Division of Pathology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Division of Urology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Int J Surg Pathol. 2023 Dec;31(8):1572-1579. doi: 10.1177/10668969231159314. Epub 2023 Mar 20.
Urinary bladder hamartoma is a rare benign proliferation with only 14 cases reported in the literature at present. Urinary bladder hamartoma is composed of a disorderly admixture of normal urinary bladder components, essentially represented by glands lined by transitional epithelium and a variable percentage of fibrous stroma, smooth muscle bundles, and adipose tissue. Urinary bladder hamartomas do not exhibit cytological or architectural abnormalities and show no necrosis or increase in mitotic activity. Clinical manifestations are usually represented by lower urinary tract symptoms, more or less frequently paired with gross hematuria. Several pediatric cases of urinary bladder hamartoma have been reported, sometimes with syndromic associations. Transurethral resection has been curative in all cases reported, with no evidence of recurrence. Here we report an additional rare urinary bladder hamartoma, clinically mimicking urothelial carcinoma, providing a review of the literature regarding this unusual entity.
膀胱错构瘤是一种罕见的良性增生,目前文献中仅报道了 14 例。膀胱错构瘤由正常膀胱成分的无序混合组成,主要由移行上皮衬里的腺体和不同比例的纤维基质、平滑肌束和脂肪组织构成。膀胱错构瘤无细胞学或结构异常,无坏死或有丝分裂活性增加。临床表现通常表现为下尿路症状,或多或少伴有肉眼血尿。已经报道了一些小儿膀胱错构瘤病例,有时伴有综合征相关性。所有报道的病例均经经尿道切除治愈,无复发证据。在这里,我们报告了另一个罕见的膀胱错构瘤病例,临床上类似于尿路上皮癌,对这一罕见实体进行了文献回顾。