Giant sigmoid colon diverticulum incarcerated in an inguinal hernia

Artúr Seli, Géza Telek, Edit Babarczi, Tibor Rudisch, Balázs Virág, Fanni Fülöp, József Sándor, Ferenc Ender
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Abstract

Introduction: The diverticulosis of the sigmoid colon may be congenital or acquired. The Giant Colonic Diverticulum (GCD), defined as a diverticulum larger than 4 cm, is a rare, but clinically important entity. The McNutt (1988) classification is used differentiate the three subgroups of giant diverticula. Type 1 diverticula are pulsion pseudo-diverticula, which enlarge gradually. Type 2 are inflammatory diverticula due to a previous subserosal perforation, where the abscess cavity is communicating with the bowel lumen and its wall would be gradually composed of fibrous scar tissue, lacking the intestinal histological layers. Type 3 are the real, congenital diverticula of the colon, containing all layers of the intestinal wall. We present a case of a 59-year-old male patient, who was admitted to our Dept. of Surgery in emergency with the diagnosis of strangulated left inguinal hernia. Abdominal CT demonstrated the herniation of the sigmoid colon into the hernia sac without the signs of bowel obstruction. The patient was operated on urgently; subsequent to a left inguinal incision, a Type 3 giant diverticulum of the sigmoid colon was found in the hernia sac. Laparotomy was performed, and the unusually large, 7-8 cm long strangulated diverticulum was liberated. There were no other pathological findings, the sigmoid colon was not damaged. The diverticulum was resected with a TA stapler, and the staple line was inverted with a layer of seromuscular sutures. The inguinal hernia orifices were reconstructed both intraabdominally and externally. The postoperative course was uneventful, the patient was discharged on the 7th day. The recommendations concerning the diagnosis and treatment GCD are briefly reviewed. Due to the McNutt Type 3 characteristics, we opted for the less invasive, simple diverticulectomy instead of sigmoid resection (Hartmann’s procedure). Our case was an extremely rare complication of the already uncommon GCD, resolved by an unusual surgical intervention leading to a successful cure.

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巨大乙状结肠憩室嵌顿于腹股沟疝
乙状结肠憩室病可能是先天性的,也可能是后天的。巨结肠憩室(GCD),定义为大于4cm的憩室,是一种罕见但临床上重要的疾病。McNutt(1988)分类法用于区分巨憩室的三个亚群。1型憩室为渐大的斥力性伪憩室。2型为炎性憩室,由于先前的浆膜下穿孔,其中脓肿腔与肠腔相通,其壁逐渐由纤维瘢痕组织组成,缺乏肠组织层。3型是真正的先天性结肠憩室,包含肠壁的所有层。我们报告一个59岁的男性病人,他在急诊中被诊断为绞窄性左腹股沟疝而进入我们的外科。腹部CT显示乙状结肠疝入疝囊,无肠梗阻征象。病人接受了紧急手术;左腹股沟切口后,在疝囊内发现乙状结肠3型巨大憩室。开腹手术,释放异常大的7- 8cm长的绞窄憩室。无其他病理表现,乙状结肠未见损伤。憩室用TA订书机切除,订书机线用一层血清肌缝合线反转。腹股沟疝口在腹内和腹外重建。术后过程顺利,患者于第7天出院。本文简要回顾了有关GCD诊断和治疗的建议。由于McNutt 3型的特点,我们选择了微创、简单的憩室切除术,而不是乙状结肠切除术(Hartmann手术)。我们的病例是一个非常罕见的并发症已经不常见的GCD,解决了一个不寻常的手术干预导致成功治愈。
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