Nuong Truong, Layan Alrahmani, Kristen Krum, Kevin Barton, Phillip J DeChirstopher, Ameet Kini, Samreen Fathima, Namisha Dhillon, Nicole Sprawka, Joana Lopes Perdigao, Srichandhana Rajamouli, Stephanie Rodriguez, Kalee Ahlin, Ann Lal
Acquired amegakaryocytic thrombocytopenia (AAT) in pregnancy is rare, with only one case report previously published on this condition. Our case is a 33-year-old G3P2002 female with severe thrombocytopenia, suspected to be due to AAT, who was managed with eltrombopag, prednisone, and cyclosporine A. The patient delivered at 32 weeks due to preeclampsia with severe features. She had an uncomplicated postpartum course, and the neonate did not have thrombocytopenia. With a multidisciplinary approach to care, our management approach to a patient with severe thrombocytopenia in pregnancy resulted in an uncomplicated delivery, without maternal or fetal complications.