Granular parakeratosis in a child.

Abstract:

:Granular parakeratosis has only recently been described and typically occurs in adults. We report the first instance of this condition affecting a child.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Trowers AB,Assaf R,Jaworsky C

doi

10.1046/j.1525-1470.2002.00044.x

subject

Has Abstract

pub_date

2002-03-01 00:00:00

pages

146-7

issue

2

eissn

0736-8046

issn

1525-1470

pii

0044

journal_volume

19

pub_type

杂志文章
  • Accessory tragus: Report of a case in a rare location on the nasal vestibule.

    abstract::A case of an accessory tragus located on the nasal vestibule is reported. This represents the third case of this entity located outside of a derivative of a branchial arch. All three of these cases were located in the nose/glabella region. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14090

    authors: Moradi S,Castiglione C,Ehrig T

    更新日期:2020-03-01 00:00:00

  • Ruvalcaba-Myhre-Smith syndrome.

    abstract::In 1980 a syndrome was first described in two adult males, consisting of macrocephaly, pigmented macules on the glans and shaft of the penis, and hamartomatous intestinal polyps. Since then, 10 additional cases have been identified. Herein, we present two new cases and review the cutaneous manifestations as well as ad...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1988.tb00880.x

    authors: Gretzula JC,Hevia O,Schachner LS,DiLiberti JH,Ruvalcaba RH,Schimschock JR,Weleber RG,Halal F,Lipson MH,Blumberg B

    更新日期:1988-02-01 00:00:00

  • Ear lobe bilateral necrosis by levamisole-induced occlusive vasculitis in a pediatric patient.

    abstract::We describe a bullous-hemorrhagic reaction of the ear lobes in a child with nephrosis after levamisole intake. This drug is used in children as an alternative treatment of corticosteroid-responsive nephrotic syndrome. Histologic evaluation of a lesion revealed necrotizing vasculitis involving mainly the large vessels ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1997.tb00695.x

    authors: Menni S,Pistritto G,Gianotti R,Ghio L,Edefonti A

    更新日期:1997-11-01 00:00:00

  • Pustular psoriasis in childhood and adolescence: a 20-year single-center experience.

    abstract::Pustular psoriasis (PP) is rare in children. The small number of reported cases makes deciding on treatment and follow-up challenging. The current study was an evaluation of treatment approaches and courses of PP in 18 children diagnosed and followed over a 20-year period. From 1992 to 2011 we treated 1,447 children w...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12296

    authors: Popadic S,Nikolic M

    更新日期:2014-09-01 00:00:00

  • Ischemic ulcers of the toes secondary to Raynaud's phenomenon in a child successfully treated with botulinum toxin.

    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

    pub_type:

    doi:10.1111/pde.14160

    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

  • Reversible neurotoxicity after an overdose of topical lindane in an infant.

    abstract::Lindane (gamma benzene hexachloride) is a widely prescribed topical scabicide because of its efficacy and cost-effectiveness. Although toxicity from a single proper application of lindane is generally not observed, the hazards of repeated applications, industrial exposure, and accidental ingestion have been well docum...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21515.x

    authors: Bhalla M,Thami GP

    更新日期:2004-09-01 00:00:00

  • Good response to pulsed dye laser in patients with capillary malformation-arteriovenous malformation syndrome (CM-AVM).

    abstract::Capillary malformation-arteriovenous malformation syndrome (CM-AVM) is an autosomal dominant disorder caused by heterozygous mutations in RASA1 and EPHB4. Capillary stains in CM-AVM are compatible with Schöbinger's phase I AVMs. Vascular laser has been classically contraindicated for the treatment of AVMs, as there is...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14095

    authors: Iznardo H,Roé E,Puig L,Vikula M,López-Sánchez C,Baselga E

    更新日期:2020-03-01 00:00:00

  • Stevens-Johnson syndrome associated with brucella infection.

    abstract::Stevens-Johnson syndrome is a potentially fatal condition that manifests mainly on the skin and mucosal surfaces but also affects other vital organs. There are no report of Stevens-Johnson syndrome caused by brucella infection in the literature. In this article, a previously healthy boy, diagnosed as Stevens-Johnson s...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00472.x

    authors: Babayigit A,Olmez D,Uzuner N,Caglayan S,Kumral A,Asilsoy SK,Ozer E,Karaman O

