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2,125 Possible Causes for Acquired Spherocytosis, Glycogen Storage Disease Type 1, Polychromasia in Peripheral Blood Smear

  • Autoimmune Hemolytic Anemia

    D58.1 Hereditary elliptocytosis D58.2 Other hemoglobinopathies D58.8 Other specified hereditary hemolytic anemias D58.9 Hereditary hemolytic anemia, unspecified D59 Acquired[icd10data.com] Peripheral blood smear showed polychromasia and spherocytosis. Haptoglobin level was 0.06 g/L ( N 0.16-2). Both hemoglobin electrophoresis and G6PD level were normal.[jahjournal.org] -Red cell morphology on review of the peripheral blood smear may demonstrate microspherocytes and polychromasia which are suggestive of a reactive reticulocytosis.[oncologynurseadvisor.com]

  • Arsine Poisoning

    Abstract Arsine poisoning is a well-recognized phenomenon generally associated with the smelting and refining of metals. However, acute episodes of arsine poisoning do occur in environments unrelated to metal processing and often go unrecognized. The incident described herein, which deals with artists working on the[…][ncbi.nlm.nih.gov]

    Missing: Polychromasia in Peripheral Blood Smear
  • Microangiopathic Hemolytic Anemia

    D58.1 Hereditary elliptocytosis D58.2 Other hemoglobinopathies D58.8 Other specified hereditary hemolytic anemias D58.9 Hereditary hemolytic anemia, unspecified D59 Acquired[icd10data.com] The peripheral blood smear revealed polychromasia, poikilocytosis, and many schistocytes. Bone marrow biopsy disclosed metastatic carcinoma.[ncbi.nlm.nih.gov] Hemosiderinuria is seen in chronic intravascular hemolysis. 4) Examination of blood smear: Careful examination of peripheral blood smear by an experienced person provides[bioline.org.br]

    Missing: Glycogen Storage Disease Type 1
  • Toxic Hemolytic Anemia

    storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] Abnormalities include hereditary cell membrane disorders (eg, hereditary spherocytosis ), acquired cell membrane disorders (eg, paroxysmal nocturnal hemoglobinuria ), disorders[merckmanuals.com] D58.1 Hereditary elliptocytosis D58.2 Other hemoglobinopathies D58.8 Other specified hereditary hemolytic anemias D58.9 Hereditary hemolytic anemia, unspecified D59 Acquired[icd10data.com]

    Missing: Polychromasia in Peripheral Blood Smear
  • Acquired Toxic Hemolytic Anemia

    Abnormalities include hereditary cell membrane disorders (eg, hereditary spherocytosis ), acquired cell membrane disorders (eg, paroxysmal nocturnal hemoglobinuria ), disorders[msdmanuals.com] storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] D58.1 Hereditary elliptocytosis D58.2 Other hemoglobinopathies D58.8 Other specified hereditary hemolytic anemias D58.9 Hereditary hemolytic anemia, unspecified D59 Acquired[icd10data.com]

    Missing: Polychromasia in Peripheral Blood Smear
  • Paroxysmal Cold Hemoglobinuria

    Spherocytes hereditary spherocytosis, immune-mediated hemolytic anemia If considered hereditary – osmotic fragility test, RBC membrane protein studies If considered acquired[medcaretips.com] storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] Tests include complete blood count (CBC) and peripheral smear.[emedicine.com]

  • Hypophosphatemia

    FANCONI SYNDROME Congenital :Cystinosis, Wilson’s disease, hereditary fructose intolerance glycogen storage disease Acquired: Multiple myeloma, SLE, amyloidosis, antiretroviral[slideshare.net]

    Missing: Polychromasia in Peripheral Blood Smear
  • Chronic Acquired Pure Red Cell Aplasia

    ,8,9 and 10 acquired hemolytic anemia,11,12 and 13 paroxysmal nocturnal hemoglobinuria,14 sickle cell anemia,15,16 and others.17,18,19 and 20 A brief period of erythroid aplasia[medtextfree.wordpress.com] storage disease グリコーゲン蓄積症,糖原病(0a型) glycogen storage disease (type 0a) グリコーゲン蓄積症,糖原病(0b型) glycogen storage disease (type 0b) グリコーゲン蓄積症,糖原病(I型) glycogen storage disease (type[jsge.or.jp] blood smear showed anisocytosis, poikilocytosis, polychromasia and leukocytosis.[ijmstrust.in]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    Corpuscular hemolytic anemias Erythrocytic membrane defects Hereditary spherocytosis Paroxysmal nocturnal hemoglobinuria ( PNH ) Description : : an acquired genetic defect[amboss.com] "Glycogen storage disease type I: diagnosis, management, clinical course and outcome.Results of the European study on glycogen storage disease type I".[cancertherapyadvisor.com] The peripheral blood smear post-splenectomy often shows crenated or spiculated spherocytes and marked polychromasia.[clinicaladvisor.com]

  • Autosomal Dominant Aplasia and Myelodysplasia

    ,8,9 and 10 acquired hemolytic anemia,11,12 and 13 paroxysmal nocturnal hemoglobinuria,14 sickle cell anemia,15,16 and others.17,18,19 and 20 A brief period of erythroid aplasia[medtextfree.wordpress.com] Chou JY, Mansfield BC: Molecular genetics of type 1 glycogen storage disease . TEM 1999, 10 :104–113. Google Scholar 9.[link.springer.com] Hgb 4.6 g/dL MCV 55 Retic 2.1% *Further history reveals he drinks 64 ounces of cows milk per day Plt 520 (H) TIBC 510 (H) Ferritin 3 (H) Case 1 Peripheral Blood Smear Normal[docslide.us]

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