PHACE syndrome with growth hormone deficiency and absence of bilateral internal carotid arteries: a case report.

abstract：:Acne mechanica is defined as being any acneiform eruption in areas of friction, pressure, stretching, rubbing, pinching, or occlusion of the skin in any individual, regardless of preexisting acne. Various causes have been reported, including prolonged back rest against a chair or bed, occlusive clothing, pressure from...

journal_title：Pediatric dermatology

authors： Mazhar M,Simpson M,Marathe K

更新日期：2019-07-01 00:00:00

abstract：:Mycosis fungoides is very rare in children. Hypopigmented lesions of this disease are usually observed in dark-skinned individuals and often show a T supressor CD8(+) phenotype. Two Caucasian children with predominantly hypopigmented lesions of mycosis fungoides are presented here. Atopy was a concomitant feature in b...

journal_title：Pediatric dermatology

authors： Onsun N,Kural Y,Su O,Demirkesen C,Büyükbabani N

更新日期：2006-09-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Epidemiologic studies of children with alopecia areata (AA) are sparse, and there are no studies that focus on the youngest children with AA. Evaluation of the clinical presentations of AA in children <4 years of age was performed in order to identify the prognostic factors for disease progression...

journal_title：Pediatric dermatology

authors： Rangu S,Rogers R,Castelo-Soccio L

更新日期：2019-11-01 00:00:00

abstract：BACKGROUND:The current treatment of keloids includes surgery, intralesional steroids, and radiotherapy, among others. Radiotherapy is not recommended in children due to its effects on growing tissues. Our aim was to study intralesional triamcinilone therapy of keloids in children and analyze the impact of body location...

journal_title：Pediatric dermatology

authors： Acosta S,Ureta E,Yañez R,Oliva N,Searle S,Guerra C

更新日期：2016-01-01 00:00:00

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

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

更新日期：2009-01-01 00:00:00

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

authors： Popadic S,Nikolic M

更新日期：2014-09-01 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：BACKGROUND:Bullous impetigo (BI) is a common skin infection of early childhood, resulting from desmoglein-1 cleavage by Staphylococcus aureus exfoliative toxins. Due to compromised barrier function and immune dysregulation, children with atopic dermatitis (AD) are at increased risk of cutaneous infections, yet no liter...

journal_title：Pediatric dermatology

authors： Mannschreck D,Feig J,Selph J,Cohen B

更新日期：2020-01-01 00:00:00

abstract：:Bullous pemphigoid (BP) is the most common autoimmune blistering disease affecting the elderly but is quite rare in childhood. The majority of pediatric cases have been reported during early childhood. Adolescence is divided into three phases: early (10-13 years), middle (14-17), and late (18-21). This review aimed to...

journal_title：Pediatric dermatology

authors： Patsatsi A,Kyriakou A,Werth VP

更新日期：2019-03-01 00:00:00

abstract：:Cutis laxa is a rare disorder resulting from degradation and clumping of elastic fibers in dermis. Type II acquired cutis laxa, shows only cutaneous changes without any systemic involvement. We describe an infant with acquired cutis laxa type II following a generalized inflammatory dermatitis. ...

journal_title：Pediatric dermatology

authors： Haider M,Alfadley A,Kadry R,Almutawa A

更新日期：2010-01-01 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：:Benign cephalic histiocytosis is a rare skin condition consisting of small tan papules on the face and upper trunk that is believed not to be associated with internal organ involvement. The infiltrating histiocytes are not Langerhans' cells (LCs). We report a 5-year-old girl who presented with diabetes insipidus 1 yea...

journal_title：Pediatric dermatology

authors： Weston WL,Travers SH,Mierau GW,Heasley D,Fitzpatrick J

更新日期：2000-07-01 00:00:00

abstract：:A young boy developed childhood keratosis lichenoides chronica. The eruption cleared spontaneously after 13 years. This is a rare condition, regarded by some as a variant of lichen planus. The great preponderance of cases occur in adults, whereas the disease in childhood is uncommon. ...

journal_title：Pediatric dermatology

authors： Torrelo A,Mediero IG,Zambrano A

更新日期：1994-03-01 00:00:00

abstract：:Menkes's syndrome (trichopoliodystrophy) is an x-linked, recessive genodermatosis characterized by hair defects, severe retardation, convulsions, progressive neurologic deterioration, and early death. Recent studies in copper metabolism suggest that Menkes's syndrome may be a storage disease in which copper is irrever...

