口腔黏膜假血管鳞状细胞癌一例罕见病例报告及文献复习。

IF 1.2 Q4 ONCOLOGY
ecancermedicalscience Pub Date : 2024-11-18 eCollection Date: 2024-01-01 DOI:10.3332/ecancer.2024.1802
Rituparna Dhekial, Rukmini Bezbaruah, Arpan Choudhury, Anupam Das, Sakshi Gupta
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引用次数: 0

摘要

鳞状细胞癌是头颈部最常见的恶性肿瘤。假血管鳞状细胞癌(PSCC)是一种罕见的变异,通常发生在头颈部皮肤。然而,口腔受累是极其罕见的,只有少数病例报道到目前为止。这种变异与不良预后有关。形态学上,肿瘤表现出明显的棘层溶解和吻合的通道,类似血管肿瘤。这种罕见的变异对病理学家提出了诊断挑战,可以通过免疫组织化学(IHC)研究做出准确的诊断。一位72岁男性患者因左侧口腔溃疡快速生长1个多月而转诊至我院。行大面积局部切除联合下颌骨节段性切除术,标本送我科。在大体检查中,在下牙槽和颊粘膜发现了一个大的、柔软的分叶状肿块。镜下肿瘤由恶性上皮细胞排列成巢状、小梁状和不规则的吻合通道组成。可见明显的棘层溶解和由非典型细胞排列的伪血管间隙。免疫组化检查显示肿瘤细胞CK、P40、P63和Vimentin阳性,CD31、CD34、S100和HMB45阴性。病理诊断为PSCC。这里将简要介绍该病例的历史和文献综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudovascular squamous cell carcinoma of the buccal mucosa-a rare case report and review of literature.

Squamous cell carcinoma is the most common malignancy of the head and neck. Pseudovascular squamous cell carcinoma (PSCC) is a rare variant that occurs commonly in the skin of the head and neck. However, oral cavity involvement is extremely rare, with only a few cases reported to date. This variant is associated with an adverse prognosis. Morphologically, the tumour shows marked acantholysis and anastomosing channels mimicking vascular neoplasms. This rare variant poses a diagnostic challenge for pathologists and the accurate diagnosis can be made with the help of immunohistochemical (IHC) studies. A 72-year-old male patient was referred to our hospital with a fast-growing left-sided oral ulcer for more than 1 month. Wide local excision with segmental mandibulectomy was performed and the specimen was sent to our department. On gross examination, a large, soft, lobulated mass was identified in the lower alveolus and the buccal mucosa. On microscopic examination, the tumour was composed of malignant epithelial cells arranged in nests, trabeculae and irregular anastomosing channels. Marked acantholysis and pseudo vascular spaces lined by atypical cells were seen. IHC examination revealed tumour cells positive for CK, P40, P63 and Vimentin and negative for CD31, CD34, S100 and HMB45. The pathological diagnosis was confirmed as PSCC. A short history of the case and a review of literature is discussed here.

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来源期刊
CiteScore
3.80
自引率
5.60%
发文量
138
审稿时长
27 weeks
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