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PedAM

Pediatric Disease Annotations & Medicines




Disease thrombocytopenia
Phenotype |anemia
Sentences 76
PubMedID- 21779188 Characteristic laboratory findings of ca-maha are anemia with schistocytes, thrombocytopenia, leukoerythroblastic anemia, decreased haptoglobin levels, and elevated serum levels of alp, ldh, and bilirubin [2, 10, 12].
PubMedID- 24754962 Her peripheral blood revealed normochromic normocytic anemia with hemoglobin of 9.5 g/dl, thrombocytopenia (55,000/ul), white blood cells of 8700/μl, including 25% of blasts.
PubMedID- 20802939 Normocytic and normochromic anemia, with leukocytosis and thrombocytopenia).
PubMedID- 24131255 anemia without thrombocytopenia did not affect bmbt with any device.
PubMedID- 25434823 The symptoms range from mild cytopenia in any lineage to severe aplastic anemia, often initially with thrombocytopenia (shimamura and alter, 2010).
PubMedID- 25075486 A higher risk of thrombocytopenia was identified in patients with severe anemia, neurologic complications, pulmonary complications, liver dysfunction, renal impairment and severe hypoglycemia.
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- 20589460 In addition to anemia, occurrence of neutropenia and/or thrombocytopenia is increasingly being reported.
PubMedID- 23304632 The traditional diagnostic criteria for this syndrome include hemolytic anemia with fragmented erythrocytes, thrombocytopenia, and renal failure [1].
PubMedID- 23961497 The overall impression on hematological examination was hemolytic anemia with thrombocytopenia and reactive marrow hyperplasia.
PubMedID- 25057402 Furthermore, reports of haemolytic anemia in conjunction with thrombocytopenia raise the possibility of oxaliplatin-induced microangiopathy.
PubMedID- 24363883 In advanced cll, isolated thrombocytopenia without anemia is more likely to have autoimmune etiology.33,34,42 because thrombocytopenia commonly seen with infections such as hepatitis c, helicobacter pylori and human immunodeficiency virus, it is prudent to investigate for these infections, and sometimes management of these infections may increase platelet counts without using corticosteroids43 (table 3).
PubMedID- 20636987 Objective: to identify and characterize the syndrome of immune-mediated hemolytic anemia (imha) with concurrent severe thrombocytopenia (
PubMedID- 21951951 Peripheral blood data revealed anemia (hemoglobin level of 7.7 g/l) and thrombocytopenia (12 × 109 platelets/l) with an increased white blood cell count (35.4 × 109 leucocytes/l), with 70% blasts.
PubMedID- 21151638 [8] reported a case of thrombocytopenia associated with hemolytic anemia in a patient with intracardiac metastasis originating from a testicular teratoma.
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- 21694933 The patient exhibited anemia with hemoglobin level of 7.9 g/dl, thrombocytopenia (platelet count of 140000/mm3), renal insuff iciency (creatinine clearance: 38 ml/min/1.73 m2) and hypertension (120/80 mmhg).
PubMedID- 26000153 Furthermore, on this occasion microcytic anemia with hyposideremia and thrombocytopenia (121,000/mm3) were also demonstrated in addition to leukopenia.
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- 21332348 Thrombotic thrombocytopenic purpura (ttp)/hemolytic uremic syndrome (hus) is characterized with fever, purpura, anemia due to microangiopathic hemolysis, thrombocytopenia, kidney damage, and neurologic symptoms.
PubMedID- 22363087 We report a rare sub-acute presentation of pernicious anemia with hemolysis, thrombocytopenia and numerous schistocytes that was initially diagnosed as a more serious ttp.
PubMedID- 22001463 A case of anemia with schistocytosis, thrombocytopenia, and acute renal failure caused by adenomyosis.
PubMedID- 25345959 The most common clinical characteristics were bone pain (65%), anemia with thrombocytopenia (63.6%) and leukoerythroblastic reaction (61%).
PubMedID- 21425920 Predominant features of perinatal onset mevalonate kinase deficiency include intrauterine growth restriction, cerebral ventriculomegaly, dysmorphic features, skeletal abnormalities, dyserythropoietic anemia with extramedullary erythropoiesis, thrombocytopenia, cholestatic liver disease, persistent diarrhea, renal failure, recurrent sepsis-like episodes, and failure to thrive.
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.

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