Evolution of congenital melanocytic nevi toward benignity: A case series.

abstract：:Alopecia areata (AA) involves the immune-related destruction of hair follicles, resulting in patches of complete hair loss, most often on the scalp. The topical sensitizer squaric acid dibutylester (SADBE) is a popular treatment option given its low side-effect profile, hair regrowth potential, and lack of cross-react...

journal_title：Pediatric dermatology

authors： Chen CA,Carlberg V,Kroshinsky D

更新日期：2017-01-01 00:00:00

abstract：:It has been clinically speculated that the use of oil for hair grooming may change detection of fungus on culture; however, the effect of hair oil on fungal cultures remains poorly studied. In this prospective case-controlled study, scalp cultures were collected from twenty-eight pediatric patients with clinically sus...

journal_title：Pediatric dermatology

authors： Wichterman CM,Kumar MG,Bayliss SJ

更新日期：2020-09-01 00:00:00

abstract：:The prevalence of persistent microalbuminuria, retinopathy, and peripheral and autonomic neuropathy was assessed in 18 children and adolescents with type 1 (insulin-dependent) diabetes mellitus (IDDM) who suffered from necrobiosis lipoidica diabeticorum (NLD) and in 40 diabetics without NLD, matched for sex, age, dura...

journal_title：Pediatric dermatology

authors： Verrotti A,Chiarelli F,Amerio P,Morgese G

更新日期：1995-09-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Vitamin B12 deficiency in infants is uncommonly reported from developed countries and generally lacks dermatologic manifestations. On the contrary, infantile vitamin B12 deficiency is common in India and cutaneous manifestations are a constant feature, although often overshadowed by neurologic and...

journal_title：Pediatric dermatology

authors： Kaur S,Goraya JS

更新日期：2018-11-01 00:00:00

abstract：BACKGROUND:Cutaneous leishmaniasis (CL) is an emerging uncontrolled tropical parasitic disease in endemic and nonendemic areas with a high prevalence in the pediatric age group. METHOD:A total of 382 individuals from Lebanon, Saudi Arabia, Pakistan, and Syria diagnosed with CL by punch biopsy/scrapings were grouped in...

journal_title：Pediatric dermatology

authors： Dunya G,Loya A,Taraif S,Adib Houreih M,Khalifeh I

更新日期：2020-07-01 00:00:00

abstract：:Henoch-Schönlein purpura (HSP) is an acute systemic vasculitis with unknown etiology, although several studies have found HSP to be related to cytokines such as tumor necrosis factor α, interleukin (IL)-1, and adhesion molecules. In the present study we determined the levels of cytokines such as IL-18 and endothelin-1...

journal_title：Pediatric dermatology

authors： Mahajan N,Kapoor D,Bisht D,Singh S,Minz RW,Dhawan V

更新日期：2013-11-01 00:00:00

abstract：:Onychomycosis is widespread in the adult population, but considered to be rare in children. A number of studies in recent years show a rise in the prevalence of toenail onychomycosis in children. Of these, only a few were population-based. Here, we present a comprehensive cross-sectional population-based survey of toe...

journal_title：Pediatric dermatology

authors： Leibovici V,Evron R,Dunchin M,Westerman M,Ingber A

更新日期：2009-01-01 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 results from three online surveys of dermatologists, allergists and immunologists, and primary care physicians (PCPs) regarding routine bathing frequency recommendations for children with atopic dermatitis (AD) are presented. The results suggest that PCPs approach bathing frequency differently than specialists, wi...

journal_title：Pediatric dermatology

authors： Cardona ID,Kempe E,Hatzenbeuhler JR,Antaya RJ,Cohen B,Jain N

更新日期：2015-07-01 00:00:00

abstract：:While the primary etiologic agent of tinea capitis in the United States has varied over the past century, the last several decades have been marked by a predominance of infection with Trichophyton tonsurans. Related anthropophilic organisms commonly isolated in other dermatophytoses are infrequently observed in tinea ...

