A Rare Case of Recurrent Pylephlebitis Secondary to Diverticulitis
Recommended Citation
Desai PA, Gordon SC, Jafri S. A Rare Case of Recurrent Pylephlebitis Secondary to Diverticulitis. Am J Gastroenterol 2023; 118(10):S2369-S2370.
Document Type
Conference Proceeding
Publication Date
10-25-2023
Publication Title
Am J Gastroenterol
Abstract
Introduction: Pylephlebitis is the thrombosis of the portal vein usually following an intra-abdominal infection. We present a patient with a history of diverticulitis who presented with acute pylephlebitis. Case Description/Methods: A 77-year-old woman with a history of Parkinson’s disease and polymyalgia rheumatica presented to the emergency department (ED) with acute-onset abdominal pain, nausea, and hematochezia with leukocytosis (WBC, 12.5 K/uL). Computed tomography scan (CT) showed diverticulitis of the distal descending colon and sigmoid colon, with extensive diverticulosis. She was discharged on oral ciprofloxacin and metronidazole. She returned to the ED 2.5 years later with dizziness, fever/chills, and nausea. Labs revealed WBC of 20.5 K/uL. CT showed portal vein thrombosis (PVT) supplying the right hepatic lobe segments 6 and 7. Blood cultures were negative and she was discharged, but one week later, she returned to the ED with continued fever/chills, negative blood cultures, and WBC was now 29.9 K/uL. Magnetic resonance imaging (MRI) revealed a bland portal vein thrombus vs pylephlebitis within the right portal vein extending into anterior and posterior branches, with associated perfusional alterations. Treatment consisted of 3 months of apixaban therapy and 4 weeks of parenteral ertapenem. A CT scan 1 month after her most recent ED visit showed persistent occlusive thrombus throughout the posterior right portal vein and distal right anterior portal vein. Patient was transitioned to a 1-week oral amoxicillin/clavulanate antibiotic therapy and continued her lifetime apixaban therapy. The patient’s symptoms of fever/chills, abdominal pain, and nausea were resolved 2 weeks after initial PVT diagnosis, with leukocytosis resolving 1 month after initial diagnosis (WBC 8.4 K/uL). CT 4 months after PVT onset showed no liver abnormalities, and CT 6 months after onset indicated portal veins were patent. Discussion: Pylephlebitis may present with abdominal pain and fever, and is diagnosed with CT, MRI, or ultrasound imaging. It is more likely to occur secondary to liver disease, hypercoagulative disorders, or recurrent abdominal infection as with this case. In the absence of underlying liver disease or more recent infections, we speculate that the patient’s initial diverticulitis/diverticulosis precipitated her subsequent pylephlebitis. Anticoagulation therapy is normally recommended, occasionally with surgery depending upon the severity of the thrombosis.
Volume
118
Issue
10
First Page
S2369
Last Page
S2370