Nevus trichilemmocysticus: report of a new case of a recently recognized entity.

abstract：:A male infant with skin lesions was born to a 28-year-old mother who was under treatment for pemphigus vulgaris (PV), diagnosed eight years earlier. Circulating IgG class pemphigus antibody was found in the infant's blood, and deposition of IgG in the intercellular spaces of the epidermis was seen. The infant's lesion...

journal_title：Pediatric dermatology

authors： Hup JM,Bruinsma RA,Boersma ER,de Jong MC

更新日期：1986-12-01 00:00:00

abstract：:Loose anagen hair syndrome (LAHS) is an uncommonly reported autosomal dominant hair disorder with incomplete penetrance that primarily affects children but is occasionally seen in adults. LAHS is characterized by the ability to easily and painlessly extract unsheathed anagen hairs from the scalp with gentle traction. ...

journal_title：Pediatric dermatology

authors： Dey V,Thawani M

更新日期：2013-09-01 00:00:00

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

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

更新日期：2003-01-01 00:00:00

abstract：:Graft-versus-host disease (GVHD) is an underappreciated complication of autologous hematopoietic stem cell transplantation (AHSCT) that can affect the skin, gastrointestinal tract, and liver. The development of this rare condition is probably due to an impairment of immunologic tolerance that can occur spontaneously t...

journal_title：Pediatric dermatology

authors： Kaffenberger J,Basak SA,Ioffreda M

更新日期：2015-03-01 00:00:00

abstract：:Harlequin ichthyosis (HI) is a rare autosomal recessive disorder of cornification in which children are born with an extremely thick stratum corneum that becomes a restrictive circumferential encasement around the orifices, limbs, chest, and abdomen, resulting in limb contractures. We present a neonate diagnosed in ut...

journal_title：Pediatric dermatology

authors： Tontchev G,Silverberg NB,Shlasko E,Henry C,Roberts JL,Roth MZ

更新日期：2014-09-01 00:00:00

abstract：:Verrucous perforating collagenoma is an extremely rare variant of acquired perforating dermatosis that has been seldom described in literature. We present the case of an 18-month-old boy who presented with an erythematous plaque with a central keratotic plug on the leg. Histopathology revealed transepidermal eliminati...

journal_title：Pediatric dermatology

authors： Aizman L,Gelman A,Marathe K

更新日期：2019-09-01 00:00:00

abstract：:We report an unusual occurrence of spontaneous pigmentary regression with a desmoplastic reaction in a neonatally eroded giant congenital melanocytic nevus. This process has been documented with photographs and skin biopsy specimens. Neonatal histology demonstrated connective tissue proliferation. Histology at age 5 y...

journal_title：Pediatric dermatology

authors： Gass JK,Grant JW,Hall PN,Atherton DJ,Burrows NP

更新日期：2006-11-01 00:00:00

abstract：:Eczema action plans (EAPs) are written, customizable documents that guide patients through the self-management of atopic dermatitis. Here, we distributed a survey regarding the use patterns and perceptions of eczema action plans to 1068 members of the Society for Pediatric Dermatology and received 87 responses. Althou...

journal_title：Pediatric dermatology

authors： Stringer T,Yin HS,Oza VS

更新日期：2018-11-01 00:00:00

abstract：:Prurigo pigmentosa (PP) is a rare inflammatory skin disease. Neutrophil-mediated inflammation is considered to be responsible for the etiopathogenesis of PP. We consider that colchicine may be an effective agent in the treatment of PP since it exerts an antiinflammatory effect by inhibiting neutrophil chemotaxis. Furt...

journal_title：Pediatric dermatology

authors： An I,Ucmak D,Ibiloglu I,Demir V,Akdeniz S

更新日期：2018-05-01 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：:Acute genital ulcers rarely occur in nonsexually active young girls. When present, they can cause significant physical and emotional distress for the patient and her parents, and prompt an evaluation for sexual abuse and sexually transmitted diseases. With this review, we aim to further characterize acute genital ulce...

journal_title：Pediatric dermatology

authors： Rosman IS,Berk DR,Bayliss SJ,White AJ,Merritt DF

更新日期：2012-03-01 00:00:00

abstract：:Pulmonary manifestations are well recognized during the acute phase of Stevens-Johnson syndrome but persistent pulmonary sequela is rarely reported. We report two boys with bronchiolitis obliterans following the acute phase of Stevens-Johnson syndrome and discuss the clinical picture and treatment of persistent pulmon...

journal_title：Pediatric dermatology

authors： Bakirtas A,Harmanci K,Toyran M,Razi CH,Turktas I

更新日期：2007-07-01 00:00:00

abstract：:Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder that is caused by a DNA repair defect. It is characterized mainly by skin, eye, and skeletal abnormalities. Cutaneous changes appear at between 3 and 6 months of age and include poikiloderma, photosensitivity, scaling, hyperkeratosis, and disturban...

