Literature DB >> 31344171

[Adequate diagnosis of acquired hemophilia A].

Claudia Patricia Casas Patarroyo1, Claudia Del Pilar Agudelo López2, Kenny Galvez3, Jimmy Lagos Ibarra4, Susan Martínez Rojas5, Linda Ibatá Bernal5.   

Abstract

Acquired hemophilia A (AHA) is a rare and life-threatening autoimmune hemorrhagic disorder where autoantibodies are developed against factor VIII. An early diagnosis is challenging and mandatory: an immediate hemostatic control is required to reduce morbidity and mortality. Laboratory features of AHA are: presence of autoantibodies against factor VIII, prolonged activated partial thromboplastin time (with normal prothrombin time and thrombin time) and decreased factor VIII levels. In some cases, the results of laboratory tests may be incorrect due to errors in analysis, blood extraction or manipulation of samples; also worth of consideration are limitations in the measurement range and low sensitivity of the tests. This review highlights the importance of adequate screening in patients with suspected AHA to make an adequate diagnosis and reduce overall fatal outcomes.

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Year:  2019        PMID: 31344171     DOI: 10.4067/S0034-98872019000300334

Source DB:  PubMed          Journal:  Rev Med Chil        ISSN: 0034-9887            Impact factor:   0.553


  1 in total

Review 1.  Idiopathic Acquired Hemophilia A, a Rare Cause of Bleeding: A Case Report and Literature Review.

Authors:  Carlos Andrés Regino; José C Alvarez; Leonardo Mejía Buriticá; Natalí Uribe Pulido; Valeria Torres Yepes; José D Torres
Journal:  Am J Case Rep       Date:  2021-02-17
  1 in total

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