Parental knowledge and practice of primary skin cancer prevention: gaps and solutions.

abstract：:The keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of the ectoderm characterized by diffuse hyperkeratotic erythroderma, keratitis with neovascularization of the cornea, and severe neurosensory hearing loss. A familial occurrence of this syndrome has been mentioned in four reports inc...

journal_title：Pediatric dermatology

authors： Koné-Paut I,Hesse S,Palix C,Rey R,Rémédiani K,Garnier JM,Berbis P

更新日期：1998-05-01 00:00:00

abstract：:Congenital midline cervical cleft is a rare anomaly of the ventral neck that heretofore has not been reported in the dermatology literature. We present a case of a midline cervical cleft that was diagnosed and managed at an early age. We also review the literature and discuss its clinical and histologic features, trea...

journal_title：Pediatric dermatology

authors： Eastlack JP,Howard RM,Frieden IJ

更新日期：2000-03-01 00:00:00

abstract：:Lymphangiomas are congenital malformations of the lymphatic system. We report a 10-year-old boy with lymphatic malformation of the scrotum, which presented as a multiloculated scrotal mass associated with edema of the left thigh and left cryptorchidism. Histopathologic examination showed scrotal lymphangioma cavernosu...

journal_title：Pediatric dermatology

authors： Vikicevic J,Milobratovic D,Vukadinovic V,Golubovic Z,Krstic Z

更新日期：2007-11-01 00:00:00

abstract：:A male infant with skin lesions was born to a 28-year-old mother who was under treatment for pemphigus vulgaris (PV), diagnosed eight years earlier. Circulating IgG class pemphigus antibody was found in the infant's blood, and deposition of IgG in the intercellular spaces of the epidermis was seen. The infant's lesion...

journal_title：Pediatric dermatology

authors： Hup JM,Bruinsma RA,Boersma ER,de Jong MC

更新日期：1986-12-01 00:00:00

abstract：:The proband in this study was a 4-year-old Mexican girl with Blau syndrome. She and her affected family members had skin rash and arthritis but no uveitis. Exome sequencing and DNA direct sequencing from blood samples revealed a novel nucleotide-binding oligomerization domain-containing protein 2 gene mutation in the ...

journal_title：Pediatric dermatology

authors： Toral-López J,González-Huerta LM,Martín-Del Campo M,Messina-Baas O,Cuevas-Covarrubias SA

更新日期：2018-05-01 00:00:00

abstract：:The first report of spinous follicular lichen nitidus with perifollicular granulomas was by Madhok and Winkelmann in 1988. Since this report, a few cases of follicular or periappendageal lichen nitidus have been described, in a more localized form or without perifollicular granulomas. We describe a 5-year-old girl wit...

journal_title：Pediatric dermatology

authors： Summe HS,Greenlaw SM,Deng A,Magro C,Wiss K

更新日期：2013-05-01 00:00:00

abstract：:Hemangiomas are classified as focal or segmental according to the morphology and distribution of lesions. Congestive cardiac failure is frequently encountered in diffuse hepatic hemangiomas due to high-volume shunting and rarely in hemangiomas confined to the skin. We report here the case of a large multifocal hemangi...

journal_title：Pediatric dermatology

authors： Khanna D,Chakravarty P,Arora P,Jain R,Mittal M

更新日期：2015-01-01 00:00:00

abstract：:Rothmund-Thomson syndrome (RTS) is a genetic disease characterized by developmental abnormalities and poikilodermatous skin changes that appear in infancy. An association with myelodysplastic syndromes is rarely reported in RTS, even though impairment of immune function and recurrent infections are described in the li...

journal_title：Pediatric dermatology

authors： Pianigiani E,De Aloe G,Andreassi A,Rubegni P,Fimiani M

更新日期：2001-09-01 00:00:00

abstract：:A 14-year-old boy presented with extensive capillaritis. Narrow-band ultraviolet B was administered on a thrice-weekly schedule followed by once-a-week maintenance. A favorable response to treatment was seen without any side effects. ...

journal_title：Pediatric dermatology

authors： Verma P

更新日期：2013-11-01 00:00:00

abstract：:Lichen planus (LP) in children is a rare entity. We report 23 cases of childhood LP seen over a period of 7 years. Ninety-six percent of the children were of Arab ancestry. There were 52% boys and 48% girls. Classic LP was the most common clinical variant (70%), followed by eruptive generalized LP (13%). A majority of...

