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	<title>Eczemaletters &#187; Research</title>
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	<link>http://www.eczemaletters.com</link>
	<description>Making sense of eczema</description>
	<pubDate>Fri, 09 May 2008 14:13:19 +0000</pubDate>
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		<title>A randomized, double-blind, vehicle-controlled study of 1% pimecrolimus cream in adult patients with perioral dermatitis.</title>
		<link>http://www.eczemaletters.com/2008/05/09/a-randomized-double-blind-vehicle-controlled-study-of-1-pimecrolimus-cream-in-adult-patients-with-perioral-dermatitis/</link>
		<comments>http://www.eczemaletters.com/2008/05/09/a-randomized-double-blind-vehicle-controlled-study-of-1-pimecrolimus-cream-in-adult-patients-with-perioral-dermatitis/#comments</comments>
		<pubDate>Fri, 09 May 2008 14:13:19 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18462835</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18462835">Related Articles</a></td></tr></table>
        <p><b>A randomized, double-blind, vehicle-controlled study of 1% pimecrolimus cream in adult patients with perioral dermatitis.</b></p>
        <p>J Am Acad Dermatol. 2008 May 5;</p>
        <p>Authors:  Schwarz T, Kreiselmaier I, Bieber T, Thaci D, Simon JC, Meurer M, Werfel T, Zuberbier T, Luger TA, Wollenberg A, Br&#xE4;utigam M</p>
        <p>BACKGROUND: Perioral dermatitis (POD) is a common dermatosis without standard therapy. OBJECTIVE: We sought to evaluate pimecrolimus cream 1% in POD. METHODS: We conducted a multicenter, randomized, double-blind, parallel-group study in adult patients with POD treated twice daily with pimecrolimus cream 1% or vehicle until clearance for up to 4 weeks. Follow-up took place 4 and 8 weeks after treatment. RESULTS: Patients treated with pimecrolimus had an average POD Severity Index score of 2.6 compared with 3.5 for patients treated with vehicle. Both groups had baseline scores of 5.2. The between-group difference was 0.9 (95% confidence level 0.4, 1.4, P = .0011). Patients with history of topical corticosteroids benefited most. Pimecrolimus-treated patients reported greater improvement in quality of life. There were no group differences regarding safety. LIMITATIONS: Pimecrolimus vehicle is not a true placebo. CONCLUSIONS: Pimecrolimus rapidly improves clinical symptoms and quality of life of patients with POD, being most effective in corticosteroid-induced POD.</p>
        <p>PMID: 18462835 [PubMed - as supplied by publisher]</p>
    ]]></description>
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		<title>Treatment of mild to moderate seborrhoeic dermatitis with MAS064D (Sebclair), a novel topical medical device: results of a pilot, randomized, double-blind, controlled trial.</title>
		<link>http://www.eczemaletters.com/2008/05/08/treatment-of-mild-to-moderate-seborrhoeic-dermatitis-with-mas064d-sebclair-a-novel-topical-medical-device-results-of-a-pilot-randomized-double-blind-controlled-trial/</link>
		<comments>http://www.eczemaletters.com/2008/05/08/treatment-of-mild-to-moderate-seborrhoeic-dermatitis-with-mas064d-sebclair-a-novel-topical-medical-device-results-of-a-pilot-randomized-double-blind-controlled-trial/#comments</comments>
		<pubDate>Thu, 08 May 2008 14:11:09 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18269596</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://www.blackwell-synergy.com/openurl?genre=article&#38;sid=nlm:pubmed&#38;issn=0926-9959&#38;date=2008&#38;volume=22&#38;issue=3&#38;spage=290"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.blackwell-synergy.com-templates-jsp-_synergy-images-synergy_linkout.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18269596">Related Articles</a></td></tr></table>
        <p><b>Treatment of mild to moderate seborrhoeic dermatitis with MAS064D (Sebclair), a novel topical medical device: results of a pilot, randomized, double-blind, controlled trial.</b></p>
        <p>J Eur Acad Dermatol Venereol. 2008 Mar;22(3):290-6</p>
        <p>Authors:  Veraldi S, Menter A, Innocenti M</p>
