Acquired progressive lymphangioma: Case report with partial response to imiquimod 5% cream.

abstract：:We report an 8-year-old boy who developed dystrophic calcinosis cutis that occurred following trauma. Multiple abrasions were observed in the inguinal folds after a soccer game. Subsequently, multiple papules with soft centers and white particles appeared in the same area. A biopsy specimen showed calcinosis cutis wit...

journal_title：Pediatric dermatology

authors： Larralde M,Giachetti A,Cáceres MR,Rodríguez M,Casas J

更新日期：2005-05-01 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：:Raynaud's phenomenon (RP) is an episodic vasospastic response to cold or emotional stress causing color changes and pain. These attacks can lead to digital ischemia, ulcers, and gangrene. Severe and refractory RP in children is a therapeutic challenge for clinicians because there are no standardized treatment protocol...

journal_title：Pediatric dermatology

authors： Quintana Castanedo L,Feito Rodríguez M,Maseda Pedrero R,Chiloeches Fernández C,de Lucas Laguna R

更新日期：2020-07-01 00:00:00

abstract：:Epidermolysis bullosa acquisita (EBA) is a rare, acquired, subepidermal blistering disease characterized by autoantibodies directed against type VII collagen, the major component of anchoring fibrils. We report a 5-year-old Chinese boy who presented with extensive lesions consisting of disseminated pruritic vesicles a...

journal_title：Pediatric dermatology

authors： Yang B,Wang C,Wang N,Pan F,Chen S,Zhou G,Yu M,Zhang F

更新日期：2012-09-01 00:00:00

abstract：:A 13-year-old Korean girl presented with a 7-year history of a pruritic, light-brown patch containing multiple 0.2- to 0.5-cm brownish-to-reddish maculopapules on the left anterior chest. When her skin was rubbed, the lesion became itchy and red. Histopathologic evaluation demonstrated marked dense dermal infiltration...

journal_title：Pediatric dermatology

authors： Ahn HJ,Park HJ,Jeong KH,Park YK,Lee MH

更新日期：2018-09-01 00:00:00

abstract：:Hereditary mucoepithelial dysplasia (HMD) is a rare genodermatosis characterized by nonscarring alopecia, fiery red gums, perineal erythema, and visual impairment. Histologically, dyskeratotic keratinocytes and a small number of desmosomes are the hallmark of the disease. We report on two unrelated patients who presen...

journal_title：Pediatric dermatology

authors： Hernández-Martín A,Colmenero I,Torrelo A

更新日期：2012-05-01 00:00:00

abstract：:A 6-month-old baby had erythema, fissuring of the skin, and craquelé due to prolonged use of a liquid soap mistakenly believed to be a moisturizer. We think these kinds of skin disorders will become increasingly common due to such misunderstandings. The proliferation of cosmetic products for baby skin care, the increa...

journal_title：Pediatric dermatology

authors： Menni S,Brauner I,Tsavdari T

更新日期：1993-09-01 00:00:00

abstract：:Bloom syndrome (congenital telangiectatic erythema) is a rare autosomal recessive disorder characterized by telangiectasias and photosensitivity, growth deficiency of prenatal onset, variable degrees of immunodeficiency, and increased susceptibility to neoplasms of many sites and types. We are reporting Bloom syndrome...

journal_title：Pediatric dermatology

authors： Sultan SJ,Sultan ST

更新日期：2010-03-01 00:00:00

abstract：:Hair loss and thinning are possible complications in those undergoing endocrine therapies with aromatase inhibitors. Alopecia in pediatric patients undergoing endocrine therapy has not been previously reported. We describe two adolescents, 14 and 16 years of age, who developed androgenetic alopecia following treatment...

journal_title：Pediatric dermatology

authors： Perper M,Herskovitz I,Tosti A

更新日期：2020-11-01 00:00:00

abstract：:X-linked chronic granulomatous disease (CGD), a defect of leukocyte bactericidal capacity, was seen in three generations of a large kindred. The association of discoid lupus erythematosus (DLE) with CGD was noted. Recurrent antigenic stimulation leading to autoantibody formation may explain the apparently increased fr...

journal_title：Pediatric dermatology

authors： Barton LL,Johnson CR

更新日期：1986-11-01 00:00:00

abstract：:We report the case of a 2.5-year-old girl with linear morphea initially diagnosed as an acquired port-wine stain (PWS). She underwent three treatments to the right face using the pulsed dye laser (PDL) before sclerotic changes were observed and the correct diagnosis was confirmed with histopathology. Treatment using t...

journal_title：Pediatric dermatology

authors： Pickert AJ,Carpentieri D,Price H,Hansen RC

更新日期：2014-09-01 00:00:00

abstract：:An 8-year-old girl had pseudoxanthoma elasticum (PXE) with the characteristic skin and ocular findings. She had no associated systemic symptoms and no family history of PXE. The disease was most likely inherited in an autosomal recessive fashion. It is reviewed with regard to etiology, inheritance, diagnosis, and, par...

journal_title：Pediatric dermatology

authors： Hacker SM,Ramos-Caro FA,Beers BB,Flowers FP

更新日期：1993-03-01 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：:A 4-month-old female infant presented with widespread pyoderma gangrenosum associated with stridor, presumed secondary to tracheal involvement. No underlying cause was revealed despite extensive investigation. Treatment with immunosuppressive agents only partially suppressed disease activity. Complete resolution follo...

