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92 Possible Causes for Anemia, Erythema Elevatum Diutinum, Polyarteritis Nodosa

  • Relapsing Polychondritis

    Polychondritis as a concomitant feature of polyarteritis nodosa. Clin Exp Dermatol 1982 ; 7 : 519 –22. 4 Conn DL, Dickson ER, Carpenter HA.[] Reports of RP patients with autoimmune hemolytic anemia (AIHA) are extremely rare and cases with the mixed-type AIHA has not been reported.[] Anemia at diagnosis was a marker for decreased survival in the entire group.[]

  • Microscopic Polyangiitis

    We reported an 11-year-old girl without respiratory symptoms with sever anemia which shows signs of hemolytic anemia in test data.[] Erythema elevatum diutinum in acquired immune deficiency syndrome: Can it be an immune reconstitution inflammatory syndrome?.[] POLYARTERITIS NODOSA WHAT IS POLYARTERITIS NODOSA?[]

  • Kawasaki Disease

    Severe hemolytic anemia (HA) is an uncommon adverse reaction of intravenous immunoglobulin (IVIg) administration.[] Erythema elevatum diutinum ; 3. Facial granuloma.[] Nodosa KAWASAKI DISEASE Kd Infantile Polyarteritis edit English Kawasaki disease Human disease in which blood vessels throughout the body become inflamed Kawasaki's disease[]

  • Sweet Syndrome

    nodosa) Erythema nodosum Bullous lesions: Bullous pyoderma gangrenosum Bullous leukocytoclastic vasculitis Autoimmune bullous diseases (eg, bullous pemphigoid, bullous systemic[] It is important to evaluate Sweet syndrome patients who have laboratory evidence of anemia for an underlying malignancy.[] Rule out following condition: Neutrophilic dermatoses - Abscess or cellulitis, bowel (intestinal) bypass syndrome, Erythema Elevatum Diutinum , granuloma faciale, leukocytoclastic[]

  • Vasculitis

    A biopsy of subcutaneous nodes finds an anatomopathologic lesion of polyarteritis nodosa.[] Blood Anemia (low hematocrit or red blood cell count) and/or a slightly elevated white blood cell count.[] elevatum diutinum and localized, chronic fibrosing vasculitis Lymphocytic, non-necrotizing vasculitis of small, superficial vessels: bilateral nonblanching purpuric and pigmented[]

  • Cutaneous Leukocytoclastic Vasculitis

    The patient was a 25-year-old man who had palpable purpura on his legs which showed leukocytoclastic vasculitis, and polyarteritis nodosa.[] CBC and other blood tests are needed to check for anemia, to determine platelet count and serum creatinine level, and to check for elevated levels of acute-phase reactants[] Erythema elevatum diutinum (EED) is a leukocytoclastic vasculitis followed by repair and fibrosis.[]

  • Cutaneous Vasculitis

    KEYWORDS: Cutaneous polyarteritis nodosa; Cutaneous vasculitis; HSP; Leukocytoclastic vasculitis; Palpable purpura; Pediatric[] […] laboratory data were increased erythrocyte sedimentation rate (40.2%), presence of serum cryoglobulins (26%), leukocytosis (24.7%), positive antinuclear antibodies (21.1%), anemia[] elevatum diutinum Malignant atrophic papulosis (Degos) Cryoglobulinaemia Recurrent cutaneous necrotising eosinophilic vasculitis ANCA -associated vasculitis Microscopic polyangiitis[]

  • Purpura

    Polyarteritis nodosa is a systemic vasculitis that affects medium or small arteries with necrotizing inflammation; renal glomeruli and arterioles, capillaries, and venules[] […] hemolytic anemia).[] Erythema elevatum diutinum (EED) 5. Granuloma faciale B.Vasculitis in medium-size and large arteries 1. Polyarteritis nodosa (PN) 2.[]

  • Erythema Elevatum Diutinum

    A diagnosis of type II refractory anemia with excess blasts was made based on a blast count of 13% by morphology with immunophenotyping detecting 16% of myeloid blasts positive[] […] for erythema elevatum diutinum.[] […] the diagnosis and monitoring of disease activity in various systemic vasculitides, including granulomatosis with polyangiitis (Wegener's), microscopic polyangiitis (MPO), polyarteritis[]

  • Hepatitis B

    nodosa (PAN) which is the most unique and spectacular extrahepatic manifestation.[] Peripheral blood examination revealed anemia, macrocytosis and severe thrombocytopenia.[] Erythema elevatum diutinum (EED) is a rare, chronic, cutaneous small vessel vasculitis of unclear pathogenesis.[]

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