Bathing Frequency Recommendations for Children with Atopic Dermatitis: Results of Three Observational Pilot Surveys.

abstract：:A 12-year-old girl presented for excision of a nevus sebaceous of the scalp. The surgery was complicated by unexpected difficult-to-control bleeding in the operating room. Numerous attempts to obtain hemostasis were unsuccessful including the use of local anesthetic containing epinephrine, direct pressure, wall suctio...

journal_title：Pediatric dermatology

authors： Bellet JS,Wagner AM

更新日期：2009-09-01 00:00:00

abstract：:Bascule syndrome is a recently described benign vasomotor dermatosis characterized by Bier anemic spots, cyanosis, and urticaria-like eruption. We report a case of a 13-year-old girl with cutaneous lesions consistent with Bascule syndrome who had had three exercise-related syncopal episodes. It would be recommended to...

journal_title：Pediatric dermatology

authors： Martín JM,Torres C,Cordero P,Sánchez S,Terradez L,Ramón D

更新日期：2018-03-01 00:00:00

abstract：:Amniotic band syndrome is one of the many causes of aplasia cutis congenita. It is usually seen as a constriction band surrounding a limb or as a membrane that adheres to some part of the body. This syndrome can be associated with various malformations. An infant with amniotic adhesions producing aplasia cutis, radial...

journal_title：Pediatric dermatology

authors： Nagore E,Sánchez-Motilla JM,Febrer MI,Cremades B,Aleu M,Aliaga A

更新日期：1999-05-01 00:00:00

abstract：BACKGROUND:Fibroblastic connective tissue nevi (FCTN) are benign skin conditions characterized by bland spindle cells infiltrating the reticular dermis and the upper subcutis with preservation of adnexal structures. A subset of FCTN expresses CD34, which may cause difficulties in the differential diagnosis, in particul...

journal_title：Pediatric dermatology

authors： Bouaoud J,Fraitag S,Soupre V,Mitrofanoff M,Boccara O,Galliot C,Bodemer C,Picard A,Khonsari RH

更新日期：2018-09-01 00:00:00

abstract：:Leukemia cutis and facial nerve palsy are rare presenting symptoms of leukemia. This report describes a case of acute T-cell lymphoblastic leukemia (ALL) presenting with only these two symptoms, a presentation of ALL that, to our knowledge, has not been previously described. It serves to alert physicians to look for u...

journal_title：Pediatric dermatology

authors： Gold HL,Grynspan D,Kanigsberg N

更新日期：2014-05-01 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：:Cerebriform intradermal nevus is a rare form of cutis verticis gyrata. Clinically it manifests as a scalp deformity resembling the surface of the brain, with cerebriform morphologic characteristics. Degeneration into malignant melanoma has been reported. Herein, a cerebriform intradermal nevus of the scalp in a 7-year...

journal_title：Pediatric dermatology

authors： Yazici AC,Ikizoglu G,Baz K,Polat A,Ustunsoy D

更新日期：2007-03-01 00:00:00

abstract：:The present study aimed to investigate the prevalence of atopic dermatitis in primary schoolchildren in Denizli, Turkey, and to determine the possible risk factors for atopic dermatitis in home environment. A self-administered questionnaire was handled to the parents of 2,100 children aged 7 to 15 years, from three ra...

journal_title：Pediatric dermatology

authors： Ergin S,Ozşahin A,Erdoğan BS,Aktan S,Zencir M

更新日期：2008-05-01 00:00:00

abstract：:Molluscum contagiosum is a common viral infection of the skin that frequently affects children. Lesions take between 6 and 18 months to resolve spontaneously and are a source of great embarrassment to both caretakers and children, often affecting attendance at school and limiting social activity. Treatment options to ...

journal_title：Pediatric dermatology

authors： Short KA,Fuller LC,Higgins EM

更新日期：2006-05-01 00:00:00

abstract：:Two native Yanomami children from the Venezuelan Amazonia with erythroderma were hospitalized on our service. Clinical, histologic, and immunofluorescence studies diagnosed endemic pemphigus foliaceous. Human leukocyte antigen class II showed DRB1*04 subtype *0411, which has not been previously associated with this di...

journal_title：Pediatric dermatology

authors： González F,Sáenz AM,Cirocco A,Tacaronte IM,Fajardo JE,Calebotta A

更新日期：2006-03-01 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：:Verruciform xanthoma (VX) is a rare finding thought to be caused by epidermal damage from trauma or inflammation and has been reported in a limited number of patients with recessive dystrophic epidermolysis bullosa (RDEB). Herein, we describe a 20-year-old woman with RDEB who developed a large, verrucous, pink plaque ...

journal_title：Pediatric dermatology

authors： Stephens M,Rubin AI,Perman MJ

更新日期：2020-03-01 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：:Blue nevi are common skin neoplasms that typically present as asymptomatic solitary papules, although they may rarely occur in an agminated configuration. We describe a case of agminated blue nevus in a segmental facial distribution associated with soft tissue hypertrophy and hypertrichosis in a 16-year-old boy and pr...

journal_title：Pediatric dermatology

authors： Hunjan MK,Mohandas D,Bridges AG,Tollefson M

更新日期：2018-01-01 00:00:00

abstract：:Langerhans cell histiocytosis affecting only the vulva of a child is very rare. We report a 1-year-old female infant with isolated Langerhans cell histiocytosis presenting as pruritic papules confined to the vulva, confirmed by histopathology with immunohistochemical staining. ...

journal_title：Pediatric dermatology

authors： Hwang C,Kim YJ,Seo YJ,Park JK,Lee JH,Lee Y

更新日期：2009-11-01 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：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：: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

abstract：:Bullous dermolysis of the newborn is a dominant or recessive inherited subtype of dystrophic epidermolysis bullosa characterized by the tendency to spontaneously stop blistering within the first months of life. Here we report two siblings with bullous dermolysis of the newborn who were born prematurely and have a nove...

journal_title：Pediatric dermatology

authors： Boccaletti V,Zambruno G,Castiglia D,Magnani C,Tognetti E,Fabrizi G,Cortelazzi C,Pagliarello C,Di Nuzzo S

更新日期：2015-03-01 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：: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：: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：: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：:One morphologic feature of Turner syndrome is increased numbers of melanocytic nevi; however, little attention has been given to their characterization. The development of a melanoma in one of our patients with Turner syndrome prompted this study. We prospectively examined 10 patients with the disease, confirmed by ka...

journal_title：Pediatric dermatology

authors： Becker B,Jospe N,Goldsmith LA

更新日期：1994-06-01 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：:Parry-Romberg syndrome (PRS) is characterized by hemiatrophy of facial structures, including skin, subcutaneous fat, muscle, bone, and cartilage. Complications associated with PRS include headaches, seizures, and chronic facial pain. Protocol for the treatment of chronic facial pain is not clear; reports on the use of...

journal_title：Pediatric dermatology

authors： Mishra K,Sood A,Smidt A,Price HN

更新日期：2019-03-01 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：: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：: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：:An 8-year-old girl had Crohn's disease of the vulva 16 months before the onset of intestinal symptoms. At the time of diagnosis she had no evidence of systemic disease. Cutaneous and intestinal lesions responded rapidly to corticosteroids and metronidazole. Crohn's disease must be considered in the differential diagno...

journal_title：Pediatric dermatology

authors： Lally MR,Orenstein SR,Cohen BA

更新日期：1988-05-01 00:00:00