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<rss version="2.0"><channel><title>Neue Studien: Psoriasis im JDDG</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/page/3/?d=1</link><description>Neue Studien: Psoriasis im JDDG</description><language>de</language><item><title>Unerw&#xFC;nschte Wirkungen von Januskinase&#x2010;Inhibitoren mit Relevanz f&#xFC;r den dermatologischen Klinik&#x2010; und Praxisalltag</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/unerw%C3%BCnschte-wirkungen-von-januskinase%E2%80%90inhibitoren-mit-relevanz-f%C3%BCr-den-dermatologischen-klinik%E2%80%90-und-praxisalltag-r256/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12435117?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">256</guid><pubDate>Fri, 10 Oct 2025 06:15:28 +0000</pubDate></item><item><title>Adverse effects of Janus kinase inhibitors with relevance for daily practice in dermatology.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/adverse-effects-of-janus-kinase-inhibitors-with-relevance-for-daily-practice-in-dermatology-r255/</link><description><![CDATA[Used since 2011 in the USA and 2012 in the EU, Janus kinase inhibitors (JAKi) are gaining increasing acceptance as a treatment for dermatological diseases such as atopic dermatitis, psoriasis, psoriatic arthritis, alopecia areata, chronic hand eczema and vitiligo. Knowledge of their mechanism of action and potential side effects is necessary for a safe and effective use. Their short half-life requires daily administration, enables good controllability and is appreciated by many patients due to the rapid onset of action and the absence of subcutaneous or intravenous injections. Common side effects are upper respiratory tract infections as well as varicella zoster virus reactivations. Serious infections can occur in rare cases, which may take a problematic course. An increased risk of cardiovascular events has been described in certain JAKi, so alternative treatment should be preferred in patients at cardiovascular risk. In studies on rheumatoid arthritis, an increased incidence of malignancies (bronchial carcinoma, lymphoma) was observed with tofacitinib. JAKi have also been associated with more aggressive progression of epithelial skin tumors. Animal studies indicate teratogenic effects during pregnancy. Older patients and those at increased risk should only receive JAKi after careful risk-benefit assessment. Appropriate preliminary examinations and regular laboratory monitoring are necessary to ensure safe therapy.<p><a href="http://europepmc.org/article/MED/40952332?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">255</guid><pubDate>Fri, 10 Oct 2025 06:15:28 +0000</pubDate></item><item><title>Successful treatment of palmoplantar pustulosis with topical ruxolitinib.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/successful-treatment-of-palmoplantar-pustulosis-with-topical-ruxolitinib-r244/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40847898?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">244</guid><pubDate>Thu, 04 Sep 2025 18:54:25 +0000</pubDate></item><item><title>Impfen in der Dermatologie 2025: Update mit Ber&#xFC;cksichtigung aktueller Empfehlungen der St&#xE4;ndigen Impfkommission</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/impfen-in-der-dermatologie-2025-update-mit-ber%C3%BCcksichtigung-aktueller-empfehlungen-der-st%C3%A4ndigen-impfkommission-r200/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12338436?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">200</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>Vitiligo</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/vitiligo-r199/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12338405?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">199</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>Vitiligo</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/vitiligo-r198/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12338427?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">198</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>Pyoderma gangrenosum and spider bites: a case series.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/pyoderma-gangrenosum-and-spider-bites-a-case-series-r197/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40417860?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">197</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>A phase IIb single-center study to assess the efficacy of apremilast for the treatment of nummular eczema.