A lichen striatuslike eruption adopting the morphology of Blaschko lines.

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：:Tuberous sclerosis with macrodactyly is a very uncommon presentation. We report a 15-year-old girl with a thick, loose hyperpigmented area on the dorsum of the left hand with macrodactyly. A skin biopsy specimen from the dorsum of the left hand revealed dense collagenization in the dermis. Radiographs showed marked ir...

journal_title：Pediatric dermatology

authors： Sahoo B,Handa S,Kumar B

更新日期：2000-11-01 00:00:00

abstract：:Knowledge of the molecular underpinnings of many epidermal nevi and epidermal nevus syndrome has expanded rapidly in recent years. In this review and update on epidermal nevus syndrome, we will cover recent genetic discoveries involving epidermal nevi, including nevus sebaceus, keratinocytic epidermal nevus, nevus com...

journal_title：Pediatric dermatology

authors： Asch S,Sugarman JL

更新日期：2018-01-01 00:00:00

abstract：:Hoyeraal-Hreidarsson syndrome is a rare telomere biology disorder that is recognized as a severe variant of dyskeratosis congenita. We present a Libyan boy with hematologic and neurologic abnormalities with typical dermatologic manifestations of dyskeratosis congenita. Death usually occurs before the age of 4 years as...

journal_title：Pediatric dermatology

authors： Bakar Ö,Işik U,Canpolat C,Alanay Y

更新日期：2015-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Rocky Mountain spotted fever (RMSF), a lethal tick-borne illness, is prevalent in the south central United States. Children younger than 10 years old have the greatest risk of fatal outcome from RMSF. The objective of the current study was to review pediatric cases of RMSF seen in the dermatology ...

journal_title：Pediatric dermatology

authors： Tull R,Ahn C,Daniel A,Yosipovitch G,Strowd LC

更新日期：2017-03-01 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：:Congenital erythropoietic porphyria is a rare form of porphyria, presenting during the neonatal period or during infancy. Clinical features include photosensitive blistering and severe anemia. Wood's lamp fluorescence of the diaper is a useful screening test. We describe a severely affected neonate with systemic invol...

journal_title：Pediatric dermatology

authors： Hogeling M,Nakano T,Dvorak CC,Maguiness S,Frieden IJ

更新日期：2011-07-01 00:00:00

abstract：:Practice guidelines for the treatment of tinea capitis (TC) from the European Society for Pediatric Dermatology are presented. Tinea capitis always requires systemic treatment because topical antifungal agents do not penetrate the hair follicle. Topical treatment is only used as adjuvant therapy to systemic antifungal...

journal_title：Pediatric dermatology

authors： Kakourou T,Uksal U,European Society for Pediatric Dermatology.

更新日期：2010-05-01 00:00:00

abstract：:Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a type of skin lymphoma. Pleomorphic T-cells infiltrate the subcutaneous tissue and mimic lobular panniculitis. We report a case occurring in a 12-year-old Chinese boy who presented with multiple indolent erythematous subcutaneous nodules on both extremities wi...

journal_title：Pediatric dermatology

authors： Hu ZL,Sang H,Deng L,Li Z

更新日期：2015-07-01 00:00:00

abstract：:Mutations in the keratinocyte lipid transporter adenosine triphosphate-binding cassette A12 (ABCA12) are known to cause harlequin ichthyosis. More recently, mutations in this gene have been demonstrated to cause other phenotypes within the spectrum of recessive congenital ichthyosis. We report the case of an infant wi...

journal_title：Pediatric dermatology

authors： Peterson H,Lofgren S,Bremmer S,Krol A

更新日期：2013-11-01 00:00:00

abstract：:Infantile acropustulosis (IA) is a condition of young children characterized by recurrent episodes of pruritic vesicles and pustules in an acral distribution. Several reports describe patients with scabies infestation prior to the diagnosis of IA, although the relationship between the two remains unclear. Furthermore,...

journal_title：Pediatric dermatology

authors： Mancini AJ,Frieden IJ,Paller AS

更新日期：1998-09-01 00:00:00

abstract：:Woolly hair nevus is a rare syndrome that presents as woolly hair in restricted areas of the scalp and may be associated with pigmented macules or epidermal nevus on the body. Here, we report a case of woolly hair nevus, linear pigmentation, and multiple epidermal nevi with a somatic HRAS c.34G>A(p.G12S) mutation. ...

journal_title：Pediatric dermatology

authors： Nishihara K,Tohyama M,Kubo A

更新日期：2019-05-01 00:00:00

abstract：BACKGROUND/OBJECTIVE:Pediatric hematopoietic stem cell transplantation (HSCT) patients are at an increased risk for skin cancers. Sun exposure is a significant modifiable environmental risk factor. While patient education on sun protection and avoidance behaviors with regular dermatology evaluations are crucial for ped...

journal_title：Pediatric dermatology

authors： Li EB,Song JS,Huang JT,Hawryluk EB,London WB,Guo D,Sridharan M,Fisher DE,Rea CJ,Lehmann LE,Duncan CN

更新日期：2019-11-01 00:00:00

abstract：:Juvenile xanthogranuloma is the most common non-Langerhans cell histiocytosis of infancy and childhood. It is a benign disorder that usually regresses spontaneously, more often without or with limited skin changes. The clinical features are very pleomorphic and recognition of the atypical presentations should facilita...

journal_title：Pediatric dermatology

authors： Imiela A,Carpentier O,Segard-Drouard M,Martin de Lassalle E,Piette F

更新日期：2004-03-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Loose anagen syndrome (LAS) is a disorder of abnormal anchorage of the hair to the scalp. Its symptoms include an inability to grow hair long and hair that is easily pulled out. METHODS:We conducted a retrospective chart review of patients with LAS over the last 10 years at the Children's Hospita...

