Acquired Glanzmann's thrombasthenia as part of multiple-autoantibody syndrome in a pediatric heart transplant patient - 24/08/11
Doi : 10.1016/j.jpeds.2003.12.040
Ajay Rawal, MD, Ravindra Sarode, MD ⁎ 
, Brian R Curtis, MS, Nitin J Karandikar, MD, Ken Friedman, MD, Zora R Rogers, MD
, Brian R Curtis, MS, Nitin J Karandikar, MD, Ken Friedman, MD, Zora R Rogers, MD From the Departments of Pathology and Pediatrics, UT Southwestern Medical Center, Dallas, Texas; and The Blood Center of Southeastern Wisconsin, Milwaukee, Wisconsin USA
Reprint requests: Ravindra Sarode, MD, Department of Pathology, UT Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390-9073.Abstract |
Although advances in immunosuppressive therapy have allowed prolonged patient survival, immune dysregulation observed in these patients has increased. We report an 11-year-old female heart transplant recipient in whom Glanzmann thrombasthenia was identified as part of a “multiple autoantibody syndrome” manifesting sequentially as autoimmune hemolytic anemia, thrombocytopenia, and neutropenia.
Le texte complet de cet article est disponible en PDF.Keywords : AA, ACE, ADP, AGT, DAT, MoAb, PTLPD
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© 2004
Elsevier Inc. Tous droits réservés.
Vol 144 - N° 5
P. 672-674 - mai 2004 Retour au numéro
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