2,590 results match your criteria Gianotti-Crosti Syndrome Papular Acrodermatitis of Childhood


Cutaneous paraneoplastic syndromes.

Semin Diagn Pathol 2019 Jan 31. Epub 2019 Jan 31.

PRW Laboratories, Charlottesville, VA, United State.

A variety of cutaneous abnormalities can be seen in patients with malignant diseases, some of which are infectious, with others representing direct involvement of the skin by the underlying disorder. Yet another group of lesions can be regarded as associated markers of the malignant process, and, as such, are termed "paraneoplastic." This review considers the latter collection of conditions, grouping them by the generic type of malignancy that is usually linked to the paraneoplasia. Read More

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http://dx.doi.org/10.1053/j.semdp.2019.01.001DOI Listing
January 2019
1 Read

Acquired acrodermatitis enteropathica secondary to sleeve gastrectomy.

Indian J Dermatol Venereol Leprol 2019 Mar-Apr;85(2):220-223

Department of Dermatology and Venerology, School of Medicine, Akdeniz University, Antalya, Turkey.

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http://dx.doi.org/10.4103/ijdvl.IJDVL_337_18DOI Listing
January 2019

Acrodermatitis enteropathica: the need for sustained high dose zinc supplementation.

Dermatol Online J 2018 Dec 15;24(12). Epub 2018 Dec 15.

Department of Dermatology, JSS Medical College and Hospital, Mysore, Karanataka.

Acrodermatitis enteropathica (AE) is a rare congenital disorder owing to an abnormality with intestinal absorption and/or transportation of zinc. We describe two male siblings, who presented with evidence of both acute and chronic zinc deficiency, despite being diagnosed with AE very early in life. We wish to highlight the importance of sustained high-dose zinc supplementation and regular monitoring in AE cases. Read More

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December 2018

Zn-DTSM, A Zinc Ionophore with Therapeutic Potential for Acrodermatitis Enteropathica?

Nutrients 2019 Jan 21;11(1). Epub 2019 Jan 21.

The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, 30 Royal Parade, Parkville, Victoria 3052, Australia.

Acrodermatitis enteropathica (AE) is a rare disease characterised by a failure in intestinal zinc absorption, which results in a host of symptoms that can ultimately lead to death if left untreated. Current clinical treatment involves life-long high-dose zinc supplements, which can introduce complications for overall nutrient balance in the body. Previous studies have therefore explored the pharmacological treatment of AE utilising metal ionophore/transport compounds in an animal model of the disease (conditional knockout (KO) of the zinc transporter, ), with the perspective of finding an alternative to zinc supplementation. Read More

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http://dx.doi.org/10.3390/nu11010206DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356714PMC
January 2019
1 Read

[Infantile atypical hand-foot-mouth disease with features of eczema herpeticum and acrodermatitis].

Arch Argent Pediatr 2019 02;117(1):e59-e62

Servicio de Pediatría, Hospital Juan Ramón Jiménez, Huelva. España.

Hand-foot-mouth disease can present atypically, including forms with more numerous lesions and/or morphologically different from the classic presentation. It may even mimic other viral diseases. We present the case of a 2-year-old child previously diagnosed with atopic dermatitis, who presented with papules and umbilicated vesicles affecting the perioral area and limbs, predominantly in pressure areas, as well as in areas with previous atopic lesions. Read More

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http://dx.doi.org/10.5546/aap.2019.e59DOI Listing
February 2019
14 Reads

Acroangiodermatitis of Mali (Pseudo-Kaposi Sarcoma) Associated with Chronic Venous Insufficiency and Obesity: A Case Report.

Wounds 2018 Nov;30(11):E105-E107

College of Medicine, Taif University, Taif, Saudi Arabia.

Introduction: Acroangiodermatitis, also known as psesudo-Kapsoi sarcoma, is a rare and benign angioproliferative malady. It presents clinically as purple-colored plaques, patches, or nodules resembling Kaposi sarcoma and is often related to chronic venous insufficiency, arteriovenous malformation of the legs, paralyzed limbs, and residual limbs. Obesity is a risk factor for venous insufficiency and could be related to acroangiodermatitis. Read More

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November 2018
16 Reads

Acrodermatitis chronica atrophicans: various faces of the late form of Lyme borreliosis.

