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            <header>
                <identifier>oai:data.mendeley.com/dm356kv35j.1</identifier>
                <datestamp>2021-12-03T15:40:18Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Rashid, Hanan</dc:creator>
    <dc:title>MMP case series, supplementary material </dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Background: The variable clinical severity of MMP often leads to a diagnostic and therapeutic delay.
Objective: To describe the characteristics in a large cohort of patients with MMP.
Methods: A retrospective review study of clinical and diagnostic characteristics and treatment response in 145 patients with MMP.
Results: Monosite involvement was seen in 41.4% and multisite involvement in 58.6% patients. The oral mucosa was affected in 86.9%, followed by the ocular mucosa (30.3%), skin (26.2%), genital mucosa (25.5%), nasal mucosa (23.4%) and pharyngeal and/or laryngeal mucosa (17.2%). Ocular disease developed during disease course in 41.7% of patients with initially other mucosal site involvement. The malignancy rate was significantly higher in patients with autoantibodies against laminin-332 compared to MMP patients without laminin-332 autoantibodies (35.3% vs. 10.9%, p=0.007). Systemic immunosuppressive or immunomodulatory therapy were administered in 77.1% of the patients, mainly in patients with multisite involvement (p&lt;0.001), ocular involvement (p&lt;0.001) and pharyngeal and laryngeal involvement (p=0.002). The remaining patients (22.9%) received topical therapy. Adverse events were frequently reported.
Limitations: retrospective design.
Conclusion: MMP presents with a heterogeneous clinical presentation and new symptoms may develop during the disease course. Cancer screening should be considered in MMP and in particular with autoantibodies against laminin-332.</dc:description>
    <dc:subject>Dermatology</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/dm356kv35j.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/dm356kv35j.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:date>2021-12-03T15:40:18Z</dc:date>
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