Prepubertal Melanoma Arising within a Medium ‐Sized Congenital Melanocytic Nevus
We report the case of an 8‐year‐old child who developed a 9.4‐mm‐deep melanoma within a medium‐sized congenital melanocytic nevus on the scalp. Genetic analysis revealed an activating NRAS Q61R mutation within the melanoma, which is more commonly associated with large or giant congenital melanocytic nevi. This case demonstrates that even a “low‐risk” congenital melanocytic nevus at a “low‐risk” age must be monitored regularly for the development of malignancy. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - August 29, 2016 Category: Dermatology Authors: Leah Lalor, Klaus Busam, Kara Shah Tags: Case Report Source Type: research

Subcutaneous Fat Necrosis of the Newborn: A 20 ‐Year Retrospective Study
Abstract Subcutaneous fat necrosis of the newborn (SFN) is a rare form of panniculitis that can be complicated by hypercalcemia and nephrocalcinosis. We conducted a 20‐year retrospective cohort study of 30 patients to describe the clinical characteristics of SFN and the prevalence of hypercalcemia and other complications. Hypoxia and therapeutic hypothermia (TH) seem to play an important role in the development of SFN. Hypercalcemia developed in 63% of patients, three of whom developed nephrocalcinosis. There is a need for well‐controlled prospective studies to determine the natural history, prevalence, and incidence o...
Source: Pediatric Dermatology - August 29, 2016 Category: Dermatology Authors: Blanca R. Del Pozzo ‐Magaña, Nhung Ho Tags: Brief Report Source Type: research

Syphilis in an Infant Acquired by Mouth ‐to‐Mouth Transfer of Prechewed Food
Abstract A 2‐year‐old infant boy presented with a large ulcerative lesion on his tongue. The grandmother who cared for the boy was in the habit of chewing food before giving it to the boy and had active syphilis. The infant was diagnosed with acquired early syphilis, which had been transmitted by prechewed food from his grandmother. Prechewing food is a custom in most parts of China. Prechewing an infant's food could be an avenue of disease transmission, although this is not fully recognized. No studies have been conducted to evaluate prechewed food as a disease transmission route. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - August 29, 2016 Category: Dermatology Authors: Ru ‐zhi Zhang, Hui‐ling Jin Tags: Brief Report Source Type: research

Atypical Scleredema Involving the Hands in an Adolescent
We present an atypical case of postinfectious scleredema involving the hands and discuss scleredema as an important potential cause of hand tightness and induration in adolescents. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - August 29, 2016 Category: Dermatology Authors: Caroline M. Lewis, April T. Sanchez, Loretta S. Davis Tags: Brief Report Source Type: research

Lymphoplasmacytic Plaque in Children: A Demonstrative Case of an Emerging Clinicopathologic Entity
We report a demonstrative case of lymphoplasmacytic plaque in a 3‐year‐old girl and discuss the clinical and pathologic experience with this entity. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - August 29, 2016 Category: Dermatology Authors: Dennis A. Porto, Molly Powers, Devika Patel, Marsha Chaffins, Tor A. Shwayder Tags: Brief Report Source Type: research

Transient Porphyrinemia in a Neonate: A Case Report
We describe a neonate with anemia, thrombocytopenia, and hyperbilirubinemia secondary to hemolytic disease of the newborn. After phototherapy for hyperbilirubinemia, the neonate developed a photodistributed eruption with high serum and urine porphyrin levels. This transient porphyrinemia resolved at 1 month. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - August 29, 2016 Category: Dermatology Authors: Brooke Boer, Alison Tisack, Tor Shwayder Tags: Case Report Source Type: research

Multiple Caf é au Lait Spots in a Group of Fair‐Skinned Children without Signs or Symptoms of Neurofibromatosis Type 1
ConclusionA subset of children, many with fair complexions and red or blond hair, has an increased number of feathery CAL spots and appears unlikely to develop NF‐1, although genetic testing was not conducted. It is important to recognize the benign nature of CAL spots in these patients so that appropriate screening and follow‐up recommendations may be made. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 27, 2016 Category: Dermatology Authors: Jessica St. John, Heather Summe, Courtney Csikesz, Karen Wiss, Beverly Hay, Leah Belazarian Tags: Original Article Source Type: research