Postepy Dermatol Alergol 2018 Oct 19;35(5):490-494. Epub 2018 Jul 19.

Department of Infectious Diseases and Neuroinfections, Medical University of Białystok, Białystok, Poland.

Introduction: Acrodermatitis chronica atrophicans (ACA) is probably the most common late and chronic manifestation of the Lyme borreliosis seen in European patients.

Aim: To analyze epidemiological data, and to investigate the effects of treatment of patients with ACA.

Material And Methods: Nine patients were included in the study. Read More

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https://www.termedia.pl/doi/10.5114/ada.2018.77240
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http://dx.doi.org/10.5114/ada.2018.77240DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232541PMC
October 2018
19 Reads

Acrodermatitis continua of Hallopeau with dense infiltration of IgG4-positive cells in the lesional dermis.

Br J Dermatol 2018 Nov 8. Epub 2018 Nov 8.

Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

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http://dx.doi.org/10.1111/bjd.17405DOI Listing
November 2018
3 Reads

Acrodermatitis chronica atrophicans in children: Report on two cases and review of the literature.

Ticks Tick Borne Dis 2019 01 26;10(1):180-185. Epub 2018 Oct 26.

Department of Infectious Diseases, University Medical Center Ljubljana, Ljubljana, Slovenia. Electronic address:

Acrodermatitis chronica atrophicans is a late manifestation of European Lyme borreliosis and is characterized by high levels of borrelial IgG antibodies, slowly expanding skin redness usually beginning on distal parts of extremities, and corresponding histologic findings. It very rarely develops in children. The main prerequisite for the diagnosis is clinical suspicion. Read More

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http://dx.doi.org/10.1016/j.ttbdis.2018.10.009DOI Listing
January 2019
1 Read

Acquired zinc deficiency in a renal transplant recipient with gastrointestinal tuberculosis responding promptly to oral correction.

Saudi J Kidney Dis Transpl 2018 Sep-Oct;29(5):1199-1202

Department of Dermatology, Jaslok Hospital and Research Center, Mumbai, Maharashtra, India.

Zinc deficiency is an uncommon condition, known to occur in two forms: inherited type, known as Acrodermatitis enteropathies and the acquired type. Cutaneous clinical manifestations observed include characteristic dermatitis on acral, periorificial, and anogenital areas through an unknown mechanism. The patient had a combination of causes which lead to a state of zinc deficiency. Read More

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http://www.sjkdt.org/text.asp?2018/29/5/1199/243962
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http://dx.doi.org/10.4103/1319-2442.243962DOI Listing
November 2018
14 Reads

Acrodermatitis Continua of Hallopeau.

JAMA Dermatol 2018 Nov;154(11):1346

Division of Dermatology, Department of Internal Medicine, The Ohio State University, Columbus.

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http://dx.doi.org/10.1001/jamadermatol.2018.3350DOI Listing
November 2018
1 Read

Acrodermatitis continua of Hallopeau successfully treated with secukinumab.

J Dermatolog Treat 2018 Sep 22:1-7. Epub 2018 Sep 22.

a Division of Dermatology , S. Chiara Hospital , Trento , Italy.

Acrodermatitis continua of Hallopeau is considered an uncommon variant of pustular psoriasis, characterised by a relapsing, sterile, pustular eruption of hands and feet. It is not easily treated by anti-psoriatic therapies, and may progress toward sclerosis and osteolysis. Numerous topical and systemic treatments have been used, with inconsistent results. Read More

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http://dx.doi.org/10.1080/09546634.2018.1527993DOI Listing
September 2018
4 Reads

Asymetric red-blue hypertrophic hand and tenosynovitis due to acrodermatitis chronica atrophicans.

Rheumatology (Oxford) 2018 Sep 19. Epub 2018 Sep 19.

Dermatology Department, and Université Paris Diderot-Paris VII, Sorbonne Paris Cité APHP, Saint-Louis Hospital, Paris, France.

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http://dx.doi.org/10.1093/rheumatology/key295DOI Listing
September 2018
6 Reads

Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East.

Dermatol Res Pract 2018 7;2018:1284568. Epub 2018 Aug 7.

