Palpation of the right upper quadrant showed tenderness but Murph

Palpation of the right upper quadrant showed tenderness but Murphy’s sign was negative. Lab tests showed slightly increased serum CRP (53 mg/L), normal white cell count, undisturbed coagulation blood tests, and liver function remained unremarkable. Tumor markers CA 19–9 and CEA were also normal, 3 kU/L and 1.1 ug/L, respectively. A CT showed portal vein aneurysm measuring 88 × 65 mm with complete thrombosis extending to superior mesenteric (SMV) and splenic (SV) veins (Figure 1). The risk of rupture being low, we decided to treat conservatively with anticoagulation therapy. We completed our investigations with an upper GI

endoscopy and thrombophilia workup; the former did not show any esophageal varices indicating portal AZD4547 ic50 hypertension, and any coagulation disorder could be detected. The patient was released after two weeks and followed on an outpatient basis. At two months, she reported decreased pain, and a RepSox control CT demonstrated the decreasing of the thrombosis, measuring 80 × 55 mm, associated with a diminished extension to superior mesenteric and splenic veins (Figure 2). Figure 1 CT-scan showing thrombosed portal AZD5363 price vein aneurysm (white arrows) with

thrombus extending to SMV (black arrows) and splenic vein (arrowheads). Figure 2 CT-scan showing decreasing size of thrombus within portal vein aneurysm (white arrows) with diminished extension to SMV (black arrows) and SV (arrowheads). Discussion Venous aneurysms remain much less common than arterial ones. The most common location for visceral venous aneurysms is portal

system with almost 200 reported cases [3]. Notwithstanding PVA incidence has increased during the last decades, very probably due to the widened use of modern imaging techniques like MR and CT scans. Most Resveratrol frequent sites are the main portal vein and the SV-SMV confluence. The mechanisms and etiologies are not well understood but appeared to be acquired or congenital. Concerning the former, portal hypertension and chronic liver disease were identified as risk factors [8, 14]. Other causes like pancreatitis, trauma and previous surgery were described as triggers [15–17]. Nevertheless, a significant number of PVA cases did not present any underlying liver disease; and embryological mechanisms causing PVA have been mentioned. The failure of complete regression of the right vitelline vein may be responsible for a venous saccular enlargement, leading to aneurysm. In our case, the patient did not present any risk factor: no underlying liver disease, no history of pancreatitis, trauma or abdominal surgery. These elements support the congenital cause. Hence, a genetic council was achieved and our workup was enlarged.

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