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/a-phase-iib-single-center-study-to-assess-the-efficacy-of-apremilast-for-the-treatment-of-nummular-eczema-r196/</link><description><![CDATA[<h4>Background</h4>The pathogenesis of nummular eczema (NE) remains unclear, and no targeted therapy has been approved. Apremilast is a small molecule inhibitor targeting phosphodiesterase-4.<h4>Patients and methods</h4>A phase IIb randomized, double-blind, placebo-controlled study evaluating the effects of apremilast or placebo in patients with NE. Patients received apremilast (30 mg BID) or placebo until week 16 followed by an open label phase in which all patients were treated with apremilast until week 32. The primary endpoint was the number of patients achieving an improvement in Physician's Global Assessment (PGA) by two or more points or an absolute PGA of 0 or 1 at week 16. Secondary endpoints included changes in skin physiology, life quality, or dermato-pathology.<h4>Results</h4>33 patients were enrolled, of whom 31 were randomized to apremilast (n  =  15) or placebo (n  =  16). 1/15 (6.7%) patients in the apremilast group and 4/16 (25.0%) in the placebo group reached the primary endpoint (p  =  0.369). There was no difference between placebo and apremilast with regard to all secondary endpoints at week 16 and week 32. The safety profile was in accordance with the known safety profile of apremilast.<h4>Conclusion</h4>Phosphodiesterase-4 inhibition by apremilast showed no beneficial effects for the treatment of NE.<p><a href="http://europepmc.org/article/MED/40548467?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">196</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>Pyoderma gangrenosum und Spinnenbisse: eine Fallserie</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/pyoderma-gangrenosum-und-spinnenbisse-eine-fallserie-r195/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12338411?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">195</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>Monozentrische Phase&#x2010;IIb&#x2010;Studie zur Wirksamkeit von Apremilast beim nummul&#xE4;rem Ekzem</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/monozentrische-phase%E2%80%90iib%E2%80%90studie-zur-wirksamkeit-von-apremilast-beim-nummul%C3%A4rem-ekzem-r194/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12338416?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">194</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>Psoriasis treated with dithranol: a pilot study on in vivo reflectance confocal microscopy.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/psoriasis-treated-with-dithranol-a-pilot-study-on-in-vivo-reflectance-confocal-microscopy-r193/</link><description><![CDATA[<h4>Background</h4>There are only limited histomorphological data on the response of psoriatic skin lesions to topical dithranol. In vivo reflectance confocal microscopy (RCM) in psoriatic skin is highly correlated with histopathological findings and allows non-invasive monitoring of treatment effects on a cellular level.<h4>Patients and methods</h4>Prospective, single-center pilot study at a university-based clinic of dermatology between January 1<sup>st</sup> and August 30<sup>th</sup>, 2016. Psoriatic lesions of 20 patients receiving dithranol treatment were assessed by RCM at baseline, day 4 and 8 of treatment.<h4>Results</h4>RCM measurements of psoriatic lesions receiving dithranol treatment revealed epidermal histomorphological changes with a strong median reduction of baseline hyperkeratosis by 45.0% (p &lt; 0.001), acanthosis by 38.2% (p &lt; 0.001), and epidermal thickness by 66.5% (p &lt; 0.001) from baseline until day 8. Moreover, semiquantitative measurements of parakeratosis also showed a significant reduction until day 8 (p &lt; 0.001). Correspondingly, RCM revealed dermal histomorphological changes with a decrease in diameter of dermal papillae by 32.1% (p &lt; 0.001), decrease in diameter of papillary vessels by 16.9% (p = 0.002) and a strong semiquantitative reduction of the inflammatory infiltrate (p &lt; 0.001).<h4>Conclusions</h4>Results from our pilot study indicate that topical dithranol treatment of psoriatic lesions may induce a rapid and marked reduction of pathologic epidermal and dermal RCM features.<p><a href="http://europepmc.org/article/MED/40790927?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">193</guid><pubDate>Sat, 23 Aug 2025 07:41:29 +0000</pubDate></item><item><title>Routineversorgung von Prurigo nodularis in Deutschland: eine retrospektive Analyse der Krankenakten (ADVANCE PN)</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/routineversorgung-von-prurigo-nodularis-in-deutschland-eine-retrospektive-analyse-der-krankenakten-advance-pn-r162/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12257052?