Mirande Mitchell H, Souza Dante L S, Thibodeaux Louis, Sutphin Cody
Department of Surgery, TriHealth, Good Samaritan Hospital, Cincinnati, OH, USA.
Department of Surgery, TriHealth, Bethesda North Hospital, Cincinnati, OH, USA.
Surg Case Rep. 2024 Jun 3;10(1):136. doi: 10.1186/s40792-024-01920-y.
A splenic artery pseudoaneurysm is a rare pathology that occurs mainly secondary to pancreatitis, abdominal trauma, peptic ulcers, pancreatic and gastric cancers, and infections. It is best diagnosed using computed tomography angiography and typically treated using endovascular embolization and, in some cases, open or laparoscopic surgery. In this report, we present a case of a ruptured mycotic splenic artery pseudoaneurysm containing Histoplasma capsulatum, which to our knowledge is the first case to report a mycotic splenic artery pseudoaneurysm of this nature.
We report a case of a 42-year-old white male with past medical history of Hepatitis C and IV drug abuse who presented to the Emergency Department with a 24-h history of severe diffuse abdominal pain. He was tachycardic and peritonitic on exam. Work-up demonstrated leukocytosis and lactic acidosis. Computed tomography of the abdomen and pelvis with intravenous contrast showed hemoperitoneum and active extravasation of contrast from the splenic artery into the splenic hilum, associated with a surrounding hematoma measuring 5.3 × 5.0 cm, concerning for ruptured splenic artery pseudoaneurysm. The patient was taken emergently for exploratory laparotomy, where a large intraperitoneal hematoma was evacuated. A ruptured splenic artery pseudoaneurysm was identified, isolated, and controlled, followed by completion splenectomy. Final pathology demonstrated a 3.0 × 1.3 × 0.3 cm pseudoaneurysm wall and a 14 × 9.5 × 5.5 cm spleen containing multiple necrotizing granulomata positive for the presence of Histoplasmosis species. The patient recovered appropriately and was discharged on post-operative day five.
This case demonstrates a successful approach to a ruptured mycotic splenic artery pseudoaneurysm resulting in a positive outcome. It is a unique case as it highlights, to our knowledge, the first report of splenic artery aneurysm secondary to Histoplasma capsulatum infection. This report helps further the understanding of the pathophysiology as well as the natural history of mycotic splenic pseudoaneurysms.
脾动脉假性动脉瘤是一种罕见的病变,主要继发于胰腺炎、腹部创伤、消化性溃疡、胰腺癌和胃癌以及感染。最佳诊断方法是计算机断层血管造影,通常采用血管内栓塞治疗,在某些情况下采用开放手术或腹腔镜手术。在本报告中,我们介绍了一例破裂的霉菌性脾动脉假性动脉瘤病例,瘤体中含有荚膜组织胞浆菌,据我们所知,这是首例报告的此类霉菌性脾动脉假性动脉瘤病例。
我们报告一例42岁的白人男性,有丙型肝炎和静脉药物滥用病史,因严重弥漫性腹痛24小时就诊于急诊科。检查发现他心动过速且有腹膜炎体征。检查显示白细胞增多和乳酸酸中毒。腹部和盆腔增强计算机断层扫描显示腹腔积血以及造影剂从脾动脉向脾门的活动性外渗,伴有一个5.3×5.0厘米的周围血肿,提示脾动脉假性动脉瘤破裂。患者紧急接受剖腹探查术,术中清除了大量腹腔内血肿。发现并分离出破裂的脾动脉假性动脉瘤并进行控制,随后完成脾切除术。最终病理显示有一个3.0×1.3×0.3厘米的假性动脉瘤壁,以及一个14×9.5×5.5厘米的脾脏,其中含有多个坏死性肉芽肿,荚膜组织胞浆菌检测呈阳性。患者恢复良好,术后第五天出院。
本病例展示了一种成功处理破裂霉菌性脾动脉假性动脉瘤并取得良好结果的方法。据我们所知,这是一例独特的病例,它首次报告了荚膜组织胞浆菌感染继发的脾动脉动脉瘤。本报告有助于进一步了解霉菌性脾假性动脉瘤的病理生理学以及自然病程。