Fulawka Lukasz, Dawiec Beata, Homola Wojciech, Halon Agnieszka
Department of Clinical and Experimental Pathology, Wroclaw Medical University, Wroclaw, Poland.
Molecular Pathology Centre Cellgen, Wroclaw, Poland.
Pathol Oncol Res. 2025 May 26;31:1612076. doi: 10.3389/pore.2025.1612076. eCollection 2025.
We report the first case of an asymptomatic woman with osteoclast-like giant cell-rich cervical squamous cell carcinoma (OGC-rich cervical SCC), where the detection of cancer was made possible only by routine cytological screening. The presence of OGCs in cervical SCCs is an extremely rare phenomenon, with only 8 cases reported to date.
Two consecutive liquid-based cytology revealed high-grade squamous intraepithelial lesion (HSIL). Molecular testing detected HPV 18. Colposcopic findings strongly supported the clinical diagnosis of HSIL/suspicious for invasion. Histopathological examination of biopsy samples revealed typical keratinizing-type cervical SCC morphology. The patient subsequently underwent LEEP (loop electrosurgical excision procedure). Microscopic examination of resection specimen confirmed the previous diagnosis. Moreover, groups of large multinucleated cells were observed at the periphery of some invasive nests. Most of them presented the morphology of osteoclasts, whereas some giant cells were similar to Langhans cells. All the giant cells were positive for vimentin and CD68, negative for pancytokeratin. Owing to positive margins following the LEEP procedure, the patient underwent hysterectomy via the Wertheim technique. No adjuvant treatment was applied, and after the 9-month follow-up, the patient was alive with no recurrence.
Detailed literature review revealed that our case is the first case of keratinizing-subtype cervical OGC-rich SCC. Moreover, it is the youngest (33 yo.) patient with a significantly smaller diameter than previously reported cases. Unfortunately, owing to the small number of reported cases, the analysis did not allow us to draw conclusions about the potential prognostic or predictive value of OGC-rich morphology.
我们报告了首例无症状女性患有富含破骨细胞样巨细胞的宫颈鳞状细胞癌(OGC 丰富型宫颈 SCC),其中癌症仅通过常规细胞学筛查得以发现。宫颈 SCC 中存在 OGC 是一种极为罕见的现象,迄今为止仅报道了 8 例。
连续两次液基细胞学检查显示高级别鳞状上皮内病变(HSIL)。分子检测发现 HPV 18。阴道镜检查结果强烈支持 HSIL/可疑浸润的临床诊断。活检样本的组织病理学检查显示典型的角化型宫颈 SCC 形态。患者随后接受了利普刀(环形电外科切除术)。切除标本的显微镜检查证实了先前的诊断。此外,在一些浸润巢的周边观察到成群的大型多核细胞。其中大多数呈现破骨细胞的形态,而一些巨细胞类似于朗汉斯细胞。所有巨细胞波形蛋白和 CD68 呈阳性,全细胞角蛋白呈阴性。由于利普刀手术后切缘阳性,患者通过韦特海姆技术接受了子宫切除术。未进行辅助治疗,经过 9 个月的随访,患者存活且无复发。
详细的文献综述显示,我们的病例是首例角化亚型宫颈 OGC 丰富型 SCC。此外,这是最年轻(33 岁)的患者,直径明显小于先前报道的病例。不幸的是,由于报道的病例数量较少,分析未能让我们就富含 OGC 的形态的潜在预后或预测价值得出结论。