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964 Possible Causes for Aplastic Anemia, Splenomegaly

  • Infectious Mononucleosis

    Infectious mononucleosis (IM) is a rare cause of aplastic anemia in adults.[] Clinical estimates of splenomegaly are fallible.[] anemia requiring bone marrow transplantation, are rare. 2 Neurologic complications occur in 1% to 5% of cases and can include Guillain-Barré syndrome, facial-nerve palsy,[]

  • Malignant Neoplasm

    PATIENTS: 1036 consecutive patients who underwent transplantation for leukemia, lymphoma, inborn diseases of the hematopoietic and immune systems, or severe aplastic anemia[] D55-D59 Hemolytic anemias D60-D64 Aplastic and other anemias and other bon...[] […] diseases D50-D89 ICD-10-CM Range D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism D50-D53 Nutritional anemias[]

  • Pharyngitis

    anemia, as well as oropharyngeal malignancies Oral mucositis, which is usually secondary to radiation or chemotherapy What laboratory studies should you order and what should[] It is characterised by : Sore throat Fever Enlarged cervical lymph nodes Enlarged tonsils and fatigue Other clinical manifestations are splenomegaly (enlarged spleen), hepatomegaly[] […] ulcers (including ulcers secondary to inflammatory bowel disease) Acute thyroiditis Behçet disease Gastroesophageal or laryngopharyngeal reflux disease Leukemia, lymphoma, aplastic[]

  • Paroxysmal Nocturnal Hemoglobinuria

    The frequency of PNH clone detected in aplastic anemia and non-aplastic anemia groups was 12.02 and 3.36%, respectively.[] PNH is associated with abdominal vein thrombosis, which can cause splenomegaly and hypersplenism.[] We describe a patient under treatment with the anti-complement antibody eculizumab who developed pancytopenia, requiring blood transfusions, due to massive splenomegaly.[]

  • Leukemia

    Aplastic Anemia. Only neutropenia is regarded as independent risk factor for severe opportunistic infection in T-LGL patients.[] CT, MRI, or abdominal ultrasonography may help assess splenomegaly or leukemic infiltration of other organs.[] In contrast to aplastic anemia, leukemia results in a highly cellular marrow.[]

  • Myelodysplasia

    Who has aplastic anemia and MDS?[] Therapy with granulocyte-colony stimulating factor (G-CSF) and granulocyte-monocyte-colony stimulating factor (GM-CSF) caused splenomegaly and severe thrombocytopenia, which[] We present a 2-year-old boy with splenomegaly, leukocytosis, thrombocytopenia, anemia, and excess myeloblasts with easily seen Auer rods, and marked dysgranulopoiesis and[]

  • Leukoerythroblastic Anemia

    ANEMIA LEUKOERYTHROBLASTIC Anemia, leukoerythroblastic Leukoerythroblastosis Myelophthisic anemia (disorder) myelophthisis edit English myelophthisic anemia aplastic anemia[] The French authors, Emil-Weil and Clerc, 1 in 1902, and Vaquez and Aubertin, 2 in 1904, first discussed a syndrome characterized by splenomegaly due to myeloid change and[] Acute Erythroblastic Leukemia Anemia, X-Linked, without Thrombocytopenia aplastic anemia Aplastic Anemia, Idiopathic Bone Marrow Failure Syndromes chronic myeloid leukemia[]

  • Systemic Lupus Erythematosus

    Other conditions Other conditions like thyroid disorders (particularly over active thyroid glands), aplastic anemia, rheumatoid arthritis, parasitic infestations, vitamin[] […] relapsing illness, with a variety of different presentations. [ 5 , 6 ] Symptoms and signs are often nonspecific - eg, fatigue (can be severe and debilitating), malaise, fever, splenomegaly[] Hematologic • Anemia (chronic disease) • Leukopenia • Lymphopenia • Thrombocytopenia • Lymphadenopathy • Splenomegaly • Auto Immune Haemolytic anemia 44.[]

  • Hypersplenism

    anemia bone marrow, and the blood stem cells that reside there, are damaged.[] While 38 patients displayed splenomegaly, 121 showed normal spleen volumes at 6 months after LDLT (LDLT).[] In aplastic anemia, the spleen is not enlarged and the marrow is fatty.[]

  • Pyruvate Kinase Deficiency

    […] more does not affect children's growth and development, and reduce life-threatening aplastic anemia.[] Significant hyperbilirubinaemia, anemia, and splenomegaly are common features in patients with severe haemolysis due to pyruvate kinase (PK) deficiency.[] She is doing well with mild splenomegaly.[]

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