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嗜酸性细胞性(柱状细胞)施奈德乳头状瘤恶变癌

Carcinoma ex oncocytic Schneiderian (cylindrical cell) papilloma.

作者信息

Kapadia S B, Barnes L, Pelzman K, Mirani N, Heffner D K, Bedetti C

机构信息

Department of Otolaryngic Pathology, Armed Forces Institute of Pathology, Washington, DC.

出版信息

Am J Otolaryngol. 1993 Sep-Oct;14(5):332-8. doi: 10.1016/0196-0709(93)90091-k.

Abstract

INTRODUCTION

This study reviews the clinicopathologic features of carcinoma presenting in oncocytic Schneiderian papilloma (OSP; cylindrical cell papilloma), a rare histologically distinctive papilloma sharing features with inverted papilloma.

MATERIALS AND METHODS

Nine cases of carcinoma ex OSP (1970-1990), six from the files of the Armed Forces Institute of Pathology (Washington, DC) and three from the surgical pathology files, Presbyterian-University Hospital and Eye and Ear Institute (Pittsburgh, PA), were studied. One case was previously reported. Clinical data were obtained from the patients' medical records. All available histologic slides were reviewed.

RESULTS

The patients (eight men, one woman) ranged in age from 48 to 83 years (mean age, 74 years). The carcinoma and OSP were synchronous in eight patients. In one case, the carcinoma occurred 8 years after OSP was diagnosed on biopsy. The presenting manifestations included nasal obstruction, "polyps," epistaxis, and proptosis. Radiographically, a sinonasal mass was present, often with extension to adjacent sites and bone destruction. Most patients received postoperative irradiation. Of six patients with follow-up, four died of carcinoma and two were alive without disease at 1.5 and 7 years, respectively. The types of carcinoma were: squamous cell (n = 6), high-grade mucoepidermoid (n = 2), and sinonasal undifferentiated (n = 1). Histologic transition was observed between carcinoma and dysplastic/benign OSP in eight cases.

CONCLUSION

Demonstration of histologic continuity between carcinoma and dysplastic OSP epithelium in eight of our nine cases indicates origin of carcinoma from the OSP, rather than a coincidence of the two neoplasms. Although histologically benign, OSP should be totally excised at diagnosis because of a potential for malignant transformation. This is a US government work. There are no restrictions on its use.

摘要

引言

本研究回顾了发生于嗜酸性细胞性施奈德乳头状瘤(OSP;柱状细胞乳头状瘤)中的癌的临床病理特征,OSP是一种罕见的组织学上独特的乳头状瘤,与内翻性乳头状瘤有共同特征。

材料与方法

研究了9例OSP来源的癌(1970 - 1990年),其中6例来自武装部队病理研究所(华盛顿特区)的档案,3例来自长老会大学医院及眼耳研究所(宾夕法尼亚州匹兹堡)的外科病理档案。1例曾有报道。临床资料取自患者病历。复查了所有可用的组织学切片。

结果

患者(8例男性,1例女性)年龄在48至83岁之间(平均年龄74岁)。8例患者的癌与OSP同时存在。1例患者在活检诊断OSP 8年后发生癌。主要表现包括鼻塞、“息肉”、鼻出血和眼球突出。影像学检查显示鼻窦有肿物,常侵犯相邻部位并伴有骨质破坏。大多数患者接受了术后放疗。6例有随访的患者中, 4例死于癌,2例分别在1.5年和7年时无病存活。癌的类型为:鳞状细胞癌(n = 6)、高级别黏液表皮样癌(n = 2)和鼻窦未分化癌(n = 1)。8例病例观察到癌与发育异常/良性OSP之间存在组织学过渡。

结论

我们9例中的8例显示癌与发育异常的OSP上皮之间存在组织学连续性,这表明癌起源于OSP,而非两种肿瘤的巧合。尽管OSP在组织学上为良性,但因其有恶变潜能,诊断时应完整切除。这是美国政府的工作。其使用不受限制。

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