Allergic contact dermatitis to triethanolamine in a child.

Abstract:

:Triethanolamine is used as an emulsifier in many cosmetics and in topical medications, yet the occurrence of contact dermatitis to cosmetics containing triethanolamine is rare in childhood. Our case highlights how young age should not be a deterrent to investigation and demonstrates the importance of patch testing with selected allergens.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Milanesi N,Berti S,Gola M

doi

10.1111/pde.12537

subject

Has Abstract

pub_date

2015-05-01 00:00:00

pages

e112-3

issue

3

eissn

0736-8046

issn

1525-1470

journal_volume

32

pub_type

杂志文章
  • Calcipotriene and corticosteroid combination therapy for vitiligo.

    abstract::Corticosteroids and photochemotherapy, using a combination of psoralen and ultraviolet A (PUVA) exposure, are the most widely prescribed therapies for vitiligo. These treatments are not uniformly effective and many patients have inadequate responses. Calcipotriene has been shown to be effective in adults and children ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21418.x

    authors: Travis LB,Silverberg NB

    更新日期:2004-07-01 00:00:00

  • Van der Woude syndrome. A case report.

    abstract::We describe several members of a family with Van der Woude syndrome, a genetic and congenital malformation syndrome with autosomal dominant inheritance and 70% to 80% penetrance with variable expressivity. It is characterized by clinical signs localized to the face, such as bilateral or unilateral pits on conical elev...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.1998.1998015459.x

    authors: Vignale R,Araujo J,Pascal G,Reissenweber N,Abulafia J,Quadrelli R,Vaglio A,Larrandaburo M,Reyno S

    更新日期:1998-11-01 00:00:00

  • Vitamin a deficiency phrynoderma associated with chronic giardiasis.

    abstract::Phrynoderma is a rare form of follicular hyperkeratosis associated with deficiencies in vitamins A or C or essential fatty acids. We report a 6-year-old boy with an unusual presentation of phrynoderma, characterized by multiple minute digitate hyperkeratoses associated with hair casts and related to a severe deficienc...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00261.x

    authors: Girard C,Dereure O,Blatière V,Guillot B,Bessis D

    更新日期:2006-07-01 00:00:00

  • Depilation in a 6-month-Old with hypertrichosis: A case report.

    abstract::Hypertrichosis in the pediatric age group can be troubling to both patients and parents. There is no well-established method for managing this problem in young children. We describe the successful use of a cream depilatory agent for removal of excess hair from the face and body of a 6-month-old girl. Excellent cosmeti...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.1999.00081.x

    authors: Wendelin DS,Mallory GB,Mallory SB

    更新日期:1999-07-01 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

  • Transient Porphyrinemia in a Neonate: A Case Report.

    abstract::We describe a neonate with anemia, thrombocytopenia, and hyperbilirubinemia secondary to hemolytic disease of the newborn. After phototherapy for hyperbilirubinemia, the neonate developed a photodistributed eruption with high serum and urine porphyrin levels. This transient porphyrinemia resolved at 1 month. ...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.12963

    authors: Boer B,Tisack A,Shwayder T

    更新日期:2016-11-01 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

  • A new case of hairy elbows syndrome (Hypertrichosis cubiti).

    abstract::Hypertrichosis cubiti, also named hairy elbows syndrome (HES), is an uncommon variety of congenital, circumscribed hypertrichosis in which a remarkable amount of long vellus hair is localized on the extensor surfaces of the upper extremities. Usually, this condition appears in infancy, increases during early childhood...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1996.tb01245.x

    authors: Escalonilla P,Aguilar A,Gallego M,Piqué E,Fariña MC,Requena L

    更新日期:1996-07-01 00:00:00

  • Temporal trends in mucocutaneous findings among human immunodeficiency virus 1-infected children in a population-based cohort.

    abstract::The objective of the study was to determine the prevalence of pediatric human immunodeficiency virus 1 (HIV-1) mucocutaneous manifestations in the era of highly active antiretroviral therapy (HAART). We conducted population-based, prospective, multicenter pediatric HIV-1 surveillance in 276 children with perinatally a...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,多中心研究

    doi:10.1111/pde.12020

    authors: Sturt AS,Anglemyer A,Berk DR,Maldonado YA

    更新日期:2013-07-01 00:00:00

  • Melanotic neuroectodermal tumor of infancy.

    abstract::Melanotic neuroectodermal tumor of infancy (MNTI) is an uncommon lesion with remarkably consistent histopathologic features that arises primarily in the pediatric population. We describe a MNTI arising in the anterior maxilla of a 6-month-old boy. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01566.x

    authors: Magliocca KR,Pfeifle RM,Bhattacharyya I,Cohen DM

    更新日期:2012-09-01 00:00:00

  • Cervical occult spinal dysraphism: MRI findings and the value of a vascular birthmark.