Acro ‐Dermato‐Ungual‐Lacrimal‐Tooth Syndrome: An Uncommon Member of the Ectodermal Dysplasias
We report a familial case of ADULT syndrome in a daughter, mother, and son and provide a brief review of the clinical characteristics of this syndrome. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 27, 2016 Category: Dermatology Authors: Adam Whittington, Sarah Stein, Brandi Kenner ‐Bell Tags: Case Report Source Type: research

Cutaneous Malignancies in Pediatric Solid Organ Transplant Recipients
The objective of this review is to provide updated information on posttransplantation skin cancer development in POTRs, including epidemiologic research on transplant patients and disease development, medication management, surveillance, and education efforts. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 27, 2016 Category: Dermatology Authors: Alexander L. Fogel, Maria Miyar, Joyce M. C. Teng Tags: Review Source Type: research

Harlequin Ichthyosis: A Surgical Perspective
This report documents a case of harlequin ichthyosis requiring surgical treatment, focusing on the importance of early surgical consultation, risks of surgery, indications for and timing of surgical intervention, and the details of the operation. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 27, 2016 Category: Dermatology Authors: Mitchell A. Pet, Deepti Gupta, Raymond W. Tse Tags: Case Report Source Type: research

Birt –Hogg–Dubé Syndrome Presenting as a Nevus Comedonicus–Like Lesion in an 8‐Year‐Old Boy
We present the case of an 8‐year‐old boy with a recently described cystic and comedonal variant of the classic fibrofolliculoma, which had been present since birth. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 27, 2016 Category: Dermatology Authors: Jessica Sprague, Joseph W. Landau Tags: Brief Report Source Type: research

Paucisymptomatic Dermoid Cyst with Fatal Outcome
We report the case of a 5‐month‐old girl who presented with a crusted lesion of the occipital region of the scalp. Clinical examination noted skin abnormalities suggestive of occult dysraphism. Magnetic resonance imaging (MRI) was recommended, however, 40 days after this evaluation, and before the MRI could be performed, the girl presented with neurologic complications. Unfortunately, the diagnosis of dermoid cyst was made after the onset of severe complications that led to her death. The findings in this case emphasize the importance of more prompt MRI evaluation, particularly in cases where cranial or spinal dysraphi...
Source: Pediatric Dermatology - July 27, 2016 Category: Dermatology Authors: Khadija Sellami, Hend Chaabane, Hela Fourati, Abderrahmen Masmoudi, Zeineb Mnif, Madiha Mseddi, Hamida Turki Tags: Case Report Source Type: research

Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
ConclusionDiagnosis of LAS should be made based on history, microscopic findings, and hair bulb and shaft features. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 18, 2016 Category: Dermatology Authors: Shane M. Swink, Leslie Castelo‐Soccio Tags: Original Article Source Type: research

Effect of Angiofibromas on Quality of Life and Access to Care in Tuberous Sclerosis Patients and Their Caregivers
ConclusionsPresence and lack of treatment of AF significantly impacts QoL in TSC patients and their caregivers. Access to care for AF is limited by multiple factors and should be addressed by clinicians working with this patient population. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 18, 2016 Category: Dermatology Authors: Cary Crall, Molly Valle, Kush Kapur, Kira A. Dies, Marilyn G. Liang, Mustafa Sahin, Jennifer T. Huang Tags: Original Article Source Type: research

