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32 Possible Causes for Hemolytic Anemia, Polyclonal Hyperglobulinemia

  • Castleman Disease

    anemia, bone marrow insufficiency, pulmonary, renal, hepatic, and gastrointestinal involvement, emphasizing the difficulty in diagnosis and treatment approach.[ncbi.nlm.nih.gov] The disease is characterized by fever, weight loss, anemia, polyclonal hyperglobulinemia, splenomegaly, thrombocytosis and peripheral lymphadenopathy.[ncbi.nlm.nih.gov] , hypoalbuminemia, polyclonal hypergammaglobulinemia, leukocytosis, thrombocytosis or splenomegaly. 1,4 In contrast to the localized form, the clinical course of the multicentric[scielo.br]

  • Multicentric Castleman's Disease

    anemia, and immune thrombocytopenic purpura (ITP). [4] Last updated: 6/25/2015 In about half of people with multicentric Castleman disease (MCD), it is caused by human herpesvirus[rarediseases.info.nih.gov] hyperglobulinemia, elevated transaminases and renal disease. 2 , 5 , 7 Dispenzieri et al. 8 analyzed the clinical spectrum of Castleman’s disease in 113 patients.[pagepress.org] Laboratory findings typical of MCD are: Autoimmune hemolytic anemia Pancytopenia Polyclonal hypergammaglobulinemia Hypoalbuminemia Elevated C-reactive protein Enhanced levels[symptoma.com]

  • Posthemorrhagic Anaemia of the Newborn

    : drug-absorption, immune complex, AutoAb Immune Hemolytic Anemias: Alloimmune Hemolytic Anemia Transfusion reaction - ABO-incompatible RBCs (intermediate) - Antibodies to[quizlet.com] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[en.wikisource.org] Stomatocytosis 282.9 Hereditary hemolytic anemia, unspecified Hereditary hemolytic anemia NOS 283 Acquired hemolytic anemias 283.0 Autoimmune hemolytic anemias Autoimmune[theodora.com]

  • Angioimmunoblastic Lymphadenopathy

    Angioimmunoblastic lymphadenopathy (AILD) is a rare disorder characterised by generalised lymphadenopathy, fever, hepatosplenomegaly, immune hemolytic anemia and polyclonal[ncbi.nlm.nih.gov] In one series, other symptoms included weight loss (58%), hepatomegaly (60%), polyclonal hyperglobulinemia (65%), and generalized adenopathy (87%).[emedicine.medscape.com] A patient presented with fever, night sweats, generalized lymphadenopathy, cold agglutinin hemolytic anemia, and thrombocytopenia.[ncbi.nlm.nih.gov]

  • Autosomal Dominant Autoimmune Lymphoproliferative Syndrome Type 1

    Bertil Glader, Immune Hemolytic Anemias, Pediatric Hematology, (151-170), (2007). Alexandra H.[doi.org] NOS ( R77.1 ) monoclonal gammopathy (of undetermined significance) ( D47.2 ) Excludes2 transplant failure and rejection ( T86 .-) D89.0 Polyclonal hypergammaglobulinemia[icd10coded.com] Cytopenias in these patients can be the result of splenic sequestration as well as autoimmune complications manifesting as autoimmune hemolytic anemia, immune-mediated thrombocytopenia[ncbi.nlm.nih.gov]

  • Hemolytic Anemia due to a Disorder of Glycolytic Enzymes

    anemia and congenital hemolytic anemia.[malacards.org] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[en.wikisource.org] […] is normal, the diagnosis of hereditary nonspherocytic hemolytic anemia should be considered.[orpha.net]

  • Anemia due to Glutathione Metabolism Disorder

    anemia.[umcutrecht.nl] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[en.wikisource.org] Diagnosis of hemolytic anemia Diagnosis of hemolytic anemia is performed in four steps: Establish that anemia exists.[web2.iadfw.net]

  • Rosai-Dorfman Disease

    A subset of patients with skin limited disease have associated immune disorders such as lupus, autoimmune hemolytic anemia, and Crohn disease.[ncbi.nlm.nih.gov] hyperglobulinemia.[ncbi.nlm.nih.gov] A 32-year-old woman with RDD, who underwent a right mandibulectomy to treat osteomyelitis, and who suffered hemolytic anemia, lymphoproliferative syndrome, and bacterial meningitis[ncbi.nlm.nih.gov]

  • Congenital Intrinsic Factor Deficiency

    Stomatocytosis 282.9 Hereditary hemolytic anemia, unspecified Hereditary hemolytic anemia NOS 283 Acquired hemolytic anemias 283.0 Autoimmune hemolytic anemias Autoimmune[theodora.com] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[en.wikisource.org] Anemia Acute Hemolytic Transfusion Reaction (see Acute Hemolytic Transfusion Reaction, [[Acute Hemolytic Transfusion Reaction]]) Autoimmune Hemolytic Anemia (AIHA) (see Autoimmune[mdnxs.com]

  • Polycythemia Neonatorum

    Excludes1 congenital stenosis and stricture of bile ducts ( Q44.3 ) Crigler-Najjar syndrome ( E80.5 ) Dubin-Johnson syndrome ( E80.6 ) Gilbert syndrome ( E80.4 ) hereditary hemolytic[icd10coded.com] NOS (R77.1) monoclonal gammopathy (of undetermined significance) (D47.2) Excludes2: transplant failure and rejection (T86.-) D89.0 Polyclonal hypergammaglobulinemia Benign[en.wikisource.org] anemias ( D55 - D58 ) Hemorrhagic and hematological disorders of newborn P61 ICD-10-CM Diagnosis Code P61 Other perinatal hematological disorders 2016 2017 2018 2019 Non-Billable[icd10data.com]

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