Create issue ticket

1,456 Possible Causes for Hemolytic Anemia, Hepatosplenomegaly

  • Infectious Mononucleosis

    Both cases involved young adults presenting with fever, pharyngitis, lymphadenopathy, hepatosplenomegaly, and atypical lymphocytosis confirmed by serologic tests, liver biopsy[] To our knowledge, this is the first case report in the literature of this specific constellation of findings, with infectious mononucleosis, warm antibody hemolytic anemia[] A 17-year-old boy with Epstein-Barr virus related infectious mononucleosis and cold antibody-mediated autoimmune hemolytic anemia with incidentally noted multiple pulmonary[]

  • Otitis Media

    Bowel sounds present in all 4 quadrants, no hepatosplenomegaly MSK: Full range of motion in all extremeties Comparing the left and right sides of the ear helps in pinpointing[] Rare, but serious reactions, including hemolytic anemia, crystalluria, Stevens-Johnson Syndrome. Most common side effects are nausea, vomiting, rash.[]

  • Castleman Disease

    For multicentric disease: multi-region CT bilateral hilar and mediastinal lymphadenopathy centrilobular nodules diffuse abdominal lymphadenopathy hepatosplenomegaly ascites[] anemia, bone marrow insufficiency, pulmonary, renal, hepatic, and gastrointestinal involvement, emphasizing the difficulty in diagnosis and treatment approach.[] […] in the groin , neck , or armpit Unintentional loss of weight In some cases fever and weakness Easy fatigue Appetite loss or extremely poor appetite Lymph node enlargement Hepatosplenomegaly[]

  • Multicentric Castleman's Disease

    Multicentric Castleman's disease (MCD) typically presents with constitutional symptoms, generalized peripheral lymphadenopathy, hepatosplenomegaly, and laboratory markers[] anemia , and immune thrombocytopenic purpura (ITP). [4] Last updated: 6/25/2015 In about half of people with multicentric Castleman disease (MCD), it is caused by human herpesvirus[] It manifests by fever, diffuse lymphadenopathy, hepatosplenomegaly, Involvement of the respiratory system and increased C-reactive protein.[]

  • Pyruvate Kinase Deficiency

    A case of congenital pyruvate kinase deficiency manifested at antenatal ultrasound as isolated hepatosplenomegaly is reported and the differential diagnosis is discussed.[] Hemolytic anemia due to deficiency of erythrocytic pyruvate kinase is a rare autosomal recessive disorder.[] The patients presented with severe haemolysis, progressive cholestasis, and hepatosplenomegaly, and both patients ultimately developed liver failure at a very young age.[]

  • Q Fever

    The patient had a new onset of Melody valve dysfunction associated with the combination of hepatosplenomegaly and pancytopenia but was afebrile.[] Meningoencephalitis, thyroiditis, pericarditis, myocarditis, mesenteric lymphadenopathy, hemolytic anemia, and nephritis are rare manifestations.[] CBC may show hemolytic anemia WBC Liver function may show mild elevation of transaminase ESR may be elevated Blood cultures are usually negative Lumbar puncture to sample[]

  • Niemann-Pick Disease

    Hepatosplenomegaly is a hallmark of both types of NPD and lymphadenopathy may occur in patients with type B.[] anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase deficiency ( E29.1 ) Metabolic disorders E75 ICD-10-CM Diagnosis Code E75[] These patients may have mild hepatosplenomegaly, but the central nervous system is profoundly affected.[]

  • Familial Hemophagocytic Lymphohistiocytosis

    Reported here is the case of a 12-year-old boy, from a poor family, with a 6-year history of visual loss and fever for 5 months, and transient hemiparesis with hepatosplenomegaly[] This case report highlights the difficulty in managing posttransplant autoimmune hemolytic anemia.[] Examination revealed fever, lymphadenopathy, and hepatosplenomegaly. Ultrasound examination revealed hepatosplenomegaly and free intra-abdominal fluid.[]

  • Thalassemia

    They have severe anemia and hepatosplenomegaly. Untreated children have severe failure to thrive and shortened life expectancy.[] Though hypertriglyceridemia has been reported with hemolytic anemias, the mechanism is unclear.[] Here, we report a novel mutation in a patient from Thailand who presented with chronic hemolytic anemia.[]

  • Wilson Disease

    He was deeply icteric with ascites, hepatosplenomegaly, hyperbilirubinemia, raised transaminases, and coagulopathy.[] Although fulminant hepatitis with nonimmune hemolytic anemia is frequently reported, chronic mild hepatitis can occur with bouts of transient hemolytic anemia.[] Chronic liver disease with portal hypertension, hepatosplenomegaly, ascites, low serum albumin concentration, and coagulopathy Fatty liver of mild to moderate degree with[]

Further symptoms

Similar symptoms