<?xml version="1.0"?>
<rss version="2.0"><channel><title>Neue Studien: Psoriasis im JDDG</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/?d=1</link><description>Neue Studien: Psoriasis im JDDG</description><language>de</language><item><title>Uneinheitliche Standards beim Tuberkulose&#x2010;Screening und der pr&#xE4;ventiven Tuberkulosetherapie vor Beginn einer systemischen Psoriasistherapie</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/uneinheitliche-standards-beim-tuberkulose%E2%80%90screening-und-der-pr%C3%A4ventiven-tuberkulosetherapie-vor-beginn-einer-systemischen-psoriasistherapie-r637/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC13238406?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">637</guid><pubDate>Mon, 29 Jun 2026 08:21:11 +0000</pubDate></item><item><title>PeakPASI as a marker of maximum psoriasis severity: a single-center, cross-sectional retrospective and questionnaire-based study.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/peakpasi-as-a-marker-of-maximum-psoriasis-severity-a-single-center-cross-sectional-retrospective-and-questionnaire-based-study-r636/</link><description><![CDATA[<h4>Background</h4>The Psoriasis Area and Severity Index (PASI) is the standard measure for psoriasis severity but reflects only a single time point and may underestimate long-term disease burden. To assess whether the highest-ever recorded PASI (PeakPASI) can serve as a marker of historical disease severity and correlate with treatment burden and comorbidities.<h4>Patients and methods</h4>A cross-sectional analysis of 308 psoriasis patients from a German university hospital was conducted. Data on PASI, PeakPASI, therapies, and comorbidities were obtained from self-report and medical records. Group comparisons used non-parametric tests; Poisson regression assessed PeakPASI as a predictor of systemic therapy use and comorbidity burden.<h4>Results</h4>Median PeakPASI (11.4 [IQR 5.9-17.0]) exceeded current PASI (2.0 [IQR 1.0-5.1]). PeakPASI ≥ 10 was associated with more systemic therapies (p &lt; 0.001), phototherapy (p &lt; 0.001), smoking (p = 0.021), and diabetes (p = 0.020). PeakPASI correlated with number of systemic (ρ = 0.296), topical therapies (ρ = 0.367), and hospital visits (ρ = 0.186). It significantly predicted systemic therapy use (β = 0.355, p &lt; 0.001), but not comorbidity burden.<h4>Conclusions</h4>PeakPASI may complement current measures by reflecting historical severity and informing treatment. While not a cumulative burden marker, it may prevent underestimation of long-term disease impact. Prospective validation is warranted.<p><a href="http://europepmc.org/article/MED/42219818?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">636</guid><pubDate>Mon, 29 Jun 2026 08:21:11 +0000</pubDate></item><item><title>S1 Guideline: Therapy of generalized pustular psoriasis.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/s1-guideline-therapy-of-generalized-pustular-psoriasis-r635/</link><description><![CDATA[The S1 guideline "Therapy of generalized pustular psoriasis (GPP)" is a German guideline developed in accordance with the criteria of the AWMF. The full version addresses clinical presentation, pathogenesis, diagnosis and differential diagnosis, comorbidities, and therapy. In addition, therapy recommendations for adults with GPP are provided. Both approved and off-label therapies are considered. The present article is a shortened version of the guideline, whose  therapy recommendations are presented in full and without omission.<p><a href="http://europepmc.org/article/MED/42290078?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">635</guid><pubDate>Mon, 29 Jun 2026 08:21:11 +0000</pubDate></item><item><title>Severe generalized pustular psoriasis complicated with staphylococcal toxic shock syndrome treated with spesolimab and antibiotics.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/severe-generalized-pustular-psoriasis-complicated-with-staphylococcal-toxic-shock-syndrome-treated-with-spesolimab-and-antibiotics-r634/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/42290097?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">634</guid><pubDate>Mon, 29 Jun 2026 08:21:11 +0000</pubDate></item><item><title>Trust in skincare and topical therapies in atopic dermatitis or psoriasis: a German cross-sectional study.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/trust-in-skincare-and-topical-therapies-in-atopic-dermatitis-or-psoriasis-a-german-cross-sectional-study-r633/</link><description><![CDATA[<h4>Background and objectives</h4>Trust in therapy impacts adherence and satisfaction in chronic inflammatory skin diseases, including atopic dermatitis (AD) and psoriasis (PSO). This study assessed and compared trust in skincare and topical therapies and explored influencing factors among AD and PSO patients.