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120 Possible Causes for Anemia, Eosinophilia, Erythema Elevatum Diutinum

  • Exfoliative Dermatitis

    Microcytic hypochromic anemia, elevated erythrocyte sedimentation rate, eosinophilia, low serum proteins and electrolytes were salient laboratory features.[] We present the first two cases of this adverse effect of the drug, combined with eosinophilia but no systemic symptoms.[] […] of skin following febrile illness Desquamation secondary to acute systemic illness Drug-induced desquamation of skin Epidermal collarette Erythema elevatum diutinum Erythema[]

  • Inflammatory Bowel Disease Type 1

    Moreover, anemia may result from IBD therapies, such as sulfasalazine, which may confound the problem. 7 Anemia of inflammation or anemia of chronic disease (ACD) is characterized[] Marjorie M Walker, Kavita R Aggarwal, Lisa SE Shim, Milan Bassan, Jamshid S Kalantar, Martin D Weltman, Michael Jones, Nicholas Powell and Nicholas J Talley, Duodenal eosinophilia[] Diagnosis of erythema elevatum diutinum secondary to Crohn's disease with associated peripheral spondyloarthritis was assumed.[]

  • Dermatitis Herpetiformis

    We report a case of a 12-year-old girl who presented with a vesiculobullous eruption on her face, neck, trunk and genital and oral mucosa, as well as anemia, sterile pyuria[] Involvement of other organs varies and includes the liver (hepatomegaly, icterus, hepatitis and hepatic encephalopathy), lymphadenopathy, eosinophilia, and others. [ 46, 338[] Erythema elevatum diutinum is a chronic form of vasculitis associated with IgA paraproteinemia.[]

  • Sweet Syndrome

    It is important to evaluate Sweet syndrome patients who have laboratory evidence of anemia for an underlying malignancy.[] […] erythema multiforme, erythema nodosum, erythema elevatum diutinum, Hansen's disease, pyoderma gangrenosum, bromoderma, leukocytoclastic vasculitis and facial granuloma with eosinophilia[] Rule out following condition: Neutrophilic dermatoses - Abscess or cellulitis, bowel (intestinal) bypass syndrome, Erythema Elevatum Diutinum , granuloma faciale, leukocytoclastic[]

  • Kawasaki Disease

    Severe hemolytic anemia (HA) is an uncommon adverse reaction of intravenous immunoglobulin (IVIg) administration.[] However, in CSS there is predominant eosinophilia ( 10%/ml) and positive ANCA in 60% to 70% of the patients, with p-ANCA pattern 20, 28.[] Moreover, overt bleeding and anemia are associated with the use of aspirin, and anemia is common in patients with KD.[]

  • Pemphigus

    None of the patients showed any clinical sign of systemic lupus erythematosus, AIH, primary biliary cirrhosis, autoimmune atrophic gastritis, or pernicious anemia.[] Erythema elevatum diutinum. Bullous diseases (Pemphigoid, mucous membrane Pemphigoid). Chronic bullous disease of childhood.[] Additionally, a peripheral blood eosinophilia may be present, occurring in half of BP patients. Diagnosis of BP is summarized in Box 1 . Box 1.[]

  • Eosinophilic Fasciitis

    It has been associated with hematologic disorders, such as aplastic anemia.[] Erythema elevatum diutinum - lacks Grenz zone. Inflammatory pseudotumour. Image: Granuloma faciale ( .[] In addition to systemic sclerosis, the prototype idiopathic fibrosing disorder, these conditions include the eosinophilia-myalgia syndrome, epidemic toxic oil syndrome, eosinophilic[]

  • Eosinophilic Angiocentric Fibrosis

    Rosai–Dorfman disease, splenic sclerosing angiomatoid nodular transformation, cutaneous plasmacytosis, perforating collagenosis, and autoimmune atrophic gastritis (pernicious anemia[] All laboratory tests were unremarkable, except the nasal discharge eosinophil count that showed a conspicuous eosinophilia.[] : A systematic review 2014 0 28 93% Erythema elevatum diutinum: a review of presentation and treatment 2014 0 46 91% Granuloma faciale: a case report and review of the literature[]

  • Vasculitis

    Blood Anemia (low hematocrit or red blood cell count) and/or a slightly elevated white blood cell count.[] All serologic studies were normal except for increased levels of rheumatoid factor and eosinophilia.[] elevatum diutinum and localized, chronic fibrosing vasculitis Lymphocytic, non-necrotizing vasculitis of small, superficial vessels: bilateral nonblanching purpuric and pigmented[]

  • Relapsing Polychondritis

    Reports of RP patients with autoimmune hemolytic anemia (AIHA) are extremely rare and cases with the mixed-type AIHA has not been reported.[] Leukocytosis is inconstant, but eosinophilia is found in 40% of cases Plasma viscosity or ESR is usually raised The rheumatoid factor and antinuclear factor are often positive[] elevatum diutinum [ 7 ], have been described in the iterature.[]

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