    abstract::Spinal dysraphism is easily recognized in the overt form as a meningocele or myelomeningocele. The closed form or occult spinal dysraphism (OSD) can be overlooked. It occurs predominantly at the lumbosacral level, but OSD at the cervical level, although very rare, also occurs. The value of magnetic resonance imaging i...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1995.tb00172.x

    authors: Enjolras O,Boukobza M,Jdid R

    更新日期:1995-09-01 00:00:00

  • Eruptive juvenile xanthogranuloma associated with relapsing acute lymphoblastic leukemia.

    abstract::Juvenile xanthogranuloma is a benign, self-healing disorder with characteristic lesions mainly involving the skin. Although most patients with juvenile xanthogranuloma have only cutaneous symptoms, recent articles have documented extracutaneous manifestations: systemic involvement of many organs has been reported and ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00721.x

    authors: Aparicio G,Mollet J,Bartralot R,Bodet D,Heras C,Bassas P,Virós A,García-Patos V

    更新日期:2008-07-01 00:00:00

  • Infantile acne treated with oral isotretinoin.

    abstract::In contrast to adolescent acne, infantile acne (IA) is a rare condition with only a limited body of available literature. In this descriptive, retrospective study, we reviewed six cases from 2002 to 2010 treated with oral isotretinoin. The average age of onset was 6.16 months (range 0-21 mos). Consistent with the prev...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12069

    authors: Miller IM,Echeverría B,Torrelo A,Jemec GB

    更新日期:2013-09-01 00:00:00

  • Head-and-neck dermatitis: Diagnostic difficulties and management pearls.

    abstract::Head-and-neck dermatitis is a variant of atopic dermatitis (AD) often seen in children and is challenging to diagnose, as it frequently overlaps with other eczematous dermatoses. Successful head-and-neck dermatitis (HND) treatment requires identification of common triggers and clinical mimickers, such as airborne derm...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13642

    authors: Maarouf M,Saberian C,Lio PA,Shi VY

    更新日期:2018-11-01 00:00:00

  • Tretinoin microsphere gel 0.04% pump for treating acne vulgaris in preadolescents: a randomized, controlled study.

    abstract::Although acne vulgaris is common in preadolescents (<13 yrs), few acne treatments are currently approved for children. This study assessed the safety and efficacy of tretinoin microsphere gel (TMG) 0.04% pump in children aged 9-11 with acne vulgaris. In this multicenter, randomized, double-blind, vehicle-controlled pi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1111/j.1525-1470.2012.01811.x

    authors: Eichenfield LF,Hebert AA,Schachner L,Paller AS,Rossi AB,Lucky AW

    更新日期:2012-09-01 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

  • Palmoplantar eccrine hidradenitis: three new cases and review.

    abstract::Palmoplantar eccrine hidradenitis (PEH) is characterized by painful erythematous papules and nodules of abrupt onset on the soles of young individuals. The histologic hallmark is a predominant neutrophilic infiltrate surrounding the eccrine gland apparatus. A total of 28 cases have been published since 1988, with a br...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.1998.1998015097.x

    authors: Landau M,Metzker A,Gat A,Ben-Amitai D,Brenner S

    更新日期:1998-03-01 00:00:00

  • Palmar hyperlinearity in early childhood atopic dermatitis is associated with filaggrin mutation and sensitization to egg.

    abstract:BACKGROUND/OBJECTIVES:Palmar hyperlinearity is a typical clinical feature of Filaggrin gene (FLG) null mutations. There are reports of FLG mutations and allergic sensitization; however, reports on the relationship between palmar hyperlinearity to sensitization are limited. This study aimed to examine the association be...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13752

    authors: Fukuie T,Yasuoka R,Fujiyama T,Sakabe JI,Taguchi T,Tokura Y

    更新日期:2019-03-01 00:00:00

  • Macrocephaly-capillary malformation presenting with fetal arrhythmia.

    abstract::Macrocephaly-capillary malformation (OMIM 602501) is a rare overgrowth and asymmetry syndrome. Cardiac arrhythmias were reported to occur in few patients. We present a case in which fetal arrhythmia was the presenting symptom of the syndrome. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01677.x

    authors: Kuint J,Globus O,Ben Simon GJ,Greenberger S

    更新日期:2012-05-01 00:00:00

  • FOXN1 Duplication and Congenital Hypertrichosis.

    abstract::We report a case of congenital hypertrichosis and FOXN1 duplication. FOXN1 is a member of the forkhead box gene family, located on chromosome 17. Its function includes differentiation of epithelial cells and regulation of keratinocytes, especially hair keratins. Loss of function of these transcription factors leads to...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13078

    authors: Gilhooley E,Gormally S,Irvine A,Lynch SA,Collins S

    更新日期:2017-03-01 00:00:00

  • Epidermolysis bullosa acquisita in an 8-year-old girl.

