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31 Possible Causes for Hyperglobulinemic, Purpuras

Did you mean: hyperglobulinemia, purpura

  • Hyperglobulinemic Purpura

    We described a patient who developed characteristic lesions of hyperglobulinemic purpura in the course of IgA myeloma.[] Other terms Hyperglobulinemic Purpuras,Purpuras, Hyperglobulinemic,Waldenstrom Hyperglobulinemic Purpura,Hyperglobulinemic Purpura, Waldenstrom,Purpura, Waldenstrom Hyperglobulinemic[] Abstract This is the first description of a patient with both polymyositis and Waldenström hyperglobulinemic purpura.[]

  • Waldenstrom Macroglobulinemia

    Cutaneous manifestations are usually nonspecific such as purpura, ulcers, and urticarial lesions.[] It is also called hyperglobulinemic purpura, macroglobulinemia, Waldenstrom purpura, and Waldenstrom syndrome.[] This suggests that the mechanism of immune thrombocytopenia in our case is different from that of idiopathic thrombocytopenic purpura.[]

  • Cutaneous Leukocytoclastic Vasculitis

    Patients with hyperglobulinemic purpura, which may be a subset of leukocytoclastic vasculitis, should be examined for associated conditions.[] The absence of IgA ACAs in Henoch-Schönlein purpura argues against their being an epiphenomenon in vasculitis.[] Purpura resolved after specific treatment of multiple myeloma and diagnosis of paraneoplastic purpura was asserted.[]

  • Erythema Elevatum Diutinum

    It seems noteworthy that purpura and hemorrhagic blisters of the soles were found in all cases and developed in one case as the initial lesions.[] Orthostatic purpura Purpura fulminans Purpura secondary to clotting disorders Purpuric agave dermatitis Pigmentary purpuric eruptions Solar purpura Traumatic purpura Waldenström hyperglobulinemic[] A case of EED in a patient with history of splenectomy for idiopathic thrombocytopenic purpura (ITP) is presented, where the late cutaneous lesions were excised and skin grafted[]

  • Bortezomib

    Abstract The treatment of refractory immune-mediated thrombocytopenia purpura (ITP) can be challenging.[] Hyperglobulinemic purpura disappeared, and prednisone tapering succeeded. Because of chronicity, no clinical changes were observed in sicca symptoms.[] Acquired thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening condition caused by autoantibody-mediated inhibition of ADAMTS13 (a disintegrin and metalloproteinase[]

  • Polyclonal Hypergammaglobulinemia

    D69.2 ICD-10-CM Diagnosis Code D69.2 Other nonthrombocytopenic purpura 2016 2017 2018 2019 Billable/Specific Code Applicable To Purpura NOS Purpura simplex Senile purpura[] […] purpura Hyperglobulinemic purpura (disorder) Monoclonal gammopathy with three clones Monoclonal gammopathy with two clones Major Diagnostic Categories M.D.C MDC Category[] […] disorders involving the immune mechanism, NEC (D89) D89.0 Polyclonal hypergammaglobulinemia Code Version: 2019 ICD-10-CM Synonyms Benign primary hypergammaglobulinemic purpura Hyperglobulinemic[]

  • Henoch-Schönlein Purpura

    Palpable purpura Palpable purpura , a manifestation of vascular inflammation, is the hallmark presentation of HSP presents regardless of age group.[] Associations dataset. thrombotic thrombocytopenic purpura Gene Set thrombotic thrombocytopenic purpura Gene Set autoimmune thrombocytopenic purpura Gene Set purpura Gene Set hyperglobulinemic[] Abstract Henoch-Schönlein purpura is the most common childhood vasculitis, but may also affect adults.[]

  • Necrotizing Vasculitis

    Purpura and focal areas of cutaneous infarction were present on the legs. There were scabies burrows on the wrists and hands, and a mite was extracted.[] […] protozoa, helminthic), serum sickness, a variety of collagen vascular diseases (systemic lupus erythematous, Sjögren's syndrome, rheumatoid arthritis, Behçet's disease) hyperglobulinemic[] Abstract A 53-year-old man with chronic hepatitis-C virus infection presented with livedo reticularis, purpura, and leg ulcers.[]

  • Monoclonal Gammopathy of Undetermined Significance

    Abstract A 79-year-old Japanese male who had been suffering from renal insufficiency of unknown causes visited us with reddish papules and purpura on both forearms of a month's[] CONCLUSIONS: CSH is characterized by the accumulation of reactive histiocytes filled with immunoglobulin crystals in various tissues and is frequently associated with systemic hyperglobulinemic[] Biomedical Sciences, Nagasaki University, Sakamoto 1-7-1, Nagasaki 852-8501, Japan. [email protected] Abstract Thrombotic microangiopathy (TMA)/thrombotic thrombocytopenic purpura[]

  • Cryoglobulinemia

    The phenomenon is generally seen after several years of chronicity predominantly in the female population resulting in arthralgias, purpuras, and other symptoms, due to vasculitis[] […] thrombocytopenic purpura, hemolytic uremic syndrome, atrial myxoma) Cryoglobulinemic hyperviscosity syndrome (type I) Proliferative: polyclonal/monoclonal gammopathy (Waldenstrom hyperglobulinemic[] D69.2 ICD-10-CM Diagnosis Code D69.2 Other nonthrombocytopenic purpura 2016 2017 2018 2019 Billable/Specific Code Applicable To Purpura NOS Purpura simplex Senile purpura[]

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