Aplasia cutis congenita and other anomalies associated with methimazole exposure during pregnancy.

abstract：:Familial cold auto-inflammatory syndrome, Muckle-Wells syndrome and chronic infantile neurologic, cutaneous, articular syndrome are related disorders associated with mutations in the CIAS1 gene. They appear to represent a continuum of one disease characterized by IL-1-mediated inflammation. Until recently, these condi...

journal_title：Pediatric dermatology

authors： O'Connell SM,O'Regan GM,Bolger T,Hoffman HM,Cant A,Irvine AD,Watson RM

更新日期：2007-01-01 00:00:00

abstract：:Although lentigines are usually benign, they can be associated with a number of genetic syndromes in which neoplasms and other multi-system pathological processes occur. Here, we report the case of a 6-year-old girl who presented with atypical lentiginosis and hyperpigmentation caused by a de novo genetic variant in t...

journal_title：Pediatric dermatology

authors： Tran AK,Pearce A,López-Sánchez M,Pérez-Jurado LA,Barnett C

更新日期：2019-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Sun protection starting in childhood is an important means of skin cancer prevention. Factors associated with sunscreen use have been previously described. However, less is known about factors associated with children's utilization of non-sunscreen sun protection strategies. We sought to examine p...

journal_title：Pediatric dermatology

authors： Schlarbaum JP,Lazovich D,Dodd E,Hanson B,Polcari IC

更新日期：2020-09-01 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：:Lymphangioma circumscriptum is a lymphatic malformation that involves the skin and may extend to subcutaneous tissue and muscle. Treatment of these lesions is challenging. Surgical excision may be performed but recurrence is common. Herein we report a child with a symptomatic lymphangioma circumscriptum that was treat...

journal_title：Pediatric dermatology

authors： Lai CH,Hanson SG,Mallory SB

更新日期：2001-11-01 00:00:00

abstract：BACKGROUND:The presence of six or more café au lait (CAL) spots is a criterion for the diagnosis of neurofibromatosis type 1 (NF-1). Children with multiple CAL spots are often referred to dermatologists for NF-1 screening. The objective of this case series is to characterize a subset of fair-complected children with re...

journal_title：Pediatric dermatology

authors： St John J,Summe H,Csikesz C,Wiss K,Hay B,Belazarian L

更新日期：2016-09-01 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：:Transient reactive papulotranslucent acrokeratoderma is a rare palmoplantar keratoderma seen predominantly in adolescent and young adult women. Clinically it is characterized by translucent white papules generally involving the palmar surfaces after exposure to water. The typical "hands-in-the-bucket" sign, which is n...

journal_title：Pediatric dermatology

authors： Neri I,Bianchi F,Patrizi A

更新日期：2006-01-01 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：BACKGROUND/OBJECTIVES:Recent technological advances and diagnostic and therapeutic innovations have resulted in an impressive improvement in the survival of newborn infants requiring intensive care. Consequently, with the use of modern invasive diagnostic and therapeutic procedures, the incidence of iatrogenic events h...

journal_title：Pediatric dermatology

authors： Csoma ZR,Meszes A,Ábrahám R,Kemény L,Tálosi G,Doró P

更新日期：2016-09-01 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：:A 15-year-old girl had a new variation of Andogsky syndrome (unilateral cataract and atopic dermatitis) in which atopic dermatitis was associated with primary bilateral cataracts and retinal degeneration with primary left retinal detachment before cataract surgery. She had no history of systemic steroid treatment. ...

journal_title：Pediatric dermatology

authors： Margolin L,Hershko K,Garcia-Rojas M,Ingber A

更新日期：2003-09-01 00:00:00

abstract：:Trichothiodystrophy (TTD) is a hair abnormality that may be associated with a large number of alterations affecting the skin phenotype and skin appendages, nervous system, eyes, bones, and immune, gonadal, and endocrine systems. We report the first case of TTD associated with a urologic malformation and primary hyperc...

journal_title：Pediatric dermatology

authors： Malvehy J,Ferrando J,Soler J,Tuneu A,Ballesta F,Estrach T

更新日期：1997-11-01 00:00:00

abstract：:A chart review was performed of all patients diagnosed with infantile hemangioma in the pediatric dermatology clinic to determine whether distance traveled by the patient affected adherence to follow-up and treatment plans. An increase in distance was associated with an increase in likelihood of nonadherence to treatm...

journal_title：Pediatric dermatology

authors： Desrosiers AS,Ibrahim JM,Jacks SK

更新日期：2019-05-01 00:00:00

abstract：:Rothmund-Thomson syndrome (RTS) is a genetic disease characterized by developmental abnormalities and poikilodermatous skin changes that appear in infancy. An association with myelodysplastic syndromes is rarely reported in RTS, even though impairment of immune function and recurrent infections are described in the li...