Coexisting Bacillus Calmette –Guérin‐Induced Lupus Vulgaris Involving the Vaccination Site and Lichen Scrofulosorum in an Immunocompetent Boy
Abstract The coexistence of Bacillus Calmette–Guérin (BCG)‐induced lupus vulgaris involving the site of vaccination with lichen scrofulosorum is rare. Herein we report a 3‐year‐old boy who presented with lupus vulgaris at the vaccination site 3 weeks after neonatal BCG vaccination followed by the development of lichen scrofulosorum approximately 2.5 years later. Characteristic clinical morphology, typical histopathology, and positive DNA polymerase chain reaction for Mycobacterium bovis confirmed the clinical diagnosis. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 13, 2016 Category: Dermatology Authors: Gnaneshwar Rao Angoori Tags: Brief Report Source Type: research

Progression of Idiopathic Eruptive Macular Pigmentation in a Girl from Childhood to Adolescence: Case Report and Literature Review
We describe the unusual disease progression of this case of idiopathic eruptive macular pigmentation, which was thought to be self‐limited. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 13, 2016 Category: Dermatology Authors: Wen‐Chien Tsai, Jui Lan, Chih‐Hung Lee Tags: Case Report Source Type: research

Recurrence of Two Nodules on the Toe of a 10 ‐Year‐Old Boy
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Zachary D. Gillooly, Tammy M. Berry, Hillary R. Elwood, Barrett J. Zlotoff Tags: Photoquiz Source Type: research

A Three ‐Year‐Old Girl Who Never Needs a Haircut
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Sarah Carlock, Matthew Hughes, Jay Kincannon Tags: Photoquiz Source Type: research

Patient Perspectives: What is a port ‐wine stain (also known as a port-wine birthmark)?
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Tags: Patient Perspectives Source Type: research

S ézary Syndrome in a 17‐Year‐Old Boy: Clinicopathologic Features and Genomic Profile
We describe the case of a 17‐year‐old Hispanic boy who had had erythroderma and diffuse lymphadenopathy for approximately 6 months. A diagnosis of Sézary syndrome was made on the basis of the histologic features of the skin; the presence of the same T‐cell clone on the skin, blood, and bone marrow; and the high CD4+ lymphocyte count with an aberrant phenotype in peripheral blood; bone marrow involvement was also present. The patient was treated with systemic gemcitabine and achieved partial remission. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Silvia Alberti ‐Violetti, Pamela Vezzoli, Laura Corti, Daniele Fanoni, Valentina Merlo, Luigia Venegoni, Alberto Reseghetti, Emilio Berti Tags: Case Report Source Type: research

A Herald Patch Almost Encircling the Trunk —Extreme Pityriasis Rosea Gigantea in a Young Child
Abstract An 18‐month‐old girl presented with pityriasis rosea gigantea. The herald patch encircled almost the entire trunk. The distribution of lesions on the trunk and proximal aspects of the limbs, the collarette scaling, the orientation of some lesions along the skin crease lines, and biopsy findings substantiated the diagnosis. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Antonio Chuh Tags: Brief Report Source Type: research

Probable Griseofulvin ‐Induced Drug Reaction with Eosinophilia and Systemic Symptoms in a Child
We present a rare case of probable DRESS secondary to griseofulvin. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Robert J. Smith, Markus D. Boos, Patrick McMahon Tags: Brief Report Source Type: research

Chikungunya: What We Need to Know
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Tags: Corrigendum Source Type: research

Generalized Hyperkeratotic Plaques in a Baby with a Milk Allergy
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Yuta Koike, Atsushi Utani Tags: Photoquiz Source Type: research

Recurrence of Two Nodules on the Toe of a 10‐Year‐Old Boy
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Zachary D. Gillooly, Tammy M. Berry, Hillary R. Elwood, Barrett J. Zlotoff Tags: Photoquiz Source Type: research

A Three‐Year‐Old Girl Who Never Needs a Haircut
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Sarah Carlock, Matthew Hughes, Jay Kincannon Tags: Photoquiz Source Type: research

Congenital Papule on the Anterior Neck
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Elizabeth Marvin, Cesar Guerrero, Peter Tang, Ilene Rothman Tags: Photoquiz Source Type: research

Patient Perspectives: What is a port‐wine stain (also known as a port-wine birthmark)?
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Tags: Patient Perspectives Source Type: research

