Generalized spinous follicular lichen nitidus with perifollicular granulomas.

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：:Phrynoderma is a rare form of follicular hyperkeratosis associated with deficiencies in vitamins A or C or essential fatty acids. We report a 6-year-old boy with an unusual presentation of phrynoderma, characterized by multiple minute digitate hyperkeratoses associated with hair casts and related to a severe deficienc...

journal_title：Pediatric dermatology

authors： Girard C,Dereure O,Blatière V,Guillot B,Bessis D

更新日期：2006-07-01 00:00:00

abstract：:Head-and-neck dermatitis is a variant of atopic dermatitis (AD) often seen in children and is challenging to diagnose, as it frequently overlaps with other eczematous dermatoses. Successful head-and-neck dermatitis (HND) treatment requires identification of common triggers and clinical mimickers, such as airborne derm...

journal_title：Pediatric dermatology

authors： Maarouf M,Saberian C,Lio PA,Shi VY

更新日期：2018-11-01 00:00:00

abstract：:To describe the characteristics of five pediatric patients with the Meyerson phenomenon associated with congenital melanocytic nevi, five cases were reviewed to retrieve information relating to clinical presentation, treatment and evolution of the eczematous phenomenon and of the nevi. Three of five patients were male...

journal_title：Pediatric dermatology

authors： Rolland S,Kokta V,Marcoux D

更新日期：2009-05-01 00:00:00

abstract：:We report the exceptional case of 11-year-old identical male twins who both developed discoid lupus erythematosus lesions. Although systemic lupus erythematosus has often been reported in identical twins, discoid lupus erythematosus has only occasionally been described, with only one other case in twin children, as fa...

journal_title：Pediatric dermatology

authors： Del Boz J,Martín T,Samaniego E,Vera A,Sanz A,Crespo V

更新日期：2008-11-01 00:00:00

abstract：:Benign cephalic histiocytosis is a rare skin condition consisting of small tan papules on the face and upper trunk that is believed not to be associated with internal organ involvement. The infiltrating histiocytes are not Langerhans' cells (LCs). We report a 5-year-old girl who presented with diabetes insipidus 1 yea...

journal_title：Pediatric dermatology

authors： Weston WL,Travers SH,Mierau GW,Heasley D,Fitzpatrick J

更新日期：2000-07-01 00:00:00

abstract：:Microcomedonal lesions can be aesthetically and psychologically displeasing. The burden of comedones increases when considering their frequency and demand for time-consuming attention. The objective of the current study was to describe a novel technique to facilitate open microcomedone extraction. The instrumentation ...

journal_title：Pediatric dermatology

authors： Naimer SA

更新日期：2016-11-01 00:00:00

abstract：:Connective tissue nevi of collagen type are now classified in four major subtypes. In addition to the clinicopathological features of papulolinear collagenoma, which is considered as a variant of isolated collagen harmatoma, the case we present has a unique arborizing pattern. ...

journal_title：Pediatric dermatology

authors： Lo LK,Tsai TF,Chen YF,Hung CM,Ko WC

更新日期：2009-01-01 00:00:00

abstract：:Halo dermatitis is a pruritic, eczematous eruption on pigmented nevi and halo nevi in young adults. It may be mistaken for nummular eczema, psoriasis, or fungal skin infection. Awareness of halo dermatitis will possibly reveal more cases in children, which have been reported only rarely. ...

journal_title：Pediatric dermatology

authors： Shifer O,Tchetchik R,Glazer O,Metzker A

更新日期：1992-09-01 00:00:00

abstract：:Hemangiomas, common proliferative vascular tumors, can grow rapidly in the first months of life. Although therapy with high-dose oral glucocorticoids is standard for lesions that threaten vital functions or are disfiguring, little is known about the endocrine consequences of this treatment. Using retrospective data, w...

journal_title：Pediatric dermatology

authors： Lomenick JP,Backeljauw PF,Lucky AW

更新日期：2006-03-01 00:00:00

abstract：:An 8-month-old male infant had fever, polymorphonuclear leukocytosis, and tender, firm, elevated erythematous plaques on his face, trunk, and extremities. Histologic examination revealed a dense, perivascular, polymorphonuclear, inflammatory cell infiltrate with nuclear dust in the dermis and intrafollicular abscesses...

journal_title：Pediatric dermatology

authors： Kibbi AG,Zaynoun ST,Kurban AK,Najjar SS

更新日期：1985-11-01 00:00:00

abstract：:We report a case of congenital hypertrichosis and FOXN1 duplication. FOXN1 is a member of the forkhead box gene family, located on chromosome 17. Its function includes differentiation of epithelial cells and regulation of keratinocytes, especially hair keratins. Loss of function of these transcription factors leads to...