Department of Infection, Immunity and Cardiovascular Disease, The Medical School, University of Sheffield, Sheffield S10 2RX, UK.

We report a family from Tabuk, Saudi Arabia, previously screened for Acrodermatitis Enteropathica (AE), in which two siblings presented with typical features of acral dermatitis and a pustular eruption but differing severity. Affected members of our family carry a rare genetic variant, p.Gly512Trp in the SLC39A4 gene which encodes a zinc transporter; disease is thought to result from zinc deficiency. Read More

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http://dx.doi.org/10.1155/2018/1284568DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106946PMC
August 2018
9 Reads

Acquired bullous acrodermatitis enteropathica as a histologic mimic of pemphigus foliaceus in a patient on parenteral nutrition.

Dermatol Online J 2018 May 15;24(5). Epub 2018 May 15.

Department of Dermatology, University of California, Davis, California.

The original article was published on July19, 2017 and corrected on May 15, 2018. The revised version of the article includes a funding source for Dr. Maija Kiuru's participation in this case report, awarded by the National Cancer Institute, National Institutes of Health grant K12CA138464. Read More

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May 2018
3 Reads

Acrodermatitis enteropathica from zinc-deficient total parenteral nutrition.

Cutis 2018 Jun;101(6):450-453

Department of Dermatology, University of Maryland School of Medicine, Baltimore, USA.

Acrodermatitis enteropathica (AE) is a rare autosomal-recessive disorder of zinc malabsorption, characterized by acral and periorificial dermatitis, alopecia, and diarrhea. Acquired AE is the result of decreased zinc intake, excessive zinc loss, or other malabsorptive processes. We present a case of a 54-year-old woman who developed characteristic skin lesions of acquired AE after zinc supplementation was removed from her total parenteral nutrition (TPN) solution. Read More

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June 2018
1 Read

Clinical and genetic differences between pustular psoriasis subtypes.

J Allergy Clin Immunol 2018 Jul 21. Epub 2018 Jul 21.

Department of Medical and Molecular Genetics, School of Basic and Medical Biosciences, King's College London, London, United Kingdom.

Background: The term pustular psoriasis indicates a group of severe skin disorders characterized by eruptions of neutrophil-filled pustules. The disease, which often manifests with concurrent psoriasis vulgaris, can have an acute systemic (generalized pustular psoriasis [GPP]) or chronic localized (palmoplantar pustulosis [PPP] and acrodermatitis continua of Hallopeau [ACH]) presentation. Although mutations have been uncovered in IL36RN and AP1S3, the rarity of the disease has hindered the study of genotype-phenotype correlations. Read More

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http://dx.doi.org/10.1016/j.jaci.2018.06.038DOI Listing
July 2018
22 Reads

Acrodermatitis Enteropathica Presenting with Recurrent Diarrhea and Vomiting in an Infant Reluctant to Breastfeed, and a Peculiar Erythemato-Eczematous Eruption around the Oral and Anogenital Regions.

Skinmed 2018 1;16(3):205-207. Epub 2018 Jun 1.

Department of Pathology, University College of Medical Sciences, and Associated Guru Teg Bahadur Hospital, Shahdara, Delhi, India.

A 6-month-old, 4-kg, dehydrated girl, an Indian native, was admitted with recurrent episodes of diarrhea that had occurred since age 2 months. She had stopped breastfeeding. She had also had concomitant vomiting and loss of appetite. Read More

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June 2018
4 Reads

Ixekizumab gegen die Acrodermatitis continua.

J Dtsch Dermatol Ges 2018 Jul;16(7):907-910

Klinik für Dermatologie und Allergologie, Technische Universität München, Deutschland.

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http://dx.doi.org/10.1111/ddg.13568_gDOI Listing
July 2018
4 Reads

Ixekizumab for acrodermatitis continua.

J Dtsch Dermatol Ges 2018 Jul 21;16(7):907-910. Epub 2018 Jun 21.

Department of Dermatology and Allergy, Technical University of Munich, Munich, Germany.

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http://dx.doi.org/10.1111/ddg.13568DOI Listing
July 2018
7 Reads

Acrodermatitis dysmetabolica in phenylketonuria.

Pediatr Neonatol 2018 May 26. Epub 2018 May 26.

Metro Health Medical Center, Case Western Reserve University, Cleveland, OH, USA.