        <p>AIM: MAS064D (Sebclair) is a novel steroid-free cream containing multiple active ingredients. Objective of this pilot study was to evaluate the efficacy and safety of MAS064D in the treatment of mild to moderate SD of the face. METHODS: Patients (n = 60) with SD were randomized to receive MAS064D (n = 40) or a matching vehicle (n = 20). The primary study endpoint was investigators' global assessment (IGA) score at day 28, compared with baseline. Secondary endpoints included: IGA score at day 14; investigators' assessment of erythema and scaling; patients' assessment of burning/stinging, pruritus and global response to MAS064D; resort to rescue medication; quality of life. RESULTS: Use of MAS064D for 4 weeks was associated with a higher percentage of success in the MAS064D group than in the vehicle group (approximately 68% vs 11%, P &#60; 0.0001). The effects of MAS064D were significantly better than those of vehicle for investigator-assessed erythema and scaling, and patients' assessed pruritus and global response to MAS064D (P 0.01). No patient in the MAS064D group required rescue medication, compared with two patients in the vehicle group. Four patients (two each in the MAS064D and vehicle groups) reported a total of six non-serious adverse events. CONCLUSIONS: MAS064D appears to be an effective and well tolerated cream for the treatment of mild to moderate SD of the face. Further clinical evaluation of MAS064D in SD is warranted.</p>
        <p>PMID: 18269596 [PubMed - indexed for MEDLINE]</p>
    ]]></description>
		<wfw:commentRss>http://www.eczemaletters.com/2008/05/08/treatment-of-mild-to-moderate-seborrhoeic-dermatitis-with-mas064d-sebclair-a-novel-topical-medical-device-results-of-a-pilot-randomized-double-blind-controlled-trial/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Clinical detection of ichthyosis vulgaris in an atopic dermatitis clinic: Implications for allergic respiratory disease and prognosis.</title>
		<link>http://www.eczemaletters.com/2008/05/07/clinical-detection-of-ichthyosis-vulgaris-in-an-atopic-dermatitis-clinic-implications-for-allergic-respiratory-disease-and-prognosis/</link>
		<comments>http://www.eczemaletters.com/2008/05/07/clinical-detection-of-ichthyosis-vulgaris-in-an-atopic-dermatitis-clinic-implications-for-allergic-respiratory-disease-and-prognosis/#comments</comments>
		<pubDate>Wed, 07 May 2008 14:07:31 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18455261</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://linkinghub.elsevier.com/retrieve/pii/S0190-9622(08)00398-8"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18455261">Related Articles</a></td></tr></table>
        <p><b>Clinical detection of ichthyosis vulgaris in an atopic dermatitis clinic: Implications for allergic respiratory disease and prognosis.</b></p>
        <p>J Am Acad Dermatol. 2008 May 1;</p>
        <p>Authors:  Bremmer SF, Hanifin JM, Simpson EL</p>
        <p>BACKGROUND: Recent genetic studies have demonstrated that filaggrin mutations, shown to underlie ichthyosis vulgaris (IV), may also predispose patients with atopic dermatitis to allergic respiratory disease. OBJECTIVE: Our objective was to determine whether the clinical presence of IV influences the severity and age at onset of atopic dermatitis or the probability of having allergic respiratory disease. METHODS: We reviewed data collected from the initial visits of 1187 patients with atopic dermatitis. RESULTS: Asthma symptoms were more common in atopic dermatitis patients with IV than in those without (39.9% vs 32.9%, odds ratio [OR] = 1.35, P = .050) and were most associated with severe IV (OR = 2.52, P = .002). This relationship remained after controlling for the baseline severity of atopic dermatitis. Clinical IV was also associated with symptoms of allergic rhinoconjunctivitis, earlier onset of atopic dermatitis, severity of atopic dermatitis, hyperlinear palms, and keratosis pilaris. LIMITATIONS: Our limitations include subjective grading, few data points in some groups, and an inability to demonstrate causality. CONCLUSION: These results suggest that clinical evidence of IV, irrespective of filaggrin genotype, serves as a potential marker for those patients with atopic dermatitis who develop allergic respiratory disease and a more severe skin phenotype.</p>
        <p>PMID: 18455261 [PubMed - as supplied by publisher]</p>
    ]]></description>
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		</item>
		<item>
		<title>Traffic-Related Air Pollution, Climate, and Prevalence of Eczema in Taiwanese School Children.</title>
		<link>http://www.eczemaletters.com/2008/05/05/traffic-related-air-pollution-climate-and-prevalence-of-eczema-in-taiwanese-school-children/</link>
