The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying Hypothesis

We report a 54-year-old patient with the association of hepatic dysfunction with cyanosis, severe hypoxemia, platypnea-orthodeoxia, diffuse cutaneous spider nevi, telangiectasia, palmar erythema, digital clubbing and findings of marked intrapulmonary vascular dilation and arterovenous shunt. The dia...

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Main Authors: Enrico Capodicasa, Federica De Bellis, Christopher Muscat
Format: Article
Language:English
Published: Karger Publishers 2010-08-01
Series:Case Reports in Gastroenterology
Subjects:
Online Access:http://www.karger.com/Article/FullText/319502
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spelling doaj-c825aecef90c4a71a36158067ede48032020-11-25T01:10:59ZengKarger PublishersCase Reports in Gastroenterology1662-06312010-08-014227327810.1159/000319502319502The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying HypothesisEnrico CapodicasaFederica De BellisChristopher MuscatWe report a 54-year-old patient with the association of hepatic dysfunction with cyanosis, severe hypoxemia, platypnea-orthodeoxia, diffuse cutaneous spider nevi, telangiectasia, palmar erythema, digital clubbing and findings of marked intrapulmonary vascular dilation and arterovenous shunt. The diagnosis of hepato-pulmonary-cutaneous syndrome, a term we think more appropriate and inclusive than that of hepato-pulmonary syndrome for this clinicopathological picture, is proposed. The putative underlying mechanism for these connected pulmonary and extrapulmonary syndromic features is discussed.http://www.karger.com/Article/FullText/319502HypoxemiaIntrapulmonary vascular dilationArterovenous shuntPlatypnea-orthodeoxiaCutaneous spider neviTelangiectasiaDigital clubbingPalmar erythema
collection DOAJ
language English
format Article
sources DOAJ
author Enrico Capodicasa
Federica De Bellis
Christopher Muscat
spellingShingle Enrico Capodicasa
Federica De Bellis
Christopher Muscat
The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying Hypothesis
Case Reports in Gastroenterology
Hypoxemia
Intrapulmonary vascular dilation
Arterovenous shunt
Platypnea-orthodeoxia
Cutaneous spider nevi
Telangiectasia
Digital clubbing
Palmar erythema
author_facet Enrico Capodicasa
Federica De Bellis
Christopher Muscat
author_sort Enrico Capodicasa
title The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying Hypothesis
title_short The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying Hypothesis
title_full The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying Hypothesis
title_fullStr The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying Hypothesis
title_full_unstemmed The Hepato-Pulmonary-Cutaneous Syndrome: Description of a Case and Suggestion of a Unifying Hypothesis
title_sort hepato-pulmonary-cutaneous syndrome: description of a case and suggestion of a unifying hypothesis
publisher Karger Publishers
series Case Reports in Gastroenterology
issn 1662-0631
publishDate 2010-08-01
description We report a 54-year-old patient with the association of hepatic dysfunction with cyanosis, severe hypoxemia, platypnea-orthodeoxia, diffuse cutaneous spider nevi, telangiectasia, palmar erythema, digital clubbing and findings of marked intrapulmonary vascular dilation and arterovenous shunt. The diagnosis of hepato-pulmonary-cutaneous syndrome, a term we think more appropriate and inclusive than that of hepato-pulmonary syndrome for this clinicopathological picture, is proposed. The putative underlying mechanism for these connected pulmonary and extrapulmonary syndromic features is discussed.
topic Hypoxemia
Intrapulmonary vascular dilation
Arterovenous shunt
Platypnea-orthodeoxia
Cutaneous spider nevi
Telangiectasia
Digital clubbing
Palmar erythema
url http://www.karger.com/Article/FullText/319502
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