Giant multilocular prostatic cystadenoma

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    文章类型: Case Reports
    巨大的多房性前列腺囊腺瘤是一种罕见的良性肿瘤,起源于前列腺。它通常在直肠和膀胱之间,并且由纤维间质中的主要囊性前列腺腺体组成,并在骨盆中广泛扩散。肿块通常通过压迫邻近器官而引起一系列阻塞性症状。在这里,我们报告了一个16岁患者的巨大多房性前列腺囊腺瘤,他是迄今为止报道的最年轻的病例,抱怨排便困难。
    Giant multilocular prostatic cystadenoma is a rare benign tumor that originates from the prostate gland. It usually is between the rectum and the bladder, and is composed of predominantly cystic enlarged prostatic glands in a fibrous stroma and spreads extensively in the pelvis. The mass usually causes a series of obstructive symptoms by compressing adjacent organs. Here we report a case of a giant multilocular prostatic cystadenoma in a 16-year-old patient, who is the youngest case reported up to now, complaining of difficulty in defecation.
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  • 文章类型: Case Reports
    BACKGROUND: The giant multilocular prostatic cystadenoma is a very rare benign tumor of the prostate gland. It is composed of predominantly cystic enlarged prostatic glands in a fibrous stroma and spreads extensively into the pelvis. Because of the large size at the time of diagnosis, it is not always possible to determine the exact point of origin for these multilocular cystic neoplasms. Thus, diagnosis before histological examination of a surgical specimen is often difficult. Here, we present a case involving one of the largest giant multilocular prostatic cystadenomas reported in the literature and discuss preoperative diagnoses and appropriate surgical approaches for this rare retroperitoneal tumor.
    METHODS: A 50-year-old man presented with a 2-year history of abdominal distension and lower urinary symptoms. Enhanced CT showed a large retroperitoneal mass with multiple septations in the pelvis and lower abdomen, measuring 30 cm in size, surrounding the rectum and displacing the bladder, prostate, and seminal vesicle to the right anterior side. MRI showed multiple cysts with a simple fluid appearance on T2-weighted images and enhanced solid components on gadolinium-enhanced fat-saturated T1-weighted images, suggesting the retroperitoneal mass as leiomyoma with cystic degeneration or perivascular epithelioid cell tumor. Biopsy of the mass showed a spindle cell tumor with focal smooth muscle differentiation. Differential diagnosis comprising leiomyoma, low-grade leiomyosarcoma, and perivascular epithelioid cell tumor was made. Complete resection of the tumor with low anterior resection of the rectum was performed. The tumor was solid with multilocular cavities containing blackish-brown fluid and measured 33 × 23 × 10 cm. Histologically, the tumor was composed of variously sized dilated glandular structures lined by prostatic epithelia surrounded by fibromuscular stroma. The prostatic nature of the lesions was confirmed by immunohistochemical staining of the epithelium for prostate-specific antigen. Thus, pathological diagnosis was a giant multilocular prostatic cystadenoma.
    CONCLUSIONS: We present our experiences with one of the largest giant multilocular prostatic cystadenomas. When a retroperitoneal huge lesion with locular cavities fills the pelvis in a male patient, the possibility of giant multilocular prostatic cystadenoma should be considered before planning for retroperitoneal tumor treatment.
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