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Trauma Image and Procedure > Volume 2(1); 2017 > Article
Choi, Lee, Ma, Lee, Yu, and Lee: Traumatic Hepatic Arterioportal Fistula Caused by Penetrating Injury

Abstract

Hepatic arterioportal fistula (APF) can be congenital, acquired, or iatrogenic. Trauma-induced APF is a rare pathologic condition. We report the case of a patient with APF accompanied by hepatic ischemia that was successfully treated using angioembolization.

CASE

A 46-year-old male was stabbed in the right chest and transported to the trauma bay. The patient was alert. His initial vital signs were as follows: blood pressure, 100/60mmHg; pulse, 122 beats/min; respiratory rate, 21 breaths/min; and body temperature, 35°C. Emergency laparotomy was performed, which revealed that hepatic segment 6 was penetrated and had a 6-cm long penetrating wound. Primary suture closure and perihepatic packing of the lacerated liver were performed. One day postoperatively, the patient’s vital signs were not optimized, and a second-look operation revealed a newly developed right adrenal gland laceration and perforation of inferior vena cava (IVC). Right adrenalectomy and primary closure of IVC were performed. At 27 days after the initial operation, abdominal CT scan revealed a hepatic APF (Fig. 1.). The APF was successfully occluded by hepatic embolization (Fig. 2.). Abdominal CT repeated 6 months after the operation (Fig. 3.) revealed that the APF and ischemic lesion of the liver had disappeared.

DISCUSSION

APF can be asymptomatic but can cause complications, such as portal hypertension, which can lead to gastrointestinal bleeding, ascites, heart failure, and intestinal ischemia [1,2]. In this patient, the hepatic ischemia might have been a complication of APF. Currently, angioembolization is the treatment of choice for most APFs [1,2]. Effective treatment requires expertise in determining the location of the fistula and achieving superselective catheterization and complete occlusion of all feeding arteries. APFs should be diagnosed early because complications can be serious and spontaneous resolution is rare. An angiography can confirm the diagnosis [1,2]. The angioembolization for the APF is curative in a high percentage of patients with little morbidity.

Notes

CONFLICT OF INTEREST

No potential conflict of interest relevant to this article was reported.

Fig. 1.
Abdominal CT scan shows arterioportal venous fistula and pseudoaneurysm on POD#27. A large ischemic area is also noted.
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Fig. 2.
Hepatic arteriogram shows an arterioportal venous fistula between the right posterior hepatic artery and portal vein (A). The pseudoaneurysm between the hepatic artery and portal vein was successfully occluded by angioembolization using microcoil and glue (B).
tip-2-1-32f2.gif
Fig. 3.
Abdominal CT performed after 6 months shows disappearance of APF and the ischemic lesion of the liver.
tip-2-1-32f3.gif

REFERENCES

1. Guzman EA, McCahill LE, Rogers FB. Arterioportal fistulas: introduction of a novel classification with therapeutic implications. Journal of gastrointestinal surgery. 2006;10(4):543-50.
crossref pmid
2. Lumsden AB, Allen R, Sreeram S, Atta H, Salam A. Hepatic arterioportal fistula. The American Surgeon. 1993;59(11):722-6.
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