Makthala Sripooja, Bains Lovenish, Lal Pawan, Bhukya Kranthi Naik
Department of Surgery, Maulana Azad Medical College, New Delhi, India.
J Med Case Rep. 2025 Aug 8;19(1):397. doi: 10.1186/s13256-025-05479-6.
Vascular complications such as hepatic vein and inferior vena cava thrombus, phlebitis, and extrahepatic biliary obstruction are rare in amebic liver abscesses. Many pathophysiological mechanisms are proposed, but the exact pathogenesis is still not known. These complications are believed to be multifactorial, with local and systemic factors acting synergistically. Here, we present a case of amebic abscess rupture into the inferior vena cava, with a thrombus extending up to the right atrium and pulmonary thromboembolism treated successfully.
A 45-year-old Indian male presented with multiple episodes of fever with chills, palpitations, dyspnea, right upper abdominal pain, bilateral lower limb edema, and petechia for 20 days. On examination, tachycardia, tender hepatomegaly, and reduced air entry in the right lower lobe of the lung were observed. Ultrasound revealed an abscess in the left lobe of the liver about 150 cc in volume, abutting the inferior vena cava with rupture into it. Contrast-enhanced computed tomography imaging showed 5.7 × 6.2 × 5.4 cm segment IV A liver abscess with capsule breach into the intrahepatic vena cava and thrombus extending up to the right atrium was observed. Computed tomography-pulmonary angiography revealed a right atrium thrombus with bilateral pulmonary artery thrombus and parenchymal infarcts. Raised D-dimer, protein C and S deficiency was observed. The patient was managed by needle aspiration of abscess, anticoagulation, and antibiotics.
Vascular complications need a high index of suspicion, good clinical knowledge, timely workup, and intervention. Direct rupture of an amebic liver abscess into the inferior vena cava, leading to pulmonary thromboembolism, is exceedingly rare and is not well-documented in the literature. Thorough investigation and timely intervention can successfully treat the patient.
血管并发症,如肝静脉和下腔静脉血栓形成、静脉炎及肝外胆管梗阻在阿米巴肝脓肿中较为罕见。虽然提出了许多病理生理机制,但确切的发病机制仍不清楚。这些并发症被认为是多因素的,局部和全身因素协同作用。在此,我们报告一例阿米巴脓肿破入下腔静脉,血栓延伸至右心房并成功治疗肺血栓栓塞的病例。
一名45岁印度男性,出现寒战、心悸、呼吸困难、右上腹疼痛、双下肢水肿和瘀点等多次发热症状20天。检查发现心动过速、肝脏肿大压痛,右肺下叶呼吸音减弱。超声显示肝左叶有一约150cc的脓肿,紧邻下腔静脉并破入其中。增强计算机断层扫描成像显示IV A段肝脓肿大小为5.7×6.2×5.4cm,包膜破裂进入肝内静脉,血栓延伸至右心房。计算机断层扫描肺动脉造影显示右心房血栓伴双侧肺动脉血栓及实质梗死。D-二聚体升高,蛋白C和S缺乏。患者接受脓肿穿刺抽吸、抗凝及抗生素治疗。
血管并发症需要高度怀疑、良好的临床知识、及时的检查和干预。阿米巴肝脓肿直接破入下腔静脉导致肺血栓栓塞极为罕见,文献记载较少。全面检查和及时干预可成功治疗患者。