Punched-out erosions with scalloped borders: Group A Streptococcal pustulosis.

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

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

abstract：:Henoch-Schönlein purpura (HSP) is the most common vasculitis of childhood. It is usually self-limiting and is characterized by an immune complex-mediated vasculitis associated with IgA deposition. We present an unusual case of HSP with mucosal lesions and coronary artery thickening. ...

journal_title：Pediatric dermatology

authors： Veetil BM,Reed AM,Mattke AC

更新日期：2012-05-01 00:00:00

abstract：:Vitiligo is a common acquired progressive depigmenting condition that can have devastating psychological effects in dark-skinned patients. We performed a retrospective review of patients younger than 16 years of age with a clinical diagnosis of vitiligo treated using phototherapy at the National Skin Center, Singapore...

journal_title：Pediatric dermatology

authors： Koh MJ,Mok ZR,Chong WS

更新日期：2015-03-01 00:00:00

abstract：:Henna is a shrub cultivated in India, Sri Lanka, and North Africa; it is used, mixed with other substances, as a hair and body dye. Several cases are reported in the literature of sensitization to para-phenylenediamine (PPD) contained in the henna tincture, but few of these are pediatric cases. We report two instances...

journal_title：Pediatric dermatology

authors： Neri I,Guareschi E,Savoia F,Patrizi A

更新日期：2002-11-01 00:00:00

abstract：:Prostaglandin E1 is commonly used in the management of cyanotic congenital heart disease. While cutaneous flushing and peripheral edema are well recognized side effects of prostaglandin E1 therapy, other cutaneous effects have not been described in the dermatologic literature. We report a neonate with transposition of...

journal_title：Pediatric dermatology

authors： Carter EL,Garzon MC

更新日期：2000-01-01 00:00:00

abstract：:Fibroadipose vascular anomaly (FAVA) is a rare, complex mesenchymal malformation combining fibrofatty replacement of the affected muscles and slow-flow vascular malformation. The condition is characterized by localized swelling, severe pain, phlebectasia, and contracture of the affected limb. Treatment paradigms are n...

journal_title：Pediatric dermatology

authors： Erickson J,McAuliffe W,Blennerhassett L,Halbert A

更新日期：2017-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVE:Pediatric hematopoietic stem cell transplantation (HSCT) patients are at an increased risk for skin cancers. Sun exposure is a significant modifiable environmental risk factor. While patient education on sun protection and avoidance behaviors with regular dermatology evaluations are crucial for ped...

journal_title：Pediatric dermatology

authors： Li EB,Song JS,Huang JT,Hawryluk EB,London WB,Guo D,Sridharan M,Fisher DE,Rea CJ,Lehmann LE,Duncan CN

更新日期：2019-11-01 00:00:00

abstract：:Trisomy 13, or Patau syndrome, is a chromosomal disorder that can occur in complete, partial, or mosaic forms. Mosaicism is observed in 6% of individuals with trisomy 13 and, in contrast to the complete form, has wide phenotypic variability, longer survival, and in some patients an unusual skin pigmentary pattern simi...

journal_title：Pediatric dermatology

authors： González-del Angel A,Estandia-Ortega B,Gaviño-Vergara A,Sáez-de-Ocariz M,Velasco-Hernández Mde L,Salas-Labadía C

更新日期：2014-09-01 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：: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

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

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

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

更新日期：1987-11-01 00:00:00

abstract：:PLACK syndrome (OMIM 616295) is a form of generalized peeling skin syndrome (GPSS; OMIM 270300). It is an autosomal recessive genodermatosis caused by pathogenic mutations in CAST, which encodes calpastatin, an endogenous specific inhibitor of calpain, a calcium-dependent cysteine protease. We present a 5-year-old gir...

journal_title：Pediatric dermatology

authors： Boggs JME,Irvine AD

更新日期：2020-10-03 00:00:00

abstract：:The keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of the ectoderm characterized by diffuse hyperkeratotic erythroderma, keratitis with neovascularization of the cornea, and severe neurosensory hearing loss. A familial occurrence of this syndrome has been mentioned in four reports inc...

journal_title：Pediatric dermatology

authors： Koné-Paut I,Hesse S,Palix C,Rey R,Rémédiani K,Garnier JM,Berbis P

更新日期：1998-05-01 00:00:00

abstract：:We recently encountered a 2-year-old boy with slightly infiltrative brown papules on the face, trunk, and extremities. Stroking of one of the papules produced an urticarial wheal (positive Darier's sign). Histopathologic tests revealed a dense infiltration of mast cells containing numerous granules and showing metachr...

journal_title：Pediatric dermatology

authors： Mitsuya J,Hara H,Fukuda N,Terui T

更新日期：2011-07-01 00:00:00

abstract：:Capillary malformation (CM) can be a "red flag" for several syndromic vascular anomalies. We identified a subset of patients with diffuse CM and fetal pleural effusion and documented the type of CM, the etiology of the pleural effusion, the potential syndromic diagnosis, and outcome. Patients with a history of CM and ...

journal_title：Pediatric dermatology

authors： Rork JF,Alomari AI,Mulliken JB,Fishman SJ,Liang MG

更新日期：2015-01-01 00:00:00

abstract：:Bloom syndrome (congenital telangiectatic erythema) is a rare autosomal recessive disorder characterized by telangiectasias and photosensitivity, growth deficiency of prenatal onset, variable degrees of immunodeficiency, and increased susceptibility to neoplasms of many sites and types. We are reporting Bloom syndrome...

