scholarly journals Diagnostic Dilemma of Thrombotic Microangiopathy in Pregnancy

Author(s):  
Kati Kaartinen ◽  
Leena Martola ◽  
Sari Aaltonen ◽  
Seppo Meri
2017 ◽  
Vol 18 (4) ◽  
pp. 348-351 ◽  
Author(s):  
Sarah Birkhoelzer ◽  
Alexandra Belcher ◽  
Helen Peet

A diagnostic dilemma occurred when thrombotic microangiopathy developed during pregnancy. The diagnostic criteria of thrombotic microangiopathy include thrombocytopenia (platelets <100) and microangiopathic haemolytic anaemia (including thrombotic thrombocytopenic purpura and haemolytic-uraemic syndrome). An urgent interdisciplinary approach is required to treat thrombotic microangiopathy in pregnancy to differentiate between thrombotic microangiopathy and HELLP syndrome (haemolysis, elevated liver enzymes, low platelets).1 This case presented with the pentad of thrombotic thrombocytopenic purpura: severe thrombocytopenia (platelets 9 × 109/L), microangiopathic haemolytic anaemia (reticular count 245 × 109/L (20–110)), LDH >5000 U/L (<425)), neurological abnormalities (Glasgow Coma Scale 10/15), renal failure (creatinine 140 µmol/L (<97)), fever (37.7℃). A Disintegrin And Metalloproteinase with a Thrombospondin type 1 motif, member 13 (ADAMTS13) activity of less than 5% and anti-ADAMTS13 antibodies retrospectively confirmed the diagnosis of acquired idiopathic thrombotic thrombocytopenic purpura in pregnancy. The immediate management in the Emergency Department with an interdisciplinary team of Consultant Nephrologists, Intensivists, Haematologists and Obstetricians facilitated prompt diagnosis resulting in immediate plasma exchange (PEX) and coordination of semi-elective delivery of the foetus.


1994 ◽  
Vol 160 (4) ◽  
pp. 217-218
Author(s):  
Frank L Clark ◽  
Peter Greenwood ◽  
Peter J G Forster

2019 ◽  
Vol 2019 ◽  
pp. 1-4
Author(s):  
Shravya Govindappagari ◽  
Michelle Nguyen ◽  
Megha Gupta ◽  
Ramy M. Hanna ◽  
Richard M. Burwick

Severe vitamin B12 deficiency may present with hematologic abnormalities that mimic thrombotic microangiopathy disorders such as hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome. We report a patient diagnosed with severe vitamin B12 deficiency, following termination of pregnancy for suspected preeclampsia and HELLP syndrome at 21 weeks’ gestation. When hemolysis and thrombocytopenia persisted after delivery, testing was performed to rule out other etiologies of thrombotic microangiopathy, including atypical hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, and vitamin B12 deficiency. This work-up revealed undetectable vitamin B12 levels and presence of intrinsic factor antibodies, consistent with pernicious anemia. Parenteral B12 supplementation was initiated, with subsequent improvement in hematologic parameters. Our case emphasizes the importance of screening for B12 deficiency in pregnancy, especially in at-risk women with unexplained anemia or thrombocytopenia. Moreover, providers should consider B12 deficiency and pernicious anemia in the differential diagnosis of pregnancy-associated thrombotic microangiopathy.


2017 ◽  
Vol 32 (suppl_3) ◽  
pp. iii187-iii187
Author(s):  
Anupma Kaul ◽  
Dharmendra Bhaduaria ◽  
Kavita Vishwakarama ◽  
Mandakini Pradhan ◽  
Narayan prasad ◽  
...  

Journal SOGC ◽  
1995 ◽  
Vol 17 (9) ◽  
pp. 904-906
Author(s):  
F.A. McAlister ◽  
P.G. Hamilton

1996 ◽  
Vol 50 (8) ◽  
pp. 399
Author(s):  
B. Rosaia ◽  
A. D'Acunto ◽  
A. Ferretti ◽  
C. Pileggi ◽  
A. Sagripanti

2012 ◽  
Vol 02 (02) ◽  
pp. 174-175 ◽  
Author(s):  
Narmatha Kangeyan ◽  
Sophia N. E. Webster ◽  
Aparna Sanyal ◽  
Remko Beukenholdt

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