journal_title：Pediatric dermatology

authors： Swink SM,Castelo-Soccio L

更新日期：2016-09-01 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：:Traumatic tattoos induced by pencil point puncture in children may result in persistent disfigurement if left untreated. The Q-switched ruby laser effectively removes darkly colored cutaneous chromophores with minimal disruption of unaffected skin. We present a young patient with pencil point induced traumatic tattooi...

journal_title：Pediatric dermatology

authors： Knoell KA,Schreiber AJ,Kutenplon M,Milgraum SS

更新日期：1997-07-01 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：:Acquired progressive lymphangioma (APL), or benign lymphangioendothelioma, is an unusual entity derived from vascular structures. Clinically and histopathologically it may resemble Kaposi's sarcoma and well-differentiated angiosarcoma, causing a diagnostic problem. We report an individual with APL initially diagnosed ...

journal_title：Pediatric dermatology

authors： Salman A,Sarac G,Can Kuru B,Cinel L,Yucelten AD,Ergun T

更新日期：2017-11-01 00:00:00

abstract：:Psychologic factors may play a significant role in acne in at least three ways. First, as many patients readily report, emotional stress can exacerbate acne. Second, it is common for patients to develop psychiatric problems as a consequence of the conditions, such as those related to low self-esteem, social phobias, o...

journal_title：Pediatric dermatology

authors： Koo JY,Smith LL

更新日期：1991-09-01 00:00:00

abstract：:Prostaglandin E1 is commonly used in the management of cyanotic congenital heart disease. While cutaneous flushing and peripheral edema are well recognized side effects of prostaglandin E1 therapy, other cutaneous effects have not been described in the dermatologic literature. We report a neonate with transposition of...

journal_title：Pediatric dermatology

authors： Carter EL,Garzon MC

更新日期：2000-01-01 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 17-year-old woman with Cornelia de Lange syndrome had asymptomatic skin lesions since the age of 4 years. These were multiple, follicular, horny papules, present on both cheeks, and surrounded by erythematous skin. Similar lesions were present on the external aspect of the arms, but amidst skin of normal coloration....

journal_title：Pediatric dermatology

authors： Flórez A,Fernández-Redondo V,Toribio J

更新日期：2002-01-01 00:00:00

abstract：:Familial hyperpigmentation, or melanosis universalis hereditaria, is a rare hyperpigmentary disorder with onset in infancy. Here, we describe monozygotic twins with similar pattern of progressive hyperpigmentation with onset in early neonatal period without any family history. Histopathological examination showed incr...

journal_title：Pediatric dermatology

authors： Gupta N,Sharma MC,Ramam M,Kabra M

更新日期：2011-01-01 00:00:00

abstract：:Febrile ulceronecrotic Mucha-Habermann disease (FUMHD) is a severe variant of pityriasis lichenoides et varioliformis acuta (PLEVA). We report a case of FUMHD in an 11-year-old boy who subsequently developed neurologic symptoms and was found to have necrotizing vasculitis on brain biopsy. Over 5 years of follow-up, he...

journal_title：Pediatric dermatology

authors： Rosman IS,Liang LC,Patil S,Bayliss SJ,White AJ

更新日期：2013-01-01 00:00:00

abstract：:Orf is a zoonotic parapoxvirus typically transmitted to humans by a bite from goats or sheep. We present an unusual case of multiple orf lesions on the fingers of a 13-month-old child who was bitten by a goat and subsequently developed progressive swelling, blistering, and necrotic papulonodules of the hand followed b...

journal_title：Pediatric dermatology

authors： Haddock ES,Cheng CE,Bradley JS,Hsu CH,Zhao H,Davidson WB,Barrio VR

更新日期：2017-11-01 00:00:00

abstract：:Perianal streptococcal dermatitis (PSD) is a recently described cutaneous entity caused by group A beta-hemolytic streptococci. It is characterized by perianal erythema, sometimes associated with functional disturbances. We describe four children (2 boys, 2 girls) who had acute guttate psoriasis and also PSD. One of t...

journal_title：Pediatric dermatology

authors： Patrizi A,Costa AM,Fiorillo L,Neri I

更新日期：1994-06-01 00:00:00

abstract：:A 40-year-old man and his 6-year-old only son had numerous, firm papulonodular lesions on their faces. Their medical histories were unremarkable and no family consanguinity was recorded. Surgical excision of several lesions was performed on each patient. All the lesions were solid tumors with the characteristic histop...

journal_title：Pediatric dermatology

authors： Pujol RM,Casanova JM,Egido R,Pujol J,de Moragas JM

更新日期：1995-12-01 00:00:00

abstract：:Orofacial granulomatosis, a rare disease in childhood, is characterized by orofacial swelling in the absence of systemic disease. We report the case of a 12-year-old girl with asymptomatic erythematous infiltration of her upper lip, cheeks, and chin that had persisted for more than 2 years; biopsy confirmed granuloma ...

journal_title：Pediatric dermatology

authors： Lalosevic J,Gajic-Veljic M,Nikolic M

更新日期：2017-11-01 00:00:00

abstract：:Skin prick tests were performed in 12 children with atopic eczema before and after 2 weeks of treatment with topical mometasone furoate and tacrolimus. Both treatments significantly suppressed the allergen wheal size. Mometasone furoate reduced the histamine wheal size as well. Skin prick testing in children treated w...

journal_title：Pediatric dermatology

authors： Gradman J,Wolthers OD

更新日期：2008-03-01 00:00:00