		<comments>http://www.eczemaletters.com/2008/05/05/traffic-related-air-pollution-climate-and-prevalence-of-eczema-in-taiwanese-school-children/#comments</comments>
		<pubDate>Mon, 05 May 2008 14:05:54 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18449213</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://dx.doi.org/10.1038/jid.2008.110"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.nature.com-images-lo_npg.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18449213">Related Articles</a></td></tr></table>
        <p><b>Traffic-Related Air Pollution, Climate, and Prevalence of Eczema in Taiwanese School Children.</b></p>
        <p>J Invest Dermatol. 2008 May 1;</p>
        <p>Authors:  Lee YL, Su HJ, Sheu HM, Yu HS, Guo YL</p>
        <p>The prevalence of childhood eczema is increasing in many countries. Epidemiological studies, however, say little of its association to outdoor air pollution and climate factors. We conducted a nationwide survey of middle-school students in Taiwan from 1995 to 1996. The 12-month prevalence of eczema was compared with air monitoring station data of temperature, relative humidity, and criteria air pollutants. A total of 317,926 children attended schools located within 2 km of 55 stations. Prevalence rates of recurrent eczema were 2.4 and 2.3% in boys and girls, respectively, with prevalence rates of flexural eczema 1.7% in both sexes. After adjustment for possible confounders, flexural eczema was found to be associated with traffic-related air pollutants, including nitrogen oxides and carbon monoxide. Recurrent eczema was associated with traffic-related air pollution only in girls. There were no associations for the highest monthly means of temperature, whereas the annual means and the lowest monthly means of temperature were negatively related to flexural eczema, but only in girls. The lowest monthly mean relative humidity was positively related to eczema. The results suggest that air pollution and climatic factors, which showed stronger associations in girls than boys, may affect the prevalence of childhood eczema.Journal of Investigative Dermatology advance online publication, 1 May 2008; doi:10.1038/jid.2008.110.</p>
        <p>PMID: 18449213 [PubMed - as supplied by publisher]</p>
    ]]></description>
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		</item>
		<item>
		<title>Prevalence and risk factors for atopic dermatitis in preschool children.</title>
		<link>http://www.eczemaletters.com/2008/05/01/prevalence-and-risk-factors-for-atopic-dermatitis-in-preschool-children/</link>
		<comments>http://www.eczemaletters.com/2008/05/01/prevalence-and-risk-factors-for-atopic-dermatitis-in-preschool-children/#comments</comments>
		<pubDate>Thu, 01 May 2008 14:02:52 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18067476</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://www.blackwell-synergy.com/openurl?genre=article&#38;sid=nlm:pubmed&#38;issn=0007-0963&#38;date=2008&#38;volume=158&#38;issue=3&#38;spage=539"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.blackwell-synergy.com-templates-jsp-_synergy-images-synergy_linkout.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18067476">Related Articles</a></td></tr></table>
        <p><b>Prevalence and risk factors for atopic dermatitis in preschool children.</b></p>
        <p>Br J Dermatol. 2008 Mar;158(3):539-43</p>
        <p>Authors:  Peroni DG, Piacentini GL, Bodini A, Rigotti E, Pigozzi R, Boner AL</p>
        <p>BACKGROUND: Atopic dermatitis (AD) is a common condition in infancy which usually disappears by 3 years of age in a significant proportion of children. The prognosis is mostly determined by severity and presence of atopic sensitization. OBJECTIVES: To investigate prevalence of AD, comorbidities and risk factors in a population of preschool children aged 3-5 years. METHODS: Children in kindergartens were evaluated. The International Study of Asthma and Allergies in Childhood written questionnaire (WQ) was used, with additional questions on risk factors. Atopy was investigated by skin prick tests. RESULTS: One thousand, four hundred and two valid WQs (92% response rate) were returned for evaluation. The prevalence of AD symptoms in the last 12 months in the whole population was 18.1% (254 cases). Seventy-two per cent of these children presented AD-specific localizations. The