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A case of incomplete duplication of the portal vein associated with multiple congenital anomalies.
Ichikawa, Tamaki; Matsumoto, Shunro; Nomura, Takakiyo; Yamamuro, Hiroshi; Tsuruya, Kota; Kawaga, Tatehiro; Yamamoto, Seiichiro; Hashimoto, Jun.
Afiliação
  • Ichikawa T; Department of Radiology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 159-1193, Japan.
  • Matsumoto S; Department of Radiology, Oita City Medical Association's Almeida Hospital, Oita, Japan.
  • Nomura T; Department of Radiology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 159-1193, Japan.
  • Yamamuro H; Department of Radiology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 159-1193, Japan.
  • Tsuruya K; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Kawaga T; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Yamamoto S; Department of Gastroenterological Surgery, Tokai University School of Medicine, Isehara, Kanagawa, Japan.
  • Hashimoto J; Department of Radiology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 159-1193, Japan.
Radiol Case Rep ; 18(8): 2785-2789, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37388262
ABSTRACT
Double portal veins are a duplication of the portal vein and normal portal vein with an accessory portal vein. We report a case of a 63-year-old asymptomatic female with double portal veins. There was fat accumulation observed in the area which was supplied by the first portal vein in normal position, and fatty sparing of the liver was observed in the area which was supplied by the second portal vein in the preduodenal position. The 2 portal veins were equal in size. Furthermore, the patient presented with multiple congenital anomalies, including double inferior vena cava, splenic lobulation, and accessory liver lobe. Therefore, double portal veins in our case were thought to be an incomplete duplication of the portal vein with multiple congenital anomalies.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article