Pregnancy and thrombosis: Adrenal vein thrombosis. A retrospective descriptive study of 14 cases

Author(s):  
Pierre Descargues ◽  
Catherine Battie ◽  
Cyril Huissoud ◽  
Nathalie Hoen ◽  
Yesim Dargaud ◽  
...  
2003 ◽  
Vol 76 (908) ◽  
pp. 566-569 ◽  
Author(s):  
M F Ryan ◽  
J P Murphy ◽  
R Jay ◽  
J Callum ◽  
D MacDonald

1963 ◽  
Vol 157 (2) ◽  
pp. 277-280 ◽  
Author(s):  
Irwin H. Krasna ◽  
Keith M. Schneider ◽  
Jerrold M. Becker ◽  
Ralph E. Moloshok

1972 ◽  
Vol 80 (1) ◽  
pp. 101-103 ◽  
Author(s):  
Elsa Valderrama ◽  
Irwin Gribetz ◽  
Lotte Strauss

2019 ◽  
Vol 12 (12) ◽  
pp. e232769
Author(s):  
Elysha A VanderVeer ◽  
Raymond P Torbiak ◽  
Ally PH Prebtani ◽  
Theodore E Warkentin

Adrenal gland infarction resulting from adrenal vein thrombosis is an infrequently recognised entity with a limited differential diagnosis. When bilateral, it can result in acute life-threatening adrenal failure. Heparin-induced thrombocytopenia (HIT) is an antibody-mediated, prothrombotic state that represents an important cause of adrenal vein thrombosis leading to associated infarction. Sometimes, the clinical picture of HIT—including the presence of HIT antibodies—occurs despite absence of proximate heparin exposure (‘spontaneous HIT syndrome’). We report a case of nearly missed adrenal failure secondary to bilateral adrenal infarction that evolved during the second week following knee arthroplasty (a known trigger of spontaneous HIT syndrome). The combination of bilateral adrenal infarction, thrombocytopenia and presence of platelet-activating HIT antibodies not explainable by preceding heparin exposure led to a diagnosis of postknee arthroplasty spontaneous HIT syndrome. The case also highlights the clinical and laboratory findings associated with rapidly progressive acute adrenal failure.


2013 ◽  
Vol 9 (1) ◽  
pp. 48-53 ◽  
Author(s):  
Anneliese M. Schleyer ◽  
Kenneth M. Jarman ◽  
Patty Calver ◽  
Joseph Cuschieri ◽  
Ellen Robinson ◽  
...  

1987 ◽  
Vol 11 (2) ◽  
pp. 216-218 ◽  
Author(s):  
Kenneth Zirinsky ◽  
Yong Ho Auh ◽  
William A. Rubenstein ◽  
Harvey S. Morrison ◽  
Scott J. Sherman ◽  
...  

2010 ◽  
Vol 20 (2) ◽  
pp. 42-50 ◽  
Author(s):  
Laura W. Plexico ◽  
Julie E. Cleary ◽  
Ashlynn McAlpine ◽  
Allison M. Plumb

This descriptive study evaluates the speech disfluencies of 8 verbal children between 3 and 5 years of age with autism spectrum disorders (ASD). Speech samples were collected for each child during standardized interactions. Percentage and types of disfluencies observed during speech samples are discussed. Although they did not have a clinical diagnosis of stuttering, all of the young children with ASD in this study produced disfluencies. In addition to stuttering-like disfluencies and other typical disfluencies, the children with ASD also produced atypical disfluencies, which usually are not observed in children with typically developing speech or developmental stuttering. (Yairi & Ambrose, 2005).


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