原发性膀胱肺泡软组织肉瘤1例。

Q4 Medicine Japanese Journal of Urology Pub Date : 2021-01-01 DOI:10.5980/jpnjurol.112.45
Akiyuki Asano, Toshinori Nishikimi, Hiroko Morikami, Tomoyoshi Ohashi, Yushi Yamauchi, Ryo Ishida, Hiroshi Yamada, Hiroaki Kobayashi, Toyonori Tsuduki
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引用次数: 1

摘要

一位32岁的女性因血尿和排尿困难被我科收治。计算机断层扫描(CT)和膀胱镜检查显示一个2厘米的带蒂肿瘤,在膀胱三角区有丰富的血液供应和光滑的表面。我们施行经尿道膀胱肿瘤切除术。病理诊断为肺泡软组织肉瘤(ASPS)。CT、骨显像、正电子发射断层扫描和骨盆磁共振成像未见其他病变;因此,她被诊断为原发性膀胱ASPS。术后随访10年,定期膀胱镜检查和ct检查未见局部复发或转移。原发性膀胱ASPS极为罕见,本病例为文献报道的第8例(日本为第2例)。
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[A PRIMARY BLADDER ALVEOLAR SOFT PART SARCOMA: A CASE REPORT].

A 32-year-old woman was admitted to our department for hematuria and dysuria.Computed tomography (CT) and cystoscopy revealed a 2-cm pedunculated tumor with rich blood supply and a smooth surface in the bladder trigone. We performed a transurethral resection of bladder tumor. The pathologic diagnosis was alveolar soft part sarcoma (ASPS). CT, bone scintigraphy, positron emission tomography, and pelvic magnetic resonance imaging revealed no other lesions; thus, she was diagnosed as having a primary bladder ASPS. Postoperative follow-up with regular cystoscopies and CTs over 10 years have shown no local recurrence or metastasis.Primary ASPS of the bladder is exceedingly rare, and this case is the 8th case (the 2nd case in Japan) reported in literature.

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Japanese Journal of Urology
Japanese Journal of Urology Medicine-Urology
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