Lichenoid sarcoidosis in a 3-year-old girl.

Abstract:

:We report a case of lichenoid sarcoidosis in a 3-year-old girl. She had numerous discrete skin-colored or erythematous, infiltrated follicular papules on the buttocks and extremities since 2 months of age. Histopathologic examination showed follicular plugging and an upper dermal granulomatous infiltrate of epithelioid cells closely surrounding the follicular ducts. No acid-fast bacilli were seen in the sections examined. Chest radiograph and high-resolution computed tomography (CT) showed no hilar lymphadenopathy or pulmonary parenchymal changes. An angiotensin-converting enzyme level was elevated. The Mantoux reaction was negative and results of ophthalmologic examinations were normal. Treatment was started with triamcinolone 0.2 mg/kg and prednicarbate ointment. Some lesions healed completely and others showed residual pitting.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Seo SK,Yeum JS,Suh JC,Na GY

doi

10.1046/j.1525-1470.2001.01958.x

subject

Has Abstract

pub_date

2001-09-01 00:00:00

pages

384-7

issue

5

eissn

0736-8046

issn

1525-1470

pii

1958

journal_volume

18

pub_type

杂志文章
  • 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

  • Confluent and reticulated papillomatosis associated with tinea versicolor in three siblings.

    abstract::We describe three teenage siblings with confluent and reticulated papillomatosis, all presenting during a 6-month period. Two of the three patients had confirmed tinea versicolor, with positive potassium hydroxide scrapings, in association with this entity. This is the largest series of siblings with confluent and ret...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22410.x

    authors: Stein JA,Shin HT,Chang MW

    更新日期:2005-07-01 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...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    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

  • Atypical maculopapular cutaneous mastocytosis showing a nevus spilus-like lesion.

    abstract::A 13-year-old Korean girl presented with a 7-year history of a pruritic, light-brown patch containing multiple 0.2- to 0.5-cm brownish-to-reddish maculopapules on the left anterior chest. When her skin was rubbed, the lesion became itchy and red. Histopathologic evaluation demonstrated marked dense dermal infiltration...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13541

    authors: Ahn HJ,Park HJ,Jeong KH,Park YK,Lee MH

    更新日期:2018-09-01 00:00:00

  • Postvaccination morphea profunda in a child.

    abstract::We report a new case of postvaccination morphea profunda (MP) in a child and discuss its different clinical presentations, prognosis, and therapy and its relationship with "solitary morphea profunda." A 2-year-old healthy girl presented with an induration of the anterior aspect of the left thigh of 9 months duration. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01548.x

    authors: Khaled A,Kharfi M,Zaouek A,Rameh S,Zermani R,Fazaa B,Kamoun MR

    更新日期:2012-07-01 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

  • Rapid response to treatment with thalidomide in an adolescent with generalized discoid lupus erythematosus.

    abstract::Discoid lupus erythematosus (DLE) is the most common variant of cutaneous chronic lupus erythematosus (CLE). Sun protection, topical corticosteroids, and antimalarials constitute the first-line options for treatment. In refractory cases, alternative antimalarials, methotrexate, retinoids, and thalidomide have been uti...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14067

    authors: Tran B,Yazdani Abyaneh MA,Wu J

    更新日期:2020-01-01 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

  • Eosinophilic pustular folliculitis of infancy suppressed with cetirizine.

    abstract::Eosinophilic pustular folliculitis of infancy is a rare inflammatory disease characterized by recurrent, itchy sterile pustules mainly located on the scalp. Topical agents are mostly effective to suppress the symptoms in the majority of cases. However, systemic agents that are safe for long-term use are required for p...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13764

    authors: Odyakmaz Demirsoy E,Demirsoy U,Ozod U,Kiran R

    更新日期:2019-05-01 00:00:00

  • Collodion baby associated with asymmetric crying facies: a case report.

