Suppr超能文献

起源于拉克氏裂囊肿壁内的鞍内涎腺样多形性腺瘤。

Intra-sellar salivary gland-like pleomorphic adenoma arising within the wall of a Rathke's cleft cyst.

作者信息

Chimelli L, Gadelha M R, Une K, Carlos S, Pereira P J, Santos J L, Filho P N, Duarte F

机构信息

Department of Pathology, University Hospital, Federal University of Rio de Janeiro, Brazil.

出版信息

Pituitary. 2000 Dec;3(4):257-61. doi: 10.1023/a:1012888315577.

Abstract

Salivary gland rests occur in the posterior lobe of the pituitary gland near or often communicating with the Rathke's cleft or its cystic subdivisions, and are usually incidental autopsy findings. They are attributed to the oropharyngeal development of the Rathke's pouch and may rarely give rise to salivary gland-like tumors in the sella. We present a pleomorphic adenoma, a rare tumor of the sellar region, that has not been previously recognized in association with Rathke's cleft cyst. It occurred in a 44-year-old man who presented with hypopituitarism and reduced vision. Magnetic resonance imaging showed a sellar mass with suprasellar extension which was totally removed. It consisted of segments of a cyst wall lined by focally ciliated columnar of cuboid epithelium containing goblet cells. An eosinophilic granular material with cholesterol clefts represented the contents of the cyst. Within its wall there was a tumor with ductal structures and non-ductal varied cellular components including hypercellular areas of spindle and ovoid cells forming interlacing fascicles. Individual cells appeared to float in abundant mucinous material. The appearances were those of a salivary gland pleomorphic adenoma arising within the wall of a Rathke's cleft cyst. The myoepithelial nature of non-ductal tumor cells was confirmed with immunocytochemistry. The existence of seromucous glands communicating with the Rathke's cleft remnants, explains the concomitant occurrence of the tumor and the cyst. This rare neoplasm from salivary gland rest should be considered in the differential diagnosis of unusual sellar and suprasellar tumors.

摘要

涎腺残余见于垂体后叶,靠近拉克氏裂或常与之相通,或位于其囊性分支内,通常是尸检时的偶然发现。它们被认为是拉克氏囊口咽发育的结果,在鞍区很少引发涎腺样肿瘤。我们报告一例多形性腺瘤,这是一种罕见的鞍区肿瘤,此前未被认为与拉克氏裂囊肿相关。该病例发生在一名44岁男性,表现为垂体功能减退和视力下降。磁共振成像显示鞍区肿物并向上延伸至鞍上,肿物被完整切除。肿物由部分囊壁组成,囊壁内衬有局灶性纤毛柱状或立方上皮,含杯状细胞。囊内容物为含胆固醇裂隙的嗜酸性颗粒物质。在囊壁内有一个肿瘤,具有导管结构和非导管性多种细胞成分,包括梭形和卵圆形细胞的高细胞区,形成交错束状。单个细胞似乎漂浮在丰富的黏液样物质中。其表现为起源于拉克氏裂囊肿壁内的涎腺多形性腺瘤。非导管性肿瘤细胞的肌上皮性质经免疫细胞化学证实。与拉克氏裂残余相通的浆液黏液性腺的存在,解释了肿瘤与囊肿的并存。在鉴别诊断不常见的鞍区和鞍上肿瘤时,应考虑这种罕见的涎腺残余肿瘤。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验