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380 Possible Causes for Cholelithiasis, Jaundice, Mild Anemia

  • Hereditary Spherocytosis

    This case also highlights the fact that physicians should consider concomitant hemolytic disease in patients in whom jaundice and infections that rarely cause jaundice coexist[ncbi.nlm.nih.gov] A 27-year-old Nigerian woman presented with mild anemia, jaundice, splenomegaly and a history of multiple blood transfusion.[ncbi.nlm.nih.gov] This is a report of an 11 years old male diagnosed case of hereditary spherocytosis who presented with jaundice, splenomegaly and cholelithiasis.[ncbi.nlm.nih.gov]

  • Cooley's Anemia

    Children develop life-threatening anemia, have failure to thrive, and may develop jaundice.[secure.ssa.gov] People with Cooley's anemia make less hemoglobin and fewer circulating red blood cells than normal, which results in mild or severe anemia.[blood.emedtv.com] In cases of symptomatic cholelithiasis, cholecystectomy may be considered. This procedure may be performed together with splenectomy.[symptoma.com]

  • Beta Thalassemia

    CASE PRESENTATION: An 8-month-old ethnic Gypsy male infant with failure to thrive from birth, mild jaundice and splenomegaly.[ncbi.nlm.nih.gov] The heterozygous form may be asymptomatic or marked by mild anemia. β-thalassemia ( beta-thalassemia ) that caused by diminished synthesis of beta chains of hemoglobin.[medical-dictionary.thefreedictionary.com] Hypersplenism, cholelithiasis, extramedullary hematopoiesis, thrombotic complications and progressive iron overload are the main clinical features that may complicate the[orpha.net]

  • Hemoglobin Bart's Disease

    […] metabolism; description of hemolytic jaundice; description of hyperbilirubinemia.[books.google.de] Homozygotes display mild hemolytic anemia and splenomegaly (enlarged spleen). The HbCSpr trait is asymptomatic.[wikilectures.eu] […] mutations. 20.2 Hemoglobin H deletion After the newborn period, the diagnosis of deletional hemoglobin H disease is often made only after the detection of complications such as cholelithiasis[thalassemia.com]

  • Hereditary Elliptocytosis

    As neonates, the nine relatives did not have any significant jaundice or anemia that was recognizable.[ncbi.nlm.nih.gov] The patient presented for a general check up when his CBC showed only mild anemia with slightly increased reticulocytes.[ncbi.nlm.nih.gov] Cholelithiasis (pigment stones) is common and may be the presenting symptom.[msdmanuals.com]

  • Pyruvate Kinase Deficiency

    Pyruvate kinase deficiency may cause pregnancy-associated jaundice.[ncbi.nlm.nih.gov] Patients presenting with hemolytic anemia, either severe or mild hemolytic anemia, should be screened for PKD in the first year of life.[ncbi.nlm.nih.gov] […] laparoscopic splenectomy and cholecystectomy is safe and effective for the management of hemolytic anemia resulting from pyruvatre kinase deficiency and associated with cholelithiasis[ncbi.nlm.nih.gov]

  • Thalassemia

    Diagnostic methods Diagnosis is suspected in infants younger than 2 years of age with severe microcytic anemia, mild jaundice and hepatosplenomegaly.[orpha.net] Mild anemia can make you feel tired. Mild anemia caused by alpha thalassemia trait might be mistaken for iron-deficiency anemia.[web.archive.org] […] hemoglobin level postinfancy, these patients developed many of the classic complications of SCD, including vaso-occlusive crisis, acute chest syndrome, avascular necrosis, and cholelithiasis[ncbi.nlm.nih.gov]

  • Erythropoietic Protoporphyria

    A 21-year-old Japanese man was admitted to our hospital because of severe abdominal pain and jaundice.[ncbi.nlm.nih.gov] Patients studied had a mild anemia and thrombocytopenia, as shown by the downward shift of hematologic parameters, which positively correlated with the amount of erythrocyte[ncbi.nlm.nih.gov] Some authors believe that EPP should be suspected when cholelithiasis presents in childhood[ 21 ].[doi.org]

  • Congenital Hemolytic Anemia

    jaundice (yellowing) and splenomegaly (enlargement of the spleen).[medicinenet.com] anemia.[ncbi.nlm.nih.gov] Early phenobarbital treatment may prevent the development of cholelithiasis in patients with chronic hemolysis.[ncbi.nlm.nih.gov]

  • Sickle Cell Disease

    Jaundice, or yellowing of the skin, eyes, and mouth. Jaundice is a common sign and symptom of sickle disease.[hopkinsmedicine.org] Partial exchange transfusion should be reserved for children with only mild anemia (Hb 9 g/dL) but deteriorating respiratory status.[ncbi.nlm.nih.gov] […] sickle complications comparing the survivors of septicemia to the non-infected patients was: subsequent death 1.76, retinopathy 4.06, avascular necrosis 1.95, symptomatic cholelithiasis[ncbi.nlm.nih.gov]

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