journal_title：Pediatric dermatology

authors： Gilhooley E,Gormally S,Irvine A,Lynch SA,Collins S

更新日期：2017-03-01 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：:Cutis laxa is a rare disorder resulting from degradation and clumping of elastic fibers in dermis. Type II acquired cutis laxa, shows only cutaneous changes without any systemic involvement. We describe an infant with acquired cutis laxa type II following a generalized inflammatory dermatitis. ...

journal_title：Pediatric dermatology

authors： Haider M,Alfadley A,Kadry R,Almutawa A

更新日期：2010-01-01 00:00:00

abstract：:Xanthoma disseminatum is a rare, usually self-healing dermatologic disease of unknown etiology. Involvement of other organs and tissues including bone marrow, bone, and brain may be seen rarely in children. However, to date, hepatic involvement has not been reported. We describe a child with xanthoma disseminatum who ...

journal_title：Pediatric dermatology

authors： Büyükavci M,Selimoglu A,Yildirim U,Ertekin V,Atasoy M

更新日期：2005-11-01 00:00:00

abstract：:Our objective was to establish the aerobic and anaerobic microbiology of nonbullous impetigo (NI) in children. We used a retrospective review of clinical microbiology laboratory and patients' records. Specimens were obtained from 40 patients with NI lesions and showed bacterial growth. Aerobic or facultative anaerobic...

journal_title：Pediatric dermatology

authors： Brook I,Frazier EH,Yeager JK

更新日期：1997-05-01 00:00:00

abstract：:Tinea capitis is a common infection of childhood. There have been several reports of tinea capitis in newborns. Our patient presented at 19 days of age to the emergency room with a scalp lesion of 5 days duration. The fungal culture grew both Trichophyton rubrum and Trichophyton mentagrophytes. The patient was success...

journal_title：Pediatric dermatology

authors： Ungar SL,Laude TA

更新日期：1997-05-01 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：:Little is known about pediatricians' counseling and clinical practices to reduce skin cancer risk among their patients. Thus our objectives were to characterize skin cancer preventive counseling and clinical practices in a sample of pediatricians and identify correlates of these practices. Physicians practicing genera...

journal_title：Pediatric dermatology

authors： Gritz ER,Tripp MK,de Moor CA,Eicher SA,Mueller NH,Spedale JH

更新日期：2003-01-01 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：: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：: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

abstract：:We report a 2-year-old boy with a plaque on the upper arm composed of multiple 2- to 3-mm leiomyomata which developed at the age of 3 months and have been unchanged since. Immunohistologically there was positive staining for the muscle intermediate filament desmin. We discuss the unusual clinical presentation and poss...

journal_title：Pediatric dermatology

authors： Henderson CA,Ruban E,Porter DI

更新日期：1997-07-01 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：:Granular parakeratosis has only recently been described and typically occurs in adults. We report the first instance of this condition affecting a child. ...

journal_title：Pediatric dermatology

authors： Trowers AB,Assaf R,Jaworsky C

更新日期：2002-03-01 00:00:00

abstract：:Mycosis fungoides (MF) is the most common form of cutaneous T-cell lymphoma. It usually occurs in middle-aged and elderly persons, although several reports have described its occurrence in young children. The aim of this study was to review the profile and outcome of childhood MF in Singapore from 1989 to 1998. A tota...

journal_title：Pediatric dermatology

authors： Tan E,Tay YK,Giam YC

更新日期：2000-09-01 00:00:00

abstract：:Nipple adenoma is an uncommon proliferative process of the breast and predominantly occurs in women aged 40-50. Its incidence is extremely low in men, and it has not been reported in a boy. Although nipple adenoma is rare and benign, being familiar with it is important because it clinically resembles Paget disease and...

journal_title：Pediatric dermatology

authors： Fujisawa K,Kato M,Kono T,Utsunomiya H,Watanabe A,Watanabe S

更新日期：2018-05-01 00:00:00

abstract：:Childhood pemphigus foliaceus typically causes erythema and scaling of the scalp. Sometimes, blisters and oozing are present, which often are misdiagnosed as either impetigo or seborrheic dermatitis. The eruption may progress to involve the trunk and limbs, the lesions often having an arcuate pattern. The diagnosis ca...

journal_title：Pediatric dermatology

authors： Jones SK,Schwab HP,Norris DA

更新日期：1986-12-01 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：:Langerhans cell histiocytosis (LCH) is a rare disorder characterized by clonal proliferation of Langerhans cells in the skin. A molluscum-like presentation of cutaneous LCH is rare but important to consider for examination and management. We present an atypical molluscum-like LCH case and review the literature for com...

journal_title：Pediatric dermatology

authors： Karpman MS,AlJasser MI,Lam JM

更新日期：2017-09-01 00:00:00