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成人下尿路纤维上皮性息肉

Fibroepithelial polyp of the lower urinary tract in adults.

作者信息

Tsuzuki Toyonori, Epstein Jonathan I

机构信息

Department of Pathology, Johns Hopkins Hospital, Baltimore, MD 21231, USA.

出版信息

Am J Surg Pathol. 2005 Apr;29(4):460-6. doi: 10.1097/01.pas.0000155153.64360.1a.

Abstract

OBJECTIVE

Fibroepithelial polyps of the urinary tract are rare with most cases reported in children.

DESIGN

We report the clinicopathologic features of 12 fibroepithelial polyps of the lower urinary tract in adults.

PATIENTS

There were 9 males, 2 females, and 1 patient where the gender was unknown (median age, 44 years; range, 17-70 years).

RESULTS

Chief clinical symptoms were hematuria, urinary urgency, and hesitancy. Five patients were asymptomatic, where the lesions were discovered incidentally. Most lesions were located near the verumontanum or the bladder neck. Ten patients were treated by transurethral resection. Of the 10 patients with follow-up information, none showed recurrence (mean, 20 months; median, 17 months). Histologically, all of the fibroepithelial polyps were lined by normal-appearing urothelium, with in one lesion the additional finding of a columnar epithelial lining. There were three overall architectural patterns seen within fibroepithelial polyps. The most common pattern (Pattern 1) seen in 5 cases consisted of a polypoid mass with club-like projections resembling a cloverleaf with florid cystitis cystica et glandularis of the nonintestinal type in the stalk. The second pattern (Pattern 2) seen in 4 cases consisted of a papillary tumor composed of numerous small, rounded fibrovascular cores containing dense fibrous tissue. The last morphologic pattern (Pattern 3) consisted of a polypoid lesion with secondary tall finger-like projections, which was seen in 3 cases. All lesions lacked prominent edema and inflammation seen in polypoid cystitis. Fibroepithelial polyps contained broader stalks with dense fibrous tissue, in contrast to the thin delicate loose fibroconnective tissue seen in the stalk of papillomas. One lesion contained atypical degenerative-appearing stromal cells.

CONCLUSIONS

Although fibroepithelial polyps have been considered to be congenital, we think that some of these polyps could develop after birth because all of our patients first showed clinical symptoms in adulthood. Because fibroepithelial polyps in adults are rare, some of these cases can be misdiagnosed as urothelial neoplasms or reactive conditions. Recognition of the precise histologic features of fibroepithelial polyp can facilitate its correct diagnosis.

摘要

目的

尿路纤维上皮性息肉罕见,多数病例报道于儿童。

设计

我们报告12例成人下尿路纤维上皮性息肉的临床病理特征。

患者

9例男性,2例女性,1例性别未知(中位年龄44岁;范围17 - 70岁)。

结果

主要临床症状为血尿、尿急和排尿踌躇。5例患者无症状,病变为偶然发现。多数病变位于精阜或膀胱颈附近。10例患者接受经尿道切除术。在有随访信息的10例患者中,均未显示复发(平均20个月;中位17个月)。组织学上,所有纤维上皮性息肉均由外观正常的尿路上皮衬覆,1例病变还额外发现柱状上皮衬覆。纤维上皮性息肉内可见三种总体结构模式。最常见的模式(模式1)见于5例,由息肉样肿物组成,有类似苜蓿叶的棒状突起,蒂部有非肠型的腺性膀胱炎伴囊性变。第二种模式(模式2)见于4例,由乳头状肿瘤组成,由众多含致密纤维组织的小圆形纤维血管核心构成。最后一种形态学模式(模式3)由有继发性长指状突起的息肉样病变组成,见于3例。所有病变均无息肉样膀胱炎中所见的明显水肿和炎症。纤维上皮性息肉含有较宽的蒂,有致密纤维组织,与乳头状瘤蒂部所见的纤细疏松纤维结缔组织不同。1例病变含有非典型退变样间质细胞。

结论

尽管纤维上皮性息肉一直被认为是先天性的,但我们认为其中一些息肉可能在出生后发生,因为我们所有患者均在成年后首次出现临床症状。由于成人纤维上皮性息肉罕见,其中一些病例可能被误诊为尿路上皮肿瘤或反应性病变。认识纤维上皮性息肉的确切组织学特征有助于正确诊断。

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