Ishii Kae, Takahashi Hidekazu, Tsuji Hiromi, Ishihara Takayoshi, Iwami Yuka, Juavijitjan Watsapol, Yokota Mitsuki, Takaichi Shohei, Paku Masakatsu, Iwamoto Kazuya, Ohashi Tomofumi, Nakahara Yujiro, Asaoka Tadafumi, Matsuda Chu, Nishikawa Kazuhiro, Omori Takeshi
Department of Gastroenterological Surgery, Osaka International Medical and Science Center, Osaka Keisatsu Hospital, Osaka, Japan.
Department of Diagnostic Pathology, Osaka International Medical and Science Center, Osaka Keisatsu Hospital, Osaka, Japan.
Cancer Diagn Progn. 2025 Jan 3;5(1):49-55. doi: 10.21873/cdp.10411. eCollection 2025 Jan-Feb.
BACKGROUND/AIM: Perianal Paget's disease (PPD) is an intraepithelial invasion of the perianal skin that is frequently associated with anorectal carcinoma. Rectal canal carcinoma with Pagetoid spread (PS) is a relatively rare disease, and few reports on its outcomes are available. The relatively rare nature of this disease makes the development of treatment recommendations difficult. This study aimed to clarify the characteristics of the disease and factors related to prognosis. We present a case report and review of 89 cases, including those from the existing literature and our own experience.
The patient was an 81-year-old man who was referred to our hospital for surgery after endoscopic examination of the lower gastrointestinal tract revealed cancer of the anal canal with PS. Physical examination revealed erythema and erosions around the anus. Lower gastrointestinal endoscopy revealed an erythematous area and a continuous raised lesion in the anal canal. We diagnosed the patient with anal canal carcinoma with PS, and robot-assisted abdominoperineal resection was performed.
Our findings indicate that the five-year survival rate for PPD patients was 63%, comparable to that of anal canal cancer without PS. The histological type and presence of lymph node metastasis may be related to the prognosis. The study suggests that early-stage patients with favorable histological types and no lymph node involvement may benefit from less invasive treatment options, such as endoscopic submucosal dissection.
背景/目的:肛周佩吉特病(PPD)是肛周皮肤的上皮内浸润,常与肛管直肠癌相关。伴有派杰样扩散(PS)的直肠肛管癌是一种相对罕见的疾病,关于其治疗结果的报道较少。这种疾病相对罕见的性质使得制定治疗建议变得困难。本研究旨在阐明该疾病的特征以及与预后相关的因素。我们报告1例病例并回顾89例病例,包括现有文献中的病例和我们自己的经验。
患者为一名81岁男性,在下消化道内镜检查发现肛管癌伴PS后转诊至我院接受手术。体格检查发现肛门周围有红斑和糜烂。下消化道内镜检查显示肛管有一个红斑区域和一个连续的隆起病变。我们诊断该患者为肛管癌伴PS,并进行了机器人辅助腹会阴联合切除术。
我们的研究结果表明,PPD患者的五年生存率为63%,与无PS的肛管癌相当。组织学类型和淋巴结转移情况可能与预后有关。该研究表明,组织学类型良好且无淋巴结受累的早期患者可能从内镜下黏膜下剥离等侵入性较小的治疗选择中获益。