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耵聍腺瘤:41例临床病理研究并文献复习

Ceruminous adenomas: a clinicopathologic study of 41 cases with a review of the literature.

作者信息

Thompson Lester D R, Nelson Brenda L, Barnes E Leon

机构信息

Department of Endocrine-Otorhinolaryngic-Head & Neck Pathology, Armed Forces Institute of Pathology, Washington, DC, USA.

出版信息

Am J Surg Pathol. 2004 Mar;28(3):308-18. doi: 10.1097/00000478-200403000-00003.

Abstract

BACKGROUND

Ceruminous gland neoplasms are rare neoplasms. To date, a large clinicopathologic study of benign ceruminous gland neoplasms has not been reported.

DESIGN

Forty-one cases of ceruminous gland adenomas diagnosed between 1970 and 2000 were retrieved from the files of the Armed Forces Institute of Pathology. Histologic features were reviewed, immunohistochemical analysis was performed (n = 21), and patient follow-up was obtained (n = 40).

RESULTS

The patients included 22 men and 19 women, 24 to 85 years of age (mean, 54.2 years). Patients presented clinically with a painless mass of the outer half of the external auditory canal (n = 33) or with hearing changes (n = 11). Symptoms were present for an average of 16.3 months. The polypoid masses affected the external auditory canal only and ranged in size from 0.4 to 2 cm in greatest dimension (mean, 1.1 cm). Histologically, the tumors demonstrated glands and small cysts lined by a tubuloglandular proliferation of inner ceruminous cells (cerumen-secreting epithelium with decapitation secretion) subtended by a spindled to cuboidal myoepithelial layer. A hyalinized stroma created an infiltrative pattern of growth; surface involvement (n = 8) was seen. Tumors were divided into ceruminous adenoma (n = 36), ceruminous pleomorphic adenoma (n = 4), and syringocystadenoma papilliferum (n = 1) types. The luminal cells were strongly and diffusely immunoreactive with CK7, while the basal cells were highlighted with CK5/6, S-100 protein, and p63. CD117 highlighted the luminal cells preferentially. The proliferation markers revealed a low index. Adenocarcinoma and middle ear adenoma are the principal differential consideration. Surgical excision was used in all patients. Four patients developed a recurrence due to incomplete excision. All patients were without evidence of disease at the last follow-up: alive (n = 28, mean 16.3 years) or dead (n = 12, mean 11.8 years).

CONCLUSION

Ceruminous gland adenomas are the most common external auditory canal tumors. They demonstrate a dual cell population of basal myoepithelial-type cells and luminal ceruminous (ceruminal) cells. Cerumen pigment, CK7, and p63 can help to distinguish this tumor from other neoplasms that occur in the region. Complete surgical excision results in an excellent long-term clinical outcome.

摘要

背景

耵聍腺肿瘤是罕见肿瘤。迄今为止,尚未见关于良性耵聍腺肿瘤的大型临床病理研究报道。

设计

从武装部队病理研究所档案中检索出1970年至2000年间诊断的41例耵聍腺腺瘤病例。回顾组织学特征,进行免疫组化分析(n = 21),并对患者进行随访(n = 40)。

结果

患者包括22名男性和19名女性,年龄24至85岁(平均54.2岁)。患者临床上表现为外耳道外半段无痛性肿物(n = 33)或听力改变(n = 11)。症状平均持续16.3个月。息肉样肿物仅累及外耳道,最大径0.4至2 cm(平均1.1 cm)。组织学上,肿瘤表现为腺体和小囊肿,内衬由内耵聍细胞呈小管状腺性增生(具有断头分泌的耵聍分泌上皮),其下方为梭形至立方形的肌上皮层。玻璃样变的间质形成浸润性生长模式;可见表面受累(n = 8)。肿瘤分为耵聍腺瘤(n = 36)、耵聍多形性腺瘤(n = 4)和乳头状汗腺囊腺瘤(n = 1)类型。管腔细胞对CK7呈强而弥漫性免疫反应,而基底细胞用CK5/6、S-100蛋白和p63突出显示。CD117优先突出管腔细胞。增殖标志物显示低指数。腺癌和中耳腺瘤是主要的鉴别诊断考虑对象。所有患者均采用手术切除。4例患者因切除不完全而复发。在最后一次随访时,所有患者均无疾病证据:存活(n = 28,平均16.3年)或死亡(n = 12,平均11.8年)。

结论

耵聍腺腺瘤是最常见的外耳道肿瘤。它们表现为基底肌上皮样细胞和管腔耵聍(耵聍腺)细胞的双细胞群。耵聍色素、CK7和p63有助于将该肿瘤与该区域发生的其他肿瘤区分开来。完整的手术切除可带来优异的长期临床结局。

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