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Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association.

Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Research Abstract Details 

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  • Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Abstract Text:

    takuro ohnoTakuro Ohno,jun muneuchiJun Muneuchi,kenji iharaKenji Ihara,tetsuji yugeTetsuji Yuge,yoshiaki kanayaYoshiaki Kanaya,shigeo yamakiShigeo Yamaki,toshiro haraToshiro Hara,takuro ohnoTakuro Ohno,jun muneuchiJun Muneuchi,kenji iharaKenji Ihara,tetsuji yugeTetsuji Yuge,yoshiaki kanayaYoshiaki Kanaya,shigeo yamakiShigeo Yamaki,toshiro haraToshiro Hara,

    BACKGROUND. Pulmonary arterial hypertension has been reported to be observed in association with acquired portal hypertension. However, the contribution of congenital anomalies occurring in the portal system to the development of pulmonary arterial hypertension remains to be elucidated. METHODS. Nine patients with congenital portosystemic venous shunt were studied from January 1990 through September 2005. RESULTS. Patent ductus venosus was detected in 5 patients, including 3 patients with an absence of the portal vein. The presence of either a gastrorenal or splenorenal shunt was evident in another 4 patients. Six patients had a history of hypergalactosemia with normal enzyme activities, as seen during neonatal screening. Six (66.7%) of the 9 patients were identified to have clinically significant pulmonary arterial hypertension (mean pulmonary artery pressure: 34-79 mm Hg; pulmonary vascular resistances: 5.12-38.07 U). The median age at the onset of pulmonary arterial hypertension was 12 years and 3 months. Histologic studies of lung specimens, which were available in 4 of the 9 patients with congenital portosystemic venous shunt, showed small arterial microthrombotic lesions in 3 patients. This characteristic finding was recognized even in the congenital portosystemic venous shunt patients without PAH. CONCLUSIONS. This study demonstrated thromboembolic pulmonary arterial hypertension to be a crucial complication in congenital portosystemic venous shunt, and this pathologic state may be latently present in patients with pulmonary arterial hypertension of unknown etiology.

    Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Publishing Authors By Initials

    t ohnoT Ohno,j muneuchiJ Muneuchi,k iharaK Ihara,t yugeT Yuge,y kanayaY Kanaya,s yamakiS Yamaki,t haraT Hara,t ohnoT Ohno,j muneuchiJ Muneuchi,k iharaK Ihara,t yugeT Yuge,y kanayaY Kanaya,s yamakiS Yamaki,t haraT Hara,

    For similar abstracts research abstracts see: abstracts research

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    Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Pediatrics

    VOLUME: 121

    Page Numbers: e892-9

    Journal Abbreviation: Pediatrics

    ISSN: 1098-4275

    DAY: 24

    MONTH: 03

    YEAR: 2008

    Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Information

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    LANGUAGE: eng

    NlmUniqueID: 376422

    Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association. Keywords Mesh Terms:

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    Grant and Affiliation Information for Pulmonary hypertension in patients with congenital portosystemic venous shunt: a previously unrecognized association.

    AFFILIATION: Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan. k-ihara@pediatr.med.kyushu-u.ac.jp.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Pediatrics

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