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http://dx.doi.org/10.1016/j.pedneo.2018.05.005DOI Listing
May 2018
2 Reads

Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation.

Clin Case Rep 2018 Jun 14;6(6):1048-1050. Epub 2018 Apr 14.

Pediatric Department Hospital of Divino Espirito Santo of Ponta Delgada, EPER São Miguel Island, Azores Portugal.

Methylmalonic aciduria children must follow an adequate diet with low protein intake and should be regularly monitored to prevent complications. Although skin lesions like acrodermatitis enteropathica are rare in this disease, their appearance should be correlated with possible low plasma isoleucine level and it can be a sign of decompensation. Read More

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http://dx.doi.org/10.1002/ccr3.1509DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986048PMC
June 2018
22 Reads

Tatami Mats: A Source of Pitted Keratolysis in a Martial Arts Athlete?

Acta Dermatovenerol Croat 2018 Apr;26(1):68-70

Daniela Ledić Drvar, MD, PhD, University Hospital Centre Zagreb, Department of Dermatology and Venereology, School of Medicine University of Zagreb, Šalata 4, 10000 Zagreb, Croatia;

Dear Editor, Pitted keratolysis (PK), also known as keratosis plantaris sulcatum, is a non-inflammatory, bacterial, superficial cutaneous infection, characterized by many discrete superficial crateriform ''pits'' and erosions in the thickly keratinized skin of the weight-bearing regions of the soles of the feet (1). The disease often goes unnoticed by the patient, but when it is noticed it is because of the unbearable malodor and hyperhidrosis of the feet, which are socially unacceptable and cause great anxiety to many of the patients. PK occurs worldwide, with the incidence rates varying based on the environment and occupation. Read More

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April 2018
24 Reads

Behandlung der Acrodermatitis continua suppurativa Hallopeau mit Ustekinumab als Monotherapie nach Versagen von TNF-Antagonisten.

J Dtsch Dermatol Ges 2018 May;16(5):610-612

Abteilung für Dermatologie, Krankenhaus San Pedro, Logroño, Spanien.

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http://dx.doi.org/10.1111/ddg.13506_gDOI Listing
May 2018
1 Read

Papular crusted rash in a child after immunisation.

Arch Dis Child 2018 May 4. Epub 2018 May 4.

Pediatric Dermatology, Hospital de Clinicas - UFPR, Curitiba, Brazil.

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http://dx.doi.org/10.1136/archdischild-2018-314922DOI Listing
May 2018
1 Read

Acute prurigo simplex in humans caused by pigeon lice.

An Bras Dermatol 2018 Mar;93(2):285-287

Department of Dermatology and Radiotherapy, Faculdade de Medicina de Botucatu, Universidade Estadual Paulista Júlio de Mesquita Filho, Botucatu, SP, Brazil.

Pigeon lice are insects that feed on feathers of these birds; their life cycle includes egg, nymph and adult and they may cause dermatoses in humans. Four persons of the same family, living in an urban area, presented with widespread intensely pruritic erythematous papules. A great number of lice were seen in their house, which moved from a nest of pigeons located on the condenser of the air-conditioning to the dormitory of one of the patients. Read More

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http://dx.doi.org/10.1590/abd1806-4841.20187120DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916410PMC
March 2018
4 Reads

Atypical Gianotti-Crosti syndrome.

An Bras Dermatol 2018 Mar;93(2):265-267

Outpatient Clinic of Pediatric Dermatology, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.

We report the case of a male 22-month-old child, with atypical presentation of Gianotti-Crosti syndrome after infection with Epstein-Barr virus. Read More

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http://dx.doi.org/10.1590/abd1806-4841.20186726DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916403PMC
March 2018
4 Reads

A case of acrodermatitis continua of Hallopeau (ACH) successfully treated with sulfasalazine.

Dermatol Ther 2018 May 25;31(3):e12595. Epub 2018 Apr 25.

Department of Dermatology, the Affiliated Hospital of Jiangsu University, Zhenjiang, China.

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http://dx.doi.org/10.1111/dth.12596DOI Listing
May 2018
3 Reads

Acrodermatitis continua of Hallopeau and geographic tongue are variants of pustular psoriasis.

