Literature DB >> 15503485

A case of patent ductus venosus with pulmonary arterio-venous fistula as a rare and unique clinical entity.

Ilker Büyükyavuz1, Saniye Ekinci, Mithat Haliloğlu, M Emin Senocak, Arbay O Ciftçi.   

Abstract

A 13-year-old boy presenting with digital and lip cyanosis, easy fatigability, and weight gain was diagnosed to have an intrapulmonary arterio-venous fistula. During his routine follow-up examinations, there was fullness on right upper quadrant of his abdomen. Abdominal ultrasonography (USG) showed a mass in portal hilus. We planned abdominal computed (CT) to gain tomography detailed information about the mass. Surprisingly abdominal CT and the color-Doppler sonography showed that the structure mimicking a mass was patent ductus venosus (PDV). We report PDV with intrapulmonary arterio-venous fistula as a unique and rare clinical entity. In addition, we underline the misdiagnosis of portal mass instead of patent ductus venosus. If there is a portal mass in USG or CT, color-Doppler sonography or, if needed, other diagnostic methods should be used to exclude PDV.

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Year:  2004        PMID: 15503485

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  1 in total

Review 1.  Insight into congenital absence of the portal vein: is it rare?

Authors:  Guo-Hua Hu; Lai-Gen Shen; Jin Yang; Jin-Hua Mei; Yue-Feng Zhu
Journal:  World J Gastroenterol       Date:  2008-10-21       Impact factor: 5.742

  1 in total

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