journal_title：Pediatric dermatology

authors： Maddox JL Jr,Odom RB,Goette DK

更新日期：1984-04-01 00:00:00

abstract：:Dyskeratosis congenita (DC) is an unusual inherited disease characterized by the triad of mucosal leukoplakia, nail dystrophy, and skin pigmentation. Hyperkeratosis of the palms and soles is another reported skin finding. This hyperkeratosis can lead to fissures, chronic erosion, and deep ulcerations. These atypical w...

journal_title：Pediatric dermatology

authors： Quintana-Castanedo L,Feito-Rodríguez M,Pérez-Conde I,Maseda-Pedrero R,Chiloeches-Fernández C,de Lucas Laguna R

更新日期：2020-11-01 00:00:00

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

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

更新日期：2012-09-01 00:00:00

abstract：:Childhood granulomatous periorificial dermatitis (CGPD) is a condition included in the spectrum of rosacea and perioral dermatitis that affects prepubescent children. It is characterized by papular eruptions located around the mouth, nose, and eyes that histopathologically show a granulomatous pattern. We report a 9-y...

journal_title：Pediatric dermatology

authors： Rodriguez-Caruncho C,Bielsa I,Fernandez-Figueras MT,Ferrándiz C

更新日期：2013-09-01 00:00:00

abstract：BACKGROUND:In recent years propranolol has become the treatment of choice for infantile hemangiomas (IHs). There is broad variation in the approach to propranolol initiation in clinical practice. This retrospective study explored the effectiveness of routine pre-treatment ECG in screening infants being considered for s...

journal_title：Pediatric dermatology

authors： Yarbrough KB,Tollefson MM,Krol AL,Leitenberger SL,Mann JA,MacArthur CJ

更新日期：2016-11-01 00:00:00

abstract：:Although the prognosis of maculopapular cutaneous mastocytosis (MPCM), also referred to as urticaria pigmentosa, is often benign, clinicians lack evidence to reliably predict those at risk of associated systemic manifestations. We sought to elucidate clinical markers of disease severity to provide better treatment and...

journal_title：Pediatric dermatology

authors： Barnes M,Van L,DeLong L,Lawley LP

更新日期：2014-05-01 00:00:00

abstract：:Hereditary progressive mucinous histiocytosis is a rare, benign, skin-limited form of non-Langerhans cell histiocytosis. We report on a 5-year-old boy who presented in infancy with self-resolving dermal nodules but later developed persistent and progressive erythematous papules on the face and scalp. Histologic evalua...

journal_title：Pediatric dermatology

authors： Nguyen NV,Prok L,Burgos A,Bruckner AL

更新日期：2015-11-01 00:00:00

abstract：:Langerhans cell histiocytosis is a rare proliferative disorder where pathologic Langerhans cells accumulate in a variety of organs. Historically, the nomenclature regarding this entity has been confusing because the disease had been subcategorized simply based upon the different clinical manifestations. In the followi...

journal_title：Pediatric dermatology

authors： Satter EK,High WA

更新日期：2008-05-01 00:00:00

abstract：:We present a 16-year-old girl with a 4-year history of chronic persistent erythema nodosum. Recurrently low serum iron values suggested the possibility of a malabsorption syndrome. The presence of antitransglutaminase and antiendomysium antibodies and the jejunal biopsy specimen findings showed an underlying celiac di...

journal_title：Pediatric dermatology

authors： Bartyik K,Várkonyi A,Kirschner A,Endreffy E,Túri S,Karg E

更新日期：2004-05-01 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：:Although many cases of follicular mucinosis are idiopathic, numerous others are associated with mycosis fungoides or, rarely, other neoplastic or inflammatory disorders. There are only three reported cases, all in adults, of follicular mucinosis arising in association with acute myelogenous leukemia, two of which invo...

journal_title：Pediatric dermatology

authors： Jefferson J,Taube J,Grossberg A

更新日期：2016-01-01 00:00:00

abstract：:Polyurethane chemicals are produced by the reaction of isocyanates and they may cause allergic contact dermatitis or precipitate asthma attacks. Contact dermatitis to polyurethane toilet seat has not been reported before. Herein we present a case of allergic contact dermatitis to polyurethane toilet seat. ...

journal_title：Pediatric dermatology

authors： Turan H,Saricaoğlu H,Turan A,Tunali S

更新日期：2011-11-01 00:00:00

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

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

更新日期：2013-11-01 00:00:00

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

authors： Burdall O,Willgress L,Goad N

更新日期：2019-01-01 00:00:00

abstract：:Depigmentation after the use of topical immune modulators is a rare but reported event. Herein we present what is to our knowledge the first case of vitiligo at a site of Candida antigen injection. ...

journal_title：Pediatric dermatology

authors： Wilmer EN,Burkhart CN,Morrell DS

更新日期：2013-11-01 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：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

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