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3,141 Possible Causes for Bronchial Mucosal Biopsy with Edema, Hemoglobinuria, Leukocytes Increased

  • Cerebral Malaria

    If not treated on time, it can lead to complications like jaundice, hemoglobinuria, tender and enlarged spleen, acute renal failure, and uremia, and is fatal in about 20%[] […] in the same pathological outcome: a severe increase in ICP leading to brainstem herniation and death from respiratory arrest.[] […] with abnormal behavior, impairment of consciousness, seizures, coma, or other neurologic abnormalities Severe anemia due to hemolysis (destruction of the red blood cells) Hemoglobinuria[]

  • Autoimmune Hemolytic Anemia

    March hemoglobinuria Paroxysmal cold hemoglobinuria Type 1 Excludes hemoglobinuria NOS ( R82.3 ) Use Additional code (Chapter 20) to identify external cause D59.6 ) The following[] Classifications of AIHA include warm AIHA, cold agglutinin syndrome, paroxysmal cold hemoglobinuria, mixed-type AIHA, and drug-induced AIHA.[] ( ICD-10-CM Diagnosis Code D59.6 Hemoglobinuria due to hemolysis from other external causes 2016 2017 2018 2019 Billable/Specific Code Applicable To Hemoglobinuria from exertion[]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Malaria

    Hemoglobinuria (blackwater fever), a darkening of the urine seen with severe RBC hemolysis, results from high parasitemia and is often a sign of impending renal failure and[] The leukocyte count is usually normal or low, but neu-trophilia with a marked increase in band forms (left shift) is present in the majority of cases.[]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Bartonella Infection

    Bartonella (formerly Rochalimaea) quintana is the etiological agent of trench fever, a disease extensively reported during the World Wars. Recent molecular biology approaches have allowed dramatic extension of the spectrum of Bartonella infections. B. quintana is now also recognized as an etiological agent of fever[…][]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Mesenteric Vein Thrombosis

    […] categories: Venous hypercoagulability – Examples of thrombophilia include factor deficiency (protein S/C or anti-thrombin III), lupus anticoagulants, paroxysmal nocturnal hemoglobinuria[] Additional laboratory studies may reveal excessive levels of acids and increased accumulations of ketone bodies in bodily tissues and fluids (ketoacidosis), increased levels[] Patients with inflammatory bowel disease and patients with certain blood disorders, including myeloproliferative neoplasms and paroxysmal nocturnal hemoglobinuria, sometimes[]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Intestinal Infarction

    A patient with paroxysmal nocturnal hemoglobinuria of 14 years duration presented with severe abdominal pain and fever.[] Peritoneal fluid may be sero-sanguinous, and contain increased protein and leukocyte levels, as the disease progresses, these levels rise further, and the fluid takes on a[] , phospholipase A 2 is activated during reperfusion, increasing the formation of cytotoxic lysophospholipids within the ischemic tissue and up-regulating the production of[]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Leukemoid Reaction

    Paroxysmal nocturnal hemoglobinuria (PNH) has been observed to evolve into myelofibrosis and acute myeloid leukemia.[] Leukemoid Reaction (LR) is defined by reactive increase in leukocyte count of more than 50,000/cu mm with increase in mature leukocytes on peripheral blood.[] (PCH)発作性寒冷血色素尿症 paroxysmal nocturnal hemoglobinuria (PNH)発作性夜間血色素尿症 peripheral blood stem cell transplantation (PBSCT)抹消血幹細胞移植 petechia出血斑 phlebotomy静脈切開、しゃ(瀉)血(ステッドマン) phosphorylation[]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Hereditary Spherocytosis

    […] usually mild; treatment is splenectomy Includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria[] Additionally, daily oral penicillin prophylaxis for 3-5 years afterwards Differential Diagnosis : 1) Autoimmune hemolytic anemia (negative family history) 2) Paroxysmal nocturnal hemoglobinuria[] CDA: congenital dyserythropoietic anemia; AIHA: autoimmune hemolytic anemia; HE: hereditary elliptocytosis; PNH: paroxysmal noctural hemoglobinuria As regards the NaCl osmotic[]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Disseminated Intravascular Coagulation

    Malignancy, including acute leukemias, but also solid-organ malignancies Intravascular hemolysis, including transfusion reaction, drug induced hemolysis, and Paroxysmal nocturnal hemoglobinuria[] leukocyte infiltration and tissue destruction in various organs 81.[] […] mixed-breed dog (12 years old) with severe anemia, bleeding tendency, increased serum indirect bilirubin concentration, acanthocytosis of the peripheral blood, and severe hemoglobinuria[]

    Missing: Bronchial Mucosal Biopsy with Edema
  • Leukemia

    […] myeloid leukemia (CML), myelodysplastic syndrome (MDS), myeloproliferative neoplasms (MPN), and bone marrow failure diseases such as aplastic anemia, paroxysmal nocturnal hemoglobinuria[] Leukemia leads to an uncontrolled increase in the number of white blood cells.[] Studies in CLL have shown that, in some individuals, there is emergence of a paroxysmal nocturnal hemoglobinuria, CD52 clone following treatment with CAMPATH-1H. 20 This clone[]

    Missing: Bronchial Mucosal Biopsy with Edema

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