Authors:
Muriel Sadlier

JAAD Case Rep 2018 Apr 7;4(3):277. Epub 2018 Mar 7.

Department of Dermatology, St James's Hospital Dublin, Dublin, Ireland.

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http://dx.doi.org/10.1016/j.jdcr.2017.08.022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909475PMC
April 2018
3 Reads

Treatment of acrodermatitis continua of Hallopeau with ustekinumab as monotherapy after failure of anti-TNF agents.

J Dtsch Dermatol Ges 2018 May 16;16(5):611-613. Epub 2018 Apr 16.

Department of Dermatology, Hospital San Pedro, Logroño, Spain.

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http://dx.doi.org/10.1111/ddg.13506DOI Listing
May 2018
3 Reads

[A 10-Year-Old Boy with a Skin Rash on the Face and on Both Forearms].

Dtsch Med Wochenschr 2018 Apr 12;143(8):549-550. Epub 2018 Apr 12.

Klinik für Dermatologie, Venerologie und Allergologie, HELIOS St. Elisabeth Krankenhaus Oberhausen, Universität Witten-Herdecke.

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http://dx.doi.org/10.1055/s-0043-123335DOI Listing
April 2018
6 Reads
0.550 Impact Factor

Acrodermatitis-Like Rash in Kawasaki Disease.

J Pediatr 2018 07 5;198:320. Epub 2018 Apr 5.

Allergy Immunology Unit Department of Pediatrics Advanced Pediatrics Center Postgraduate Institute of Medical Education and Research Chandigarh, India.

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http://dx.doi.org/10.1016/j.jpeds.2018.02.051DOI Listing
July 2018
3 Reads

Generalized pustular psoriasis: a review and update on treatment.

J Eur Acad Dermatol Venereol 2018 Oct 11;32(10):1645-1651. Epub 2018 Apr 11.

Department of Dermatology, Rutgers-New Jersey Medical School, Newark, NJ, USA.

Generalized pustular psoriasis (GPP) is a subtype of pustular psoriasis characterized by painful and occasionally disfiguring cutaneous manifestations with sepsis-like systemic symptoms. Affecting any age and race, GPP can occur with other forms of psoriasis or by itself. Stimuli for flares include medications, infections and environmental triggers. Read More

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http://doi.wiley.com/10.1111/jdv.14949
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http://dx.doi.org/10.1111/jdv.14949DOI Listing
October 2018
15 Reads

MKLN1 splicing defect in dogs with lethal acrodermatitis.

PLoS Genet 2018 03 22;14(3):e1007264. Epub 2018 Mar 22.

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Lethal acrodermatitis (LAD) is a genodermatosis with monogenic autosomal recessive inheritance in Bull Terriers and Miniature Bull Terriers. The LAD phenotype is characterized by poor growth, immune deficiency, and skin lesions, especially at the paws. Utilizing a combination of genome wide association study and haplotype analysis, we mapped the LAD locus to a critical interval of ~1. Read More

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http://dx.doi.org/10.1371/journal.pgen.1007264DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863938PMC
March 2018
4 Reads

Acquired bullous acrodermatitis enteropathica as a histologic mimic of pemphigus foliaceus in a patient on parenteral nutrition.

Dermatol Online J 2017 Jul 15;23(7). Epub 2017 Jul 15.

Department of Dermatology, Hofstra Northwell School of Medicine, New Hyde Park, New York. vsharon@ northwell.edu.

Acquired zinc deficiency can develop as a consequence of poor nutritional intake or from dependence on total parenteral nutrition. Acquired zinc deficiency dermatitis classically manifests with erosions and scaly plaques in a periorificial and acral distribution. We present a case of a woman on parenteral nutrition who presented with bullous acrodermatitis mimicking pemphigus foliaceus histopathologically. Read More

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July 2017
8 Reads

The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin.

Nutrients 2018 Feb 16;10(2). Epub 2018 Feb 16.

Division of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Tokyo 142-8555, Japan.

