Idiopathic thrombocytopenic purpura (ITP) is an autoimmune disease characterized by a low platelet count despite normalcy in bone marrow. Here we present a patient who developed severe ITP after surgery. A 74-year-old man with a squamous cell carcinoma in the lower gingiva received a segmental resection of the mandible, supraomohyoid neck dissection and a reconstruction using pectoral major myocutaneous flap and titanium plates. Preoperative blood test data showed no abnormalities, and blood loss during the operation was 310mL. On the first day after surgery, the patient presented with thrombocytopenia (1.9×10
4 platelets/μL) and was referred to a hematologist. Drug induced thrombocytopenic purpura (DITP), heparin induced thrombocytopenia (HIT), disseminated intravascular coagulation (DIC), ITP and leukemia were considered as differential diagnoses of thrombocytopenia. As the platelet count decreased continuously despite the immediate withdrawal of medication, DITP was excluded. Due to normal values of the HIT antibody, fibrin degradation product (FDP) and D-dimer, HIT and DIC were excluded. A bone marrow biopsy revealed normal blood cells, thus leukemia was also excluded, and the patient was diagnosed with ITP. On the 6th day after surgery the patient was given steroid pulse therapy for 4 days, and was administered Romiplostim (Romiplate
Ⓡ), which caused the platelet count to return to the normal range.
In most cases ITP can be managed by preoperative treatments. In this case, however, critical thrombocytopenia occurred in the perioperative period. Acute ITP can cause severe bleeding, so early diagnosis and effective treatment are essential.
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