prevalence of eczema as a doctor's diagnosis in the total population was 15.4%. Positive atopic sensitization was present in 18.6% of the total and in 32.2% of the AD study population, respectively. Multiple sensitivities were observed in 58.2% of sensitized children. The prevalence of sensitization demonstrated that the most common sensitizing allergens in children with AD were mites and grass pollen. Rhinitis symptoms and wheezing were present in 32.2% and 24.2%, respectively, of children with AD. Allergic sensitization to egg, cat, grass pollen and mites, as well as the presence of symptoms of rhinitis, and a positive family history of atopy were all significant risk factors for AD. CONCLUSIONS: The study demonstrates a high prevalence of AD and a close relationship with rhinitis symptoms. Significant risk factors for AD were sensitization to food or inhalant allergens as well as parental history of atopy.</p>
        <p>PMID: 18067476 [PubMed - indexed for MEDLINE]</p>
    ]]></description>
		<wfw:commentRss>http://www.eczemaletters.com/2008/05/01/prevalence-and-risk-factors-for-atopic-dermatitis-in-preschool-children/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Assessment of health state utilities of controlled and uncontrolled psoriasis and atopic eczema: a population-based study.</title>
		<link>http://www.eczemaletters.com/2008/04/28/assessment-of-health-state-utilities-of-controlled-and-uncontrolled-psoriasis-and-atopic-eczema-a-population-based-study/</link>
		<comments>http://www.eczemaletters.com/2008/04/28/assessment-of-health-state-utilities-of-controlled-and-uncontrolled-psoriasis-and-atopic-eczema-a-population-based-study/#comments</comments>
		<pubDate>Mon, 28 Apr 2008 13:57:39 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18070214</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://www.blackwell-synergy.com/openurl?genre=article&#38;sid=nlm:pubmed&#38;issn=0007-0963&#38;date=2008&#38;volume=158&#38;issue=2&#38;spage=351"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.blackwell-synergy.com-templates-jsp-_synergy-images-synergy_linkout.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18070214">Related Articles</a></td></tr></table>
        <p><b>Assessment of health state utilities of controlled and uncontrolled psoriasis and atopic eczema: a population-based study.</b></p>
        <p>Br J Dermatol. 2008 Feb;158(2):351-9</p>
        <p>Authors:  Schmitt J, Meurer M, Klon M, Frick KD</p>
        <p>BACKGROUND: Health utilities are used to express relevant trade-offs for resource allocation. The absence of valid and generalizable utilities for atopic eczema (AE) and psoriasis limits the validity of previous cost-utility analyses. OBJECTIVES: (i) To assess health utilities of standardized scenarios of controlled and uncontrolled AE and psoriasis in participants from the general population and in patients using the time trade-off (TTO) method; (ii) to test the association of the utilities obtained with demographic and patient characteristics; and (iii) to compare these utilities with other health economic outcomes [utilities assessed on visual analogue scale (VAS), willingness to pay (WTP)]. METHODS: A single-centre study conducted in 2006 at the Department of Dermatology, Dresden, Germany. Standardized interactive computer-assisted interviews in a random sample from the general population (n=139), and patients with AE (n=58) and psoriasis (n=62). Information on health states included characteristic clinical pictures and a short text explaining aetiology, signs, symptoms and quality of life impact. RESULTS: In participants from the general population median utilities (TTO) of controlled and uncontrolled AE were 0.97 and 0.64, respectively. For psoriasis the corresponding utilities were 0.93 and 0.56. Utilities were independent of sex and socioeconomic position, and tended to be lower in patients with psoriasis. Correlations between TTO, VAS and WTP responses were weak. CONCLUSIONS: To avoid uncontrolled psoriasis or eczema participants chose an approximately 40% shorter life expectancy. This indicates that severe chronic inflammatory skin diseases may be considered as severe as angina pectoris, chronic anxiety, rheumatoid arthritis, multiple sclerosis or regional oesophageal cancer. The different economic outcomes assessed are not interchangeable.</p>
        <p>PMID: 18070214 [PubMed - indexed for MEDLINE]</p>