<h4>Patients and methods</h4>Cross-sectional surveys of AD or PSO patients were conducted at two dermatological university centers in Germany. Group differences were analyzed using Mann-Whitney U and Kruskal-Wallis tests; associations between trust (6-point Likert scale: 1 = very high, 6 = none) and demographics, disease severity, pruritus, pain, and quality of life (QoL) using Spearman correlations. All analyses were exploratory.<h4>Results</h4>Among 253 AD or PSO patients (median age 53.0 years, interquartile range 36.0-63.0; 43.9% female) median trust in skin care and topical therapies was moderate. AD patients reported significantly higher trust than PSO patients. In AD, trust in skin care correlated with pruritus intensity (p &lt; 0.001), pain intensity (p &lt; 0.05), and QoL (p &lt; 0.001); trust in topical therapy correlated with QoL (p &lt; 0.01). No significant correlations were observed in PSO.<h4>Conclusions</h4>Trust levels were higher in AD than in PSO but tended to decline with increasing disease burden and poorer QoL. Enhancing patient education and shared decision-making may help improve trust and adherence.<p><a href="http://europepmc.org/article/MED/42290123?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">633</guid><pubDate>Mon, 29 Jun 2026 08:21:11 +0000</pubDate></item><item><title>Unterschiedliche anatomische Spezifit&#xE4;ten des residualen PASI bei Biologikatherapien der Psoriasis</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/unterschiedliche-anatomische-spezifit%C3%A4ten-des-residualen-pasi-bei-biologikatherapien-der-psoriasis-r622/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC13140128?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">622</guid><pubDate>Mon, 25 May 2026 08:01:34 +0000</pubDate></item><item><title>Dermal lipomatous metaplasia in chronic plaque psoriasis: A clinicopathological case report.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/dermal-lipomatous-metaplasia-in-chronic-plaque-psoriasis-a-clinicopathological-case-report-r621/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/42144885?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">621</guid><pubDate>Mon, 25 May 2026 08:01:34 +0000</pubDate></item><item><title>Dupilumab-Induced Psoriasis in a Patient with Bullous Pemphigoid.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/dupilumab-induced-psoriasis-in-a-patient-with-bullous-pemphigoid-r620/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/42101339?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">620</guid><pubDate>Thu, 14 May 2026 18:05:27 +0000</pubDate></item><item><title>Safety of biologic therapy in psoriasis patients with a previous malignancy: Retrospective study using TriNetX.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/safety-of-biologic-therapy-in-psoriasis-patients-with-a-previous-malignancy-retrospective-study-using-trinetx-r609/</link><description><![CDATA[<h4>Background and objectives</h4>Evidence-based recommendations for the treatment of patients with psoriatic disease (PsO) and a prior history of malignancy are limited. This study aimed to compare the incidence of newly diagnosed neoplasms among patients with PsO and a previous malignancy receiving treatment with conventional systemic therapies, apremilast, or biologic agents.<h4>Patients and methods</h4>Retrospective observational study using TriNetX. PsO patients (ICD10:L40) with a previous diagnosis of cancer (ICD10:C00-D49) less than 5 years prior to systemic therapy initiation were selected. Outcomes evaluated included new documentation of neoplasms and all-cause mortality.<h4>Results</h4>Patients under biologic therapy had a significantly lower new neoplasm documentation rate and all-cause mortality compared to classical agents (HR 0.857 and HR 0.705, respectively) and apremilast (HR 0.782 and HR 0.803, respectively) at 3 years follow-up. Only TNFi exhibited a significantly lower new neoplasm rate (HR 0.867, p &lt; 0.0001) compared to classical agents; however, all biologic agents significantly decreased mortality. IL-23i was the only biologic therapy to significantly lower cancer recurrence risk (RR 0.878) compared to TNFi, with no differences in all-cause mortality.<h4>Conclusions</h4>Biologic therapy for PsO may represent a safe treatment option in patients with a history of malignancy, compared with conventional systemic therapies or apremilast. Among biologic agents, IL-23 inhibitors appear to be associated with the most favorable safety profile.<p><a href="http://europepmc.org/article/MED/41978521?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">609</guid><pubDate>Thu, 23 Apr 2026 06:10:08 +0000</pubDate></item><item><title>Evidence- and consensus-based guideline on lichen sclerosus.