PedAM
Pediatric Disease Annotations & Medicines
| Disease | thrombocytopenia |
| Symptom | C0005779|coagulopathy |
| Sentences | 12 |
| PubMedID- 20733375 | Kasabach-merritt syndrome is a life-threatening and localized consumption coagulopathy, characterized with profound thrombocytopenia and microangiopathic anemia. |
| PubMedID- 20601131 | There was no difference in prevalence of significant coagulopathy between patients with severe thrombocytopenia who underwent invasive procedure and bled (3/10; 30%) and those who did not bleed (10/22; 45%). |
| PubMedID- 25692091 | A severe coagulopathy with profound thrombocytopenia (27,000×109/l) and elevated d-dimer level (84,369 mcg/l) were observed, all of which supported the diagnosis of kasabach-merritt phenomenon (kmp). |
| PubMedID- 19476462 | coagulopathy due to thrombocytopenia was implicated in one case. |
| PubMedID- 23327286 | In this case, the patient developed coagulopathy with hemolytic anemia, thrombocytopenia, and low fibrinogen. |
| PubMedID- 22824775 | Kasabach–merrit syndrome is an uncommon complication, which involves coagulopathy with fibrinolysis and thrombocytopenia associated with a hemangioma. |
| PubMedID- 26435870 | Kasabach-merritt phenomenon is characterized by vascular tumour and consumptive coagulopathy with life-threatening thrombocytopenia, prolonged prothrombin time (pt), and activated partial thromboplastin time (aptt), hypofibrinogenemia, and the presence of d-dimer and fibrin split products 2. |
| PubMedID- 20359440 | Subsequently, consumption coagulopathy with thrombocytopenia and haemolysis, colicky pain in the epigastrium and acute renal failure developed. |
| PubMedID- 23185153 | Although lc is commonly associated with coagulopathy, including thrombocytopenia and hypoprothrombinemia, iliopsoas hematoma in lc patients has been rarely reported. |
| PubMedID- 25354539 | Consumptive coagulopathy have the features of intense thrombocytopenia, fibrinogen depletion and increased clotting times (menoret et al. |
| PubMedID- 26157953 | The patient then developed marked thrombocytopenia with coagulopathy (pt 19.1, ptt 48.5, ldh 446 u/l, d-dimer >20 μg/ml, and fibrinogen 129 mg/dl). |
| PubMedID- 20863161 | Kasabach-merritt phenomenon (kmp) is a serious coagulopathy with severe thrombocytopenia (<10,000/mm(3)) that occurs in the presence of an enlarging vascular tumor such as kaposiform hemangioendothelioma (khe) and tufted angioma (ta). |
Page: 1