    abstract::Epidermolysis bullosa acquisita is an autoimmune blistering disease with the distinct feature of having an autoantibody directed against an antigen located below the basement membrane of human skin and mucous membrane. We identified this disease in an 8-year-old girl, the youngest patient documented by immunoelectron ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1986.tb00532.x

    authors: Borok M,Heng MC,Ahmed AR

    更新日期:1986-09-01 00:00:00

  • A new variant of trichothiodystrophy with recurrent infections, failure to thrive, and death.

    abstract::Two brothers demonstrated a severe variant of trichothiodystrophy. Both had brittle hair, developmental delay with severe failure to thrive, recurrent infections, cataracts, and angioendotheliomas of the liver at autopsy. The elder died at 12 weeks, the younger at 6 months. The younger had the typical appearance of ba...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.1998.1998015031.x

    authors: Petrin JH,Meckler KA,Sybert VP

    更新日期:1998-01-01 00:00:00

  • Tissue-engineered skin in the healing of wound stumps from limb amputations secondary to purpura fulminans.

    abstract::Currently wound treatment options of amputation stumps due to purpura fulminans include healing by secondary intention from wound debridement, split-thickness skin grafting, tissue and muscle flaps, plantar skin free transfer, skin expansion, artificial skin, and hyperbaric oxygen therapy. We saw a 6-month-old girl wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.20218.x

    authors: Greenberg JE,Falabella AF,Bello YM,Schachner LA

    更新日期:2003-03-01 00:00:00

  • Infantile Bullous Pemphigoid Treated Using Intravenous Immunoglobulin: Case Report and Review of the Literature.

    abstract::We report a 5-month-old girl diagnosed with bullous pemphigoid who initially did not respond to systemic corticosteroids and dapsone but rapidly improved after the addition of intravenous immunoglobulin (IVIG) infusions. A literature search revealed anecdotal cases of infantile bullous pemphigoid treated with IVIG, al...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12635

    authors: Tekin B,Yücelten AD

    更新日期:2015-09-01 00:00:00

  • Aleukemic congenital leukemia cutis.

    abstract::A newborn girl had typical "blueberry muffin" skin lesions, which showed histopathologic features of myelomonocytic leukemia cutis. We could not demonstrate leukemic infiltration of bone marrow in four aspirates. Her course was complicated with primary pulmonary hypertension, which led to death at 7 months of age. We ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21408.x

    authors: Torrelo A,Madero L,Mediero IG,Baño A,Zambrano A

    更新日期:2004-07-01 00:00:00

  • Verruciform xanthoma in a patient with recessive dystrophic epidermolysis bullosa: Case report and literature review.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.14079

    authors: Stephens M,Rubin AI,Perman MJ

    更新日期:2020-03-01 00:00:00

  • Tuberous Sclerosis Complex: An Update for Dermatologists.

    abstract::Tuberous sclerosis complex is an autosomal dominant disorder that often manifests early in life with cutaneous features, and it is important that dermatologists who care for children remain up to date on its diagnosis and management. This article provides an update regarding the most recent guidelines for diagnosis pu...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12567

    authors: Jacks SK,Witman PM

    更新日期:2015-09-01 00:00:00

  • Outpatient pediatric dermatologic surgery: experience in 296 patients.

    abstract::From January 2010 to December 2012, 296 skin biopsies were performed in pediatric patients using only local anesthesia (cream and infiltration). The biopsies were divided into three groups: biopsies of skin neoplasms, biopsies of skin rashes and biopsies of follicular-centered lesions. Our data demonstrate the possibi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12414

    authors: D'Acunto C,Raone B,Neri I,Passarini B,Patrizi A

    更新日期:2015-05-01 00:00:00

  • Cutaneous ultrasound and its utility in Pediatric Dermatology: Part II-Developmental anomalies and vascular lesions.

    abstract::High-frequency ultrasonography represents a promising tool for pediatric dermatologists. It is a noninvasive and harmless diagnostic technique that is especially appealing when working with children. It can be easily performed at the patient's bedside, avoiding diagnostic delays, sedation, or multiple visits. It repre...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13897

    authors: Rodríguez Bandera AI,Sebaratnam DF,Feito Rodríguez M,de Lucas Laguna R

    更新日期:2020-01-01 00:00:00

  • Congenital midline cervical cleft: case report and review of the English language literature.

    abstract::Congenital midline cervical cleft is a rare anomaly of the ventral neck that heretofore has not been reported in the dermatology literature. We present a case of a midline cervical cleft that was diagnosed and managed at an early age. We also review the literature and discuss its clinical and histologic features, trea...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.2000.01727.x

    authors: Eastlack JP,Howard RM,Frieden IJ

    更新日期:2000-03-01 00:00:00