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">162</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>Evaluation of routine care of prurigo nodularis in Germany: retrospective chart review study (ADVANCE PN).</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/evaluation-of-routine-care-of-prurigo-nodularis-in-germany-retrospective-chart-review-study-advance-pn-r161/</link><description><![CDATA[<h4>Background and objectives</h4>Knowledge on patient care gaps of prurigo nodularis (PN) is limited. This retrospective chart review (ADVANCE PN) investigated unmet medical needs and gaps in diagnostics, treatment, and management of patients with PN in routine care in Germany.<h4>Patients and methods</h4>Medical records for adults newly diagnosed with PN between January 2012 and December 2022 from dermatologic clinics and office-based dermatologists were analyzed. Baseline demographics, treatment patterns, diagnostics, symptoms, patient-reported outcomes (PROs), and disease-specific scores are reported.<h4>Results</h4>Records of 363 patients from 42 sites were analyzed. Median age (range) was 67 (19-95) years; most patients were female (61.7%), Caucasian (73.4%), and retired (57.3%). Overall, 209 (62.2%) patients had comorbidities (most common: hypertension [28.3%]). Clinically, most patients had nodules (81.1%) or papules (66.7%). PROs, disease-specific scores, and laboratory assessments were performed for 32 (8.8%), 12 (3.3%), and 71 (19.7%) patients, respectively. Topical corticosteroids (TCS) were the most common overall (90.9%) and first-line therapy (84.9%); for second-line therapy, 'no further treatment' was most commonly documented (58.6%).<h4>Conclusions</h4>The findings of ADVANCE PN indicate a high unmet need in the current state of medical care, evidenced by shortcomings in PRO assessment, PN documentation, and adherence to guidelines on PN.<p><a href="http://europepmc.org/article/MED/40484725?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">161</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>Erkennen &#x2013; Der klinische Blick auf die kutane Tuberkulose</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/erkennen-der-klinische-blick-auf-die-kutane-tuberkulose-r160/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12257059?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">160</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>Recognising cutaneous tuberculosis.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/recognising-cutaneous-tuberculosis-r159/</link><description><![CDATA[Tuberculosis (TB) continues to be a leading cause of death in many countries, and also remains a significant concern in Germany, particularly due to migration. The diagnosis of rare cutaneous tuberculosis is challenging as it manifests in various clinical forms that resemble more common dermatological conditions. Especially in paucibacillary forms, gold-standard diagnostic tests may yield negative results, complicating the identification of the disease. Therefore, a strong clinical suspicion based on the clinical presentation is essential for guiding further or repeated diagnostic evaluations. In this article, we present various forms of cutaneous tuberculosis, using excerpts from the image collection of the Department of Dermatology and Allergy at Biederstein, Technical University of Munich, to improve clinical recognition of cutaneous TB and raise awareness of this condition also as a potential differential diagnosis.<p><a href="http://europepmc.org/article/MED/40613433?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">159</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>Glutenbedingte Hauterkrankungen: Klinik, Diagnostik und Therapie</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/glutenbedingte-hauterkrankungen-klinik-diagnostik-und-therapie-r158/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12257071?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">158</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>Gluten-related skin disorders: clinical presentation, diagnostic and treatments.