    更新日期:2007-07-01 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

  • Prevalence of inflammatory bowel disease among pediatric patients with hidradenitis suppurativa and the potential role of screening with fecal calprotectin.

    abstract:BACKGROUND/OBJECTIVES:Previous studies have demonstrated an increased prevalence of inflammatory bowel disease (IBD) in adults with hidradenitis suppurativa (HS). Whether the same association exists in pediatric patients is unknown. Fecal calprotectin (FC) is used to screen and monitor disease activity in IBD. There ar...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14417

    authors: Lloyd-McLennan AM,Ali S,Kittler NW

    更新日期:2020-10-25 00:00:00

  • Diaper dermatitis: a therapeutic dilemma. Results of a double-blind placebo controlled trial of miconazole nitrate 0.25%.

    abstract::Diaper dermatitis, an acute inflammation of the skin in the diaper area, is the most common dermatologic disorder of infancy. This placebo-controlled, randomized, double-blind, parallel-group trial compared the efficacy and safety of miconazole nitrate 0.25% in a zinc oxide/petrolatum base with that of the ointment ba...

    journal_title:Pediatric dermatology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1046/j.1525-1470.2001.018002149.x

    authors: Concannon P,Gisoldi E,Phillips S,Grossman R

    更新日期:2001-03-01 00:00:00

  • Juvenile xanthogranuloma: a congenital giant form leading to a wide atrophic sequela.

    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

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21206.x

    authors: Imiela A,Carpentier O,Segard-Drouard M,Martin de Lassalle E,Piette F

    更新日期:2004-03-01 00:00:00

  • Skin cancer prevention counseling and clinical practices of pediatricians.

    abstract::Little is known about pediatricians' counseling and clinical practices to reduce skin cancer risk among their patients. Thus our objectives were to characterize skin cancer preventive counseling and clinical practices in a sample of pediatricians and identify correlates of these practices. Physicians practicing genera...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.03004.x

    authors: Gritz ER,Tripp MK,de Moor CA,Eicher SA,Mueller NH,Spedale JH

    更新日期:2003-01-01 00:00:00

  • Novel KIT mutation presenting as marked lentiginosis.

    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

    pub_type:

    doi:10.1111/pde.13952

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

    更新日期:2019-11-01 00:00:00

  • Histologic changes resembling the verrucous phase of incontinentia pigmenti within epidermal nevi: report of two cases.

    abstract::A wide spectrum of histopathologic changes has been reported to occur within epidermal nevi. We saw two patients with warty nevoid lesions in which histopathologic features of incontinentia pigmenti, verrucous phase, were present. The diagnosis of incontinentia pigmenti was excluded because both patients were male, la...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1985.tb00490.x

    authors: Fletcher V,Williams ML,Lane AT

    更新日期:1985-11-01 00:00:00

  • Crisaborole Topical Ointment, 2% in Patients Ages 2 to 17 Years with Atopic Dermatitis: A Phase 1b, Open-Label, Maximal-Use Systemic Exposure Study.

    abstract:BACKGROUND:Phosphodiesterase-4 (PDE4) is a promising target in atopic dermatitis (AD) treatment. The pharmacokinetics (PK), safety, and efficacy of crisaborole topical ointment, 2% (formerly AN2728) (Anacor Pharmaceuticals, Palo Alto, CA), a boron-based benzoxaborole PDE4 inhibitor, were evaluated in children with mild...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,多中心研究

    doi:10.1111/pde.12872

    authors: Zane LT,Kircik L,Call R,Tschen E,Draelos ZD,Chanda S,Van Syoc M,Hebert AA

    更新日期:2016-07-01 00:00:00

  • A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.14076

    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

  • Epidermal nevus syndrome: case report and review of clinical manifestations.

    abstract::The epidermal nevus syndrome is a disorder characterized by epidermal nevi and associated neurologic, skeletal, and other abnormalities. We cared for a 3-month-old male with multiple epidermal nevi and severe central nervous system involvement. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1989.tb00917.x

    authors: Eichler C,Flowers FP,Ross J

    更新日期:1989-12-01 00:00:00

  • Unusual cystic scalp lesions in Gorlin syndrome: a brief report.

