Lopez Yamil
Loma Linda University Medical Center, Loma Linda, CA, USA.
J Oral Maxillofac Pathol. 2019 Feb;23(Suppl 1):87-89. doi: 10.4103/jomfp.JOMFP_276_18.
Pseudovascular squamous cell carcinoma (SCC) is a rare variant of SCC characterized by acantholysis and necrosis with preservation of vascular-like cords and spaces mimicking glands or vascular differentiation. Only three cases of this variant in the oral cavity have been reported in the literature. However, none of these cases were eosinophil-rich, which is considered to be a good prognostic indicator for conventional SCC. We report one case of an eosinophil-rich pseudovascular adenoid SCC in the oral cavity. A 38-year-old previously healthy African-American female presented with an enlarging inner left cheek mass with overlying ulcer of 2 months duration. A computed tomography scan with contrast demonstrated a large irregularly outlined peripherally enhancing mass located between the anterior margin of the ramus of the left mandible and maxilla protruding outward. An incisional biopsy was performed followed by a wide local excision 3 weeks later. She recovered well postoperatively but refused to follow-up chemoradiation therapy. Six months later, she presented with altered mental status secondary to hypercalcemia from bony metastases. She was discharged to a hospice facility as per her family's request. Histologic sections of the specimens revealed a diffuse hypercellular pleomorphic ill-circumscribed lesion with extensive necrosis. The viable areas exhibited slit vascular-like spaces and micropapillary architectural patterns with stromal eosinophilia. Focal small cellular nests with features of SCC were present. Immunohistochemistry displayed positivity for vimentin, p53, AE1/AE3 and CAM 5.2 (focally positive). All tumor cells were negative for desmin and CD34.
假血管性鳞状细胞癌(SCC)是SCC的一种罕见变体,其特征为棘层松解和坏死,同时保留类似血管的条索和间隙,类似腺体或血管分化。文献中仅报道了3例口腔内的这种变体病例。然而,这些病例均无丰富的嗜酸性粒细胞,而丰富的嗜酸性粒细胞被认为是传统SCC的良好预后指标。我们报告1例口腔内富含嗜酸性粒细胞的假血管性腺样SCC。一名38岁既往健康的非裔美国女性,左颊内侧肿物增大伴表面溃疡2个月。增强计算机断层扫描显示,一个大的、轮廓不规则、周边强化的肿物位于左下颌骨升支前缘与上颌骨之间并向外突出。进行了切开活检,3周后进行了广泛局部切除。她术后恢复良好,但拒绝接受后续的放化疗。6个月后,她因骨转移导致高钙血症继发精神状态改变。根据其家人的要求,她被送往临终关怀机构。标本的组织学切片显示为弥漫性细胞增多、多形性、边界不清的病变,伴有广泛坏死。存活区域可见裂隙样血管间隙和微乳头结构模式,伴有间质嗜酸性粒细胞增多。存在具有SCC特征的局灶性小细胞巢。免疫组化显示波形蛋白、p53、AE1/AE3和CAM 5.2呈阳性(局灶阳性)。所有肿瘤细胞结蛋白和CD34均为阴性。