Varied Presentations of Pediatric Lipoblastoma: Case Series and Review of the Literature.

abstract：:Intralesional corticosteroid injections are frequently used to treat various musculoskeletal and dermatologic conditions, including keloid scarring. While a number of adverse events may be associated with these injections, hypopigmentation without atrophy is rare. We report a case of a pediatric patient with temporary...

journal_title：Pediatric dermatology

authors： Bjorklund KA,Fernandez Faith E

更新日期：2020-01-01 00:00:00

abstract：:This report describes the clinical, radiologic, and autopsy findings of a newborn with PHACE syndrome (posterior fossa malformations, hemangioma, arterial anomalies, cardiac defects, and eye anomalies) and fetal alcohol spectrum disorder. To our knowledge, the concurrence of these conditions has not been reported in t...

journal_title：Pediatric dermatology

authors： Oza VS,Feigenbaum DF,Jacquot C,Hess CP,Siegel D,Frieden IJ

更新日期：2016-05-01 00:00:00

abstract：:Cutaneous manifestations are becoming increasingly well-documented in adults with COVID-19. There is now also a growing body of literature regarding skin involvement in children, with reports of papulovesicular, petechial and widespread macular and papular lesions, and chilblains (pernio). We describe the case of a 13...

journal_title：Pediatric dermatology

authors： Klimach A,Evans J,Stevens J,Creasey N

更新日期：2020-09-01 00:00:00

abstract：INTRODUCTION:Extravasation injuries are a common and challenging problem in hospitalized newborns. Accidental infusion leakage into the surrounding tissues in immature infants may frequently result in skin necrosis, with significant risk of functional and cosmetic impairment. MATERIAL AND METHODS:In the present study ...

journal_title：Pediatric dermatology

authors： Kostogloudis N,Demiri E,Tsimponis A,Dionyssiou D,Ioannidis S,Chatziioannidis I,Nikolaidis N

更新日期：2015-11-01 00:00:00

abstract：:Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a variety of underlying abnormalities. The phenotype includes parchment-like hyperkeratosis, pseudocontractures, ectropion, eclabium, absence of eyebrows, and sparse hair. Asymmetric crying facies is caused by congenital hyp...

journal_title：Pediatric dermatology

authors： Akcakus M,Gunes T,Kurtoglu S,Ozturk A

更新日期：2003-03-01 00:00:00

abstract：:Oral-facial-digital syndrome type 1 (OMIM #311200) is an X-linked dominant, developmental disorder. Among the 13 described clinical variants of oral-facial-digital syndrome, oral-facial-digital syndrome type 1 is of significance to dermatologists due to presence of congenital milia and hypotrichosis, not described in ...

journal_title：Pediatric dermatology

authors： Nanda A,Sharaf A,Alsaleh QA

更新日期：2010-11-01 00:00:00

abstract：:Leukemia cutis and facial nerve palsy are rare presenting symptoms of leukemia. This report describes a case of acute T-cell lymphoblastic leukemia (ALL) presenting with only these two symptoms, a presentation of ALL that, to our knowledge, has not been previously described. It serves to alert physicians to look for u...

journal_title：Pediatric dermatology

authors： Gold HL,Grynspan D,Kanigsberg N

更新日期：2014-05-01 00:00:00

abstract：:We report an unusual occurrence of spontaneous pigmentary regression with a desmoplastic reaction in a neonatally eroded giant congenital melanocytic nevus. This process has been documented with photographs and skin biopsy specimens. Neonatal histology demonstrated connective tissue proliferation. Histology at age 5 y...

journal_title：Pediatric dermatology

authors： Gass JK,Grant JW,Hall PN,Atherton DJ,Burrows NP

更新日期：2006-11-01 00:00:00

abstract：BACKGROUND:Children with congenital melanocytic nevi (CMN) were historically managed with surgical removal to lower the risk of malignant transformation. The evolving literature over the last decade has indicated a significantly lower risk than previously estimated. Indications for excision currently revolve around aes...

journal_title：Pediatric dermatology

authors： Mosa A,Ho ES,Heinelt M,Wong K,Neuhaus K

更新日期：2019-11-01 00:00:00

abstract：:Keratitis ichthyosis deafness syndrome is a rare congenital ectodermal disorder. It appears to be genetically heterogeneous and may be caused by mutations in the connexin 26 (Cx26) gene (GJB2) or in the connexin 30 gene. It is characterized by the association of ichthyosis-like skin lesions, hearing loss, and vascular...