    abstract::Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is a rare, autosomal dominant syndrome that is known to have variable expressivity in multiple organ systems. We describe the case of a young male child with nevoid basal cell carcinoma syndrome and scalp lesions, including a branchial cleft cyst with respiratory ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01110.x

    authors: Findley AB,Pride H

    更新日期:2010-03-01 00:00:00

  • Congenital curved nail of the fourth toe--three different clinical presentations.

    abstract::A congenital curved nail of the fourth toe (NIM 219070) is a rare nail deformity with no other associated abnormalities. Three patients with this congenital anomaly are reported here. Radiologic examination in all three revealed distal symphalangism of the fourth toes bilaterally. The clinical manifestations in these ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00454.x

    authors: Lin YC,Wu YH,Scher RK

    更新日期:2007-07-01 00:00:00

  • Neonatal skin care: Developments in care to maintain neonatal barrier function and prevention of diaper dermatitis.

    abstract:BACKGROUND:Understanding the importance of the barrier function of the skin of preterm and term neonates is crucial in effective neonatal skin and diaper care. This literature search aimed to review the development of different practices in neonatal care to maintain skin barrier function, in turn preventing diaper derm...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13714

    authors: Burdall O,Willgress L,Goad N

    更新日期:2019-01-01 00:00:00

  • Erythema multiforme possibly triggered by rabies vaccine in a 10-year-old boy.

    abstract::This report documents a possible rabies vaccine-induced erythema multiforme manifestation in a 10-year-old boy. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2012.01842.x

    authors: Verma P

    更新日期:2013-11-01 00:00:00

  • 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...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1992.tb00632.x

    authors: Williams ML

    更新日期:1992-12-01 00:00:00

  • Nodular lichen myxedematosus during childhood: a case report.

    abstract::Nodular lichen myxedematosus (LM) is a rare disease and is one of the five subtypes of localized LM. It is distinctly characterized by multiple nodules on the trunk and limbs with or without papular lesions. A healthy 6-year-old boy presented with complaints of "knots" on his right chest, upper limb, and thigh for 4 m...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12376

    authors: Zeng R,Li M,Jiang Y,Liu W

    更新日期:2014-11-01 00:00:00

  • Psoriasis first presenting around an enteral feeding tube in three pediatric patients: an important consideration for timely diagnosis and management.

    abstract::Pediatric dermatologists may care for patients with percutaneous enteral feeding tubes. Although ostomy complications such as allergic contact and irritant dermatitis are common, psoriasis may be misdiagnosed. We report three novel cases of childhood psoriasis first presenting around an enteral feeding tube site. Loca...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12211

    authors: Zitelli KB,Lucky AW

    更新日期:2014-01-01 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

    pub_type: 杂志文章

    doi:10.1111/pde.13779

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

    更新日期:2019-05-01 00:00:00

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

    abstract::Aplasia cutis congenita (ACC) is a congenital defect consisting of a circumscribed absence of skin that usually involves the scalp. The etiology is uncertain, and several teratogenic agents such as methimazole have been involved. We report two cases of ACC and other anomalies in newborns exposed to methimazole during ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01572.x

    authors: Rodríguez-García C,González-Hernández S,Hernández-Martín A,Pérez-Robayna N,Sánchez R,Torrelo A

    更新日期:2011-11-01 00:00:00

  • Streptococcal exanthem in a blaschkolinear pattern: clinical evidence for genetic mosaicism in hypomelanosis of ito.

    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

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2002.00119.x

    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

  • Perforating folliculitis in a patient with cystic fibrosis.

    abstract::We report a case of a young man with perforating folliculitis and cystic fibrosis with complications including chronic obstructive pulmonary disease, insulin dependent diabetes mellitus, and liver cirrhosis. We demonstrate increased TGF-β1 immunohistochemical staining in the perforating folliculitis lesions of our pat...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01329.x

    authors: Tuttle MS,Kwon EJ,Tamburro J,Honda K

    更新日期:2010-11-01 00:00:00

  • Generalized lupus panniculitis and antiphospholipid syndrome in a patient without complement deficiency.

    abstract::Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report a 13-year-old girl with extensive lupus panniculitis since the age of 8 months and no e...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.1999.00060.x

    authors: Nousari HC,Kimyai-Asadi A,Santana HM,Diglio GM,Tausk FA,Cohen BA

    更新日期:1999-07-01 00:00:00