Literature DB >> 21311642

Successful treatment of a spontaneous haemothorax with recombinant factor VIIa in a haemophilic child with inhibitors.

D Gidaris1, M Economou, R Valeri, N Gombakis, M Athanasiou-Metaxa.   

Abstract

Haemophilia A is an X-linked disorder caused by a deficiency of factor VIII. Haemorrhage in various sites may occur spontaneously or secondary to trauma depending on the severity of the deficiency. Common manifestations include haemarthrosis, epistaxis, gastrointestinal haemorrhage and haematuria. Spontaneous haemothorax has rarely been reported both in children and adults1,2. We report the case of a haemophiliac child presenting with spontaneous haemothorax due to the rarity of this clinical presentation in order to raise the awareness among clinicians.

Entities:  

Keywords:  haemophilia; haemothorax; inhibitors; prophylaxis; recombinant factor VIIa

Year:  2010        PMID: 21311642      PMCID: PMC3031328     

Source DB:  PubMed          Journal:  Hippokratia        ISSN: 1108-4189            Impact factor:   0.471


  10 in total

1.  Spontaneous hemopneumothorax in a hemophiliac.

Authors:  J F BURKE; E W SALZMAN
Journal:  J Am Med Assoc       Date:  1959-04-04

2.  Haemothorax in children with congenital coagulopathy.

Authors:  A Obitko-Pludowska; P Laguna; A Adamowicz-Salach; M Brzewski; K S Del Campo
Journal:  Haemophilia       Date:  2010-04-07       Impact factor: 4.287

3.  [Successful treatment of hemothorax with recombinant factor VIIa in a hemophilic child with inhibitor].

Authors:  M Hulíková; P Galajda; P Kubisz
Journal:  Vnitr Lek       Date:  1998-09

4.  [Conservative treatment of hemophiliac bleeding].

Authors:  S Bulvik; M Barhum; S Burstein; I Tatarsky
Journal:  Harefuah       Date:  1990-06-01

5.  Cardiac tamponade in a patient with moderate hemophilia A and factor VIII Inhibitors.

Authors:  Nina Ghosh; Patrick Teefy; Lori Laudenbach; Georges-Etienne Rivard
Journal:  Can J Cardiol       Date:  2006-01       Impact factor: 5.223

6.  [Hemorrhagic parapneumonic effusion in a 64 year-old patient as the first symptom of hemophilia B].

Authors:  Elzbieta M Grabczak; Rafał Krenke; Magdalena Jeleńska; Iwan Komarow; Urszula Ambroziak; Adam Fangrat; Ryszarda Chazan
Journal:  Pneumonol Alergol Pol       Date:  2009

Review 7.  Prophylaxis of bleeding episodes and surgical interventions in patients with rare inherited coagulation disorders.

Authors:  Giancarlo Castaman
Journal:  Blood Transfus       Date:  2008-09       Impact factor: 3.443

8.  Feasibility of prophylaxis and immune tolerance induction regimens in haemophilic children using fully implantable central venous catheters.

Authors:  Maria Elisa Mancuso; Pier Mannuccio Mannucci; Angelo Sartori; Andrea Agliardi; Elena Santagostino
Journal:  Br J Haematol       Date:  2008-04-10       Impact factor: 6.998

Review 9.  Central venous access devices in haemophilia.

Authors:  L A Valentino; B Ewenstein; R J Navickis; M M Wilkes
Journal:  Haemophilia       Date:  2004-03       Impact factor: 4.287

Review 10.  The epidemiology of inhibitors in haemophilia A: a systematic review.

Authors:  J Wight; S Paisley
Journal:  Haemophilia       Date:  2003-07       Impact factor: 4.287

  10 in total

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