journal_title：Pediatric dermatology

authors： De Raeve L,Bonduelle M,Deconinck H,Roseeuw D,Stene JJ

更新日期：2008-07-01 00:00:00

abstract：:Subcutaneous granuloma annulare is a benign inflammatory disorder that primarily affects healthy children and manifests as a rapidly growing, painless, nonmobile mass, most commonly located in the leg. The current case highlights the sonographic appearance of subcutaneous granuloma annulare. Ultrasound color Doppler i...

journal_title：Pediatric dermatology

authors： Vázquez-Osorio I,Quevedo A,Rodríguez-Vidal A,Rodríguez-Díaz E

更新日期：2018-05-01 00:00:00

abstract：:A newborn girl had typical "blueberry muffin" skin lesions, which showed histopathologic features of myelomonocytic leukemia cutis. We could not demonstrate leukemic infiltration of bone marrow in four aspirates. Her course was complicated with primary pulmonary hypertension, which led to death at 7 months of age. We ...

journal_title：Pediatric dermatology

authors： Torrelo A,Madero L,Mediero IG,Baño A,Zambrano A

更新日期：2004-07-01 00:00:00

abstract：:We present a special case of an 8-year-old girl diagnosed with severe drug reaction with eosinophilia and systemic symptoms due to trimethoprim-sulfamethoxazole for urinary tract infection prophylaxis for congenital vesicoureteral reflux. The patient is believed to have developed drug reaction with eosinophilia and sy...

journal_title：Pediatric dermatology

authors： Maarouf M,Wickenheiser M,Krase JM,Wolter S,Shi VY

更新日期：2018-11-01 00:00:00

abstract：:Autosomal recessive congenital ichthyosis is a genetically and phenotypically heterogenous group of scaling skin disorders. We describe a patient with ARCI caused by homozygous variants in NIPAL4, in whom the dermatologic phenotype and an associated arthropathy, markedly improved with ustekinumab. ...

journal_title：Pediatric dermatology

authors： Poulton C,Gration D,Murray K,Baynam G,Halbert A

更新日期：2019-11-01 00:00:00

abstract：:We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous p...

journal_title：Pediatric dermatology

authors： Musumeci ML,Nasca MR,De Pasquale R,Schwartz RA,Micali G

更新日期：2006-05-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Despite rising skin cancer rates in children, multiple studies reveal inadequate youth sun-protective behavior (eg, sunscreen use). Using Healthy Passages data for fifth-graders, we set out to determine sunscreen adherence in these children and investigated factors related to sunscreen performance...

journal_title：Pediatric dermatology

authors： Correnti CM,Klein DJ,Elliott MN,Veledar E,Saraiya M,Chien AT,Schwebel DC,Mrug S,Tortolero SR,Cuccaro PM,Schuster MA,Chen SC

更新日期：2018-09-01 00:00:00

abstract：: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. ...

journal_title：Pediatric dermatology

authors： Boer B,Tisack A,Shwayder T

更新日期：2016-11-01 00:00:00

abstract：:Acquired ichythosis has been described in adult hematopoietic stem cell transplant recipients. While some authors have suggested the association of acquired ichythosis with cutaneous graft-versus-host disease, the evidence to support this association is rare. We describe a patient who developed enteritis secondary to ...

journal_title：Pediatric dermatology

authors： Huang J,Pol-Rodriguez M,Silvers D,Garzon MC

更新日期：2007-01-01 00:00:00

abstract：:Demand for pediatric dermatologic care far exceeds the supply of pediatric dermatologists. Teledermatology has been proposed as a solution to improve access to care, however, data regarding teledermatology use for pediatric patients are lacking. Surveys assessing use and experience with teledermatology were administer...

journal_title：Pediatric dermatology

authors： Fieleke DR,Edison K,Dyer JA

更新日期：2008-03-01 00:00:00

abstract：:Aplasia cutis congenita (ACC) is characterized by the complete or partial absence of skin at birth, with 85% of cases of ACC involving the scalp vertex. The etiology of ACC is unclear and appears to be multifactorial. We present the case of a 3-month-old boy who presented with a diagnosis of non-scalp ACC affecting ap...

journal_title：Pediatric dermatology

authors： Davis MJ,Voller LM,Gonzalez SR,Abu-Ghname A,Davies LW,Bedwell JR,Lee GL,Hunt RD,Phung TL,Buchanan EP

