Lymphangioma circumscriptum treated with pulsed dye laser.

abstract：:Montelukast was effective in treating refractory abdominal and urinary symptoms in a child with systemic mastocytosis. ...

journal_title：Pediatric dermatology

authors： Turner PJ,Kemp AS,Rogers M,Mehr S

更新日期：2012-03-01 00:00:00

abstract：:Condylomata acuminata (CA), or anogenital warts, are typically benign lesions caused by human papillomavirus infection. Although they are rare, immunocompromised individuals are at a higher risk of CA undergoing transformation into invasive anal squamous cell carcinoma (SCC). These patients need aggressive evaluation ...

journal_title：Pediatric dermatology

authors： Paul S,Cheng CE,Kroshinsky D

更新日期：2015-07-01 00:00:00

abstract：:Loose anagen hair syndrome (LAHS) is an uncommonly reported autosomal dominant hair disorder with incomplete penetrance that primarily affects children but is occasionally seen in adults. LAHS is characterized by the ability to easily and painlessly extract unsheathed anagen hairs from the scalp with gentle traction. ...

journal_title：Pediatric dermatology

authors： Dey V,Thawani M

更新日期：2013-09-01 00:00:00

abstract：:Fibro-osseous pseudotumor of the digits is a benign neoplasm that originates in the soft tissue adjacent to the short bones of the hands and feet. We present a case in a 13-year-old girl that was initially misdiagnosed as pyogenic granuloma. Familiarity with this entity and imaging and histologic studies are necessary...

journal_title：Pediatric dermatology

authors： Gómez-Zubiaur A,Pericet-Fernández L,Vélez-Velázquez MD,Cabrera-Hernández A,Piteiro-Bermejo AB,Beá-Ardebol S,Medina-Montalvo S,Trasobares-Marugán L

更新日期：2017-05-01 00:00:00

abstract：:One hundred and twenty-one children with plantar warts were treated with a topical preparation containing salicylic acid, 30%; podophyllin, 5%; and cantharidin, 1%. One hundred patients or their families were reached 6 months to 1 year later. This treatment was effective in 81 cases. ...

journal_title：Pediatric dermatology

authors： Coskey RJ

更新日期：1984-07-01 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：: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：: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：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：: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：:Microgeodic disease, similar to chilblains (pernio), is characterized by painful, erythematous swelling, as well as small, punched-out erosions found in affected phalanges. Although they share a similar appearance and proposed pathogenesis, chilblains has rarely been diagnosed in children with microgeodic disease, and...

journal_title：Pediatric dermatology

authors： Prindaville B,Antaya RJ

更新日期：2013-03-01 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：:Proteus syndrome is an extremely rare mosaic condition characterized by progressive overgrowth of tissues due to a somatic activating mutation of the AKT1 gene. Distinct cutaneous features, including cerebriform connective tissue nevi, epidermal nevi, vascular malformations, and adipose abnormalities, can alert the de...

journal_title：Pediatric dermatology

authors： Rodenbeck DL,Greyling LA,Anderson JH,Davis LS

更新日期：2016-09-01 00:00:00

abstract：:We report a child with bilateral congenital triangular alopecia. Shaving the scalp and inserting intravenous cannulas into scalp vessels during the neonatal period was misconstrued by the parents as the cause of hair loss, and resulted in medicolegal implications. ...

journal_title：Pediatric dermatology

authors： Armstrong DK,Burrows D

更新日期：1996-09-01 00:00:00

abstract：BACKGROUND:Acrodermatitis acidemica is a recently proposed term for the rash that is similar to acrodermatitis enteropathica, which is encountered in organic acidemias. However, acrodermatitis enteropathica-like eruption may be seen in metabolic disorders other than organic acidemias. OBJECTIVE:The aim of this study w...

journal_title：Pediatric dermatology

authors： Tabanlioğlu D,Ersoy-Evans S,Karaduman A

更新日期：2009-03-01 00:00:00

abstract：:Due to the presence of two different clones of cells in early embryogenesis, numerous congenital and acquired dermatoses have a linear distribution following the lines of Blaschko. Acquired inflammatory skin diseases are rarely observed in linear patterns. Our patient was born with macrocephaly, left eye glaucoma, and...