    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...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.20208.x

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

    更新日期:2003-03-01 00:00:00

  • Childhood onset vulvar lichen sclerosus does not resolve at puberty: a prospective case series.

    abstract::When vulvar lichen sclerosus occurs in prepubertal children it is widely believed that it is likely to remit at puberty. However when it occurs in adult women it is accepted that remission is unlikely and that in addition untreated or inadequately treated disease may be complicated by significant disturbance of vulvar...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.01022.x

    authors: Smith SD,Fischer G

    更新日期:2009-11-01 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

  • Serum sickness-like reaction in children due to cefditoren.

    abstract::We describe the case of a 7-year-old boy with urticaria, fever, and arthritis that appeared 10 days after starting cefditoren therapy for acute tonsillopharyngitis, which was diagnosed as a serum sickness-like reaction due to this medication. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01539.x

    authors: Misirlioglu ED,Duman H,Ozmen S,Bostanci I

    更新日期:2012-05-01 00:00:00

  • Xp microdeletion syndrome characterized by pathognomonic linear skin defects on the head and neck.

    abstract::We describe a new case of a rare syndrome characterized by ocular abnormalities and pathognomonic linear skin defects. This syndrome is the result of an unbalanced translocation resulting in a deletion of the distal end of the short arm of the X chromosome. We report the thirteenth case and review the clinical and cyt...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1997.tb00422.x

    authors: Paulger BR,Kraus EW,Pulitzer DR,Moore CM

    更新日期:1997-01-01 00:00:00

  • Epidermolysis bullosa simplex with mottled pigmentation due to a rare keratin 5 mutation: cutaneous findings in infancy.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12206

    authors: Geller L,Kristal L,Morel KD

    更新日期:2013-09-01 00:00:00

  • Aeromonas hydrophila folliculitis associated with an inflatable swimming pool: mimicking Pseudomonas aeruginosa infection.

    abstract::Aeromonas species are ubiquitous, facultative, anaerobic, gram-negative flagellated rods, mainly found in aquatic ecosystems worldwide. Skin and soft-tissue infections, including cellulitis and wound infections, are the second most frequent location of isolations of Aeromonas spp. in clinical samples, after the gastro...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00993.x

    authors: Julià Manresa M,Vicente Villa A,Gené Giralt A,González-Enseñat MA

    更新日期:2009-09-01 00:00:00

  • Hypomelanosis of ito-whorled hyperpigmentation combination: a mirror image presentation.

    abstract::We hereby report a 2-year-old boy who presented with a peculiar combination of hyperpigmented and hypopigmented skin lesions along the lines of Blaschko, sharply demarcated at the midline, both on the anterior and posterior trunk. Although combinations of hyperpigmented and hypopigmented skin lesions distributed along...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00529.x

    authors: Thapa R,Dhar S,Malakar R,Chakrabartty S

    更新日期:2007-09-01 00:00:00

  • Less common clinical manifestations of atopic dermatitis: prevalence by age.

    abstract::The common manifestations of atopic dermatitis (AD) appear sequentially with involvement of the cheeks in infancy, flexural extremities in childhood, and hands in adulthood. Although less common clinical manifestations are well described, they have not been the subject of epidemiologic studies to describe their preval...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2012.01739.x

    authors: Julián-Gónzalez RE,Orozco-Covarrubias L,Durán-McKinster C,Palacios-Lopez C,Ruiz-Maldonado R,Sáez-de-Ocariz M

    更新日期:2012-09-01 00:00:00

  • Phacomatosis pigmentokeratotica: a follow-up report documenting additional cutaneous and extracutaneous anomalies.

    abstract::This is a follow-up report on a boy with phacomatosis pigmentokeratotica. At the age of 10 years he had, in addition to a sebaceous nevus and a speckled lentiginous nevus, multiple lesions of a collagen nevus localized on the chin and in the lumbar area. On the left shoulder, a small telangiectatic spot was present wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00588.x

    authors: Boente Mdel C,Asial RA,Happle R

    更新日期:2008-01-01 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

  • Hair casts: a clinical and electron microscopic study.

    abstract::Hair casts were seen in 22 girls ranging in age from 4 to 13 years. They were localized to the frontal, vertex, and temporal areas. The number of affected hairs varied from one-tenth to one-third. Twenty of the 22 girls styled their hair in ponytails or pigtails. Compound root sheath casts were present in six of nine ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1990.tb01023.x

    authors: Zhu WY,Xia MY,Wu JH,Do DA

    更新日期:1990-12-01 00:00:00

  • Accessory tragus: report of two cases and review of the literature.

