PedAM
Pediatric Disease Annotations & Medicines
| Disease | hemolytic anemia |
| Phenotype | C0040034|thrombocytopenia |
| Sentences | 27 |
| PubMedID- 21151638 | [8] reported a case of thrombocytopenia associated with hemolytic anemia in a patient with intracardiac metastasis originating from a testicular teratoma. |
| PubMedID- 23827373 | Hemolytic and uremic syndrome (hus) is a classical form of thrombotic microangiopathies characterized by the association of hemolytic anemia with schizocytes, thrombocytopenia, and acute renal failure. |
| PubMedID- 21559455 | The criteria for hus diagnosis were microangiopathic hemolytic anemia with schizocytes, thrombocytopenia (platelet count <150×109/l) and acute renal failure (serum creatinine level higher than the normal values considering the age of the patient). |
| PubMedID- 23961497 | The overall impression on hematological examination was hemolytic anemia with thrombocytopenia and reactive marrow hyperplasia. |
| PubMedID- 20436664 | Thrombotic microangiopathies (tma) represent a rare and heterogeneous group of diseases defined by microangiopathic hemolytic anemia with peripheral thrombocytopenia and organ failure of variable severity. |
| PubMedID- 21776377 | A 15-year-old female was admitted to our hospital because of thrombocytopenia with hemolytic anemia. |
| PubMedID- 24013519 | A mixed-type autoimmune hemolytic anemia with immune thrombocytopenia related with myositis and post-transplantation lymphoproliferative disorder. |
| PubMedID- 23772412 | The lowest platelet count occurred at postoperative day 9. to identify the reason for the refractory response to platelet transfusion, a study for antibody to platelet and additional immune workup were performed on postoperative days 9 and 10. the findings included hemolytic anemia with thrombocytopenia (hemoglobin=7.6 g/dl, platelet=15,000/µl, schistocytosis(+) in a peripheral blood smear), negative direct and indirect coombs tests, decreased haptoglobin (3 mg/dl), normal ranges of an international normalized ratio (inr 1.13), activated partial thromboplastin time (38.2 seconds) and fibrinogen (287 mg/dl), slightly elevated d-dimer (3.3 µg/ml), hyperbilirubinemia (total bilirubin 3.28 mg/dl, direct bilirubin 1.9 mg/dl), increased lactate dehydrogenase (580 mg/dl), normal serum alanine aminotransferase (10 iu/l) and aspartate aminotransferase (15 iu/l), increased blood urea nitrogen (51 mg/dl), normal creatinine (0.8 mg/dl), microscopic hematuria (red blood cell >30/hpf), negative human immunodeficiency virus antibody, and positive hepatitis b surface antibody. |
| PubMedID- 20056203 | Result(s): both patients developed a very rare complication after surgery of severe thrombocytopenia with microangiopathic hemolytic anemia leading to acute renal failure. |
| PubMedID- 23304632 | The traditional diagnostic criteria for this syndrome include hemolytic anemia with fragmented erythrocytes, thrombocytopenia, and renal failure [1]. |
| PubMedID- 23758712 | Hemangioma-thrombocytopenia syndrome associated with microangiopathic hemolytic anemia has been documented in children. |
| PubMedID- 23602056 | thrombocytopenia together with microangiopathic hemolytic anemia is mandatory for the diagnosis of ttp and if these two criteria met in a patient, tpe should be performed immediately. |
| PubMedID- 22929300 | 59. thrombocytopenia associated with mechanical hemolytic anemia should suggest tma, even in the absence of organ failure (strong agreement). |
| PubMedID- 20399168 | hemolytic anemia with schistocytes, thrombocytopenia without evidence of disseminated intravascular coagulation, and renal failure are consistently found. |
| PubMedID- 22374533 | It is important to suspect ttp when hemolytic anemia with thrombocytopenia is observed, and to check the activity and antigen of adamts13 immediately for the diagnosis. |
| PubMedID- 25821808 | Eryptosis is triggered by hemolytic uremic syndrome (hus), characterized by hemolytic anemia with fragmented erythrocytes, thrombocytopenia, and acute renal failure [198]. |
| PubMedID- 26576277 | The combination of severe anemia, acute kidney injury, and indeterminate platelet count suggested a preliminary differential diagnosis of a thrombotic microangiopathy, autoimmune hemolytic anemia with immune thrombocytopenia, or disseminated intravascular coagulation (dic) secondary to sepsis. |
| PubMedID- 20636987 | Objective: to identify and characterize the syndrome of immune-mediated hemolytic anemia (imha) with concurrent severe thrombocytopenia ( |
| PubMedID- 21151550 | Peripheral blood smear examination revealed schistocytes and thrombocytopenia consistent with microangiopathic hemolytic anemia (fig. |
| PubMedID- 21295897 | We report the first case to our knowledge of a patient who developed an acute decrease in kidney function, nonimmune microangiopathic hemolytic anemia with schistocytes, and thrombocytopenia after 4 intravitreal injections of ranibizumab. |
| PubMedID- 20331741 | Recognition of cancer-associated microangiopathic hemolytic anemia with thrombocytopenia (ca-mha) is paramount to avoid inappropriate pe therapy and delays in cancer-specific chemotherapy. |
| PubMedID- 23989401 | For thrombotic thrombocytopenic purpura and hemolytic uremic syndrome (ttp-hus) the diagnosis of coombs negative hemolytic anemia together with thrombocytopenia should lead to the detection of fragmentocytes in peripheral blood smears. |
| PubMedID- 21772952 | Evans syndrome (es) is an autoimmune disorder characterized by thrombocytopenia and/or neutropenia associated with hemolytic anemia (aha).1–3 it is a potentially life-threatening condition that may be associated with other underlying autoimmune or lymph-proliferative disorders.4 standard treatment consists of transfusions, corticosteroids and immunoglobulins (ivig); second-line treatment in es evolved over the last decade, and includes at present anti-cd20 rituximab, vincristine, alkalizing agents, mycophenolate mofetil (mmf) or cyclosporine (cya).5–6,8–14 long-term remissions induced by splenectomy are less frequent than in uncomplicated immune thrombocytopenia purpura (itp). |
| PubMedID- 23943710 | A congenital or acquired deficiency of adamts-13 can result in accumulation of the ultralarge vwf multimers leading to microangiopathic thromboses and severe thrombocytopenia with resultant hemolytic anemia and thrombotic sequelae.6 in the rare familial forms of ttp, mutations of the adamts-13 gene can be found resulting in significant risk of ttp in pregnancy in affected women.6 acquired ttp is postulated to be secondary to viral infections that trigger production of antibodies targeted against adamts-13.7 women with acquired ttp also have a high risk of recurrence in a subsequent pregnancy.6 it has been proposed that specific proteins found in the placental circulation serve as antigens that trigger maternal antibody production against adamts-13. |
| PubMedID- 21961487 | He was diagnosed to have es at the age of 8, during another bout of thrombocytopenia, this time associated with coombs-positive hemolytic anemia. |
| PubMedID- 24490094 | There are many reported cases of hemolytic anemia with or without thrombocytopenia in gastric cancer. |
| PubMedID- 23842487 | Background: hemolytic anemia with thrombocytopenia and schistocytosis is suggestive of thrombotic thrombocytopenic purpura (ttp). |
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