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

Papular mucinosis with IgG(K) M component

F W Danby, C W Danby, W Pruzanski

    Canadian Medical Association Journal
    |May 22, 1976
    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

    'Invasive proliferative gelatinous mass' of hidradenitis suppurativa contains distinct inflammatory components.

    The British journal of dermatology·2019
    Same author

    Personal history of rosacea and risk of incident cancer among women in the US.

    British journal of cancer·2015
    Same author

    Diverse activity of human secretory phospholipases A2 on the migration of human vascular smooth muscle cells.

    Inflammation research : official journal of the European Histamine Research Society ... [et al.]·2015
    Same author

    Preliminary findings suggest hidradenitis suppurativa may be due to defective follicular support.

    The British journal of dermatology·2013
    Same author

    New, relevant information and innovative interventions in the management of acne.

    Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia·2011
    Same author

    Reducing government spending.

    Canadian Medical Association journal·2010

    This study reports a rare case of papular mucinosis associated with an IgG kappa M component. The findings suggest papular mucinosis may be a systemic condition linked to plasma cell disorders.

    Area of Science:

    • Dermatology
    • Hematology
    • Immunology

    Background:

    • Papular mucinosis is a rare skin condition characterized by mucin deposition in the dermis.
    • Monoclonal gammopathies, such as M components, can be associated with various systemic diseases.

    Observation:

    • A 59-year-old woman presented with papular mucinosis and an immunoglobulin G kappa (IgG(K)) M component in her serum.
    • This specific combination of papular mucinosis and IgG(K) M component is exceptionally rare, with only three prior reported cases.

    Findings:

    • The case highlights the association between papular mucinosis and a specific type of monoclonal gammopathy (IgG(K)).
    • Papular mucinosis appears to be a systemic disease rather than confined to the skin.
    • The condition is often linked to plasma cell dyscrasias.

    Related Experiment Videos

    Implications:

    • Early identification of M components in patients with papular mucinosis is crucial for understanding potential systemic involvement.
    • The generally benign course of papular mucinosis should be considered, as chemotherapy might have adverse effects.
    • Further research is warranted to elucidate the precise relationship between papular mucinosis and plasma cell dyscrasias.