Refractory symptoms successfully treated with leukotriene inhibition in a child with systemic mastocytosis.

Abstract:

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

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Turner PJ,Kemp AS,Rogers M,Mehr S

doi

10.1111/j.1525-1470.2011.01576.x

subject

Has Abstract

pub_date

2012-03-01 00:00:00

pages

222-3

issue

2

eissn

0736-8046

issn

1525-1470

journal_volume

29

pub_type

杂志文章
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    abstract::Over the past two decades there have been significant efforts in the United States to heighten awareness about skin cancer. Our goal was to assess parental knowledge, practice, and source of information about sun protection for their children. A questionnaire was administered to 158 parents of children at a dermatolog...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2001.1861996.x

    authors: Weinstein JM,Yarnold PR,Hornung RL

    更新日期:2001-11-01 00:00:00

  • Sequestrated meningocele of the scalp: diagnostic value of hair anomalies.

    abstract::Clinical aspects of sequestrated meningocele can be varied, causing difficulties in histopathological diagnosis. The meningeal tissue is scanty and appears as nonspecific connective tissue, therefore it may be overlooked. One classical and two unusual clinical presentations of sequestrated meningocele are described: o...

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    doi:10.1111/j.1525-1470.1994.tb00095.x

    authors: Khallouf R,Fétissof F,Machet MC,Stephanov E,Lechrist J,Lorette G

    更新日期:1994-12-01 00:00:00

  • Extensive orf infection in a toddler with associated id reaction.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.13259

    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

  • Novel ABCA-12 mutations leading to recessive congenital ichthyosis.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01695.x

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

    更新日期:2013-11-01 00:00:00

  • Acute genital ulcers in nonsexually active young girls: case series, review of the literature, and evaluation and management recommendations.

    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

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    doi:10.1111/j.1525-1470.2011.01589.x

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

    更新日期:2012-03-01 00:00:00

  • A case series of demodicosis in children.

    abstract::Demodex mites are commensal inhabitants of the pilosebaceous unit that are typically absent or at low numbers in childhood. When they are present, they can cause a primary eruption or exacerbate an underlying facial dermatosis. Here we report five cases of demodicosis occurring in childhood, the clinical presentations...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13852

    authors: Douglas A,Zaenglein AL

    更新日期:2019-09-01 00:00:00

  • Fatal nodular xanthomatosis in an infant.

    abstract::We describe a unique and puzzling case of a 7-month-old baby with a non-X hypertriglyceridemic histiocytoxanthomatosis. The disease was characterized by a massive nodular eruption that was clinically, histologically, and ultrastructurally consistent with juvenile xanthogranuloma, but it had a rapid, fatal evolution. ...

    journal_title:Pediatric dermatology

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    authors: Caputo R,Ermacora E,Gelmetti C,Gianni E

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  • Autologous graft-versus-host disease in a child with stage IV neuroblastoma.

    abstract::Graft-versus-host disease (GVHD) is an underappreciated complication of autologous hematopoietic stem cell transplantation (AHSCT) that can affect the skin, gastrointestinal tract, and liver. The development of this rare condition is probably due to an impairment of immunologic tolerance that can occur spontaneously t...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12407

    authors: Kaffenberger J,Basak SA,Ioffreda M

    更新日期:2015-03-01 00:00:00

  • Bullous Impetigo Rapid Diagnostic and Therapeutic Quiz: A Model for Assessing Basic Dermatology Knowledge of Primary Care Providers.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12974

    authors: Simkin DJ,Grossberg AL,Cohen BA

    更新日期:2016-11-01 00:00:00

  • Colchicine may be of therapeutic benefit in prurigo pigmentosa.

    abstract::Prurigo pigmentosa (PP) is a rare inflammatory skin disease. Neutrophil-mediated inflammation is considered to be responsible for the etiopathogenesis of PP. We consider that colchicine may be an effective agent in the treatment of PP since it exerts an antiinflammatory effect by inhibiting neutrophil chemotaxis. Furt...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13480

    authors: An I,Ucmak D,Ibiloglu I,Demir V,Akdeniz S

    更新日期:2018-05-01 00:00:00

  • Frequency and severity of diaper dermatitis with use of traditional Chinese cloth diapers: observations in 3- to 9-month-old children.

    abstract::Chinese cloth diapers differ from disposable diapers in several respects that are central to our understanding of the etiology of diaper dermatitis (DD), yet there are no published reports on the dermatological correlates of this manner of infant care, which is prevalent among the world's second-largest pediatric popu...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01494.x

    authors: Liu N,Wang X,Odio M

    更新日期:2011-07-01 00:00:00

  • Raynaud phenomenon after treatment of verruca vulgaris of the sole with intralesional injection of bleomycin.

    abstract::Intralesional injection of bleomycin (BLM) for the treatment of warts resistant to all conventional therapies is of certain interest because of the drug's low toxicity and its efficacy. However, delayed side effects may appear, particularly Raynaud phenomenon. Accordingly, some precautions must be taken in patients wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2001.018003249.x

    authors: Vanhooteghem O,Richert B,de la Brassinne M

    更新日期:2001-05-01 00:00:00

  • Idiopathic infantile pyoderma gangrenosum with stridor responsive to infliximab.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00825.x

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

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  • Endemic pemphigus foliaceus in Venezuela: report of two children.