The first manifestations that appear under zinc deficiency are skin defects such as dermatitis, alopecia, acne, eczema, dry, and scaling skin. Several genetic disorders including acrodermatitis enteropathica (also known as Danbolt-Closs syndrome) and Brandt's syndrome are highly related to zinc deficiency. However, the zinc-related molecular mechanisms underlying normal skin development and homeostasis, as well as the mechanism by which disturbed zinc homeostasis causes such skin disorders, are unknown. Read More

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http://dx.doi.org/10.3390/nu10020219DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852795PMC
February 2018
4 Reads

Zinc and Skin Disorders.

Nutrients 2018 Feb 11;10(2). Epub 2018 Feb 11.

Department of Dermatology, Faculty of Medicine, University of Yamanashi, Yamanashi 409-3898, Japan.

The skin is the third most zinc (Zn)-abundant tissue in the body. The skin consists of the epidermis, dermis, and subcutaneous tissue, and each fraction is composed of various types of cells. Firstly, we review the physiological functions of Zn and Zn transporters in these cells. Read More

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http://www.mdpi.com/2072-6643/10/2/199
Publisher Site
http://dx.doi.org/10.3390/nu10020199DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852775PMC
February 2018
8 Reads

Acrodermatitis Continua of Hallopeau with Bone Resorption in an 8-Year-Old Patient: A Case Report.

Case Rep Dermatol 2017 Sep-Dec;9(3):259-264. Epub 2017 Dec 18.

Department of Dermatology, King Saud University Medical City, Riyadh, Saudi Arabia.

Acrodermatitis continua of Hallopeau (ACH) is an uncommon inflammatory disease manifesting as sterile pustular eruption of the fingers and toes. The disease is of a chronic relapsing nature and is often refractory to treatment. With longstanding disease, osteitis with consequent bone resorption of the underlying phalanges can occur, leading to disability. Read More

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http://dx.doi.org/10.1159/000485370DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803711PMC
December 2017
7 Reads

Autoinflammatory keratinization diseases: An emerging concept encompassing various inflammatory keratinization disorders of the skin.

J Dermatol Sci 2018 May 1;90(2):105-111. Epub 2018 Feb 1.

Department of Dermatology, Fujita Health University School of Medicine, Toyoake, Japan.

Classifying inflammatory skin diseases is challenging, especially for the expanding group of disorders triggered by genetic factors resulting in hyperactivated innate immunity that result in overlapping patterns of dermal and epidermal inflammation with hyperkeratosis. For such conditions, the umbrella term "autoinflammatory keratinization diseases" (AIKD) has been proposed. AIKD encompasses diseases with mixed pathomechanisms of autoinflammation and autoimmunity, and includes IL-36 receptor antagonist (IL-36Ra)-related pustulosis, CARD14-mediated pustular psoriasis, pityriasis rubra pilaris (PRP) type V, and familial keratosis lichenoides chronica (KLC). Read More

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http://dx.doi.org/10.1016/j.jdermsci.2018.01.012DOI Listing
May 2018
8 Reads

ACRODERMATITIS ENTEROPATHICA: CLINICAL MANIFESTATIONS AND PEDIATRIC DIAGNOSIS.

Rev Paul Pediatr 2018 Apr-Jun;36(2):238-241. Epub 2018 Jan 15.

Universidade de São Paulo, Ribeirão Preto, São Paulo, Brasil.

Objective: To report a case of acrodermatitis enteropathica, a rare disease with autosomal recessive inheritance.

Case Description: An 11-month-old boy was presenting symmetrical erythematous and yellowish-brownish crusted lesions on his face, feet, hands and knees, intermittent diarrhea, fever, and recurrent infections since the age of six months. He was thin and had scarce hair on the scalp. Read More

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http://dx.doi.org/10.1590/1984-0462/;2018;36;2;00010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038791PMC
January 2019
2 Reads

Nail psoriasis: clinical features, pathogenesis, differential diagnoses, and management.

Authors:
Eckart Haneke

Psoriasis (Auckl) 2017 16;7:51-63. Epub 2017 Oct 16.

Department of Dermatology, Inselspital, University of Bern, Bern, Switzerland.

Psoriasis is the skin disease that most frequently affects the nails. Depending on the very nail structure involved, different clinical nail alterations can be observed. Irritation of the apical matrix results in psoriatic pits, mid-matrix involvement may cause leukonychia, whole matrix affection may lead to red lunulae or severe nail dystrophy, nail bed involvement may cause salmon spots, subungual hyperkeratosis, and splinter hemorrhages, and psoriasis of the distal nail bed and hyponychium causes onycholysis whereas that of the proximal nail fold causes psoriatic paronychia. Read More

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http://dx.doi.org/10.2147/PTT.S126281DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774607PMC
October 2017
12 Reads

[Acrodermatitis enteropathica].