Issue Information ‐ Table of Contents
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Tags: Issue Information Source Type: research

Issue Information ‐ Editorial Board
(Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Tags: Issue Information Source Type: research

Sézary Syndrome in a 17‐Year‐Old Boy: Clinicopathologic Features and Genomic Profile
We describe the case of a 17‐year‐old Hispanic boy who had had erythroderma and diffuse lymphadenopathy for approximately 6 months. A diagnosis of Sézary syndrome was made on the basis of the histologic features of the skin; the presence of the same T‐cell clone on the skin, blood, and bone marrow; and the high CD4+ lymphocyte count with an aberrant phenotype in peripheral blood; bone marrow involvement was also present. The patient was treated with systemic gemcitabine and achieved partial remission. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Silvia Alberti‐Violetti, Pamela Vezzoli, Laura Corti, Daniele Fanoni, Valentina Merlo, Luigia Venegoni, Alberto Reseghetti, Emilio Berti Tags: Case Report Source Type: research

Seizures and Methemoglobinemia After Topical Application of Eutectic Mixture of Lidocaine and Prilocaine on a 3.5‐Year‐Old Child with Molluscum Contagiosum and Atopic Dermatitis
We report a case of generalized seizures and methemoglobinemia after topical application of EMLA for curettage of molluscum contagiosum lesions in a 3.5‐year‐old girl with atopic dermatitis. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Yong Se Cho, Bo Young Chung, Chun Wook Park, Hye One Kim Tags: Brief Report Source Type: research

Incontinentia Pigmenti Coxsackium
We present a case of incontinentia pigmenti coxsackium in which a coxsackievirus infection triggered reactivation of IP and cutaneous viral lesions were concentrated in areas of IP. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Julie Jefferson, Anna Grossberg Tags: Brief Report Source Type: research

A Herald Patch Almost Encircling the Trunk—Extreme Pityriasis Rosea Gigantea in a Young Child
Abstract An 18‐month‐old girl presented with pityriasis rosea gigantea. The herald patch encircled almost the entire trunk. The distribution of lesions on the trunk and proximal aspects of the limbs, the collarette scaling, the orientation of some lesions along the skin crease lines, and biopsy findings substantiated the diagnosis. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Antonio Chuh Tags: Brief Report Source Type: research

Acne Knowledge of Hispanic Parents of Teenagers with Mild to Moderate Acne
Abstract We performed a cross‐sectional study of Hispanic and non‐Hispanic parents of children with acne using a survey designed to determine their level of awareness of acne and its treatment; 82% of Hispanic parents and 40% of non‐Hispanic parents agreed that a health care provider should treat mild acne (p
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Isha Lopez, Lucio Zapata, Juan Jesús Sosa, Clifford Rodgers, Maria Ruiz, Susan Oh, Linda S. Hynan, Alexa B. Kimball, Amit G. Pandya Tags: Brief Report Source Type: research

Probable Griseofulvin‐Induced Drug Reaction with Eosinophilia and Systemic Symptoms in a Child
We present a rare case of probable DRESS secondary to griseofulvin. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Robert J. Smith, Markus D. Boos, Patrick McMahon Tags: Brief Report Source Type: research

Infantile Hemangiomas of the Lip: Patterns, Outcomes, and Implications
This study examined sizes, patterns, and locations of lip hemangiomas, their prognostic value, and their implications in hemangioma pathogenesis. MethodsRecords of 106 patients seen for lip hemangiomas from 2006 to 2013 at Nationwide Children's Hospital were reviewed. Localized hemangiomas were mapped to a location on the lip based on their focus. Size, location, and morphology were assessed with regard to outcome. Poor outcomes were considered to be marked anatomic deformity, scarring, functional complications, and ulceration. ResultsOf 72 untreated hemangiomas with discernible outcomes, 92% of segmental lip hemangiomas w...
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Daniel A. Yanes, Gregory D. Pearson, Patricia M. Witman Tags: Original Article Source Type: research

