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

Histiocytosis X: a clinical presentation.

J S McDonald, R L Miller, M L Bernstein

    Journal of Oral Pathology
    |November 1, 1980
    PubMed
    Summary

    This case study details a 56-year-old male with chronic oral ulcers, revealing diffuse alveolar bone destruction and diabetes insipidus. Further tests confirmed a diagnosis of histiocytosis X, a rare disorder.

    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

    Impact of the coronavirus disease 2019 (COVID-19) pandemic on the presentation of paediatric acute appendicitis: an observational study.

    Clinical radiology·2022
    Same author

    Effect of Systemic Therapies on Outcomes following Vertebroplasty among Patients with Multiple Myeloma.

    AJNR. American journal of neuroradiology·2016
    Same author

    RNA-Sequencing Analysis of Messenger RNA/MicroRNA in a Rabbit Aneurysm Model Identifies Pathways and Genes of Interest.

    AJNR. American journal of neuroradiology·2015
    Same author

    Racial and health insurance disparities of inpatient spine augmentation for osteoporotic vertebral fractures from 2005 to 2010.

    AJNR. American journal of neuroradiology·2014
    Same author

    Pelvic pain.

    Journal of back and musculoskeletal rehabilitation·2014
    Same author

    Pretreatment advanced imaging in patients with stroke treated with IV thrombolysis: evaluation of a multihospital data base.

    AJNR. American journal of neuroradiology·2013

    Area of Science:

    • Oncology
    • Pathology
    • Endocrinology

    Background:

    • Histiocytosis X, now known as Langerhans cell histiocytosis (LCH), is a rare clonal proliferative disorder of Langerhans cells.
    • LCH can affect multiple organ systems, presenting with diverse clinical manifestations.

    Observation:

    • A 56-year-old male presented with chronic oral ulcers.
    • Initial investigations showed diffuse alveolar bone destruction and diabetes insipidus.
    • Biopsy results were suggestive of histiocytosis X.

    Findings:

    • Histiocytosis X was confirmed through further diagnostic tests.
    • The case highlights the importance of considering rare systemic diseases in patients with seemingly localized symptoms.
    • The discussion includes a clinical differential diagnosis and follow-up of the patient.

    Implications:

    • This case underscores the varied presentations of Langerhans cell histiocytosis, emphasizing the need for comprehensive diagnostic workups.
    • Early recognition and diagnosis are crucial for effective management of histiocytosis X.
    • Understanding the spectrum of LCH manifestations aids clinicians in patient care and differential diagnosis.

    Related Experiment Videos