    ]]></description>
		<wfw:commentRss>http://www.eczemaletters.com/2008/04/28/assessment-of-health-state-utilities-of-controlled-and-uncontrolled-psoriasis-and-atopic-eczema-a-population-based-study/feed/</wfw:commentRss>
		</item>
		<item>
		<title>Generalized xerotic dermatitis with neutrophilic spongiosis induced by erlotinib (Tarceva).</title>
		<link>http://www.eczemaletters.com/2008/04/28/generalized-xerotic-dermatitis-with-neutrophilic-spongiosis-induced-by-erlotinib-tarceva/</link>
		<comments>http://www.eczemaletters.com/2008/04/28/generalized-xerotic-dermatitis-with-neutrophilic-spongiosis-induced-by-erlotinib-tarceva/#comments</comments>
		<pubDate>Mon, 28 Apr 2008 13:57:39 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18182820</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://content.karger.com/produktedb/produkte.asp?typ=fulltext&#38;file=000112936"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.karger.com-images-sk_nlm_ft.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18182820">Related Articles</a></td></tr></table>
        <p><b>Generalized xerotic dermatitis with neutrophilic spongiosis induced by erlotinib (Tarceva).</b></p>
        <p>Dermatology. 2008;216(3):247-9</p>
        <p>Authors:  L&#xFC;bbe J, Masouy&#xE9; I, Dietrich PY</p>
        <p>Erlotinib is a small molecule tyrosine kinase inhibitor that is used as an anticancer agent. Most patients develop a pustular facial dermatitis within the first week of treatment. Pyogenic granulomas of the nail folds are another typical adverse event occurring in about 10-15% of cases. We report on a patient who developed a generalized dermatitis characterized by neutrophilic spongiosis. Neutrophilic inflammation has been observed in several drugs that interfere with EGFR signaling, suggesting a class effect. The present case may be yet another manifestation of this particular reaction pattern.</p>
        <p>PMID: 18182820 [PubMed - indexed for MEDLINE]</p>
    ]]></description>
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		</item>
		<item>
		<title>Autoimmune progesterone dermatitis. Case report with histologic overlap of erythema multiforme and urticaria.</title>
		<link>http://www.eczemaletters.com/2008/04/28/autoimmune-progesterone-dermatitis-case-report-with-histologic-overlap-of-erythema-multiforme-and-urticaria/</link>
		<comments>http://www.eczemaletters.com/2008/04/28/autoimmune-progesterone-dermatitis-case-report-with-histologic-overlap-of-erythema-multiforme-and-urticaria/#comments</comments>
		<pubDate>Mon, 28 Apr 2008 13:57:39 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18377604</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://www.blackwell-synergy.com/openurl?genre=article&#38;sid=nlm:pubmed&#38;issn=0011-9059&#38;date=2008&#38;volume=47&#38;issue=4&#38;spage=380"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.blackwell-synergy.com-templates-jsp-_synergy-images-synergy_linkout.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18377604">Related Articles</a></td></tr></table>
        <p><b>Autoimmune progesterone dermatitis. Case report with histologic overlap of erythema multiforme and urticaria.</b></p>
        <p>Int J Dermatol. 2008 Apr;47(4):380-2</p>
        <p>Authors:  Walling HW, Scupham RK</p>
        <p>BACKGROUND: Autoimmune progesterone dermatitis is a rare eruption that recurs monthly as progesterone levels peak during the menstrual cycle. Clinical and histologic features are variable, and the eruption is thought to represent a hypersensitivity response to endogenous progesterone. METHODS: We present the case of a 38-year-old woman with a pruritic intermittent facial eruption of 18 months' duration that recurred predictably in the days surrounding menses. RESULTS: The histology showed interface dermatitis with features of both erythema multiforme and urticaria. Intradermal injection of medroxyprogesterone acetate was positive. Her symptoms responded to antihistamine therapy. CONCLUSION: This unusual case is particularly distinctive both in terms of the histologic findings and the response to therapy.</p>
        <p>PMID: 18377604 [PubMed - indexed for MEDLINE]</p>
    ]]></description>
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		</item>
		<item>
		<title>Possible Pathogenic Role of Th17 Cells for Atopic Dermatitis.</title>
		<link>http://www.eczemaletters.com/2008/04/28/possible-pathogenic-role-of-th17-cells-for-atopic-dermatitis/</link>
