Literature DB >> 31776647

Methicillin-resistant Staphylococcus aureus (MRSA) is an important pathogen in erythrodermic cutaneous T-cell lymphoma (CTCL) patients.

Drew A Emge1,2, Roland L Bassett3, Madeleine Duvic4, Auris O Huen4.   

Abstract

Erythroderma can occur in cutaneous T-cell lymphoma (CTCL). Staphylococcus aureus (S. aureus) prevalence is increased in CTCL patients and contributes to CTCL disease flares. Our primary aim was to describe S. aureus infections, including resistance patterns and the antibiotic treatment regimens used, in erythrodermic CTCL patients. This was a retrospective chart review of erythrodermic CTCL patients who had S. aureus infection or colonization and were treated at the UT MD Anderson Cancer Center's Melanoma Skin Center between 2012 and 2016. Twenty-six erythrodermic CTCL patients had 50 documented S. aureus colonization or infection events. Patients had an improvement in body surface area (BSA) or modified Severity Weighted Assessment Tool (mSWAT) in 53% events treated for S. aureus. Seventeen of the 50 (34%) events were due to methicillin-resistant S. aureus (MRSA). One-third (33%) of MRSA events were initially treated with dicloxacillin. The MRSA isolates were sensitive to trimethoprim-sulfamethoxazole (92%) and doxycycline (88%). Patients treated in the outpatient setting (OR 0.073; 95% CI 0.008-0.627; p = 0.017) and patients with a previous history of topical anti-S. aureus decolonization treatments before S. aureus event as stand-alone (OR 0.125; 95% CI 0.018-0.887; p = 0.038) or in combination treatment with systemic antibiotics (OR 0.094; 95% CI 0.009-0.944; p = 0.045) were less likely to see improvement in BSA or mSWAT from S. aureus treatment. Treatment of S. aureus improved CTCL skin score in a high number of erythrodermic patients. The MRSA prevalence was high in erythrodermic CTCL patients. Clinicians should consider using empiric MRSA antibiotic coverage for these patients.

Entities:  

Keywords:  Cutaneous T-cell lymphoma (CTCL); Erythroderma; Methicillin-resistant Staphylococcus aureus (MRSA); Mycosis fungoides (MF); Staphylococcus aureus; Sézary syndrome (SS)

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Substances:

Year:  2019        PMID: 31776647     DOI: 10.1007/s00403-019-02015-7

Source DB:  PubMed          Journal:  Arch Dermatol Res        ISSN: 0340-3696            Impact factor:   3.017


  3 in total

Review 1.  Transcriptional Heterogeneity and the Microbiome of Cutaneous T-Cell Lymphoma.

Authors:  Philipp Licht; Volker Mailänder
Journal:  Cells       Date:  2022-01-19       Impact factor: 6.600

Review 2.  The Skin Microbiome in Cutaneous T-Cell Lymphomas (CTCL)-A Narrative Review.

Authors:  Magdalena Łyko; Alina Jankowska-Konsur
Journal:  Pathogens       Date:  2022-08-18

3.  Multimodal single-cell analysis of cutaneous T-cell lymphoma reveals distinct subclonal tissue-dependent signatures.

Authors:  Alberto Herrera; Anthony Cheng; Eleni P Mimitou; Angelina Seffens; Dean George; Michal Bar-Natan; Adriana Heguy; Kelly V Ruggles; Jose U Scher; Kenneth Hymes; Jo-Ann Latkowski; Niels Ødum; Marshall E Kadin; Zhengqing Ouyang; Larisa J Geskin; Peter Smibert; Terkild B Buus; Sergei B Koralov
Journal:  Blood       Date:  2021-10-21       Impact factor: 25.476

  3 in total

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