Bilgin, Aynur UgurKaraselek, Mehmet AliBilgin, Rasim2024-02-232024-02-2320151473-0502https://doi.org/10.1016/j.transci.2015.01.001https://hdl.handle.net/20.500.12452/12653Immune thrombocytopenia (ITP) is an acquired immune-mediated disease characterized by persistant thrombocytopenia. Onset of the disease and the clinical course is highly variable, but the disease typically has a benign course. Patients rarely develop serious life-threatening bleeding. Herein, a case with refractory ITP and massive alveolar hemorrhage who was successfully treated with a fast and sequential approach is presented for the first time. (C) 2015 Elsevier Ltd. All rights reserved.eninfo:eu-repo/semantics/closedAccessRefractory ItpLife-Threatening HemorrhageFviiaArticle522214216256347872-s2.0-84930477561Q3WOS:000356738500017Q410.1016/j.transci.2015.01.001