Commonly Employed African Neonatal Skin Care Products Compromise Epidermal Function in Mice
ConclusionSome neonatal skin care products that are widely used in Africa perturb important epidermal functions, including permeability barrier homeostasis in mice. Should these products have similar effects on newborn human skin, they could cause a defective epidermal permeability barrier, which can increase body fluid loss, impair thermoregulation, and contribute to the high rates of neonatal morbidity and mortality seen in Africa. Accordingly, alternative products that enhance permeability barrier function should be identified, particularly for use in preterm infants. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Mao‐Qiang Man, Richard Sun, George Man, Dale Lee, Zelee Hill, Peter M. Elias Tags: Original Article Source Type: research

Notalgia Paresthetica and Multiple Endocrine Neoplasia Syndrome 2A: A Case Report
We report a 9‐year‐old girl diagnosed with MEN 2A and notalgia paresthetica. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 10, 2016 Category: Dermatology Authors: Francisco Alcántara, Marta Feito, Fátima Albizuri, María Beato, Raúl De Lucas Tags: Case Report Source Type: research

Early Recognition of Proteus Syndrome
We present a series of photographs documenting the skin and musculoskeletal changes in a patient with Proteus syndrome over the first 2 years of life to emphasize the key signs that a dermatologist can recognize to facilitate an earlier diagnosis in these patients. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 3, 2016 Category: Dermatology Authors: Dorothy L. Rodenbeck, Laura A. Greyling, John H. Anderson, Loretta S. Davis Tags: Case Report Source Type: research

Successful Treatment of Pediatric Alopecia Areata of the Scalp Using Topical Bimatoprost
Abstract Alopecia areata (AA) is a genetic and immune‐mediated disease that targets anagen hair follicles. Despite limited evidence supporting the efficacy of corticosteroid treatments, they are often prescribed as first‐line therapy because of their favorable safety profile. Prostaglandin analogues are currently being studied as an alternate therapy for scalp AA in adults. Herein we present a case of steroid‐resistant multifocal AA that was successfully treated with topical bimatoprost. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - July 3, 2016 Category: Dermatology Authors: Alvin W. Li, Richard J. Antaya Tags: Brief Report Source Type: research

Use of Propranolol for Treating Hemangiomas in Infants with Previously Diagnosed Hypoglycemic Conditions
We report three cases of infants with preexisting hypoglycemic conditions requiring diazoxide whose complicated hemangiomas were successfully and safely treated with oral propranolol. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Ting ‐Lin B. Yang, Patrick McMahon, Diva D. De Léon, James R. Treat Tags: Case Report Source Type: research

A Typical Vascular and Pigmentary Dermoscopic Pattern of Capillary Malformations in Capillary Malformation –Arteriovenous Malformation Syndrome: Report of Four Cases
We report dermoscopic characteristics of cutaneous capillary malformations in four patients with capillary malformation–arteriovenous malformation (CM‐AVM) syndrome. We observed a mixed vascular and pigmentary pattern with branched linear vessels and an underlying homogeneous brown background. Disappearance of the vascular pattern on pressure revealed an underlying faint pigmentary reticular pattern. Our results suggest that this typical biphasic pattern on dermoscopy may be useful for the diagnosis of CM‐AVM syndrome. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Claudine Gandon, Bertille Bonniaud, Evelyne Collet, Sophie Dalac, G éraldine Jeudy, Pierre Vabres Tags: Case Report Source Type: research

Tuberous Sclerosis Complex Associated with Vascular Anomalies or Overgrowth
ConclusionHemihypertrophy and vascular anomalies may be more frequent in the setting of TSC than previously appreciated. A common pathogenetic mechanism may tie these manifestations together. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: David Jenkins, Catherine McCuaig, Beth A. Drolet, Dawn Siegel, Susan Adams, John A. Lawson, Orli Wargon Tags: Original Article Source Type: research

