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23 Possible Causes for Eruptions, Polyclonal Hyperglobulinemia

  • Multicentric Castleman's Disease

    hyperglobulinemia, elevated transaminases and renal disease. 2 , 5 , 7 Dispenzieri et al. 8 analyzed the clinical spectrum of Castleman’s disease in 113 patients.[] A 65-year-old man was admitted with relapsing and remitting fever, scattered skin eruptions and hepatosplenomegaly following combination antiretroviral therapy for his HIV[] […] or thrombocytosis, hypoalbuminemia, renal dysfunction or proteinuria, polyclonal hypergammaglobulinemia, constitutional symptoms, hepatosplenomegaly, effusions or edema, eruptive[]

  • HIV Infection

    The patient reported unprotected sexual contacts a few months before the eruptions. The unilateral distribution was highly suggestive of herpes zoster.[] Hyperactivation is reflected in dramatic polyclonal hyperglobulinemia, only a portion of which is directed against HIV antigens;(59) bone marrow plasmacytosis;(60) heightened[] Demodicosis Inflammatory conditions Seborrhoeic dermatitis Psoriasis (new onset and severe forms, including pustular psoriasis and erythroderma ) Eczema Pruritic papular eruption[]

  • Pyoderma

    One feature is a phenomenon known as pathergy, in which trauma to the skin can cause new eruptions of ulcers in patients with the disease.[] Monoclonal or polyclonal hyperglobulinemia may also be associated with PG.[ 3 ] However, the immunological abnormalities associated with PG are not always consistently observed[] 2016 2017 2018 2019 Billable/Specific Code Type 1 Excludes specified type of rash- code to condition vesicular eruption ( R23.8 ) pustular L08.0 ICD-10-CM Codes Adjacent[]

  • Angioimmunoblastic Lymphadenopathy

    RESULTS: A transient morbilliform eruption of the trunk was seen most often. Other cutaneous features were infiltrated plaques and purpuric or urticarial lesions.[] In one series, other symptoms included weight loss (58%), hepatomegaly (60%), polyclonal hyperglobulinemia (65%), and generalized adenopathy (87%).[] Transient acantholytic dermatosis is a papulovesicular cutaneous eruption first described in 1970.[]

  • Rosai-Dorfman Disease

    […] xanthoma, generalized eruptive histiocytoma, Juvenile xanthogranuloma, inflammatory malignant fibrous histiocytoma, Lepromatous leprosy, Hodgkin's lymphoma.[] hyperglobulinemia.[] BCH overlaps with generalized eruptive histiocytosis, progressive nodular histiocytosis, papular xanthomas, and multiple JXG. 52 Generalized eruptive histiocytosis (GEH) is[]

  • Castleman Disease

    38oC), weight loss, or fatigue ( 2 CTCAE lymphoma score for B-symptoms) †Large spleen and/or liver †Fluid accumulation: edema, anasarca, ascites, or pleural effusion †Eruptive[] The disease is characterized by fever, weight loss, anemia, polyclonal hyperglobulinemia, splenomegaly, thrombocytosis and peripheral lymphadenopathy.[] […] symptom 1 Weakness and fatigue Enlarged liver or spleen: 41-78% of iMCD patients were reported to have this symptom 1 Peripheral neuropathy (numbness in the hands and feet) Eruption[]

  • H Syndrome

    Upper medial incisors erupt late, often after the age of 6 years.[] […] development of spasticity (abnormally stiff muscles and restricted movements) Seizures (these are rare) Some teeth may be already present at birth (natal teeth) Dentition (eruption[] […] of teeth) is delayed, and the first teeth to erupt are the deciduous molars, not the incisors as usual.[]

  • Hyperglobulinemic Purpura

    Other immunologic abnormalities include a polyclonal hyperglobulinemia and positive tests for cryoglobulins; these cryoglobulins may contain monoclonal IgMK proteins.[] Ensure that you’re up to speed with the hottest topics in dermatology, including drug eruptions from new medications, new therapeutics for melanoma, as well as viral infections[] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[]

  • Allergic Gastritis

    Such eruptions are treated immediate cancellation of the medicine.[] Elevated serum IgE, elevated levels of tumor necrosis factor (TNF-α) and interleukin-5 (IL-5) [ 17 ], polyclonal hyperglobulinemia, and good response to steroids are additional[] No eruption was present and neurological exam was grossly intact. The patient gave written consent for publication of this report.[]

  • Polyclonal Hypergammaglobulinemia

    A description is given of two patients with peculiar multiple skin eruptions, asymptomatic generalized lymphadenopathy, and polyclonal hypergammaglobulinemia.[] NOS ( R77.1 ) monoclonal gammopathy (of undetermined significance) ( D47.2 ) Excludes2 transplant failure and rejection ( T86 .-) D89.0 Polyclonal hypergammaglobulinemia[] A syndrome of peculiar multiple skin eruptions, generalized lymphadenopathy, and polyclonal hypergammaglobulinemia. ( 3777978 ) Watanabe S....Mori S. 1986 21 Helper T-cell[]

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