journal_title：Pediatric dermatology

authors： Sultan SJ,Sultan ST

更新日期：2010-03-01 00:00:00

abstract：:Clinical and pathologic features of five cases of epidermolysis bullosa simplex, Dowling-Meara type (EBS-DM), are described. Four patients were children, and two were related (father and daughter). Clinical history revealed blistering at birth in three patients; in all of them the signs and symptoms improved with age....

journal_title：Pediatric dermatology

authors： Puddu P,Angelo C,Faraggiana T,Onetti Muda A,Colonna L,Paradisi M

更新日期：1996-05-01 00:00:00

abstract：:We report an Italian prepubescent girl with the typical clinical and histologic features of prurigo pigmentosa associated with an atopic diathesis. The dermatitis disappeared after treatment with minocycline, leaving a brown, reticulated hyperpigmentation, with no recurrence. The association with an atopic diathesis c...

journal_title：Pediatric dermatology

authors： Cota C,Donati P,Amantea A

更新日期：2007-05-01 00:00:00

abstract：:Benign fibrous histiocytoma is a common soft tissue tumor that usually occurs in adults and is relatively rare in childhood. This report describes a 7-month-old Caucasian boy with an enlarging firm congenital nodule on his occipital scalp. Histologic analysis revealed a benign fibrous histiocytoma with osteoclast-like...

journal_title：Pediatric dermatology

authors： Stinehelfer SE,Woosley JT,Losken HW,Morrell DS

更新日期：2007-09-01 00:00:00

abstract：:We cared for 124 pediatric patients with a histologic diagnosis of Langerhans' cell histiocytosis (histiocytosis X) over a period of 14 years. Clinical, laboratory, and radiographic findings were analyzed. The most frequent manifestations were bone lesions, lymph node involvement, and skin infiltration. Liver disease ...

journal_title：Pediatric dermatology

authors： Rivera-Luna R,Martinez-Guerra G,Altamirano-Alvarez E,Martinez-Avalos A,Cardenas-Cardoz R,Ayon-Cardenas A,Ruiz-Maldonado R,Lopez-Corella E

更新日期：1988-08-01 00:00:00

abstract：:The prevalence of persistent microalbuminuria, retinopathy, and peripheral and autonomic neuropathy was assessed in 18 children and adolescents with type 1 (insulin-dependent) diabetes mellitus (IDDM) who suffered from necrobiosis lipoidica diabeticorum (NLD) and in 40 diabetics without NLD, matched for sex, age, dura...

journal_title：Pediatric dermatology

authors： Verrotti A,Chiarelli F,Amerio P,Morgese G

更新日期：1995-09-01 00:00:00

abstract：:Trichothiodystrophy is characterized by sparse, short, sulfur-deficient hair. Numerous symptom complexes have been described in which the hair abnormality represents a constant feature. We report a boy with trichothiodystrophy, ichthyotic skin changes, onychodystrophy, chronic neutropenia, osteosclerosis, hypothyroidi...

journal_title：Pediatric dermatology

authors： Hersh JH,Klein LR,Joyce MR,Hordinsky MK,Tsai MY,Paller A,Hyzer R,Zax RH

更新日期：1993-06-01 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：: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

authors： Moradi S,Castiglione C,Ehrig T

更新日期：2020-03-01 00:00:00

abstract：:Childhood lichen sclerosus (LS) is a rare and often misdiagnosed inflammatory dermatitis with an unpredictable course. The complications of LS are architectural changes of the vulva; malignant transformation is possible. The objective of our study was to define the background and the long-term course of childhood LS. ...

journal_title：Pediatric dermatology

authors： Lagerstedt M,Karvinen K,Joki-Erkkilä M,Huotari-Orava R,Snellman E,Laasanen SL

更新日期：2013-07-01 00:00:00

abstract：BACKGROUND:Cutaneous leishmaniasis (CL) is an emerging uncontrolled tropical parasitic disease in endemic and nonendemic areas with a high prevalence in the pediatric age group. METHOD:A total of 382 individuals from Lebanon, Saudi Arabia, Pakistan, and Syria diagnosed with CL by punch biopsy/scrapings were grouped in...

journal_title：Pediatric dermatology

authors： Dunya G,Loya A,Taraif S,Adib Houreih M,Khalifeh I

更新日期：2020-07-01 00:00:00

abstract：BACKGROUND:Dermatologic conditions comprise a significant number of emergency department visits in the pediatric population in the United States. Understanding key predictors of emergency department utilization for dermatologic conditions is important to reduce inappropriate use. METHODS:A total of 44 554 sampled pati...

journal_title：Pediatric dermatology

authors： Collier EK,Yang JJ,Sangar S,Chen ST,Huang JT,Bach DQ

更新日期：2020-12-18 00:00:00

abstract：:A new type of organoid epidermal nevus, characterized by the presence of multiple trichilemmal cysts disposed in a linear arrangement, was recently recognized and named nevus trichilemmocysticus. We report a 10-year-old girl with a congenital linear dermatosis affecting the head, neck, trunk, limbs, palms, and soles. ...

journal_title：Pediatric dermatology

authors： Larralde M,Boggio P,Abad ME,Corbella C,Happle R

更新日期：2011-05-01 00:00:00

abstract：:A 3 year-old boy presented to our clinic with a 3-day history of itchy rash involving the face and limbs and recent contact with a caterpillar. A diagnosis of caterpillar dermatitis was suspected. This condition has rarely been reported and may be underestimated in the pediatric population who may suffer more systemic...

journal_title：Pediatric dermatology

authors： Jadoo AS,Treat JR

更新日期：2020-05-01 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