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炎性肌纤维母细胞性膀胱肿瘤:一种非常罕见的表现。

Inflammatory myofibroblastic bladder tumor: A very rare presentation.

作者信息

Fachini Cipriani Raphael Flavio, Cavalli Alexandre Cavalheiro, Andrade Joaquim Lorenzetti, Sfredo Luciano Ricardo, Martins da Silva Ivam Vargas, de Souza Digner Ingridy

机构信息

Urology Resident, Universidade Federal do Paraná, Hospital de Clínicas, Curitiba, Brazil.

Division of Urology, Universidade Federal do Paraná, Hospital de Clínicas, Curitiba, Brazil.

出版信息

Urol Case Rep. 2021 Sep 27;39:101863. doi: 10.1016/j.eucr.2021.101863. eCollection 2021 Nov.

Abstract

Inflammatory myofibroblastic tumor (IMT) is a rare benign lesion with similarities to malignant lesions due to possible aggressive behavior. Although highly uncommon, this condition usually occurs in lungs and retroperitoneum. The involvement of the genitourinary tract represents a singular occasion. May present with nonspecific manifestations such as painless hematuria, dysuria, voiding urgency and low abdominal pain. We describe a Case of a 55-year-old patient who presented to the urology service complaining of hematuria. Imaging studies showed a 62mm lesion on the upper right side of the bladder and the diagnosis of IMT was confirmed by immunohistochemical evaluation after laparoscopic partial cystectomy.

摘要

炎性肌纤维母细胞瘤(IMT)是一种罕见的良性病变,因其可能具有侵袭性而与恶性病变有相似之处。尽管极为罕见,但这种情况通常发生在肺部和腹膜后。泌尿生殖道受累则是一种特殊情况。可能表现为无痛性血尿、排尿困难、尿急和下腹痛等非特异性症状。我们描述了一例55岁的患者,该患者因血尿就诊于泌尿外科。影像学检查显示膀胱右上侧有一个62mm的病变,经腹腔镜部分膀胱切除术后通过免疫组化评估确诊为IMT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c5/8487991/241297adb01e/gr3.jpg

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