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    更新日期:2006-03-01 00:00:00

  • Eccrine angiomatous hamartoma: a report of symmetric and painful lesions of the wrists.

    abstract::Eccrine angiomatous hamartoma (EAH) is a rare, benign cutaneous lesion histologically defined as a proliferation of eccrine glands within a closely associated vascular stroma. Typically EAH presents as a solitary flesh-colored, hyperhidrotic, painful papule or plaque appearing at birth or during childhood. Only two pr...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.2001.018002117.x

    authors: Morrell DS,Ghali FE,Stahr BJ,McCauliffe DP

    更新日期:2001-03-01 00:00:00

  • A prospective survey of pediatric dermatology clinic patients in Kuwait: an analysis of 10,000 cases.

    abstract::Skin diseases are common in children. However, only a very few prospective epidemiologic surveys are available in the literature. The present survey was directed at determining the spectrum and pattern of skin diseases of children in Kuwait. A total of 10,000 consecutive new patients were studied; 96% were children of...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

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  • Multiple milia in a newborn with congenital malformations: oral-facial-digital syndrome type 1.

    abstract::Oral-facial-digital syndrome type 1 (OMIM #311200) is an X-linked dominant, developmental disorder. Among the 13 described clinical variants of oral-facial-digital syndrome, oral-facial-digital syndrome type 1 is of significance to dermatologists due to presence of congenital milia and hypotrichosis, not described in ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01334.x

    authors: Nanda A,Sharaf A,Alsaleh QA

    更新日期:2010-11-01 00:00:00

  • Onychodystrophy in lichen striatus.

    abstract::Lichen striatus is a common childhood eruption, but only rare reports link cutaneous manifestations and onychodystrophy. We report a case of lichen striatus and onychodystrophy in a 12-year-old girl, only the eighth such patient in the dermatologic literature. Nail changes may precede the rash of lichen striatus and s...

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  • Approach to the jewelry aficionado.

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    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13379

    authors: Ivey LA,Limone BA,Jacob SE

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  • Ichthyosis: mechanisms of disease.

    abstract::The disorders of cornification (ichthyoses) comprise acquired and inherited disorders characterized clinically by generalized scaling and histologically by hyperkeratosis. They may arise through defects in the production or maintenance of a normal cornified cell compartment, or both. The stratum corneum is composed of...

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  • Resolution of diffuse facial verruca plana following nonavalent human papillomavirus immunization.

    abstract::Treatment of verruca plana is often challenging, and multiple treatment modalities, both pharmacologic and destructive, are frequently necessary to clear lesions. We report a case of a 16-year-old girl with a 2-year history of extensive verruca plana of the forehead, temples, and upper periorbital skin, recalcitrant t...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14384

    authors: Johnson NM,Pickard CM

    更新日期:2020-10-08 00:00:00

  • Adams-Oliver syndrome: a sporadic occurrence with minimal disease expression.

    abstract::Adams-Oliver syndrome is a congenital condition comprising congenital scalp defects and distal limb abnormalities. We report a child with the sporadic form of the disease who had minimal disease expression, illustrating the wide clinical spectrum of the syndrome. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00598.x

    authors: Narang T,Kanwar AJ,Dogra S

    更新日期:2008-01-01 00:00:00

  • Dermatofibrosarcoma protuberans in a pediatric patient with ataxia telangiectasia syndrome.

    abstract::Ataxia telangiectasia (AT) is a rare autosomal recessive neurodegenerative disorder caused by a mutation in the ATM gene. An impaired immune response due to the gene mutation leads to an increased risk of infection and malignancy. We present a rare case of dermatofibrosarcoma protuberans arising in a patient with AT. ...

    journal_title:Pediatric dermatology

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    doi:10.1111/pde.13779

    authors: Duffy R,Liaqat M,Lawrence N,Manders S

    更新日期:2019-05-01 00:00:00

  • Febrile ulceronecrotic Mucha-Habermann disease with central nervous system vasculitis.

    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...

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

    更新日期:2013-01-01 00:00:00

  • Cutaneous tuberculosis in children.

    abstract::Cutaneous tuberculosis is a rare form of extrapulmonary tuberculosis that accounts for 1% to 2% of cases. Childhood skin tuberculosis represents 18% to 82% of all cutaneous tuberculosis cases. Scrofuloderma and lupus vulgaris are the two most common clinical forms in children. An increase in the number of tuberculids,...

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    authors: Sethuraman G,Ramesh V

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  • Molluscum Contagiosum-Like Presentation of Langerhans Cell Histiocytosis: A Case and Review.

    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...

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    doi:10.1111/pde.13223

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  • Lichen planus in a child requiring circumcision.

    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...

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    abstract::Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a variety of underlying abnormalities. The phenotype includes parchment-like hyperkeratosis, pseudocontractures, ectropion, eclabium, absence of eyebrows, and sparse hair. Asymmetric crying facies is caused by congenital hyp...

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    authors: Akcakus M,Gunes T,Kurtoglu S,Ozturk A

    更新日期:2003-03-01 00:00:00

  • Rapp-Hodgkin syndrome with pili canaliculi.

    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...

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  • Neonatal urticaria due to prostaglandin E1.

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    更新日期:2000-01-01 00:00:00