journal_title：Pediatric dermatology

authors： Pianigiani E,De Aloe G,Andreassi A,Rubegni P,Fimiani M

更新日期：2001-09-01 00:00:00

abstract：:Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant inherited blistering skin disease characterized by nonscarring blistering and reticulated hyperpigmentation. It is most commonly due to a heterozygous point mutation, P25L, in the nonhelical V1 domain of keratin 5 (KRT5). Here we...

journal_title：Pediatric dermatology

authors： Geller L,Kristal L,Morel KD

更新日期：2013-09-01 00:00:00

abstract：:Eruptive vellus hair cysts are benign lesions that can be difficult to distinguish from other skin conditions, including molluscum contagiosum and acne vulgaris. Diagnosis can be corroborated with histopathology. We emphasize differing dermoscopy features to help distinguish eruptive vellus hair cysts from molluscum c...

journal_title：Pediatric dermatology

authors： Alfaro-Castellón P,Mejía-Rodríguez SA,Valencia-Herrera A,Ramírez S,Mena-Cedillos C

更新日期：2012-11-01 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：:Isolated benign primary cutaneous plasmacytosis in a child is a very rare and benign disease. Herein we present a case of this condition occurring in a child who showed good response to topical corticosteroid. ...

journal_title：Pediatric dermatology

authors： On HR,Lee SE,Kim YC,Kim SC

更新日期：2014-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Bullous impetigo (BI) is a common dermatologic condition, particularly in children, yet confusion regarding its diagnosis and treatment persists. This study measured pediatricians' ability to diagnose and appropriately treat BI and explored factors that might influence pediatricians' accuracy in m...

journal_title：Pediatric dermatology

authors： Simkin DJ,Grossberg AL,Cohen BA

更新日期：2016-11-01 00:00:00

abstract：:Imatinib mesylate was the first of several tyrosine kinase inhibitors approved for use in the treatment of a number of human cancers. Adverse cutaneous reactions to imatinib are common. Pseudoporphyria has been infrequently reported in adults undergoing imatinib therapy for chronic myeloid leukemia. We present two chi...

journal_title：Pediatric dermatology

authors： Mahon C,Purvis D,Laughton S,Bradbeer P,Teague L

更新日期：2014-09-01 00:00:00

abstract：:Lichen planus is a rare disorder in infants and children where it usually has the classical cutaneous pattern and only exceptionally involves the mucosa and skin appendages. A 9-year-old boy was referred to our department with a 4-month history of erythematous keratotic papules on the trunk and the upper and lower lim...

journal_title：Pediatric dermatology

authors： Aste N,Pau M,Ferreli C,Biggio P

更新日期：1997-03-01 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：: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：: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：:Sixty novice Buddhist monks with tinea capitis confirmed according to clinical presentation and mycological laboratory finding were included in this study. Mixed-type clinical presentation was observed in approximately half of all cases, together with scarring alopecia (95%) and superficial fungal skin infection at lo...

journal_title：Pediatric dermatology

authors： Bunyaratavej S,Leeyaphan C,Rujitharanawong C,Muanprasat C,Matthapan L

更新日期：2017-05-01 00:00:00

abstract：:Papular epidermal nevus with "skyline" basal cell layer (PENS), a variant of epidermal nevus, was recently described in otherwise normal children. We describe herein a patient with multiple, typical PENS lesions associated with peculiar facies, bilateral Achilles tendon shortening, and mild psychomotor delay. The asso...

journal_title：Pediatric dermatology

authors： Rodríguez-Díaz E,Gonzalvo P,Colmenero I,Requena L,Hernández-Martín A,Torrelo A

更新日期：2013-07-01 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：:Prurigo nodularis is an uncommon pediatric cutaneous disorder that is associated with intense pruritus. We report a teenager with prurigo nodularis as the presenting sign of stage IIA Hodgkin's disease, primarily in the mediastinum. The pruritus and associated cutaneous lesions resolved with combination chemotherapy d...

journal_title：Pediatric dermatology

authors： Shelnitz LS,Paller AS

更新日期：1990-06-01 00:00:00

abstract：:Down syndrome is the most common chromosomal abnormality affecting numerous organs, including the skin. Our aim was to study mucocutaneous findings in this syndrome. To do so, 100 children with Down syndrome attending Schools for Children with Special Educational Needs and centers affiliated to the Welfare and Rehabil...

journal_title：Pediatric dermatology

authors： Daneshpazhooh M,Nazemi TM,Bigdeloo L,Yoosefi M

更新日期：2007-05-01 00:00:00