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/evidence-and-consensus-based-guideline-on-lichen-sclerosus-r582/</link><description><![CDATA[The German-language, consensus- and evidence-based S3 guideline on lichen sclerosus (LS) was developed based on the European "EuroGuiDerm Guideline on lichen sclerosus" under the leadership of the German Dermatological Society (DDG) and the German Society for Gynecology and Obstetrics (DGGG). Particular emphasis was placed on adapting the recommendations to the healthcare conditions in German-speaking countries. The interdisciplinary guideline development group consisted of 24 experts from 16 medical societies and actively included patient representatives in the development process. The guideline provides comprehensive recommendations on diagnosis, patient management, follow-up care, and patient education, as well as the treatment of both genital and extragenital LS in women, men, girls, and boys. Regardless of age or sex, ultrapotent or potent topical glucocorticosteroids in combination with emollients remain the standard therapy for genital LS. In male patients with LS-associated phimosis who do not respond sufficiently to standard therapy, circumcision with complete removal of the foreskin is indicated. For extragenital LS, phototherapy with UV light is recommended as an adjunct to topical treatment. Topical calcineurin inhibitors are second-line therapy.<p><a href="http://europepmc.org/article/MED/41778748?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">582</guid><pubDate>Fri, 10 Apr 2026 10:21:31 +0000</pubDate></item><item><title>Evidenz&#x2010; und konsensbasierte (S3) Leitlinie: Lichen sclerosus</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/evidenz%E2%80%90-und-konsensbasierte-s3-leitlinie-lichen-sclerosus-r581/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC13059059?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">581</guid><pubDate>Fri, 10 Apr 2026 10:21:31 +0000</pubDate></item><item><title>The role of inflammatory cell death in type 1 dominant inflammatory skin diseases.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/the-role-of-inflammatory-cell-death-in-type-1-dominant-inflammatory-skin-diseases-r580/</link><description><![CDATA[While there has been significant progress in the development of new therapies for psoriasis and atopic dermatitis in recent years, innovation in the field of type 1 dominant skin diseases is still limited. This category comprises diseases characterized by a cytotoxic immune reaction directed against resident skin cells. The histological correlate is interface dermatitis, defined by a subepidermal inflammatory infiltrate associated with epidermal keratinocyte apoptosis. Representative conditions include lichen planus, cutaneous lupus erythematosus, erythema multiforme, alopecia areata, and vitiligo. Immunologically, there is a dominance of Th1 cells, which mediate their effects through interferon-γ and tumor necrosis factor-α. Recent findings have shown that, in addition to apoptosis, other forms of cell death are also activated by this immune response, such as necroptosis. In contrast to apoptosis, necroptosis represents a strong immunological stimulus and thus further intensifies the local inflammatory response. These findings open new therapeutic perspectives, as numerous necroptosis inhibitors are currently under investigation for various inflammatory diseases. The present review summarizes the immunopathogenesis of type 1-dominant skin diseases and highlights emerging therapeutic strategies, including the inhibition of inflammatory cell death.<p><a href="http://europepmc.org/article/MED/41937512?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">580</guid><pubDate>Fri, 10 Apr 2026 10:21:31 +0000</pubDate></item><item><title>Should TNF inhibitors be avoided in psoriasis patients with latent tuberculosis?</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/should-tnf-inhibitors-be-avoided-in-psoriasis-patients-with-latent-tuberculosis-r579/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41954303?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">579</guid><pubDate>Fri, 10 Apr 2026 10:21:31 +0000</pubDate></item><item><title>Palmoplantare Pustulose: Entstehung, Differentialdiagnose und Therapie</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/palmoplantare-pustulose-entstehung-differentialdiagnose-und-therapie-r578/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC13059063?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">578</guid><pubDate>Fri, 10 Apr 2026 10:21:31 +0000</pubDate></item><item><title>Palmoplantar pustulosis: pathogenesis, differential diagnosis, and treatment.