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2,173 Possible Causes for Anemia, Cholestasis

  • Cystic Fibrosis

    Female sex and chronic anemia were independent predictors of readmission.[] We present a rare presentation of cystic fibrosis with neonatal cholestasis.[] When CF is not treated for a longer period, a child may develop symptoms of malnutrition, including anemia, bloating, and, paradoxically, appetite loss.[]

  • Progressive Familial Intrahepatic Cholestasis

    […] cea mai frecventa cauza de crestere usoara a bilirubinei neconjugate (pg 280)\*\Which is the most frequent cause of a mild rise in unconjugated bilirubin (s 280) a) [ ] \*\anemia[] […] as well as intrahepatic cholestasis of pregnancy.[] […] de Fanconi #227650 #227645 #614082 #300514 Anemia Diseritropoiética Congénita #224120 #224100 Anemia hemolítica por déficit de hexoquinasa #235700 Anemia megaloblástica sensible[]

  • Otitis Media

    Rare, but serious reactions, including hemolytic anemia, crystalluria, Stevens-Johnson Syndrome. Most common side effects are nausea, vomiting, rash.[] Tuberculosis was suspected after a positive ELlspot tests with appearance of biologic markers of hepatic dysfunction like cholestasis and hepatic cytolysis.[]

  • Autoimmune Hemolytic Anemia

    Cold antibody hemolytic anemia is common among the elderly, while warm antibody hemolytic anemia affects all age groups.[] […] autoimmune hemolytic anemia (AHA) is a very rare disease characterized by early onset and severe clinical manifestations, including immune hemolytic anemia and hepatitis with cholestasis[] A complicated with autoimmune hemolytic anemia, prolonged cholestasis, and false-positive immunoglobulin M anti-hepatitis E virus: a case report.[]

  • Hereditary Spherocytosis

    To date only three siblings with coinheritance of sickle cell anemia (SCA) and hereditary spherocytosis (HS) have been reported.[] Mutations in the ABCB11 gene, encoding the bile salt export pump, can entail progressive familial intrahepatic cholestasis and benign recurred intrahepatic cholestasis.[] Hereditary spherocytosis (HS) and pyruvate kinase (PK) deficiency are the most common causes of congenital hemolytic anemia.[]

  • Pyruvate Kinase Deficiency

    Pyruvate kinase deficiency is a rare cause of hemolytic anemia and, in its most severe form, requires splenectomy in childhood.[] Unexpected severe cholestasis is part of the presentation in some neonates with hemolytic anemia but is usually self-resolving.[] We report an autopsy case of pyruvate kinase deficiency anemia with severe hemochromatosis. This anemia is rarely associated with hemochromatosis.[]

  • Dengue Hemorrhagic Fever

    She had no serious complications except for postpartum anemia. The newborn became febrile at the 48th hour of life.[] […] prooxidant, cytotoxic, mutagenic and teratogenic in higher concentration, especially when unbound to protein, and an endogenous form of vitamin A intoxication is recognized in cholestasis[] The patient developed diffuse pulmonary hemorrhage and anemia requiring multiple transfusions. She eventually sustained multi-organ system failure and expired.[]

  • Intrahepatic Cholangiocarcinoma

    The major toxic effect was grade 3 anemia, occurring in 1 patient (4.5%).[] This suggests that the cancer development could be related to intrahepatic cholestasis.[] The median age of patients with intrahepatic cholangiocarcinoma was 63 years, and most of them presented with cholestasis and intrahepatic biliary ductal dilation.[]

  • Ehrlichiosis

    5-year-old boy who was referred to the Hematology-Oncology Clinic to consider a bone marrow etiologic process after his pediatrician discovered progressive neutropenia, anemia[] Cholestasis was evident in 6 cases, sometimes with bile duct epithelial injury.[] Patients exhibit diagnostically important hematological changes, including anemia and thrombocytopenia, although the basis of the abnormalities is unknown.[]

  • Primary Sclerosing Cholangitis

    After ruling out all the other causes of autoimmunity and hemolytic anemia, she was diagnosed as leukemoid reaction due to autoimmune hemolytic anemia with primary sclerosing[] In conclusion, chronic cholestasis in PSC induces adaptive changes in expression of BA transporters and FXR in the intestine.[] Primary sclerosing cholangitis (PSC) is rarely associated with autoimmune hemolytic anemia (AIHA), and the presence of specific autoantibodies has not been reported previously[]

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