Ben Mahmoud Ahmed, Hammami Mahdi, Atri Souhaib, Sebai Amine, Haddad Anis, Kacem Montassar
Department of General Surgery, Hopital la Rabta, Tunis, Tunisia.
Department of General Surgery, Hopital la Rabta, Tunis, Tunisia.
Int J Surg Case Rep. 2025 Apr;129:111207. doi: 10.1016/j.ijscr.2025.111207. Epub 2025 Mar 25.
Gastrointestinal stromal tumors (GISTs) are rare mesenchymal neoplasms, comprising less than 1 % of gastrointestinal tumors. Arising from interstitial cells of Cajal, GISTs are frequently found in the stomach and small intestine. Typically asymptomatic, GISTs can occasionally present as acute abdominal emergencies, including hemorrhage, obstruction, or perforation. This report presents a case of spontaneous perforation of a large ileal GIST, leading to peritonitis.
An 82-year-old man arrived at the emergency department with severe abdominal pain, fever, vomiting, and diarrhea. Physical examination showed abdominal tenderness and distension, and laboratory findings indicated elevated inflammatory markers. A computed tomography (CT) scan revealed a 15 cm mass in the lower right abdomen, with free fluid and extraluminal air suggesting perforation. Emergency laparotomy confirmed a perforated tumor, with purulent peritonitis. Surgical resection of the affected ileum and cecum was performed, followed by anastomosis and enterostomy. Histopathology confirmed a high-risk GIST, and the patient recovered well post-operatively, subsequently beginning adjuvant imatinib therapy.
GISTs commonly remain asymptomatic until complications arise. Peritonitis due to tumor perforation is rare and necessitates prompt surgical intervention. Surgical resection remains the standard treatment for localized GISTs, with adjuvant imatinib recommended for high-risk cases. CT imaging is critical for diagnosis and surgical planning.
While GIST perforation leading to peritonitis is rare, it requires urgent surgery. High-risk GIST patients benefit from adjuvant imatinib and should undergo long-term follow-up. This case highlights the importance of a multidisciplinary approach for complex GIST presentations and associated complications.
胃肠道间质瘤(GIST)是罕见的间叶性肿瘤,占胃肠道肿瘤的比例不到1%。GIST起源于 Cajal 间质细胞,常见于胃和小肠。GIST通常无症状,偶尔可表现为急性腹部急症,包括出血、梗阻或穿孔。本报告介绍了一例回肠巨大GIST自发穿孔导致腹膜炎的病例。
一名82岁男性因严重腹痛、发热、呕吐和腹泻到急诊科就诊。体格检查显示腹部压痛和腹胀,实验室检查结果显示炎症标志物升高。计算机断层扫描(CT)显示右下腹有一个15厘米的肿块,有游离液体和腔外气体提示穿孔。急诊剖腹手术证实肿瘤穿孔,伴有化脓性腹膜炎。对受累的回肠和盲肠进行了手术切除,随后进行了吻合术和肠造口术。组织病理学证实为高危GIST,患者术后恢复良好,随后开始辅助伊马替尼治疗。
GIST通常在出现并发症之前无症状。肿瘤穿孔导致的腹膜炎很少见,需要及时进行手术干预。手术切除仍然是局限性GIST的标准治疗方法,高危病例推荐辅助伊马替尼治疗。CT成像对诊断和手术规划至关重要。
虽然GIST穿孔导致腹膜炎很少见,但需要紧急手术。高危GIST患者从辅助伊马替尼治疗中获益,应进行长期随访。本病例强调了多学科方法处理复杂GIST表现及相关并发症的重要性。