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/palmoplantar-pustulosis-pathogenesis-differential-diagnosis-and-treatment-r577/</link><description><![CDATA[Palmoplantar pustulosis (PPP) is a chronic inflammatory and often painful disease characterized by sterile pustules on the palms and soles, significantly impairing quality of life. Women are more frequently affected than men, and smoking is a major trigger. Under biologic therapies, especially TNF antagonists, a paradoxical PPP may occur. PPP is associated with psoriasis vulgaris and may be accompanied by osteoarticular involvement. Pathogenetically, PPP likely begins around the acrosyringium, with the pustules consisting almost exclusively of infiltrating neutrophilic granulocytes attracted by chemotactic factors secreted by activated keratinocytes. Inflammation is sustained through a self-amplifying cytokine network, including interleukin (IL)-17, IL-19, and related mediators. Treatment options for PPP include topical treatments, UV-phototherapies - particularly topical PUVA (Psoralen plus UVA) therapy- and systemic therapies. Systemic agents comprise conventional treatments such as acitretin, methotrexate, fumaric acid esters, and ciclosporin, newer small molecules like apremilast and Janus kinase inhibitors, as well as biologics. Conventional systemic therapies are often not sufficiently effective in PPP and associated with side effects. Currently, among systemic therapies, only acitretin is approved for PPP. In recent years, placebo-controlled studies have demonstrated a significant effect of apremilast, brodalumab, guselkumab and risankizumab on PPP, and further studies with topical and systemic Janus kinase inhibitors as well as IL-17A/F inhibitors are underway.<p><a href="http://europepmc.org/article/MED/41948989?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">577</guid><pubDate>Fri, 10 Apr 2026 10:21:31 +0000</pubDate></item><item><title>Ixekizumab optimization in moderate-to-severe plaque psoriasis in real clinical practice: a retrospective multicenter study.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/ixekizumab-optimization-in-moderate-to-severe-plaque-psoriasis-in-real-clinical-practice-a-retrospective-multicenter-study-r539/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/MED/41830197?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">539</guid><pubDate>Mon, 30 Mar 2026 08:02:13 +0000</pubDate></item><item><title>Psychoeducational schema therapy for psoriasis and atopic dermatitis: a randomized controlled pilot crossover trial.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/psychoeducational-schema-therapy-for-psoriasis-and-atopic-dermatitis-a-randomized-controlled-pilot-crossover-trial-r538/</link><description><![CDATA[<h4>Background and objectives</h4>Atopic dermatitis and psoriasis are chronic inflammatory skin diseases often linked to psychological stress. Integrative care models are lacking. This randomized pilot study aimed to develop and test a psychoeducational intervention for dermatology patients.<h4>Patients and methods</h4>Patients with a PHQ-2 score ≥ 3 at an outpatient inflammation center were randomized into an intervention or control group. The intervention group received three standardized educational sessions focusing on maladaptive schemas, coping strategies, psychoeducation, and emotion-focused techniques (e.g. chair-dialogues, imaginary rescripting).<h4>Results</h4>19 patients received the intervention; 13 were in the control group. Post-intervention, significant improvements were observed in dermatological quality of life (DLQI), subjective well-being (WHO-5), and depressive symptoms (PHQ-9, BDI-II). Psychological benefits were largely independent of disease severity (PASI, EASI). Qualitative feedback highlighted usability, learning specific techniques, and a trusting therapeutic relationship.<h4>Conclusions</h4>A brief psychoeducational intervention significantly reduced psychological stress in dermatology outpatients. Further studies are needed to evaluate long-term effects and broader implementation.<p><a href="http://europepmc.org/article/MED/41854066?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">538</guid><pubDate>Mon, 30 Mar 2026 08:02:13 +0000</pubDate></item><item><title>Simulation der Auswirkungen eines edukativen und digitalen Ansatzes unter Verwendung von Patient&#x2010;Journey&#x2010;Modellen, um praktische Herausforderungen bei der Behandlung der chronischen spontanen Urtikaria in Deutschland zu bew&#xE4;ltigen</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/simulation-der-auswirkungen-eines-edukativen-und-digitalen-ansatzes-unter-verwendung-von-patient%E2%80%90journey%E2%80%90modellen-um-praktische-herausforderungen-bei-der-behandlung-der-chronischen-spontanen-urtikaria-in-deutschland-zu-bew%C3%A4ltigen-r508/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12968974?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">508</guid><pubDate>Wed, 11 Mar 2026 05:52:25 +0000</pubDate></item><item><title>Lebensqualit&#xE4;t bei Patienten mit vernarbender und nicht vernarbender Alopezie: eine explorative Querschnittsstudie</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/lebensqualit%C3%A4t-bei-patienten-mit-vernarbender-und-nicht-vernarbender-alopezie-eine-explorative-querschnittsstudie-r507/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12968979?