygopalatine fossa/retroantral mass. Excisional biopsy was performed and revealed pathology consistent with PEComa. Upon review of the literature, there have been 43 reported cases of PEComa of the head and neck. There is only one previously reported case of PEComa in the skull base, and none reported in the pterygopalatine fossa. Of note, the previously reported case of skull base PEComa involved an aggressive tumor with widespread metastasis. Here, we report the first case of a PEComa of the pterygopalatine fossa/retroantral region, which was treated conservatively. This rare pathology should be considered in the differential diagnosis for atypical skull base tumors.

摘要

血管周上皮样细胞肿瘤(PEComas)是一组与结节性硬化症相关的罕见间叶性肿瘤。这些肿瘤通常采用手术切除治疗,很少复发或表现出恶性行为。一名78岁女性因偶然发现翼腭窝/鼻窦后肿块就诊。进行了切除活检,病理结果显示符合PEComa。查阅文献发现,头颈部PEComa已有43例报道。此前仅有1例颅底PEComa的报道,翼腭窝尚无报道。值得注意的是,此前报道的颅底PEComa病例是一例具有广泛转移的侵袭性肿瘤。在此,我们报告首例翼腭窝/鼻窦后区域的PEComa病例,该病例采用了保守治疗。对于非典型颅底肿瘤的鉴别诊断应考虑这种罕见的病理情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d74/7069881/ab79f1222c00/CCR3-8-553-g001.jpg

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