继发于组织胞浆菌病的霉菌性脾动脉假性动脉瘤自发性破裂:病例报告。

IF 0.7 Q4 SURGERY Surgical Case Reports Pub Date : 2024-06-03 DOI:10.1186/s40792-024-01920-y
Mitchell H Mirande, Dante L S Souza, Louis Thibodeaux, Cody Sutphin
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引用次数: 0

摘要

背景: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。最好通过计算机断层扫描血管造影术进行诊断,通常采用血管内栓塞治疗,在某些情况下也可采用开腹或腹腔镜手术治疗。在本报告中,我们介绍了一例含有荚膜组织胞浆的霉菌性脾动脉假性动脉瘤破裂的病例,据我们所知,这是第一例报告这种性质的霉菌性脾动脉假性动脉瘤的病例:我们报告了一例既往有丙型肝炎病史和静脉吸毒史的 42 岁白人男性病例。他心动过速,腹膜炎。检查显示白细胞增多和乳酸酸中毒。腹部和盆腔静脉注射造影剂的计算机断层扫描显示腹腔积血,造影剂从脾动脉外渗至脾门,周围伴有 5.3 × 5.0 厘米的血肿,考虑为脾动脉假性动脉瘤破裂。患者被紧急送往剖腹探查手术室,腹腔内的巨大血肿被清除。确定、分离并控制了破裂的脾动脉假性动脉瘤,随后完成了脾脏切除术。最终病理结果显示,假性动脉瘤壁为 3.0 × 1.3 × 0.3 厘米,脾脏为 14 × 9.5 × 5.5 厘米,内含多个坏死性肉芽肿,组织胞浆菌阳性。患者恢复良好,术后第五天出院:本病例展示了一种成功治疗霉菌性脾动脉假性动脉瘤破裂的方法,并取得了良好的疗效。据我们所知,这是第一例继发于组织胞浆菌感染的脾动脉瘤,因此是一个独特的病例。该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和自然史。
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Spontaneous rupture of a mycotic splenic artery pseudoaneurysm secondary to histoplasmosis: a case report.

Background: 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.

Case presentation: 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.

Conclusions: 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.

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