Munuswamy Nivetha, Kumar Pola Govardhan, Shanmugasundaram Rajendran, Venkatesh Sreedevi B
Department of General Surgery, Sree Balaji Medical College and Hospital, Chennai, India.
Department of Surgical Gastroenterology, Sree Balaji Medical College and Hospital, Chennai, India.
Iran J Med Sci. 2025 Feb 1;50(2):124-128. doi: 10.30476/ijms.2024.104038.3751. eCollection 2025 Feb.
Gastrointestinal stromal tumors (GIST) are less prevalent mesenchymal tumors, accounting for 1% of gastrointestinal malignancies. Spontaneous hemoperitoneum (SH) following gastric GIST rupture is a rare occurrence. The present study described a case of a 67-year-old female who presented with acute onset abdominal pain. Vital signs at the time of presentation were unstable. Contrast-enhanced computed tomography (CECT) of the abdomen revealed a mixed-density mass lesion with multiple hyperdense areas within. A hemogram indicated a low hemoglobin level. An emergency laparotomy revealed a ruptured pedunculated, friable mass with active bleeding arising from the lesser curvature of the stomach. A wedge resection was carried out to achieve a gross negative margin of the mass. Final pathology confirmed GIST epitheloid type with positive margins (pT3N0M0-pathologically tumor size within 10 cm with no nodal or distant metastasis) and positive for CD117, DOG1. Given the tumor rupture and positive margins, the patient was started on imatinib mesylate therapy. As demonstrated in this case, GIST rarely ruptures, resulting in hemoperitoneum. The primary treatment approach is surgical exploration and resection.
胃肠道间质瘤(GIST)是一种较为少见的间叶组织肿瘤,占胃肠道恶性肿瘤的1%。胃GIST破裂后自发性血腹(SH)是一种罕见的情况。本研究描述了一例67岁女性患者,该患者突发腹痛。就诊时生命体征不稳定。腹部增强计算机断层扫描(CECT)显示一个混合密度肿块病变,内部有多个高密度区域。血常规显示血红蛋白水平较低。急诊剖腹探查发现一个带蒂的、易碎的肿块破裂,胃小弯处有活动性出血。进行了楔形切除术,以实现肿块的大体阴性切缘。最终病理证实为上皮样型GIST,切缘阳性(pT3N0M0 - 病理上肿瘤大小在10 cm以内,无淋巴结或远处转移),CD117、DOG1阳性。鉴于肿瘤破裂且切缘阳性,患者开始接受甲磺酸伊马替尼治疗。如本病例所示,GIST很少破裂导致血腹。主要的治疗方法是手术探查和切除。