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8,446 Possible Causes for Anemia, Cutaneous Vasculitis, Diffuse Hepatic Steatosis

  • Rheumatoid Arthritis

    However, many cases of cutaneous and systemic vasculitis related to TNF-α inhibitors have been reported in the literature.[] Erythropoiesis-stimulating agents have been used to treat anemia, one of the extra-articular manifestations of RA.[] Abnormal retention of lipids within hepatocytes Cholangitis Inflammation of bile ducts Reactive hepatitis Aspecific and mild inflammatory cell infiltrate of portal spaces[]

  • Non-Hodgkin Lymphoma

    Cutaneous vasculitis in non Hodgkin's lymphoma Haematologica January 1995 80: 529-531; doi: Abstract Cutaneous vasculitis has been described in association with various hematological[] In the first case, the laboratory tests showed anemia, thrombocytosis, elevated inflammatory biomarkers, a low level of iron, and hypoproteinemia.[] We report the case of a 53-year-old woman with underlying systemic lupus erythematosus and autoimmune hemolytic anemia that were in remission.[]

    Missing: Diffuse Hepatic Steatosis
  • Hypocomplementemic Vasculitis

    Cutaneous vasculitis. J Am Acad Dermatol. 2003;48:311-40. [ Links ] 3. Chen KR, Carlson JA. Clinical approach to cutaneous vasculitis.[] At the latest follow-up visit in August 2016 she was doing well, no signs of skin or eye relapses, her anemia was compensated (Hd 12,0 g/dL), urinalysis became normal, and[] Abdominal ultrasound showed diffuse hepatic steatosis and thorax x-ray was unremarkable.[]

  • Systemic Lupus Erythematosus

    Along with the production of autoantibodies, these patients can develop a syndrome of arthritis/arthralgias, cutaneous vasculitis, and serositis. ( See "Drug-induced lupus[] Anemia is a common finding in children with systemic lupus erythematosus (SLE).[] vasculitis : palpable purpura or urticarial vasculitis Livedo reticularis (a network pattern of blood vessels ) in 20–30% patients with SLE Papular mucinosis (deposits of[]

    Missing: Diffuse Hepatic Steatosis
  • Leukemia

    ( 3 ) with or without lymphadenopathy, hepatomegaly, splenomegaly, or anemia.[] The patient does not have an enlarged liver or spleen, anemia, or low levels of platelets.[] If untreated, the white cell count can rise so high that blood flow slows down and anemia becomes severe.[]

    Missing: Diffuse Hepatic Steatosis
  • Sjögren Syndrome

    Leukocytoclastic cutaneous vasculitis, hypocomplementemia, and HCV infection are associated with the presence of cryoglobulins in the sera of patients with primary SS.[] On admission, she presented with anemia, elevated C-reactive protein levels, anasarca, and hepato-splenomegaly.[] Laboratory investigations suggested anemia, thrombocytopenia, significantly increased lactic dehydrogenase, schistocytes in peripheral blood smear, and a disintegrin-like[]

    Missing: Diffuse Hepatic Steatosis
  • Polyarteritis Nodosa

    Gibson Cutaneous Vasculitis Rheum Dis Clin North Am, 21 (1995), pp. 1097-1112 [3.] M.J. Dillon, B.M.[] A 73-year-old gentleman who presented with progressive anemia and scant hemoptysis developed acute kidney injury over the course of hospital admission.[] […] infections Indications for Testing Unexplained systemic illness with multiple system involvement (renal, neurologic, dermatologic) Laboratory Testing Nonspecific testing CBC – anemia[]

    Missing: Diffuse Hepatic Steatosis
  • Cryoglobulinemia

    The patient had a complete clinical response, with the disappearance of serum cryoglobulins and all signs of cutaneous vasculitis and with the normalization of kidney-function[] A 76-year-old woman was diagnosed with chronic active Epstein-Barr virus (EBV) infection (CAEBV) with sustained fever, anemia, numbness of the lower limbs, and liver dysfunction[] Ten days after she received the second dose, painful necrotic and bullous purpura of the legs, suggestive of cutaneous vasculitis, developed. The lesion . . .[]

    Missing: Diffuse Hepatic Steatosis
  • Hairy Cell Leukemia

    We present a 37-year-old man with paraneoplastic leukocytoclastic vasculitis complicating newly diagnosed HCL.[] Here, we describe a patient with HCL who initially presented with pancytopenia and received a diagnosis of aplastic anemia.[] Hairy cell leukemia Chronic leukemia Aplastic anemia Cladribine Pentostatin AlphaMed Press[]

    Missing: Diffuse Hepatic Steatosis
  • Kawasaki Disease

    cutaneous vasculitis.[] Severe hemolytic anemia (HA) is an uncommon adverse reaction of intravenous immunoglobulin (IVIg) administration.[] Moreover, overt bleeding and anemia are associated with the use of aspirin, and anemia is common in patients with KD.[]

    Missing: Diffuse Hepatic Steatosis

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