Papagrigoriadis Savvas, Brandimarte Giovanni, Tursi Antonio
IASO Hospital, Athens, Greece.
One Welbeck Digestive Health Centre, London, United Kingdom.
Front Med (Lausanne). 2025 Mar 13;12:1500053. doi: 10.3389/fmed.2025.1500053. eCollection 2025.
Diverticular disease (DD) of the colon has a number of phenotypes, including asymptomatic diverticulosis and complicated diverticulitis with bowel perforation or bleeding. The factor that affects the phenotype of this condition and leads to a wide range of clinical presentations is unknown. The formation of fistulas associated with diverticulitis has long been recognized, and they are treated according to indications. We hypothesized that the formation of fistulas in diverticular disease exhibits such a wide range of variable anatomic features that it may be considered a distinct form of the condition, fistulating diverticulitis (FD).
We conducted a narrative review based on 50 years of publications covering a wide range of diverticulitis-associated fistulas, both common and uncommon.
While there is abundant literature on common fistulas, such as colovesical and colovaginal fistulas, little is known about rarer fistulas, such as coloenteric fistulas, colocutaneous fistulas, and genitourinary tract fistulas. The majority of these fistulas are treated surgically, which is in contrast to the trend toward conservative management that is predominant in acute or chronic diverticulitis.
Epidemiological and histological evidence support the hypothesis that FD may be a feature of chronic DD that requires individual management. Histopathology shows similarities with Crohn's disease. It remains unknown which underlying immune or genetic factors may be affecting the clinical presentation of these patients, leading to fistulation. We contend that there is adequate published evidence to characterize a distinct phenotype of FD that can involve the entire GI tract and other organs. Surgical guidelines may need to be modified to treat this small but important group, which predominantly requires surgical treatment.
结肠憩室病(DD)有多种表型,包括无症状憩室病以及伴有肠穿孔或出血的复杂性憩室炎。影响这种疾病表型并导致广泛临床表现的因素尚不清楚。与憩室炎相关的瘘管形成早已被认识到,并且根据适应症进行治疗。我们假设憩室病中瘘管的形成表现出如此广泛的可变解剖特征,以至于它可能被认为是该疾病的一种独特形式,即瘘管性憩室炎(FD)。
我们基于50年的出版物进行了一项叙述性综述,涵盖了广泛的与憩室炎相关的瘘管,包括常见的和不常见的。
虽然有大量关于常见瘘管的文献,如结肠膀胱瘘和结肠阴道瘘,但对于较罕见的瘘管,如结肠小肠瘘、结肠皮肤瘘和泌尿生殖道瘘,了解甚少。这些瘘管大多通过手术治疗,这与急性或慢性憩室炎中占主导地位的保守治疗趋势形成对比。
流行病学和组织学证据支持FD可能是慢性DD的一种特征,需要个体化管理这一假设。组织病理学显示与克罗恩病有相似之处。尚不清楚哪些潜在的免疫或遗传因素可能影响这些患者的临床表现并导致瘘管形成。我们认为有足够的已发表证据来描述一种独特的FD表型,它可能累及整个胃肠道和其他器官。可能需要修改手术指南来治疗这个规模虽小但很重要的群体,他们主要需要手术治疗。