| Literature DB >> 29503871 |
Yoshio Naya1,2, Natsuki Takaha1, Takako Okubo3, Koji Shiota2, Issei Hayashi2, Masaru Mori2, Seiki Date2, Tsuneharu Miki4, Osamu Ukimura5.
Abstract
Background: Cystoscopy using white light is a standard procedure for diagnosing bladder cancer; however, white light can result in missed lesions that are present, but not visible, such as in cases of carcinoma in situ (CIS). In this case report, we describe observing the nuclei of urothelial carcinoma cells in situ that were not visible with cystoscopy under white light using probe-based confocal laser endomicroscopy (pCLE) with acrinol and fluorescein during transurethral resection of a bladder tumor (TURBT). Case Presentation: A 59-year-old male with a medical history of neurogenic bladder dysfunction with multiple bladder diverticula was referred to the urology department for gross hematuria. TURBT was performed with the assistance of pCLE, using acrinol as a novel dye. Standard cystoscopy under white light could not detect any bladder tumor; however, pCLE using acrinol could detect the abnormal nuclei of bladder CIS. Subsequent histopathologic analysis of the specimen confirmed a diagnosis of bladder CIS. To our knowledge, this is the first reported case of bladder CIS diagnosed with the assistance of pCLE using acrinol in a patient undergoing a TURBT.Entities:
Keywords: acrinol; carcinoma in situ of bladder; endomicroscopy; laser optical fiber
Year: 2018 PMID: 29503871 PMCID: PMC5831980 DOI: 10.1089/cren.2017.0114
Source DB: PubMed Journal: J Endourol Case Rep ISSN: 2379-9889

Representative images from white light cystoscopy and pCLE dependent on intravenous administration of acrinol and fluorescein. (A) White light cystoscopy with irregular mucosa in a bladder diverticulum. The 2.7 mm imaging probe is visible at the bottom of the image. (B) pCLE of intravesically stained tumor cells at irregular mucosa. (C) Pathologic examination of the biopsy sample obtained from the irregular mucosa revealed carcinoma in situ of bladder. pCLE, probe-based confocal laser endomicroscopy.