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/gluten-related-skin-disorders-clinical-presentation-diagnostic-and-treatments-r157/</link><description><![CDATA[Gluten-related disorders (GRDs) encompass a spectrum of clinical manifestations triggered by gluten ingestion in genetically susceptible individuals. These disorders include celiac disease (CD) and non-celiac gluten sensitivity (NCGS) and present with both intestinal and extraintestinal symptoms, including skin manifestations. Besides the well-known association between CD and dermatitis herpetiformis, considered as the cutaneous manifestation of CD, other dermatoses have been associated to GRDs. In this paper, we provide a concise overview of the clinical appearance, diagnosis and therapeutic management of GRDs, a tool which we hope will facilitate clinicians when faced with this challenging group of diseases.<p><a href="http://europepmc.org/article/MED/40631603?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">157</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>A case of successful treatment of nail psoriasis with abrocitinib.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/a-case-of-successful-treatment-of-nail-psoriasis-with-abrocitinib-r156/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40677022?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">156</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>Optimizing biologics for chronic plaque psoriasis: insights on non-medical interruptions of IL-17, IL-12/23, and IL-23 inhibitors.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/optimizing-biologics-for-chronic-plaque-psoriasis-insights-on-non-medical-interruptions-of-il-17-il-1223-and-il-23-inhibitors-r155/</link><description><![CDATA[<h4>Background and objectives</h4>Continuous biologic treatment is recommended for patients with psoriasis; however, treatment interruption in daily practice is inevitable. The impact of treatment interruption is difficult to study in a real-world setting. In Taiwan, biologics are reimbursed by the National Health Insurance for moderate-to-severe psoriasis for a 2-year course, followed by regulatory discontinuation. Thus, our study provides pragmatic data on the impact of the interruption of biologics treatment for non-medical reasons on therapy effectiveness.<h4>Patients and methods</h4>This single-center retrospective cohort study recruited patients who underwent two consecutive 2-year courses of biologics between 2012 to 2021.<h4>Results</h4>A total of 192 treatment courses from 61 patients were analyzed, with secukinumab and ustekinumab being the most frequently administered biologics. Among patients who continued with the same biologic across two consecutive courses, the time to achieve PASI 75 was shorter during the first course compared to the second, while overall maintenance effects remained similar. Switching to a different biologic usually produced superior results in the second course of treatment.<h4>Conclusions</h4>Although the overall effectiveness after interruption and resumption of treatment with secukinumab or ustekinumab was comparable, the time to achieve PASI 75 was longer following an interruption. Continuous, uninterrupted treatment with a given biologic is therefore recommended whenever possible.<p><a href="http://europepmc.org/article/MED/40719449?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">155</guid><pubDate>Thu, 31 Jul 2025 12:43:38 +0000</pubDate></item><item><title>Secukinumab for erythrodermic psoriasis combined with sepsis: three case reports.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/secukinumab-for-erythrodermic-psoriasis-combined-with-sepsis-three-case-reports-r144/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40641260?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">144</guid><pubDate>Sat, 12 Jul 2025 18:34:11 +0000</pubDate></item><item><title>Generalized pustular psoriasis in a patient with asthma following dupilumab and tezepelumab therapy.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/generalized-pustular-psoriasis-in-a-patient-with-asthma-following-dupilumab-and-tezepelumab-therapy-r122/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/40560362?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">122</guid><pubDate>Thu, 26 Jun 2025 16:19:30 +0000</pubDate></item><item><title>Verl&#xE4;ngerung der Dosierungsintervalle von IL&#x2010;17&#x2010; und IL&#x2010;23&#x2010;Inhibitoren bei erwachsenen Patienten mit Psoriasis: eine Pilotstudie aus der Praxis</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/verl%C3%A4ngerung-der-dosierungsintervalle-von-il%E2%80%9017%E2%80%90-und-il%E2%80%9023%E2%80%90inhibitoren-bei-erwachsenen-patienten-mit-psoriasis-eine-pilotstudie-aus-der-praxis-r85/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12152519?