Leishmaniasis Gone Viral: Social Media and an Outbreak of Cutaneous Leishmaniasis
This report details how social media communication was used in a group of teens to diagnose cutaneous leishmaniasis that they acquired during a trip to Israel. Their posts quickly brought the cluster to the attention of the teens and their parents, leading to prompt recognition of the true etiology of their lesions and appropriate treatment. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Kanokporn Mongkolrattanothai, Santhosh M. Nadipuram, Andrew C. Krakowski, Margaret M. Stone, Paul Krogstad, Deborah Lehman Tags: Brief Report Source Type: research

Vascular Stains: Proposal for a Clinical Classification to Improve Diagnosis and Management
Abstract Vascular stains are a common reason for consultation in pediatric dermatology clinics. Although vascular stains include all vascular malformations, the term is most often used to refer to capillary malformations, but capillary malformations include a wide range of vascular stains with different clinical features, prognoses, and associated findings. The discovery of several mutations in various capillary malformations and associated syndromes has reinforced these differences, but clinical recognition of these different types of capillary vascular stains is sometimes difficult, and the multitude of classifications a...
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Eduardo Rozas ‐Muñoz, Ilona J. Frieden, Esther Roé, Luis Puig, Eulalia Baselga Tags: Review Source Type: research

Effectiveness and Safety of Acitretin in Children with Plaque Psoriasis: A Multicenter Retrospective Analysis
Abstract BackgroundAcitretin is licensed for and is most commonly used to treat psoriasis. Little information exists about its efficacy and safety in childhood and adolescent psoriasis. MethodsRetrospective analysis of a group of children and adolescents (
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Vito Di Lernia, Domenico Bonamonte, Claudia Lasagni, Anna Belloni Fortina, Stefano Cambiaghi, Monica Corazza, Sergio Di Nuzzo, Paolo Gisondi, Michele Panzone, Claudio Guarneri, Iria Neri Tags: Original Article Source Type: research

Muckle –Wells Syndrome: A Case Report with an NLRP3 T348M Mutation
We report a 5‐year‐old girl with MWS that manifested as a recurrent skin rash without fever episodes or intracranial hypertension with papilledema. Genetic analysis revealed a T348M mutation of the NLRPR 3 gene in the patient and her mother. She was successfully treated with the interleukin‐1β antagonist receptor anakinra. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Elena Naz Villalba, Enrique Gomez de la Fuente, Dolores Caro Gutierrez, Fernando Pinedo Moraleda, Julio Yanguela Rodilla, Diana Mazagatos Angulo, Jose Luis L ópez Estebaranz Tags: Case Report Source Type: research

Muckle–Wells Syndrome: A Case Report with an NLRP3 T348M Mutation
We report a 5‐year‐old girl with MWS that manifested as a recurrent skin rash without fever episodes or intracranial hypertension with papilledema. Genetic analysis revealed a T348M mutation of the NLRPR 3 gene in the patient and her mother. She was successfully treated with the interleukin‐1β antagonist receptor anakinra. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Elena Naz Villalba, Enrique Gomez de la Fuente, Dolores Caro Gutierrez, Fernando Pinedo Moraleda, Julio Yanguela Rodilla, Diana Mazagatos Angulo, Jose Luis López Estebaranz Tags: Case Report Source Type: research

Coexisting Bacillus Calmette–Guérin‐Induced Lupus Vulgaris Involving the Vaccination Site and Lichen Scrofulosorum in an Immunocompetent Boy
Abstract The coexistence of Bacillus Calmette–Guérin (BCG)‐induced lupus vulgaris involving the site of vaccination with lichen scrofulosorum is rare. Herein we report a 3‐year‐old boy who presented with lupus vulgaris at the vaccination site 3 weeks after neonatal BCG vaccination followed by the development of lichen scrofulosorum approximately 2.5 years later. Characteristic clinical morphology, typical histopathology, and positive DNA polymerase chain reaction for Mycobacterium bovis confirmed the clinical diagnosis. (Source: Pediatric Dermatology)
Source: Pediatric Dermatology - June 30, 2016 Category: Dermatology Authors: Gnaneshwar Rao Angoori Tags: Brief Report Source Type: research