Literature DB >> 23214340

A case of severe ADAMTS13 deficiency presenting as thrombotic thrombocytopenic purpura in pregnancy.

Marinos Nikolaou1, Marina Karakantza, George Adonakis, George Theodorou, Nikolaos Zoumbos, George Decavalas.   

Abstract

INTRODUCTION: Thrombotic thrombocytopenic purpura is a rare life-threatening disorder characterized by thrombocytopenia and microangiopathic hemolytic anemia. It is caused by the absent or severe deficiency of the von Willebrand Factor-cleaving protease named ADAMTS13. Pregnancy is a well recognized factor precipitating the appearance of the disease both in women that had reduced levels of ADAMTS13 activity prior to gestation and in those with other inherited or acquired thrombophilic syndromes. CASE REPORT: We report a 25-year old woman with severe ADAMTS13 deficiency presented early in her 1st pregnancy and relapsed in two subsequent gestations. This presentation is uncommon for thrombotic thrombocytopenic purpura is associated with pregnancy (ADAMTS13 deficiency < 5%, without an inhibitor). In the first pregnancy she started with daily plasma exchange 1.5 x volume, corticosteroids and IV immunoglobulin and finally entered remission after 23 sessions and termination of pregnancy. In the second pregnancy she did not receive prophylactic treatment and relapsed in the 3rd trimester. Prophylactic treatment during the third pregnancy with plasma infusions proved also ineffective to prevent relapse. DISCUSSION: Many issues regarding treatment and prevention of thrombotic thrombocytopenic purpura relapses in subsequent pregnancies are unclear. Proposed guidelines recommend that the same treatment should be performed on pregnant and non pregnant patients without modification of plasma replacement dose according to ADAMTS13 levels. In addition, many authors suggest that pregnant patients with history of thrombotic thrombocytopenic purpura and severe deficiency of ADAMTS13 levels should received prophylactic treatment for prevention of relapses in the subsequent pregnancies.
CONCLUSION: Severe ADAMTS 13 deficiency may present as thrombotic thrombocytopenic purpura of pregnancy. Pregnant women with thrombotic thrombocytopenic purpura and especially with severe deficiency of ADAMTS13 levels require specific consideration regarding treatment and prophylaxis in subsequent pregnancies.

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Year:  2012        PMID: 23214340     DOI: 10.2298/mpns1210436n

Source DB:  PubMed          Journal:  Med Pregl        ISSN: 0025-8105


  4 in total

Review 1.  A new biological marker candidate in female reproductive system diseases: Matrix metalloproteinase with thrombospondin motifs (ADAMTS).

Authors:  Kadir Demircan; İsmail Cömertoğlu; Sümeyya Akyol; Beyza Nur Yiğitoğlu; Esma Sarıkaya
Journal:  J Turk Ger Gynecol Assoc       Date:  2014-12-01

2.  Maternal and fetal outcomes of pregnancy occurring after a diagnosis of immune-mediated thrombotic thrombocytopenic purpura.

Authors:  Jenna Brown; Bindu Potugari; Marshall A Mazepa; Ruhail Kohli; Alison R Moliterno; Robert A Brodsky; Jason A Vaught; Richard Burwick; Shruti Chaturvedi
Journal:  Ann Hematol       Date:  2022-08-06       Impact factor: 4.030

3.  Unfavorable course in pregnancy-associated thrombotic thrombocytopenic purpura necessitating a perimortem Cesarean section: a case report.

Authors:  Ernesto González-Mesa; Isidoro Narbona; Marta Blasco; Isaac Cohen
Journal:  J Med Case Rep       Date:  2013-04-29

4.  A Race against the Clock: A Case Report and Literature Review Concerning the Importance of ADAMTS13 Testing in Diagnosis and Management of Thrombotic Thrombocytopenic Purpura during Pregnancy.

Authors:  Melinda Ildiko Mitranovici; Lucian Pușcașiu; Ioan Emilian Oală; Izabella Petre; Marius Lucian Craina; Antonia Rebeka Mager; Kinga Vasile; Diana Maria Chiorean; Adrian-Horațiu Sabău; Sabin Gligore Turdean; Ovidiu Simion Cotoi
Journal:  Diagnostics (Basel)       Date:  2022-06-27
  4 in total

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