上颌牙槽透明细胞鳞状细胞癌1例诊断缺陷报告。

IF 4.1
Mahija Janardhanan, Rakesh Suresh, Vindhya Savithri, Thara Aravind, Lisha Mathew, V Ravi
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摘要

背景:透明细胞肿瘤是一组异质性的良性和恶性肿瘤,其特征是在组织学检查中存在透明细胞。虽然在头颈部不常见,但广泛的不同细胞来源的口腔内肿瘤可能表现出明显的细胞变化。虽然独特的组织形态学特征通常允许准确的诊断,但广泛的透明细胞改变与重叠模式可能构成重大的诊断挑战。本文强调了这些挑战,并采取了系统的方法来建立最终诊断。方法:我们报告一例罕见的口腔鳞状细胞癌(CCSCC)透明细胞变异累及上颌牙槽,58岁的女性。临床和组织学上,病变模拟牙源性肿瘤、唾液腺肿瘤、黑色素瘤和颌骨转移性病变。在特殊染色和免疫组织化学的支持下,进行了详细的组织形态学评估以达到明确的诊断。结果:组织病理学显示上皮透明细胞岛,其特征与唾液腺和牙源性肿瘤以及黑色素瘤重叠。特殊染色排除黏液表皮样癌、钙化上皮性牙源性肿瘤和转移性肾细胞癌。免疫组织化学显示CK19、EMA和泛细胞角蛋白呈阳性,HMB-45、S100、P63、calretinin和CK10呈阴性。深层切片检查显示严重的上皮发育不良伴间质浸润,证实了CCSCC的诊断。结论:口腔CCSCC是一种非常罕见且具有诊断挑战性的疾病。准确的诊断需要临床、影像学、组织病理学和免疫组织化学的结合。鉴于其具有侵略性的临床行为,早期识别至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clear Cell Squamous Cell Carcinoma of Maxillary Alveolus-A Case Report with Diagnostic Pitfalls.

Background: Clear cell neoplasms are a heterogeneous group of benign and malignant tumours characterized by the presence of clear cells on histological examination. Although uncommon in the head and neck, a wide range of intraoral tumours of varied cellular origins may exhibit clear cell changes. While distinctive histomorphological features often allow accurate diagnosis, extensive clear cell alterations with overlapping patterns can pose significant diagnostic challenges. This paper highlights such challenges and the systematic approach undertaken to establish the final diagnosis.

Methods: We report a rare case of the clear cell variant of oral squamous cell carcinoma (CCSCC) involving the maxillary alveolus in a 58-year-old female. Clinically and histologically, the lesion mimicked odontogenic tumours, salivary gland neoplasms, melanoma, and metastatic lesions of the jaws. Detailed histomorphological assessment, supported by special stains and immunohistochemistry, was performed to reach a definitive diagnosis.

Results: Histopathology revealed epithelial islands of clear cells with features overlapping those of salivary gland and odontogenic tumours, as well as melanoma. Special stains excluded mucoepidermoid carcinoma, calcifying epithelial odontogenic tumour, and metastatic renal cell carcinoma. Immunohistochemistry demonstrated positivity for CK19, EMA and pan-Cytokeratin, with negativity for HMB-45, S100, P63, calretinin & CK10. Examination of deeper sections showed severe epithelial dysplasia with stromal invasion, confirming the diagnosis of CCSCC.

Conclusion: CCSCC of the oral cavity is an exceptionally rare and diagnostically challenging entity. Accurate diagnosis requires correlation of clinical, imaging, histopathology, and immunohistochemistry. Early recognition is essential, given its aggressive clinical behaviour.

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