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22 Possible Causes for Eczema, Pancytopenia, Polyclonal Hyperglobulinemia

  • HIV Infection

    […] osteomalacia* Protease inhibitors with statins: myopathy Hematologic or oncologic Anemia of chronic disease Lymphoma, multiple myeloma Bone marrow infiltration (leading to pancytopenia[] Hyperactivation is reflected in dramatic polyclonal hyperglobulinemia, only a portion of which is directed against HIV antigens;(59) bone marrow plasmacytosis;(60) heightened[] […] ectoparasites Insect bites Scabies Demodicosis Inflammatory conditions Seborrhoeic dermatitis Psoriasis (new onset and severe forms, including pustular psoriasis and erythroderma ) Eczema[]

  • Multicentric Castleman's Disease

    Diffuse lymph-node enlargement, splenomegaly and pancytopenia were detected. Induction with Rituximab was made because pancytopenia was present.[] hyperglobulinemia, elevated transaminases and renal disease. 2 , 5 , 7 Dispenzieri et al. 8 analyzed the clinical spectrum of Castleman’s disease in 113 patients.[] Abstract An HIV positive black African woman presented with widespread lymphadenopathy and pancytopenia that had been ascribed to tuberculosis.[]

  • Primary Myelofibrosis

    This is then followed by pancytopenia (a reduction in the number of red and white blood cells, as well as platelets).[] Polyclonal hyperglobulinemia may be present. Patients with sporadic idiopathic or familial pulmonary hypertension have significant marrow fibrosis.[] The clinical manifestations of PMF include splenomegaly, consequent to extramedullary hematopoiesis, pancytopenias, and an array of potentially debilitating constitutional[]

  • Castleman Disease

    There is often significant anemia which may be hemolytic, often reflecting pancytopenia or hemophagocytic syndrome (Stebbing 2009).[] The disease is characterized by fever, weight loss, anemia, polyclonal hyperglobulinemia, splenomegaly, thrombocytosis and peripheral lymphadenopathy.[] , hypoalbuminemia, polyclonal hypergammaglobulinemia, leukocytosis, thrombocytosis or splenomegaly. 1,4 In contrast to the localized form, the clinical course of the multicentric[]

  • Angioimmunoblastic Lymphadenopathy

    Laboratory findings included progressive pancytopenia, hyperuricemia, and acute renal failure. Bone marrow biopsy showed a T cell lymphoid neoplasm that had ...[] In one series, other symptoms included weight loss (58%), hepatomegaly (60%), polyclonal hyperglobulinemia (65%), and generalized adenopathy (87%).[] V 26766; 2678 Page 1774 and 1775: 1763 valve of coronary sinus26759 v Page 1776 and 1777: 1765 vanillylmandelic acid* valvula Page 1778 and 1779: 1767 vascular dementiai eczema[]

  • Autosomal Dominant Autoimmune Lymphoproliferative Syndrome Type 1

    […] lymphoproliferative syndrome (ALPS) is a rare, newly recognized, chronic lymphoproliferative disorder in children and is characterized by lymphadenopathy, splenomegaly, pancytopenia[] NOS ( R77.1 ) monoclonal gammopathy (of undetermined significance) ( D47.2 ) Excludes2 transplant failure and rejection ( T86 .-) D89.0 Polyclonal hypergammaglobulinemia[] Severe autoimmune cytopenias (requiring immunosuppressive treatment at least twice a year), lymphadenopathy, and IgG level were predictive of ALPS (B), whereas pancytopenia[]

  • Congenital Intrinsic Factor Deficiency

    Gene GIF (AR) Diagnostic Test Plasma Vitamin B12, Folate Neurological Ataxia, dystonia Non-Neurological Megaloblastic anemia, pancytopenia Treatment HydroxyCobalamin Level[] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[] The GIF splice site mutation (c.79 1G A) was also found in a 15 year old boy with megaloblastic anemia with pancytopenia, slight proteinuria and slightly elevated methylmalonate[]

  • Posthemorrhagic Anaemia of the Newborn

    […] with malformations 284.1 Pancytopenia Excludes: pancytopenia (due to) (with): aplastic anemia NOS (284.9) bone marrow infiltration (284.2) constitutional red blood cell aplasia[] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[] This causes a depression of all blood elements: (pancytopenia): red blood cells (anemia), white blood cells (leukopenia), and platelets (thrombocytopenia).[]

  • Polycythemia Neonatorum

    Excludes1: pancytopenia (due to) (with): aplastic anemia (D61.-) bone marrow infiltration (D61.82) congenital (pure) red cell aplasia (D61.01) drug induced (D61.1) hairy[] Eczema - Nummular (Nummular Eczema) Eczema (Atopic Dermatitis) Eczema with infection Edema - Peripheral, Peripheral Edema (Foot, Leg, and Ankle Swelling) Edema (Swelling)[] […] bronchitis 慢性支氣管炎 Chronic nasopharyngitis 慢性鼻咽炎 Chronic sinusitis 慢性鼻竇炎 Congenital anomaly,unspecified 先天畸形未明示者 Conjunctivitis 結膜炎 Constipation 便秘 Contact dermatitis and other eczema[]

  • Pediatric Chronic Granulomatous Disease

    He developed pancytopenia, hypofibrinogenemia, transaminitis, and elevated ferritin of 11 783 ng/mL.[] Polyclonal hyperglobulinemia 3. Elevated acute phase reactants such as ESR or CRP 4. Normal studies of T and B lymphocyte immunity Diagnostic test 1.[] CGD can cause many types of skin infections that are hard to treat, including: Blisters or sores on the face (impetigo) Eczema Growths filled with pus (abscesses) Pus-filled[]

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