上颌龈血管肉瘤1例:组织病理学分析

F. Hartanto, S. Lau
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引用次数: 2

摘要

背景:血管肉瘤是一种罕见的恶性肿瘤,多发生于皮肤和软组织。它发生在头颈部,尤其是口腔内,是罕见的。本病例报告的目的是强调组织病理学检查的重要性,并强调血管肉瘤的特征。病例报告:一名52岁女性,在她的磨牙牙间区右侧上颌部分生长。这种增长已经持续了大约一个月。计算机断层扫描(CT)显示转移瘤在肺、肝、骨和上颌龈软组织。口腔内检查发现右侧腭龈一柔软可移动的带梗卵形肿块;肿块呈红蓝色。进行了切口活检以确认诊断并计划进一步治疗。组织病理学检查显示恶性内皮细胞以血管形成的方式生长,有许多血管通道排列着肿瘤内皮形成的腔内芽、突起和乳头。这些突出物中散布着肿瘤细胞。免疫组化分析显示这些内皮细胞对CD31、因子VIII和fl -1具有很强的阳性免疫反应性。诊断为血管肉瘤。讨论:由于口腔内血管肉瘤是罕见的,其临床表现与其他血管病变相似,因此对临床医生和病理学家来说是一个具有挑战性的诊断。在本病例中,诊断为口腔内血管肉瘤是基于临床和组织病理学结果。恶性内皮细胞的显微镜特征和腔内投射的存在,以及CD31、因子VIII和fl -1的阳性免疫反应,证实了诊断。结论:由于血管肉瘤在口腔内的罕见发生,对牙科医生和口腔病理学家提出了诊断挑战。组织病理学检查是准确诊断的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case report of angiosarcoma of maxillary gingiva: Histopathology aspects
Background: Angiosarcoma is a rare malignant tumor, which most often occurs in the skin and soft tissue. Its occurrence in the head and neck region, and the intraoral region in particular, is uncommon. The aim of this case report is to highlight the importance of histopathological examination and to underscore the characteristic features of angiosarcoma. Case report: A 52-year-old female presented with a growth in the right maxillary portion of the interdental region of her molar teeth. The growth had been present for approximately one month. A computerized tomography (CT) scan showed metastatic tumors in the lungs, liver, bone, and soft tissue of maxillary gingiva. Intraoral examination found a soft and mobile pedunculated ovoid mass at the right palatal gingiva; the mass was reddish-blue in color. An incisional biopsy was performed to confirm the diagnosis and plan for further treatment. Histopathologic examination revealed malignant endothelial cells in a vasoformative growth pattern, with numerous vascular channels lined with neoplastic endotheliumforming intraluminal buds, projections, and papillae. These projections were interspersed with the tumor cells. Immunohistochemistry analysis showed these endothelial cells demonstrated strong positive immunoreactivity with CD31, factor VIII, and FLi-1. A diagnosis of angiosarcoma was made. Discussion: Because intraoral angiosarcoma is rare and its clinical presentation can resemble other vascular lesions, it can be a challenging diagnosis for clinicians and pathologists. In the present case, the diagnosis of intraoral angiosarcoma was made based on clinical and histopathology findings. The microscopic features of malignant endothelial cells and the presence of intraluminal projections, supported by positive immunoreactivity with CD31, factor VIII, and FLi-1, confirmed the diagnosis. Conclusion: Angiosarcoma poses a diagnostic challenge to dental practitioners and oral pathologists due to the rarity of occurrence in the oral cavity. Histopathological examination is critical for an accurate diagnosis.
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