journal_title：Pediatric dermatology

authors： Durán-McKinster C,Moises C,Rodríguez-Jurado R,Tamayo-Sánchez L,Orozco-Covarrubias L,Ruiz-Maldonado R

更新日期：2002-09-01 00:00:00

abstract：:Cranioectodermal dysplasia is a rare syndrome characterized by craniofacial and skeletal anomalies and ectodermal dysplasia. Life-threatening associated conditions (i.e., kidney failure and abnormal regulation of the parathyroid-bone axis) can also develop. We report a patient whose features are suggestive of an inapp...

journal_title：Pediatric dermatology

authors： Zannolli R,Mostardini R,Carpentieri ML,Gatti MG,Galluzzi P,Terrosi Vagnoli P,Giorgetti R,Calvieri S,Morgese G

更新日期：2001-07-01 00:00:00

abstract：:Post-transplantation lymphoproliferative disorder (PTLD) is one of the most common de novo malignancies in patients who receive immunosuppressive therapy after solid organ transplantation. We report a case of a 5-year-old girl who presented with indurated violaceous skin nodules 3.5 years post-liver transplantation, d...

journal_title：Pediatric dermatology

authors： Chen KY,Lin CY,Kuo TT,Shih LY,Chang CH,Chen WT,Yang CY

更新日期：2019-09-01 00:00:00

abstract：:Acute genital ulcers rarely occur in nonsexually active young girls. When present, they can cause significant physical and emotional distress for the patient and her parents, and prompt an evaluation for sexual abuse and sexually transmitted diseases. With this review, we aim to further characterize acute genital ulce...

journal_title：Pediatric dermatology

authors： Rosman IS,Berk DR,Bayliss SJ,White AJ,Merritt DF

更新日期：2012-03-01 00:00:00

abstract：:Rat bite fever is a rare but potentially fatal Gram-negative infection that predominantly affects populations with exposure to rats, notably children. The clinical presentation is nonspecific and requires a high threshold of suspicion to elicit a history of rat exposure. We report here a case of a child whose diagnosi...

journal_title：Pediatric dermatology

authors： Lewis BK,Vanderhooft S

更新日期：2012-11-01 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：:An adolescent boy whose initial presentation consisted of an asymmetric, nonvesicular rash was eventually diagnosed with dermatitis herpetiformis (DH). Certain factors, including lesions limited to the genitals, an initial biopsy revealing nonspecific findings on microscopy studies, and the absence of characteristic d...

journal_title：Pediatric dermatology

authors： Clark K,Powers R,Kovach R

更新日期：2014-07-01 00:00:00

abstract：:Follicular mucinosis (FM) is an uncommon reaction pattern in which the accumulation of mucin in the follicular epithelium is the main pathologic finding. FM may be idiopathic (primary follicular mucinosis [PFM]), in association with mycosis fungoides or cutaneous T-cell lymphoma, or in association with other neoplasti...

journal_title：Pediatric dermatology

authors： Santos-Briz A,Cañueto J,García-Dorado J,Alonso MT,Balanzategui A,González-Díaz M

更新日期：2013-11-01 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：: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：:Precalcaneal congenital fibrolipomatous hamartomas are uncommon, congenital, nontender papules located on the medial plantar aspects of the heel. We report the occurrence of this rare disorder in two half brothers, suggesting that it may occur in a familial pattern. ...

journal_title：Pediatric dermatology

authors： Fangman WL,Prose NS

更新日期：2004-11-01 00:00:00

abstract：:Epidermolysis bullosa-associated nevi are recently described dysplastic nevi found in patients with epidermolysis bullosa. These lesions display clinical features of unusual nevi suggestive of malignancy but thus far cases with malignant transformation have not been reported. We describe a case of epidermolysis bullos...

journal_title：Pediatric dermatology

authors： Mollet T,Henderson FW,Groben PA,Burkhart CN,Morrell DS

更新日期：2011-01-01 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 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：: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