journal_title：Pediatric dermatology

authors： Nanda A,Al-Ajmi HS,Al-Sabah H,Al-Hasawi F,Alsaleh QA

更新日期：2001-01-01 00:00:00

abstract：:A 3-year-old girl presented with longer hair on the left side of her scalp, coarse hair of abnormal length on her extremities, and a tuft of hair in the lumbosacral region, with all hair distributed on normally pigmented skin. Neither similar or relevant family history nor associated extracutaneous abnormalities was d...

journal_title：Pediatric dermatology

authors： Sotiriadis D,Patsatsi A,Lazaridou E,Sotiriou E,Devliotou-Panagiotidou D

更新日期：2009-07-01 00:00:00

abstract：BACKGROUND:The current treatment of keloids includes surgery, intralesional steroids, and radiotherapy, among others. Radiotherapy is not recommended in children due to its effects on growing tissues. Our aim was to study intralesional triamcinilone therapy of keloids in children and analyze the impact of body location...

journal_title：Pediatric dermatology

authors： Acosta S,Ureta E,Yañez R,Oliva N,Searle S,Guerra C

更新日期：2016-01-01 00:00:00

abstract：:The October 2018 report from the United Nations Intergovernmental Panel on Climate Change predicts significant threats to human health secondary to anthropogenic global warming; children have been and will continue to be disproportionately affected by these weather-related changes. Multiple physician groups have ackno...

journal_title：Pediatric dermatology

authors： Schachtel A,Boos MD

更新日期：2019-07-01 00:00:00

abstract：:Superficial granulomatous pyoderma is a rare entity thought to be a variant of pyoderma gangrenosum and is often mistaken for classic pyoderma gangrenosum. Superficial granulomatous pyoderma has mainly been described in adults. We describe a case of Superficial granulomatous pyoderma in an 11-year-old girl and present...

journal_title：Pediatric dermatology

authors： Tollefson MM,Cook-Norris RH,Theos A,Davis DM

更新日期：2010-09-01 00:00:00

abstract：:Diaper dermatitis results from the action of a number of physical and chemical factors on the skin. While its etiology is complex, there is agreement that prolonged contact between wet diapers and the skin leading to excessive hydration of the stratum corneum and reduced barrier function is a primary factor. Recent re...

journal_title：Pediatric dermatology

authors： Davis JA,Leyden JJ,Grove GL,Raynor WJ

更新日期：1989-06-01 00:00:00

abstract：:Granular cell tumors are uncommon in the vulva. We cared for a child who had a solitary vulvar tumor since infancy. ...

journal_title：Pediatric dermatology

authors： Guenther L,Shum D

更新日期：1993-06-01 00:00:00

abstract：:Acne fulminans is a severe form of acne vulgaris accompanied by systemic symptoms. A 17-year-old Chinese boy presented with an outbreak of necrotic lesions on his face eight days after the onset of palpable purpura, arthralgia, fever, abdominal pain, and proteinuria. He was successfully treated with oral prednisolone ...

journal_title：Pediatric dermatology

authors： Xu X,Li X,Pradhan S,Li W

更新日期：2020-11-01 00:00:00

abstract：:We report a rare presentation of vulvar lymphangiectasia that developed secondary to gastrointestinal tuberculosis in a teenager, and its spontaneous resolution after anti-tuberculous treatment was completed. ...

journal_title：Pediatric dermatology

authors： Ho VPY,Koh MJA

更新日期：2020-01-01 00:00:00

abstract：:We report an unusual congenital vesiculopustular eruption arising in a neonate as the result of the transient myeloproliferative disorder (TMD) associated with trisomy 21. In this instance, the neonate was phenotypically normal, making the diagnosis more elusive. Initially the lesions were clinically suspicious for he...

journal_title：Pediatric dermatology

authors： Solky BA,Yang FC,Xu X,Levins P

更新日期：2004-09-01 00:00:00

abstract：:Stevens-Johnson syndrome is a potentially fatal condition that manifests mainly on the skin and mucosal surfaces but also affects other vital organs. There are no report of Stevens-Johnson syndrome caused by brucella infection in the literature. In this article, a previously healthy boy, diagnosed as Stevens-Johnson s...