journal_title：Pediatric dermatology

authors： Abdel-Rahman SM,Penny J,Alander SW

更新日期：2004-01-01 00:00:00

abstract：:Hidradenitis suppurativa is a chronic relapsing disorder of follicular occlusion that is often recalcitrant to therapy. Topical and systemic antibiotics, hormonal therapies, oral retinoids, immunosuppressant agents, and surgical treatment are some of the therapeutic alternatives used for this often recalcitrant and fr...

journal_title：Pediatric dermatology

authors： Lam J,Krakowski AC,Friedlander SF

更新日期：2007-09-01 00:00:00

abstract：:Cutaneous myxomas are rare, benign, connective tissue tumors composed of stellate cells set in a loose mucoid stroma containing delicate reticulin fibers running in various directions. They are also called angiomyxomas to reinforce their vascular component. These lesions have been recognized as part of Carney complex....

journal_title：Pediatric dermatology

authors： Martí N,Jordá E,Monteagudo C,Gámez L,Reig I,Calduch L

更新日期：2011-07-01 00:00:00

abstract：:Infantile myofibromatosis is a rare benign tumor of infancy and childhood that occurs in solitary, multiple, and generalized forms with similar histology but different clinicopathologic and prognostic implications. Even solitary tumors need follow-up, as the type of presentation will be determined over time. It is nec...

journal_title：Pediatric dermatology

authors： Jurcić V,Perković T,Pohar-Marinsek Z,Hvala A,Lazar I

更新日期：2003-07-01 00:00:00

abstract：:Bullous mastocytosis (diffuse cutaneous mastocytosis) is a rare form of mast cell disease that begins during the first month of life and causes extensive blisters that mimic scalded skin syndrome or bullous erythema multiforme. Discrete pigmented macules, papules, and nodules are absent and the characteristic leathery...

journal_title：Pediatric dermatology

authors： Golitz LE,Weston WL,Lane AT

更新日期：1984-04-01 00:00:00

abstract：:Anogenital (AG) warts in 31 prepubertal children were HPV typed by nonisotopic in situ hybridization (NISH) using digoxigenin-labeled probes for human papilloma virus (HPV) types 1-5, 6, 11, 16, 18, 31, and 33. Mode of transmission was determined from historical, clinical, and laboratory data independent of HPV typing...

journal_title：Pediatric dermatology

authors： Handley J,Hanks E,Armstrong K,Bingham A,Dinsmore W,Swann A,Evans MF,McGee JO,O'Leary J

更新日期：1997-09-01 00:00:00

abstract：:An unselected cohort of 4,641 newborns was ascertained prospectively for the purpose of detecting any cutaneous lesion. These were catalogued into pigmented lesions, vascular lesions, and miscellaneous lesions. Several important findings were elucidated: congenital nevocellular nevi are speckled at their borders; no w...

journal_title：Pediatric dermatology

authors： Alper JC,Holmes LB

更新日期：1983-07-01 00:00:00

abstract：:Harlequin ichthyosis (HI) is a rare autosomal recessive disorder of cornification in which children are born with an extremely thick stratum corneum that becomes a restrictive circumferential encasement around the orifices, limbs, chest, and abdomen, resulting in limb contractures. We present a neonate diagnosed in ut...

journal_title：Pediatric dermatology

authors： Tontchev G,Silverberg NB,Shlasko E,Henry C,Roberts JL,Roth MZ

更新日期：2014-09-01 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：:An 11-year-old girl with a history of diabetes mellitus type I and celiac disease presented with multiple, depressed patches of purple-brown skin on the right lower extremity and central back, with histopathologic features of early morphea. Though morphea may coexist with other autoimmune diseases, its presentation wi...

journal_title：Pediatric dermatology

authors： Firoz EF,Kamino H,Lehman TJ,Orlow SJ

更新日期：2010-01-01 00:00:00

abstract：:Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy [HSAN] type V) is a rare disorder of pain perception in which pain sensation is absent from birth, with no other neurologic deficits. We report five Saudi patients (three male and two female) age 10 months to 23 years who lacked pain sensati...

