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儿童肾源性腺瘤:21例形态学和免疫组织化学研究

Nephrogenic adenomas in pediatric patients: a morphologic and immunohistochemical study of 21 cases.

作者信息

Kao Chia-Sui, Kum Jennifer B, Fan Rong, Grignon David J, Eble John N, Idrees Muhammad T

机构信息

Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Pediatr Dev Pathol. 2013 Mar-Apr;16(2):80-5. doi: 10.2350/12-10-1261-OA.1.

Abstract

Similar to nephrogenic adenomas in adults, those in children are rare benign lesions that often occur in the setting of previous surgery or chronic irritation of the urinary tract. These lesions often present with hematuria and/or as polypoid or papillary lesions on cystoscopy, which may indicate malignancy. We sought to evaluate the various patterns of nephrogenic adenoma occurring in the pediatric population and better characterize the immunophenotype of these lesions. We reviewed 21 cases of nephrogenic adenomas from urinary bladder biopsies of 16 patients. Most patients had a history of urinary bladder augmentation with recurrent urinary stones and urinary tract infections. Many cases presented as a papillary or polypoid mass on cystoscopy. The most common morphologic patterns are papillary, tubulocystic, and a mixed pattern of papillary and tubulocystic, followed by cystic and tubular. On immunostaining, PAX-2, PAX-8, CK7, and MUC-1 provided the most diffuse and intense positive reactivity for nephrogenic adenoma, whereas CD10 and P504S were focal and lesser in intensity when positive. p63 and PAX-5 were consistently negative. We conclude that, although rare in children, nephrogenic adenoma should be included in the differential diagnosis of papillary/polypoid lesions in the urinary tract, especially in the context of previous surgery, chronic irritation from recurrent urinary tract infections, or stones. The immunohistochemistry profile of nephrogenic adenomas in our study also provides evidence that these are derived from distal renal tubular cells. In difficult cases, an immunohistochemical panel consisting of cytokeratin 7, PAX-2, PAX-8, and MUC-1 may be useful.

摘要

与成人肾源性腺瘤相似,儿童肾源性腺瘤是罕见的良性病变,常发生于既往手术或尿路慢性刺激的情况下。这些病变常表现为血尿和/或膀胱镜检查时呈息肉样或乳头状病变,这可能提示恶性肿瘤。我们试图评估儿童人群中肾源性腺瘤的各种模式,并更好地描述这些病变的免疫表型。我们回顾了16例患者膀胱活检的21例肾源性腺瘤病例。大多数患者有膀胱扩大病史,伴有复发性尿路结石和尿路感染。许多病例在膀胱镜检查时表现为乳头状或息肉样肿物。最常见的形态学模式是乳头状、小管囊性以及乳头状和小管囊性混合模式,其次是囊性和管状。免疫染色时,PAX - 2、PAX - 8、CK7和MUC - 1对肾源性腺瘤呈现最弥漫和强烈的阳性反应,而CD10和P504S阳性时呈局灶性且强度较弱。p63和PAX - 5始终为阴性。我们得出结论,尽管肾源性腺瘤在儿童中罕见,但在尿路乳头状/息肉样病变的鉴别诊断中应考虑到,特别是在既往手术、复发性尿路感染或结石引起慢性刺激的情况下。我们研究中肾源性腺瘤的免疫组化特征也提供了证据,表明这些病变源自远端肾小管细胞。在疑难病例中,由细胞角蛋白7、PAX - 2、PAX - 8和MUC - 1组成的免疫组化检测组合可能有用。

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