journal_title：Pediatric dermatology

authors： Rajan N,Das S,Taylor A,Abinun M,Spencer D,Carmichael A

更新日期：2009-01-01 00:00:00

abstract：:Two sporadic cases of Heck disease in Polish girls were associated with human papillomavirus 13. No other children and nobody from their surroundings had similar lesions. The course of the disease was chronic in both patients. The lesions regressed spontaneously in one girl within several years after some of the papul...

journal_title：Pediatric dermatology

authors： Obalek S,Janniger C,Jablonska S,Favre M,Orth G

更新日期：1993-09-01 00:00:00

abstract：:Skin and thymus were obtained from abortuses of varying ages and from neonatal autopsies to determine if S100-protein-containing dendritic cells were present. Using an unlabeled antibody peroxidase-antiperoxidase method, we could not detect these dendritic cells in epidermis prior to live birth, but did detect them at...

journal_title：Pediatric dermatology

authors： Penneys NS,Kott-Blumenkranz R,Buck BE,Nadji M,Gould E,Ibe M

更新日期：1986-06-01 00:00:00

abstract：:A 20-year-old woman and her 12-year-old brother had hypohidrotic ectodermal dysplasia, cleft lip and palate, midfacial hypoplasia with narrow nose from the nasal bridge to the tip, narrow dysplastic nails, and conical teeth and hypodontia, and hypospadias and hypoplastic uvula in the boy. The woman had major underdeve...

journal_title：Pediatric dermatology

authors： Camacho F,Ferrando J,Pichardo AR,Sotillo I,Jorquera E

更新日期：1993-03-01 00:00:00

abstract：:Discoid lupus erythematosus (DLE) is rare in childhood. We report the case of a 5-year-old girl who presented with erythematous scaly plaques, with scarring alopecia, involving approximately 40% of her scalp. Histopathology confirmed the diagnosis of DLE. Treatment with intravenous methylprednisolone, hydroxychloroqui...

journal_title：Pediatric dermatology

authors： Miettunen PM,Bruecks A,Remington T

更新日期：2009-05-01 00:00:00

abstract：:We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous p...

journal_title：Pediatric dermatology

authors： Musumeci ML,Nasca MR,De Pasquale R,Schwartz RA,Micali G

更新日期：2006-05-01 00:00:00

abstract：:Acne fulminans is a severe form of acne characterized by painful, inflammatory nodules that progress into ulcers and concurrent systemic symptoms. Treatment of acne with isotretinoin can precipitate a syndrome called isotretinoin-induced acne fulminans without systemic symptoms. An exuberant granulation tissue respons...

journal_title：Pediatric dermatology

authors： Li AW,Antaya RJ

更新日期：2018-03-01 00:00:00

abstract：:We report a new case of postvaccination morphea profunda (MP) in a child and discuss its different clinical presentations, prognosis, and therapy and its relationship with "solitary morphea profunda." A 2-year-old healthy girl presented with an induration of the anterior aspect of the left thigh of 9 months duration. ...

journal_title：Pediatric dermatology

authors： Khaled A,Kharfi M,Zaouek A,Rameh S,Zermani R,Fazaa B,Kamoun MR

更新日期：2012-07-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Sun exposure during childhood is a modifiable risk factor for skin cancer. Social media (including parenting blogs) represent promising platforms for understanding misinformation about pediatric photoprotection. This study's objective was to qualitatively and quantitatively evaluate the digital so...

journal_title：Pediatric dermatology

authors： Tamminga MA,Lipoff JB

更新日期：2020-10-16 00:00:00

abstract：:Hand-foot-mouth disease (HFMD) is a contagious enteroviral infection occurring primarily in children and characterized by a vesicular palmoplantar eruption and erosive stomatitis. Nail matrix arrest has been associated with a variety of drug exposures and systemic illnesses, including infections, and may result in a v...

journal_title：Pediatric dermatology

authors： Clementz GC,Mancini AJ

更新日期：2000-01-01 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：: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：: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：:Congenital nevi both small and large are frequently removed. We attempted to study the removal rate and etiologic aspects of congenital nevi as well as their psychosocial effects through the use of a quality test. A questionnaire sent to a sample population of individuals with congenital nevocytic nevi (n=192) collect...

journal_title：Pediatric dermatology

authors： Berg P,Lindelöf B

更新日期：2002-07-01 00:00:00

abstract：:Verrucous perforating collagenoma is an extremely rare variant of acquired perforating dermatosis that has been seldom described in literature. We present the case of an 18-month-old boy who presented with an erythematous plaque with a central keratotic plug on the leg. Histopathology revealed transepidermal eliminati...

journal_title：Pediatric dermatology

authors： Aizman L,Gelman A,Marathe K

更新日期：2019-09-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Chromhidrosis is a rare condition of which there are only a few case reports in the literature. The aim of this study was to evaluate clinical, laboratory, and possible environmental factors in 13 patients with chromhidrosis to elucidate causative agents. METHODS:Data were obtained from the medic...

journal_title：Pediatric dermatology

authors： Erdol S,Karakaya S,Saglam H,Tarim O

更新日期：2018-07-01 00:00:00

abstract：:Identification of melanoma or worrisome moles is often taught as an important part of routine skin checks. We sought to evaluate the efficacy of gamified education vs. traditional ABCDEs education on melanoma identification and self-confidence in identifying worrisome moles. We report that in our cohort (n = 271), par...

journal_title：Pediatric dermatology

authors： Jia JL,Shen A,Tabata MM,Sarin KY

更新日期：2020-07-01 00:00:00