Yang Run-Zi, Ma Ming-Shen, Liu Rui, Ren Ting-Ting, Li Jing, Wang Nan, Xu Liang-Yuan, Guo Qi-Han, Ma Jian-Min
Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China.
Department of Ophthalmology, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China.
Int J Ophthalmol. 2025 Sep 18;18(9):1650-1657. doi: 10.18240/ijo.2025.09.05. eCollection 2025.
To examine carcinoma ex pleomorphic adenoma (CXPA) and its development to provide information for its clinical assessment and prognosis.
The clinical data of 26 patients with pathologically diagnosed CXPA were included for analysis. The patients' medical histories and data (., gender, age, eye laterality, clinical manifestations, pathologic and immunohistochemical indices, treatments, and prognosis) were recorded.
The average age of the 26 patients was 59.6±15.7y. There was no significant difference in the gender distribution. The incidence of CXPA bone destruction was approximately 57.7%, and the incidence of optic nerve involvement and extraocular muscle involvement was approximately 15.4% and 19.2%, respectively. The most common pathological type was adenocarcinoma (34.6%), followed by ductal carcinoma (26.9%). Five patients had recurrence or metastasis (19.2%). The 5-year recurrence-free survival rate was 59.0%. There were no significant differences in survival rates among patients with different pathologic types and stages (>0.05). Bone destruction, nerve invasion, and peripheral tissue invasion did not significantly affect survival rate (>0.05). Surgery combined with I radiation therapy leads to a better survival prognosis (<0.05).
CXPA has a variety of pathologic classifications, with characteristics of bone destruction and peripheral tissue invasion. Surgery combined with I endoradiotherapy is a preferable treatment option. However, long-term follow-up and close observation for recurrence or metastasis should be performed.
研究多形性腺瘤恶变(CXPA)及其发展情况,为其临床评估和预后提供信息。
纳入26例经病理诊断为CXPA患者的临床资料进行分析。记录患者的病史及数据(如性别、年龄、患眼侧别、临床表现、病理及免疫组化指标、治疗情况和预后)。
26例患者的平均年龄为59.6±15.7岁。性别分布无显著差异。CXPA骨破坏的发生率约为57.7%,视神经受累和眼外肌受累的发生率分别约为15.4%和19.2%。最常见的病理类型是腺癌(34.6%),其次是导管癌(26.9%)。5例患者出现复发或转移(19.2%)。5年无复发生存率为59.0%。不同病理类型和分期患者的生存率无显著差异(>0.05)。骨破坏、神经侵犯和周围组织侵犯对生存率无显著影响(>0.05)。手术联合I放射治疗可带来更好的生存预后(<0.05)。
CXPA有多种病理分类,具有骨破坏和周围组织侵犯的特点。手术联合I内放射治疗是较好的治疗选择。然而,应进行长期随访并密切观察复发或转移情况。