更新日期：2021-01-22 00:00:00

abstract：:In addition to the evaluation of melanocytic growths (Part I), dermoscopy is helpful in the identification and management of vascular tumors, skin infections, and inflammatory conditions. In this practical review, we present the classic dermoscopic findings of the following: vascular tumors, infectious conditions (mol...

journal_title：Pediatric dermatology

authors： Natsis NE,Gordon SC,Kaushik A,Seiverling EV

更新日期：2020-09-01 00:00:00

abstract：:The present study aimed to investigate the prevalence of atopic dermatitis in primary schoolchildren in Denizli, Turkey, and to determine the possible risk factors for atopic dermatitis in home environment. A self-administered questionnaire was handled to the parents of 2,100 children aged 7 to 15 years, from three ra...

journal_title：Pediatric dermatology

authors： Ergin S,Ozşahin A,Erdoğan BS,Aktan S,Zencir M

更新日期：2008-05-01 00:00:00

abstract：:PLACK syndrome (OMIM 616295) is a form of generalized peeling skin syndrome (GPSS; OMIM 270300). It is an autosomal recessive genodermatosis caused by pathogenic mutations in CAST, which encodes calpastatin, an endogenous specific inhibitor of calpain, a calcium-dependent cysteine protease. We present a 5-year-old gir...

journal_title：Pediatric dermatology

authors： Boggs JME,Irvine AD

更新日期：2020-10-03 00:00:00

abstract：:Bullous pemphigoid (BP) is the most common autoimmune blistering disease affecting the elderly but is quite rare in childhood. The majority of pediatric cases have been reported during early childhood. Adolescence is divided into three phases: early (10-13 years), middle (14-17), and late (18-21). This review aimed to...

journal_title：Pediatric dermatology

authors： Patsatsi A,Kyriakou A,Werth VP

更新日期：2019-03-01 00:00:00

abstract：:Kwashiorkor is a common affliction of children worldwide. It occurs less often in developed countries, but has been reported under a variety of circumstances, including poverty, neurologic disease, and malabsorption. Because of its rare occurrence in the United States and because the affected child has an edematous ra...

journal_title：Pediatric dermatology

authors： Eastlack JP,Grande KK,Levy ML,Nigro JF

更新日期：1999-03-01 00:00:00

abstract：:We evaluated the prevalence of acanthosis nigricans among urban youth. Youth (7-17 years) at nine pediatric practices completed surveys on demographics and family history of diabetes and had weight and height measured. Acanthosis nigricans was scored and digital photography of the neck performed. A total of 618 youth ...

journal_title：Pediatric dermatology

authors： Brickman WJ,Binns HJ,Jovanovic BD,Kolesky S,Mancini AJ,Metzger BE,Pediatric Practice Research Group.

更新日期：2007-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Drug reaction with eosinophilia and systemic symptoms (DRESS) is rare but potentially fatal in children. Fever and rash, which are salient features of DRESS, may mimic other commonly encountered pediatric conditions. We profiled the DRESS cases in a tertiary children's hospital in Singapore. METH...

journal_title：Pediatric dermatology

authors： Han XD,Koh MJ,Wong SMY

更新日期：2019-05-01 00:00:00

abstract：:Triethanolamine is used as an emulsifier in many cosmetics and in topical medications, yet the occurrence of contact dermatitis to cosmetics containing triethanolamine is rare in childhood. Our case highlights how young age should not be a deterrent to investigation and demonstrates the importance of patch testing wit...

journal_title：Pediatric dermatology

authors： Milanesi N,Berti S,Gola M

更新日期：2015-05-01 00:00:00

abstract：:A 2-year-old African American, Hispanic boy presented with well-defined, violaceous, annular dermal plaques without scale over the upper extremities, face, lower extremities, and buttocks. The clinical presentation and laboratory studies were consistent with a diagnosis of subacute cutaneous lupus erythematous (SCLE)....

journal_title：Pediatric dermatology

authors： Berry T,Walsh E,Berry R,DeSantis E,Smidt AC

更新日期：2014-05-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Epidemiologic studies of children with alopecia areata (AA) are sparse, and there are no studies that focus on the youngest children with AA. Evaluation of the clinical presentations of AA in children <4 years of age was performed in order to identify the prognostic factors for disease progression...

journal_title：Pediatric dermatology

authors： Rangu S,Rogers R,Castelo-Soccio L

更新日期：2019-11-01 00:00:00