Document Detail


Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber syndrome in the same family.
MedLine Citation:
PMID:  10895551     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The authors present the case of three patients from the same family in whom hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber syndrome was diagnosed. The disease is rare and occurs with multiple telangiectases of the skin and mucosa, and pulmonary arteriovenous fistulae. The clinical status of our patients included multiple telangiectases of the skin and mucosa, recurrent epistaxis, exertion dyspnea and cyanosis. Polycythemia and hypoxemia were observed in the blood. The clinical status and conventional radiological examination of the thoracic region, with the suspicion of arteriovenous (A-V) fistulae, pointed to HHT. A-V fistulae were confirmed by pulmonary angiography. The pulmonary A-V fistulae were operated in all three patients and diagnosis was confirmed by histopathological examination of the operated samples. Clinical improvement was observed after the operation and cyanosis, dyspnea, hypoxemia and polycythemia disappeared.
Authors:
S Kukulj; Z Ivanovi-Herceg; Z Slobodnjak
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Collegium antropologicum     Volume:  24     ISSN:  0350-6134     ISO Abbreviation:  Coll Antropol     Publication Date:  2000 Jun 
Date Detail:
Created Date:  2000-08-02     Completed Date:  2000-08-02     Revised Date:  2009-02-04    
Medline Journal Info:
Nlm Unique ID:  8003354     Medline TA:  Coll Antropol     Country:  CROATIA    
Other Details:
Languages:  eng     Pagination:  241-7     Citation Subset:  IM    
Affiliation:
Clinical Hospital for Lung Diseases, Zagreb, Croatia.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Female
Humans
Male
Telangiectasia, Hereditary Hemorrhagic / diagnosis,  genetics*

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