    abstract::Accessory tragus is a fairly common congenital malformation of the external ear. In the vast majority of cases it is an isolated developmental defect not associated with other abnormalities. However, the remote possibility exists that it could be associated with other abnormalities of the first and second branchial ar...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.2000.017005391.x

    authors: Jansen T,Romiti R,Altmeyer P

    更新日期:2000-09-01 00:00:00

  • Cutaneous involvement of polymorphic post-transplant lymphoproliferative disorder in a child after liver transplantation.

    abstract::Post-transplantation lymphoproliferative disorder (PTLD) is one of the most common de novo malignancies in patients who receive immunosuppressive therapy after solid organ transplantation. We report a case of a 5-year-old girl who presented with indurated violaceous skin nodules 3.5 years post-liver transplantation, d...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13903

    authors: Chen KY,Lin CY,Kuo TT,Shih LY,Chang CH,Chen WT,Yang CY

    更新日期:2019-09-01 00:00:00

  • Chilblains in children in the setting of COVID-19 pandemic.

    abstract:BACKGROUND:Different skin manifestations of COVID-19 are being reported. Acral lesions on the hands and feet, closely resembling chilblains, have been recognized during the peak incidence of the COVID-19 pandemic. MATERIAL AND METHODS:A retrospective review of 22 children and adolescents with chilblain-like lesions se...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14215

    authors: Andina D,Noguera-Morel L,Bascuas-Arribas M,Gaitero-Tristán J,Alonso-Cadenas JA,Escalada-Pellitero S,Hernández-Martín Á,de la Torre-Espi M,Colmenero I,Torrelo A

    更新日期:2020-05-01 00:00:00

  • Fetal Alcohol Exposure and PHACE Syndrome: A Case and Autopsy Report.

    abstract::This report describes the clinical, radiologic, and autopsy findings of a newborn with PHACE syndrome (posterior fossa malformations, hemangioma, arterial anomalies, cardiac defects, and eye anomalies) and fetal alcohol spectrum disorder. To our knowledge, the concurrence of these conditions has not been reported in t...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.12837

    authors: Oza VS,Feigenbaum DF,Jacquot C,Hess CP,Siegel D,Frieden IJ

    更新日期:2016-05-01 00:00:00

  • Early morphea mimicking acquired port-wine stain.

    abstract::We report the case of a 2.5-year-old girl with linear morphea initially diagnosed as an acquired port-wine stain (PWS). She underwent three treatments to the right face using the pulsed dye laser (PDL) before sclerotic changes were observed and the correct diagnosis was confirmed with histopathology. Treatment using t...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12116

    authors: Pickert AJ,Carpentieri D,Price H,Hansen RC

    更新日期:2014-09-01 00:00:00

  • Multiple nevoid hypertrichosis as an isolated developmental defect.

    abstract::A 3-year-old girl presented with longer hair on the left side of her scalp, coarse hair of abnormal length on her extremities, and a tuft of hair in the lumbosacral region, with all hair distributed on normally pigmented skin. Neither similar or relevant family history nor associated extracutaneous abnormalities was d...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00948.x

    authors: Sotiriadis D,Patsatsi A,Lazaridou E,Sotiriou E,Devliotou-Panagiotidou D

    更新日期:2009-07-01 00:00:00

  • Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement.

    abstract:BACKGROUND:Spiny hyperkeratosis refers to a rare clinical phenotype characterized by nonfollicular keratotic projections and sometimes associated with other acquired and inherited conditions. We describe a case of congenital patterned spiny hyperkeratosis. METHODS:To identify the cause of this disorder, we used a comb...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12848

    authors: Eskin-Schwartz M,Metzger Y,Peled A,Weissglas-Volkov D,Malchin N,Gat A,Vodo D,Mevorah B,Shomron N,Sprecher E,Sarig O

    更新日期:2016-05-01 00:00:00

  • Revisiting childhood herpes zoster.

    abstract::Herpes zoster is rare in otherwise healthy children, but it is more common in association with immunosuppression. Maternal varicella infection during pregnancy and varicella occurring in the newborn represent risk factors for childhood herpes zoster. However, some controversies persist about risk factors, diagnosis, a...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21104.x

    authors: Nikkels AF,Nikkels-Tassoudji N,Piérard GE

    更新日期:2004-01-01 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