journal_title：Pediatric dermatology

authors： Babayigit A,Olmez D,Uzuner N,Caglayan S,Kumral A,Asilsoy SK,Ozer E,Karaman O

更新日期：2007-07-01 00:00:00

abstract：:Burns and scalds are relatively common injuries in children. Formation of hypertrophic scars or keloids is feared complications. A 2-year-old girl who spilled a cup of hot coffee onto herself developed widespread hypertrophic scars and beginning keloids on her upper chest, despite application of pressure garments and ...

journal_title：Pediatric dermatology

authors： Eisendle K,Pichler M,De Luca J,Thuile T

更新日期：2020-01-01 00:00:00

abstract：:Granular cell tumors are uncommon, usually benign tumors of neural origin. They are most often diagnosed in the third to sixth decades of life and are infrequently seen in the pediatric population. Although they can be found in a wide distribution throughout the body, more than half occur in the oral cavity and other ...

journal_title：Pediatric dermatology

authors： Abraham T,Jackson B,Davis L,Yu J,Peterson C

更新日期：2007-05-01 00:00:00

abstract：:A 2-year-old boy had hundreds of discrete, small, flat yellow to brown colored papules distributed over the face, neck, and trunk. Biopsy revealed a well-demarcated infiltrate within the papillary dermis composed of histiocytes and some Touton giant cells and eosinophils. The cells were negative for protein S-100 and ...

journal_title：Pediatric dermatology

authors： Torrelo A,Juarez A,Hernández A,Colmenero I

更新日期：2009-03-01 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：:Eczema action plans (EAPs) are written, customizable documents that guide patients through the self-management of atopic dermatitis. Here, we distributed a survey regarding the use patterns and perceptions of eczema action plans to 1068 members of the Society for Pediatric Dermatology and received 87 responses. Althou...

journal_title：Pediatric dermatology

authors： Stringer T,Yin HS,Oza VS

更新日期：2018-11-01 00:00:00

abstract：:We report on four children born with medium to large congenital melanocytic nevi (CMN) with color heterogeneity and irregular surface rugosity. As these patients aged, their nevi evolved to become more homogeneous and lighter in color, and developed a smoother, more even texture. We propose that given this evolution t...

journal_title：Pediatric dermatology

authors： Cotton CH,Goldberg GN

更新日期：2019-03-01 00:00:00

abstract：:Although acne vulgaris is common in preadolescents (<13 yrs), few acne treatments are currently approved for children. This study assessed the safety and efficacy of tretinoin microsphere gel (TMG) 0.04% pump in children aged 9-11 with acne vulgaris. In this multicenter, randomized, double-blind, vehicle-controlled pi...

journal_title：Pediatric dermatology

authors： Eichenfield LF,Hebert AA,Schachner L,Paller AS,Rossi AB,Lucky AW

更新日期：2012-09-01 00:00:00

abstract：:A congenital curved nail of the fourth toe (NIM 219070) is a rare nail deformity with no other associated abnormalities. Three patients with this congenital anomaly are reported here. Radiologic examination in all three revealed distal symphalangism of the fourth toes bilaterally. The clinical manifestations in these ...

journal_title：Pediatric dermatology

authors： Lin YC,Wu YH,Scher RK

更新日期：2007-07-01 00:00:00

abstract：:PHACE syndrome is characterized by posterior fossa malformations (P), large facial hemangiomas (H), arterial anomalies (A), cardiac anomalies or coarctation of aorta (C), and eye anomalies (E) and has striking female predominance. Endocrine abnormalities have recently been described in these patients, involving the th...

journal_title：Pediatric dermatology

authors： Altin H,Alp H,Sap F,Karataş Z,Baysal T,Karaaslan S

更新日期：2012-05-01 00:00:00

abstract：:Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder that is caused by a DNA repair defect. It is characterized mainly by skin, eye, and skeletal abnormalities. Cutaneous changes appear at between 3 and 6 months of age and include poikiloderma, photosensitivity, scaling, hyperkeratosis, and disturban...

journal_title：Pediatric dermatology

authors： Narayan S,Fleming C,Trainer AH,Craig JA

更新日期：2001-05-01 00:00:00