Portal vein aneurysm with complete spontaneous regression after 10 years using conservative treatment
Autor: | Kenichiro Takase, Masayasu Aikawa, Kojun Okamoto, Isamu Koyama, Yukihiro Watanabe, Katsuya Okada |
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Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
Portal vein Conservative Treatment Asymptomatic 03 medical and health sciences 0302 clinical medicine Aneurysm Internal medicine medicine Humans Aged Ultrasonography Portal Vein business.industry Gastroenterology General Medicine Hepatology medicine.disease Colorectal surgery Liver 030220 oncology & carcinogenesis cardiovascular system Etiology Female 030211 gastroenterology & hepatology Radiology medicine.symptom business Abdominal surgery Rare disease |
Zdroj: | Clinical Journal of Gastroenterology. 13:940-945 |
ISSN: | 1865-7265 1865-7257 |
DOI: | 10.1007/s12328-020-01131-6 |
Popis: | Portal vein aneurysms are rare vascular findings for which there are no optimal treatment guidelines. The scarce knowledge about their etiology, natural history, and management mean that there are limited treatment options. Here, we describe the case of a 69-year-old woman who presented with a 35-mm hypoechoic area in the hilar region of the liver that was accidentally detected by ultrasonography. Color Doppler ultrasonography demonstrated a mass with internal flow contiguous with portal vein, which was confirmed to be a portal vein aneurysm by computed tomography. Given that she experienced no symptoms of impending rupture or thrombosed aneurysms, we adopted a conservative treatment. Follow-up imaging demonstrated slow progression of the aneurysm diameter, from 35 to 43 mm at 3 years, and to 48 mm at 6 years; subsequent imaging after 6 years did not show any change in the diameter from 48 mm. However, the portal vein aneurysm completely regressed with no complications at a follow-up of over 10 years. This case suggests that long-term observation with periodic imaging may be an acceptable therapeutic option for asymptomatic portal vein aneurysms that show no short-term improvement. This case report contributes to a better understanding of how to treat this rare disease. |
Databáze: | OpenAIRE |
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