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">85</guid><pubDate>Sat, 14 Jun 2025 05:52:56 +0000</pubDate></item><item><title>Treatment adjustment in biologic therapies for moderate-to-severe plaque psoriasis: a German retrospective chart review (TABU).</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/treatment-adjustment-in-biologic-therapies-for-moderate-to-severe-plaque-psoriasis-a-german-retrospective-chart-review-tabu-r62/</link><description><![CDATA[<h4>Background and objectives</h4>Flexible biologic therapy dosing regimens in psoriasis management are common, but data from routine care in Germany are scarce. This study evaluated treatment adjustments for biologic therapies commonly prescribed in Germany.<h4>Patients and methods</h4>Charts for up to 100 consecutive patients treated at 29 centers were reviewed. Data were extracted for adults (aged 18-65 years) with moderate-to-severe plaque psoriasis treated with adalimumab, guselkumab, ixekizumab, secukinumab, or ustekinumab for ≥ 36 weeks. The primary endpoint was time to first treatment adjustment. Secondary endpoints included frequency of and reasons for treatment adjustments. Time to treatment adjustment was analyzed using Kaplan-Meier methods.<h4>Results</h4>Among 982 patients, 297 treatment adjustments in 240 (24.4%) patients were identified. The mean (median; interquartile range) time to first treatment adjustment (n = 223) was 8.4 (4.0; 2.0-12.0) months (secukinumab: 14.1 [10.0; 4.0-21.0], adalimumab: 11.0 [7.0; 3.0-14.5], ustekinumab: 11.0 [6.0; 2.0-16.0], ixekizumab: 5.8 [3.0; 2.0-8.5], guselkumab: 5.1 [3.0; 2.0-7.0]). The most frequent adjustment type was starting concomitant treatment(s) (10.4% of patients); insufficient skin effectiveness was the most frequent reason for adjustment.<h4>Conclusions</h4>Biological treatment adjustments are frequent in moderate-to-severe psoriasis; flexible dosing regimens would support optimal management.<p><a href="http://europepmc.org/article/MED/39073011?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">62</guid><pubDate>Sun, 01 Jun 2025 17:24:13 +0000</pubDate></item><item><title>Is Kaposi sarcoma a novel comorbidity of cutaneous lymphoma? A systematic review of the literature.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/is-kaposi-sarcoma-a-novel-comorbidity-of-cutaneous-lymphoma-a-systematic-review-of-the-literature-r51/</link><description><![CDATA[<h4>Background and objectives</h4>Patients with cutaneous lymphomas (CL) are at an increased risk of developing secondary malignancies. This study aimed to assess the frequency of association between CL and Kaposi sarcoma (KS) and to identify factors that may promote the co-occurrence of these two diseases.<h4>Patients and methods</h4>On January 25, 2024, we conducted a systematic search of four electronic medical databases to identify all published cases of KS associated with CL. The clinical course and outcomes of these patients were summarized. For critical appraisal, we applied the JBI Checklist for Case Reports. The study was registered in the PROSPERO database (CRD42022313204).<h4>Results</h4>A total of 40 articles reporting on 45 patients were assessed for eligibility. We included 27 cases in the final analysis (26 cutaneous T-cell lymphomas, 1 cutaneous B-cell lymphoma). In 71% of cases, the diagnosis of CL preceded KS. Nearly half (48%) of the patients had erythrodermic mycosis fungoides or Sézary syndrome. KS lesions were predominantly limited to the skin, with complete remission achieved in 53% of cases.<h4>Conclusions</h4>The association between KS and CL is rare, limiting our study due to the small sample size and potential reporting bias. Skin-targeted therapies, a restricted T-cell repertoire, and impaired T-cell responses in erythrodermic CTCL patients may contribute to the development of KS.<p><a href="http://europepmc.org/article/MED/39817814?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">51</guid><pubDate>Fri, 30 May 2025 15:05:38 +0000</pubDate></item><item><title>Keine orale Beteiligung in einer gro&#xDF;en Kohorte von Frauen mit Lichen sclerosus der Vulva &#x2013; eine multizentrische prospektive Studie</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/keine-orale-beteiligung-in-einer-gro%C3%9Fen-kohorte-von-frauen-mit-lichen-sclerosus-der-vulva-eine-multizentrische-prospektive-studie-r50/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC11636959?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">50</guid><pubDate>Fri, 30 May 2025 15:05:38 +0000</pubDate></item></channel></rss>