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">507</guid><pubDate>Wed, 11 Mar 2026 05:52:25 +0000</pubDate></item><item><title>Erfolgreiche Behandlung einer palmoplantaren Pustulose mit Bimekizumab und topischer Photochemotherapie bei gleichzeitig bestehender Hidradenitis suppurativa</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/erfolgreiche-behandlung-einer-palmoplantaren-pustulose-mit-bimekizumab-und-topischer-photochemotherapie-bei-gleichzeitig-bestehender-hidradenitis-suppurativa-r506/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12968939?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">506</guid><pubDate>Wed, 11 Mar 2026 05:52:25 +0000</pubDate></item><item><title>S3 Guideline for the Treatment of Psoriasis vulgaris, adapted from EuroGuiDerm - part 2: Specific clinical and comorbid situations.</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/s3-guideline-for-the-treatment-of-psoriasis-vulgaris-adapted-from-euroguiderm-part-2-specific-clinical-and-comorbid-situations-r460/</link><description><![CDATA[The present Part 2 of the updated German S3 guideline on the treatment of psoriasis vulgaris provides recommendations for therapy selection in special clinical situations and in the presence of comorbidities. A major focus of this update is the chapter on screening for tuberculosis as well as therapy selection and management in latent tuberculosis. The recommendations regarding the use of interferon-gamma release assays and the indication for chest radiography have been extensively revised. In addition, the guidance on the suitability of systemic psoriasis therapies in patients with latent tuberculosis and on the need for preventive antituberculous treatment has been thoroughly updated. In the chapter on inflammatory bowel diseases, risankizumab and guselkumab have been added as recommended treatment options, as both agents have recently been approved for the indications Crohn's disease and ulcerative colitis. Further substantial revisions are included in the chapters on patients with a history of malignancy and viral hepatitis.<p><a href="http://europepmc.org/article/MED/41641952?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">460</guid><pubDate>Sun, 22 Feb 2026 17:23:04 +0000</pubDate></item><item><title>Wohlbefinden bei Patienten mit Vitiligo mit Beteiligung der sichtbaren Hautareale und der Genitalregion in Deutschland&#x2013; eine fragebogengest&#xFC;tzte Pilotstudie</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/wohlbefinden-bei-patienten-mit-vitiligo-mit-beteiligung-der-sichtbaren-hautareale-und-der-genitalregion-in-deutschland-eine-fragebogengest%C3%BCtzte-pilotstudie-r449/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12875177?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">449</guid><pubDate>Tue, 10 Feb 2026 08:00:26 +0000</pubDate></item><item><title>Schambezogene St&#xF6;rungen bei Patienten mit atopischer Dermatitis und Psoriasis &#x2013; eine explorative, Querschnitts&#x2010;Interviewstudie zu Pr&#xE4;valenz und Korrelaten k&#xF6;rperdysmorpher St&#xF6;rungen und sozialer Angstst&#xF6;rungen</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/schambezogene-st%C3%B6rungen-bei-patienten-mit-atopischer-dermatitis-und-psoriasis-eine-explorative-querschnitts%E2%80%90interviewstudie-zu-pr%C3%A4valenz-und-korrelaten-k%C3%B6rperdysmorpher-st%C3%B6rungen-und-sozialer-angstst%C3%B6rungen-r448/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12875169?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">448</guid><pubDate>Tue, 10 Feb 2026 08:00:26 +0000</pubDate></item><item><title>S3 Guideline for the Treatment of Psoriasis vulgaris, adapted from EuroGuiDerm &#x2013; part 2: Specific clinical and comorbid situations</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/s3-guideline-for-the-treatment-of-psoriasis-vulgaris-adapted-from-euroguiderm-part-2-specific-clinical-and-comorbid-situations-r447/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12875186?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">447</guid><pubDate>Tue, 10 Feb 2026 08:00:26 +0000</pubDate></item><item><title>S3&#x2010;Leitlinie zur Therapie der Psoriasis vulgaris, adaptiert von EuroGuiDerm &#x2013; Teil 2: Hilfestellungen f&#xFC;r besondere klinische Situationen und bei Vorliegen von Komorbidit&#xE4;ten</title><link>https://www.psoriasis-news.de/articles.html/2_psoriasis-im-jddg/s3%E2%80%90leitlinie-zur-therapie-der-psoriasis-vulgaris-adaptiert-von-euroguiderm-teil-2-hilfestellungen-f%C3%BCr-besondere-klinische-situationen-und-bei-vorliegen-von-komorbidit%C3%A4ten-r446/</link><description><![CDATA[<small>No abstract supplied.</small><p><a href="http://europepmc.org/article/PMC/PMC12875179?source=rss" rel="external nofollow">Weiterlesen</a></p>]]></description><guid isPermaLink="false">446</guid><pubDate>Tue, 10 Feb 2026 08:00:26 +0000</pubDate></item></channel></rss>
