Zhang Zhengwei, Sun Song
*MMed †MD Department of Ophthalmology, Wuxi No. 2 Hospital Affiliated to Nanjing Medical University, Wuxi, Jiangsu Province, China (both authors).
Optom Vis Sci. 2014 Mar;91(3):e72-5. doi: 10.1097/OPX.0000000000000154.
To describe a case of sebaceous carcinoma of the caruncle and review relevant literature to raise awareness about this rare disease.
A 63-year-old Chinese man presented with a nontender mass that had developed within the right lacrimal caruncle more than 3 years previously and had been growing in size. The patient was admitted to the hospital, and no systemic diseases were noted on physical and instrumental examinations. The mass was removed intact, and 10 small map biopsies of the surrounding conjunctiva and deeper tissues were performed. Thereafter, 0.04% mitomycin C was applied to the surgical defect for 5 minutes before repair by conjunctival autografting. The gross specimen was observed to be firm and yellow. Microscopic examination revealed that the tumor consisted of lobules, composed of pleomorphic vacuolated cells with central necrosis. The pathologic diagnosis was a well-differentiated sebaceous cell carcinoma of the caruncle that did not extend to the deep surgical margins. Moreover, no tumor recurrence was noted 12 months after surgery.
The occurrence of sebaceous cell carcinoma in the caruncle is rare. In general, this neoplasm is often both clinically and histopathologically misdiagnosed as a benign condition, resulting in both a delay in correct diagnosis and increased morbidity and mortality. Therefore, this malignancy should be considered in the differential diagnosis of caruncular lesions. The suspected neoplasm should be removed by margins that are as wide as possible; map biopsies are considered to be useful to rule out the subclinical spread of the tumor.
描述一例泪阜皮脂腺癌病例,并回顾相关文献以提高对这种罕见疾病的认识。
一名63岁的中国男性患者,右侧泪阜出现一个无痛性肿物,3年多前出现,且肿物大小不断增大。患者入院,体格检查和器械检查未发现全身性疾病。完整切除肿物,并对周围结膜和深层组织进行了10次小块地图状活检。此后,在结膜自体移植修复前,将0.04%丝裂霉素C应用于手术缺损处5分钟。大体标本质地硬且呈黄色。显微镜检查显示肿瘤由小叶组成,小叶由多形性空泡状细胞组成,伴有中央坏死。病理诊断为泪阜高分化皮脂腺癌,未累及手术切缘深部。此外,术后12个月未发现肿瘤复发。
泪阜皮脂腺癌的发生较为罕见。一般来说,这种肿瘤在临床和组织病理学上常被误诊为良性病变,导致正确诊断延迟,发病率和死亡率增加。因此,在泪阜病变的鉴别诊断中应考虑这种恶性肿瘤。对于疑似肿瘤,应尽可能广泛地切除边缘组织;地图状活检被认为有助于排除肿瘤的亚临床扩散。