journal_title：Pediatric dermatology

authors： Karkashan EM,Joharji HS,Al-Harbi NN

更新日期：2002-07-01 00:00:00

abstract：:Dyshidrotic eczema is one of the rare cutaneous adverse effects of intravenous immunoglobulin therapy, usually seen in adults. We herein report the first pediatric case of severe dyshidrotic eczema occurring after intravenous immunoglobulin therapy for Kawasaki syndrome. ...

journal_title：Pediatric dermatology

authors： Shiraishi T,Yamamoto T

更新日期：2013-05-01 00:00:00

abstract：:Early recognition of the hyperlipoproteinemias is a crucial element in preventing premature coronary artery disease. Xanthomas provide a cutaneous marker of the silent, underlying pathology. Identifying them, and understanding their relation to the inherited hyperlipoproteinemias may facilitate early diagnosis of hype...

journal_title：Pediatric dermatology

authors： Maher-Wiese VL,Marmer EL,Grant-Kels JM

更新日期：1990-09-01 00:00:00

abstract：:Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome is a recently described syndrome similar to Proteus syndrome but lacking the progressive or distorting bony overgrowth of Proteus syndrome. We describe a neonate with features of CLOVE syndrome and nevus unius lateris. ...

journal_title：Pediatric dermatology

authors： Harit D,Aggarwal A

更新日期：2010-05-01 00:00:00

abstract：:Over the past two decades there have been significant efforts in the United States to heighten awareness about skin cancer. Our goal was to assess parental knowledge, practice, and source of information about sun protection for their children. A questionnaire was administered to 158 parents of children at a dermatolog...

journal_title：Pediatric dermatology

authors： Weinstein JM,Yarnold PR,Hornung RL

更新日期：2001-11-01 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：:Lichen sclerosus is a T-lymphocyte mediated chronic cutaneous disorder with predilection for the vulva. In prepubertal girls, lichen sclerosus presents as vulvar discomfort, pruritus, bruising/bleeding, discharge, dysuria, or painful defecation. Diagnosis and treatment of lichen sclerosus is of utmost importance in th...

journal_title：Pediatric dermatology

authors： Yousefi M,Pride H,Elston D

更新日期：2009-05-01 00:00:00

abstract：BACKGROUND:Kindler syndrome is a rare genodermatosis. Major clinical criteria include acral blistering in infancy and childhood, progressive poikiloderma, skin atrophy, abnormal photosensitivity, and gingival fragility. METHODS:FERMT1 gene was sequenced in 5 patients with a clinical diagnosis of Kindler syndrome. RES...

journal_title：Pediatric dermatology

authors： Valinotto LE,Natale MI,Lusso SB,Cella E,Gutiérrez O,Sebastiani F,Manzur GB

更新日期：2020-03-01 00:00:00

abstract：:The epidermal nevus syndrome is a disease complex consisting of the association of an epidermal nevus with various developmental abnormalities of the skin, eyes, nervous, skeletal, cardiovascular, and urogenital systems. The epidermal nevi are classified according to their predominant component; nevus sebaceus (sebace...

journal_title：Pediatric dermatology

authors： Demerdjieva Z,Kavaklieva S,Tsankov N

更新日期：2007-09-01 00:00:00

abstract：:We aimed to better understand the pathogenesis, clinical features, prognosis, and treatment of neonatal autoimmune blistering diseases (AIBDs). We searched Medline, Embase, PubMed, Latin American and Caribbean Health Sciences Literature, and reference lists of identified articles. Inclusion criteria were articles publ...

journal_title：Pediatric dermatology

authors： Zhao CY,Chiang YZ,Murrell DF

更新日期：2016-07-01 00:00:00

abstract：:Granulomatous mycosis fungoides (GMF) is a rare form of mycosis fungoides (MF) characterized by an infiltrate of atypical lymphocytes, histiocytes, and multinucleated giant cells. Clinically, GMF has a slowly progressing course with a worse prognosis than other forms of MF. With its peak incidence being in the fifth t...

journal_title：Pediatric dermatology

authors： Wieser I,Wohlmuth C,Duvic M

更新日期：2016-09-01 00:00:00