central venous thrombosis
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2021 ◽  
Vol 3 (14) ◽  
pp. 1576-1578
Author(s):  
Andrés Obeso ◽  
Laura Romero Vázquez ◽  
Jorge Fernández Noya

2021 ◽  
Vol 2021 ◽  
pp. 1-5
Author(s):  
Erdem Gönüllü ◽  
Nesrin Özkan ◽  
Ahmet Soysal ◽  
Engin Acıoğlu ◽  
Emine Betül Tavil ◽  
...  

Implementation of the Haemophilus influenzae type B (Hib) conjugate vaccine brought about a reduction in the number of cases and morbidity from type B but an increase in nontypeable strain infections. Nontypeable Haemophilus influenzae (NTHi) commonly colonizes children’s upper respiratory tract and causes otitis media, sinusitis, and bronchitis. Invasive NTHi diseases, such as meningitis and septicemia, have rarely been reported. Herein, we discuss a previously healthy, fully immunized 3-year-old girl presented with otitis media and mastoiditis leading to meningitis caused by NTHi complicated with central venous thrombosis. She was treated with antibiotics, mastoidectomy and ventilation tube insertion, and anticoagulation therapy and recovered uneventfully. Through this case, we wish to share our unique clinical experience that NTHi should be born in mind as a potential pathogen that can cause meningitis in previously healthy children, which may be helpful in future cases.


Author(s):  
Adriana Watts Soares ◽  
Maria Maia ◽  
João Espirito Santo ◽  
Ana Palricas Costa ◽  
Artur Pereira ◽  
...  

The authors present the case of a 27-year-old patient who suffered from spontaneous bleeding during infancy and from a severe and central venous thrombosis in adult years. The patient underwent a thorough laboratory work-up on both occasions and was diagnosed with hypofibrinogenaemia as well as protein S deficiency, 2 diseases that contrast in their intrinsic bleeding/thrombotic risk. The patient´s high-risk pregnancy was carried out up to a successful full-term eutocic delivery which required fibrinogen concentrate to reduce life-threatening bleeding. The patient´s child was also diagnosed with hypofibrinogenaemia, later on confirmed with the pathogenic mutation Fibrinogen Marseilles II. This case was used to conduct a literature review of congenital fibrinogen disorders, rare entities that require more awareness for early diagnosis and accurate management.


2019 ◽  
Vol 28 (1) ◽  
pp. 43-47
Author(s):  
Kemal Magden ◽  
◽  
Bilal Toka ◽  
Ibrahim Yildirim ◽  
Gursel Yildiz ◽  
...  

2018 ◽  
Vol 14 (3) ◽  
pp. 214
Author(s):  
Adam M. Gwozdz ◽  
Justinas Silickas ◽  
Alberto Smith ◽  
Prakash Saha ◽  
Stephen A. Black

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