		<comments>http://www.eczemaletters.com/2008/04/28/possible-pathogenic-role-of-th17-cells-for-atopic-dermatitis/#comments</comments>
		<pubDate>Mon, 28 Apr 2008 13:57:38 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18432274</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://dx.doi.org/10.1038/jid.2008.111"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.nature.com-images-lo_npg.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18432274">Related Articles</a></td></tr></table>
        <p><b>Possible Pathogenic Role of Th17 Cells for Atopic Dermatitis.</b></p>
        <p>J Invest Dermatol. 2008 Apr 24;</p>
        <p>Authors:  Koga C, Kabashima K, Shiraishi N, Kobayashi M, Tokura Y</p>
        <p>The critical role of IL-17 has recently been reported in a variety of conditions. Since IL-17 deeply participates in the pathogenesis of psoriasis and keratinocyte production of certain cytokines, the involvement of T helper cell 17 (Th17) in atopic dermatitis (AD) is an issue to be elucidated. To evaluate the participation of Th17 cells in AD, we successfully detected circulating lymphocytes intracellularly positive for IL-17 by flow cytometry, and the IL-17(+) cell population was found exclusively in CD3(+)CD4(+) T cells. The percentage of Th17 cells was increased in peripheral blood of AD patients and associated with severity of AD. There was a significant correlation between the percentages of IL-17(+) and IFN-gamma(+) cells, although percentage of Th17 cells was not closely related to Th1/Th2 balance. Immunohistochemically, IL-17(+) cells infiltrated in the papillary dermis of atopic eczema more markedly in the acute than chronic lesions. Finally, IL-17 stimulated keratinocytes to produce GM-CSF, TNF-alpha, IL-8, CXCL10, and VEGF. A marked synergistic effect between IL-17 and IL-22 was observed on IL-8 production. The number of Th17 cells is increased in the peripheral blood and acute lesional skin of AD. Th17 cells may exaggerate atopic eczema.Journal of Investigative Dermatology advance online publication, 24 April 2008; doi:10.1038/jid.2008.111.</p>
        <p>PMID: 18432274 [PubMed - as supplied by publisher]</p>
    ]]></description>
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		</item>
		<item>
		<title>Facing psoriasis and atopic dermatitis: are there more similarities or more differences?</title>
		<link>http://www.eczemaletters.com/2008/04/24/facing-psoriasis-and-atopic-dermatitis-are-there-more-similarities-or-more-differences/</link>
		<comments>http://www.eczemaletters.com/2008/04/24/facing-psoriasis-and-atopic-dermatitis-are-there-more-similarities-or-more-differences/#comments</comments>
		<pubDate>Thu, 24 Apr 2008 13:45:56 +0000</pubDate>
		<dc:creator>Jeanne Louw</dc:creator>
		
		<category><![CDATA[Research]]></category>

		<guid isPermaLink="false">PubMed:18424378</guid>
		<description><![CDATA[
	<table border="0" width="100%"><tr><td align="left"><a href="http://www.john-libbey-eurotext.fr/medline.md?issn=1167-1122&#38;vol=18&#38;iss=2&#38;page=172"><img src="http://www.ncbi.nlm.nih.gov/entrez/query/egifs/http:--www.john-libbey-eurotext.fr-images-medline-1167-1122.gif"></a> </td><td align="right"><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&#38;cmd=Display&#38;dopt=PubMed_PubMed&#38;from_uid=18424378">Related Articles</a></td></tr></table>
        <p><b>Facing psoriasis and atopic dermatitis: are there more similarities or more differences?</b></p>
        <p>Eur J Dermatol. 2008 Mar-Apr;18(2):172-80</p>
        <p>Authors:  Wilsmann-Theis D, Hagemann T, Jordan J, Bieber T, Novak N</p>
        <p>Atopic dermatitis (AD) and psoriasis vulgaris (Pso) represent the most frequent chronic inflammatory skin diseases. It has been assumed for a long time that these diseases have a completely different background. Recent findings about the genetic, epidemiologic and pathophysiologic factors of both diseases have remarkably improved our knowledge about the complex mechanisms underlying AD and Pso. Beyond that, in view of these findings, the question arises, which similarities and differences between AD and Pso exist. In order to address this point, we provide an overview about the current knowledge in the field of AD and Pso.</p>
        <p>PMID: 18424378 [PubMed - in process]</p>
    ]]></description>
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