Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Cholecystitis associated with Enterobacter agglomerans.

C Nilakul, S Sukroongreung, S Fucharoen

    The Southeast Asian Journal of Tropical Medicine and Public Health
    |June 1, 1984
    PubMed
    Summary
    This summary is machine-generated.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Co-inheritance of α<sup>0</sup> -thalassemia elevates Hb A<sub>2</sub> level in homozygous Hb E: Diagnostic implications.

    International journal of laboratory hematology·2017
    Same author

    Diagnosis of common hemoglobinopathies among South East Asian population using capillary isoelectric focusing system.

    International journal of laboratory hematology·2016
    Same author

    ICSH recommendations for assessing automated high-performance liquid chromatography and capillary electrophoresis equipment for the quantitation of HbA2.

    International journal of laboratory hematology·2015
    Same author

    Tandem measurements of iron and creatinine by cross injection analysis with application to urine from thalassemic patients.

    Talanta·2014
    Same author

    Red blood cell microparticles in hemoglobin E disorders.

    International journal of laboratory hematology·2014
    Same author

    Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis.

    Clinical genetics·2013

    A case of chronic cholecystitis caused by Enterobacter agglomerans in a patient with beta-thalassemia was successfully treated with surgery and antibiotics. This highlights potential predisposing factors like immune deficiency in such infections.

    Area of Science:

    • Infectious Diseases
    • Gastroenterology
    • Hematology

    Background:

    • Chronic cholecystitis is gallbladder inflammation. Beta-thalassemia is a genetic blood disorder. Enterobacter agglomerans is a bacterium.
    • Patients with chronic illnesses and immune deficits are susceptible to infections.

    Observation:

    • A 54-year-old female with homozygous beta-thalassemia presented with chronic cholecystitis.
    • The causative agent identified was Enterobacter agglomerans.

    Findings:

    • The patient underwent successful cholecystectomy (gallbladder removal).
    • Post-operative treatment with sulfamethoxazole and trimethoprim resolved the infection.
    • The exact source of Enterobacter agglomerans infection remained undetermined.

    Related Experiment Videos

    Implications:

    • Cystic duct obstruction and immune deficiency are potential predisposing factors for Enterobacter agglomerans-related cholecystitis in beta-thalassemia patients.
    • This case underscores the importance of considering unusual pathogens in immunocompromised individuals.
    • Prompt diagnosis and appropriate antimicrobial therapy combined with surgical intervention are crucial for managing complex cases.