journal_title：Pediatric dermatology

authors： Narayan S,Fleming C,Trainer AH,Craig JA

更新日期：2001-05-01 00:00:00

abstract：:We report a 2-year-old boy with a plaque on the upper arm composed of multiple 2- to 3-mm leiomyomata which developed at the age of 3 months and have been unchanged since. Immunohistologically there was positive staining for the muscle intermediate filament desmin. We discuss the unusual clinical presentation and poss...

journal_title：Pediatric dermatology

authors： Henderson CA,Ruban E,Porter DI

更新日期：1997-07-01 00:00:00

abstract：:We described two adolescent girls with untreated, consistently annular, plaque-type psoriasis without pustules, a presentation that is to our knowledge, not previously described. No typical confluent plaque-type lesions were present. The plaques in our patients resembled other entities such as tinea corporis and eryth...

journal_title：Pediatric dermatology

authors： Guill CL,Hoang MP,Carder KR

更新日期：2005-01-01 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：:A 4-year-old girl with an established diagnosis of atopic dermatitis, previously severe and treated with cyclosporine, developed widespread papules that demonstrated changes consistent with epidermodysplasia verruciformis on biopsy. Human papilloma virus (HPV) typing was performed and was consistent with epidermodyspl...

journal_title：Pediatric dermatology

authors： Fernandez KH,Rady P,Tyring S,Stone MS

更新日期：2014-05-01 00:00:00

abstract：:Follicular mucinosis (FM) is an uncommon reaction pattern in which the accumulation of mucin in the follicular epithelium is the main pathologic finding. FM may be idiopathic (primary follicular mucinosis [PFM]), in association with mycosis fungoides or cutaneous T-cell lymphoma, or in association with other neoplasti...

journal_title：Pediatric dermatology

authors： Santos-Briz A,Cañueto J,García-Dorado J,Alonso MT,Balanzategui A,González-Díaz M

更新日期：2013-11-01 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：:Lichen planus is an uncommonly encountered dermatosis in children. In the present study of 50 children the limbs were the most common site of involvement (70.0%). A majority of the children (60.0%) presented with the classic form of the disease. Hypertrophic lesions were present in 26.0% of children while linear lesio...

journal_title：Pediatric dermatology

authors： Sharma R,Maheshwari V

更新日期：1999-09-01 00:00:00

abstract：:Hair loss and thinning are possible complications in those undergoing endocrine therapies with aromatase inhibitors. Alopecia in pediatric patients undergoing endocrine therapy has not been previously reported. We describe two adolescents, 14 and 16 years of age, who developed androgenetic alopecia following treatment...

journal_title：Pediatric dermatology

authors： Perper M,Herskovitz I,Tosti A

更新日期：2020-11-01 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：: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：:Infliximab, a chimeric antitumor necrosis factor alpha monoclonal antibody (anti-TNF alpha), has been recently shown to have a beneficial effect on pyoderma gangrenosum associated with inflammatory bowel disease. Patients with the syndromic triad of pyogenic sterile arthritis, pyoderma gangrenosum, and acne, an autoin...

journal_title：Pediatric dermatology

authors： Stichweh DS,Punaro M,Pascual V

更新日期：2005-05-01 00:00:00

abstract：:Leukemia cutis and facial nerve palsy are rare presenting symptoms of leukemia. This report describes a case of acute T-cell lymphoblastic leukemia (ALL) presenting with only these two symptoms, a presentation of ALL that, to our knowledge, has not been previously described. It serves to alert physicians to look for u...

journal_title：Pediatric dermatology

authors： Gold HL,Grynspan D,Kanigsberg N

更新日期：2014-05-01 00:00:00

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

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

更新日期：2019-03-01 00:00:00

abstract：:We describe the clinicopathologic features of an unusual case of fibromatosis colli. The lesion was rock hard, lateral, tightly affixed to the clavicle, and with overlying hypertrichosis. ...

journal_title：Pediatric dermatology

authors： Amin A,Loftis B,Shwayder TA

更新日期：2010-09-01 00:00:00

abstract：:Keratitis ichthyosis deafness syndrome is a rare congenital ectodermal disorder. It appears to be genetically heterogeneous and may be caused by mutations in the connexin 26 (Cx26) gene (GJB2) or in the connexin 30 gene. It is characterized by the association of ichthyosis-like skin lesions, hearing loss, and vascular...

journal_title：Pediatric dermatology

authors： De Raeve L,Bonduelle M,Deconinck H,Roseeuw D,Stene JJ

更新日期：2008-07-01 00:00:00

abstract：:Phrynoderma is a distinctive form of follicular hyperkeratosis associated with nutritional deficiency. Although originally thought to represent vitamin A deficiency, several studies have demonstrated multiple etiologies. Characteristic skin lesions are hyperkeratotic papules that first appear on the extensor surfaces ...

journal_title：Pediatric dermatology

authors： Maronn M,Allen DM,Esterly NB

更新日期：2005-01-01 00:00:00

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

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

更新日期：2018-11-01 00:00:00