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146 Possible Causes for Acute Cholecystitis, Hemoglobin Decreased

  • Hereditary Spherocytosis

    All experienced an increase in hemoglobin and decrease in reticulocyte count early after LPS and at last follow-up. Twenty-two were sent for genetic analysis.[] Pigmented gallstones (calcium bilirubinate) Elevated reticulocyte count, indirect bilirubin, serum LDH Treatment : Folic acid supplementation Splenectomy Complications : Acute[] Post-splenectomy blood changes include an increased hemoglobin level, decreased reticulocyte count, and the appearance of specific inclusion bodies and target cells.[]

  • Viral Hepatitis

    In total, 40.8% patients with acute hepatitis B virus developed immunity.[] CMV may also invade the hepatobiliary tract in AIDS patients causing hepatitis, pancreatitis, and acute acalculous cholecystitis 6,7 .[] The most frequently reported symptom was fatigue (73.7%), and the most common complications were cholecystitis (0.4%) and fulminant hepatitis (0.4%).[]

  • Subphrenic Abscess

    cholecystitis.[] Subdiaphragmatic abscess is usually a complication of inflammation of the abdominal cavity: perforated appendicitis, perforated gastric and duodenal ulcers, severe acute cholecystitis[] Symptoms are often misdiagnosed as acute cholecystitis.[]

  • Cooley's Anemia

    Cooley's anemia disease causes a dramatic decrease in the production of hemoglobin, resulting in anemia. This anemia can cause people to be more tired than normal.[] Early recognition and stabilization of acute complications—i.e., sepsis, transfusion reactions, drug reactions, or cholecystitis—require close communication between the primary[] However, hemoglobin (Hb) levels often decrease over time, splenomegaly appears, and progressive iron overload occurs from increased gastrointestinal iron absorption.[]

  • Sickle Cell Disease

    Mean decrease in sickle hemoglobin levels was higher in automated-red blood cell exchange (p 0.001) and permitted a higher sickle hemoglobin level decrease per volume removed[] Cholelithiasis may be asymptomatic or result in acute cholecystitis, requiring surgical intervention. The liver may also become involved.[] By inhibiting sickling, increased levels of fetal hemoglobin might decrease the frequency of painful crises.[]

  • Cystic Fibrosis

    […] and development while decreasing or eliminating transfusional iron overload, which is the leading life-threatening factor in patients with this disease.[ 134 ] Butyrate analogs[] The development of an effective therapy to increase hemoglobin levels in homozygous β-thalassemia, without the use of red blood cell transfusions, could allow normal growth[] […] are able to induce erythroid differentiation[ 135 – 137 ] and stimulate hemoglobin F production in human erythroid progenitors in vitro .[ 138 – 140 ] In vivo , they reactivate[]

  • Tuberculosis

    Increases were also seen in hemoglobin concentration and red blood cell parameters ( P 0.015), reflecting resolution of microcytic anemia as treatment progressed.[] Of the hematological parameters investigated, platelet count, neutrophil count, and monocyte count decreased during the course of treatment ( P 0.0018), but lymphocyte count[] Decreases in erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) ( P 1.24 10 12 ) and an increase in serum albumin concentration ( P 5.17 10 21 ) were also seen[]

  • Peptic Ulcer

    cholecystitis and peptic ulcer disease.[] Cholelithiasis Esophageal perforation Inflammatory bowel disease Irritable bowel syndrome Rarely mistaken Abdominal aortic aneurysm Acute coronary syndrome Barrett esophagus[] SCB Medical College, Cuttack, Odisha, India. Abstract We report a case of duodenal adenocarcinoma, who presented to the emergency ward, with features of acute[]

  • Acute Hepatic Porphyria

    Acute hepatic porphyria is a term encompassing four types of porphyria, in which the production of toxic heme precursors occurs in the liver and causes acute attacks of abdominal pain, nausea, neurological and mental changes, as well as hypertension and pain in the head and neck and/or chest. The diagnosis is[…][]

  • Acute Intermittent Porphyria

    Acute intermittent porphyria (AIP) belongs to a group of hereditary diseases known as porphyrias which are characterized by defective heme metabolism, leading to excessive cellular secretion of porphyrins and their precursors. Patients with AIP will experience abdominal pain, neuropathies and constipation without[…][]

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