Bol Med Hosp Infant Mex 2017 Jul - Aug;74(4):295-300. Epub 2017 Jul 5.

Servicio de Infectología Pediátrica, Centro Médico Nacional 20 de Noviembre, ISSSTE, Ciudad de México, México.

Introduction: Acrodermatitis enteropathica is a low-incidence disease due to inherited or acquired zinc deficiency. It is characterized by acral dermatitis, alopecia, diarrhea and growth retardation. The dermatological condition may mimic a cutaneous fungal infection or other pathogen-related skin diseases. Read More

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http://dx.doi.org/10.1016/j.bmhimx.2017.05.002DOI Listing
July 2017
2 Reads

Disorders of metal metabolism.

Transl Sci Rare Dis 2017 Dec 18;2(3-4):101-139. Epub 2017 Dec 18.

Section on Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, USA.

Trace elements are chemical elements needed in minute amounts for normal physiology. Some of the physiologically relevant trace elements include iodine, copper, iron, manganese, zinc, selenium, cobalt and molybdenum. Of these, some are metals, and in particular, transition metals. Read More

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http://dx.doi.org/10.3233/TRD-170015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764069PMC
December 2017
3 Reads

Acrodermatitis acidaemica.

Clin Exp Dermatol 2018 Apr 15;43(3):315-318. Epub 2018 Jan 15.

Department of Dermatology, St George's Healthcare NHS Trust, London, UK.

Methylmalonic acidaemia (MMA) is an inborn error of amino acid metabolism that may be associated with cutaneous manifestations mimicking other diagnoses, including staphylococcal scalded skin syndrome (SSSS), psoriasis and acrodermatitis enteropathica. Whether this is due to the underlying metabolic disorder itself or occurs as a consequence of dietary restriction has yet to be elucidated. Skin biopsies typically show histological features shared by a number of other metabolic disorders and nutritional deficiency-associated diseases. Read More

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http://dx.doi.org/10.1111/ced.13369DOI Listing
April 2018
8 Reads

Acroangiodermatitis mimicking Kaposi's sarcoma in an HIV-positive man.

Int J STD AIDS 2018 06 16;29(7):729-731. Epub 2018 Jan 16.

3 Department of Dermatopathology, Salford Royal Foundation Trust, Salford, UK.

Kaposi's sarcoma (KS) is the commonest human immunodeficiency virus (HIV)-related malignancy with its characteristic cutaneous morphological appearance and histopathological features. However, it can be simulated by other co-morbid opportunistic infections and unrelated dermatological conditions. We describe such a case of acroangiodermatitis in an HIV co-infected man, based on exclusion of KS histologically and the absence of human herpesvirus 8, the causative agent of KS. Read More

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http://dx.doi.org/10.1177/0956462417750709DOI Listing
June 2018
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Pustular psoriasis and related pustular skin diseases.

Authors:
H Bachelez

Br J Dermatol 2018 03 15;178(3):614-618. Epub 2018 Jan 15.

Department of Dermatology, AP-HP Hôpital Saint-Louis, 1 Avenue Claude Vellefaux, Paris CEDEX 10, 75475, France.

Patients with pustular psoriasis or related pustular diseases may have genetic abnormalities impairing the function of key players of the innate skin immune system. Recently, identification of these abnormalities has changed the paradigm of several of these diseases. These include generalized pustular psoriasis, palmoplantar pustular psoriasis and acrodermatitis continua of Hallopeau, and also drug-induced acute exanthematous generalized pustular eruption. Read More

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http://dx.doi.org/10.1111/bjd.16232DOI Listing
March 2018
4 Reads

Rash on extensor surfaces of a child.

BMJ 2018 01 11;360:j5547. Epub 2018 Jan 11.

St John's Institute of Dermatology, Guy's and St Thomas' Hospital, London, UK.

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http://dx.doi.org/10.1136/bmj.j5547DOI Listing
January 2018
2 Reads