scholarly journals Rare case of combined factor V and factor X deficiency in pregnancy: presenting as secondary postpartum haemorrhage in first pregnancy and successful outcome in second pregnancy

2013 ◽  
Vol 6 (3) ◽  
pp. 134-135
Author(s):  
Aniket Kakade ◽  
Tushar Panchanadikar ◽  
Yashwant Kulkarni
Author(s):  
Shilpa Venkatesh ◽  
Cecil Ross ◽  
Vani Ramkumar

2015 ◽  
Vol 2 (4) ◽  
Author(s):  
Kaivan Vaidya ◽  
Clare Arnott ◽  
Amber Biscoe ◽  
Simon Eggleton ◽  
Timothy Brighton

2008 ◽  
Vol 25 (3) ◽  
pp. 189-192 ◽  
Author(s):  
Giuseppe Chiossi ◽  
Joel Spero ◽  
Emmanuel Esaka ◽  
Kristin Novic ◽  
Jennifer Celebrezze ◽  
...  

Haemophilia ◽  
2004 ◽  
Vol 10 (5) ◽  
pp. 665-668 ◽  
Author(s):  
C. Romagnolo ◽  
S. Burati ◽  
S. Ciaffoni ◽  
E. Fattori ◽  
M. Franchi ◽  
...  

2018 ◽  
Vol 5 (4) ◽  
pp. 28
Author(s):  
Fadime Ersoy Dursun ◽  
Erdal Akyar ◽  
Gokhan Uygun ◽  
Zafer Baslar ◽  
Bengu Cobanoglu

Introduction: Isolated and combined factor deficiencies are known to occur in systemic primary amyloidosis. The most common factor deficiency known in these cases is isolated factor X deficiency. Other factor deficiencies are relatively less frequent. Isolated factor VII deficiency occurs very rarely in cases of systemic primary amyloidosis.Case report: A 58-year-old male patient previously presenting to another health center with complaints of generalized edema, fatigue, and itching had proteinuria and then he was diagnosed with systemic primary amyloidosis after the renal biopsy for proteinuria etiology. The patient’s laboratory tests showed prolongation of prothrombin time and factor VII deficiency. The patient responded well to the treatment for primary amyloidosis and factor VII deficiency.Discussion: In cases of systemic primary amyloidosis, if the etiology of prolonged prothrombin time involves no liver disease, warfarin use, or malabsorption, physicians should always keep in mind rare factor deficiencies such as factor VII deficiency, along with common factor deficiencies.


2021 ◽  
Vol 2021 ◽  
pp. 1-3
Author(s):  
Ayrton Bangolo ◽  
Trupti Waykole ◽  
Bilal Niazi ◽  
Chandini Sajja ◽  
Mahabuba Akhter ◽  
...  

Factor X deficiency is a rare coagulopathy that can be inherited or acquired. Acquired factor X deficiency has been associated with plasma cell dyscrasias, amyloids, and use of vitamin K antagonists. Of plasma cell dyscrasias, most cases in the literature have been associated with multiple myeloma with or without concomitant AL amyloidosis. Here, we present a rare case of acquired isolated factor X deficiency in an elderly patient with immunoglobulin A (Ig A) monoclonal gammopathy of undetermined significance (MGUS). Herein, we highlight a rare cause of acquired factor X deficiency, and we hope to contribute to the growing literature of plasma cell dyscrasias associated with factor X deficiency.


2018 ◽  
Vol 9 (2) ◽  
pp. 72
Author(s):  
PrakasKumar Mandal ◽  
Debraj Basu ◽  
Mostafa Kamal

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