Congenital self-healing reticulohistiocytosis: report of a patient with a strikingly large tumor mass.

abstract：:Treatment of verruca plana is often challenging, and multiple treatment modalities, both pharmacologic and destructive, are frequently necessary to clear lesions. We report a case of a 16-year-old girl with a 2-year history of extensive verruca plana of the forehead, temples, and upper periorbital skin, recalcitrant t...

journal_title：Pediatric dermatology

authors： Johnson NM,Pickard CM

更新日期：2020-10-08 00:00:00

abstract：:Traumatic tattoos induced by pencil point puncture in children may result in persistent disfigurement if left untreated. The Q-switched ruby laser effectively removes darkly colored cutaneous chromophores with minimal disruption of unaffected skin. We present a young patient with pencil point induced traumatic tattooi...

journal_title：Pediatric dermatology

authors： Knoell KA,Schreiber AJ,Kutenplon M,Milgraum SS

更新日期：1997-07-01 00:00:00

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

authors： Stephens M,Rubin AI,Perman MJ

更新日期：2020-03-01 00:00:00

abstract：:We describe a bullous-hemorrhagic reaction of the ear lobes in a child with nephrosis after levamisole intake. This drug is used in children as an alternative treatment of corticosteroid-responsive nephrotic syndrome. Histologic evaluation of a lesion revealed necrotizing vasculitis involving mainly the large vessels ...

journal_title：Pediatric dermatology

authors： Menni S,Pistritto G,Gianotti R,Ghio L,Edefonti A

更新日期：1997-11-01 00:00:00

abstract：:Hoyeraal-Hreidarsson syndrome is a rare telomere biology disorder that is recognized as a severe variant of dyskeratosis congenita. We present a Libyan boy with hematologic and neurologic abnormalities with typical dermatologic manifestations of dyskeratosis congenita. Death usually occurs before the age of 4 years as...

journal_title：Pediatric dermatology

authors： Bakar Ö,Işik U,Canpolat C,Alanay Y

更新日期：2015-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Previous studies have demonstrated an increased prevalence of inflammatory bowel disease (IBD) in adults with hidradenitis suppurativa (HS). Whether the same association exists in pediatric patients is unknown. Fecal calprotectin (FC) is used to screen and monitor disease activity in IBD. There ar...

journal_title：Pediatric dermatology

authors： Lloyd-McLennan AM,Ali S,Kittler NW

更新日期：2020-10-25 00:00:00

abstract：:Childhood pemphigus foliaceus typically causes erythema and scaling of the scalp. Sometimes, blisters and oozing are present, which often are misdiagnosed as either impetigo or seborrheic dermatitis. The eruption may progress to involve the trunk and limbs, the lesions often having an arcuate pattern. The diagnosis ca...

journal_title：Pediatric dermatology

authors： Jones SK,Schwab HP,Norris DA

更新日期：1986-12-01 00:00:00

abstract：:We report a case of a young man with perforating folliculitis and cystic fibrosis with complications including chronic obstructive pulmonary disease, insulin dependent diabetes mellitus, and liver cirrhosis. We demonstrate increased TGF-β1 immunohistochemical staining in the perforating folliculitis lesions of our pat...

journal_title：Pediatric dermatology

authors： Tuttle MS,Kwon EJ,Tamburro J,Honda K

更新日期：2010-11-01 00:00:00

abstract：:Stevens-Johnson syndrome and toxic epidermal necrolysis comprise a spectrum of severe mucocutaneous hypersensitivity reactions. A paucity of data limits current understanding of the etiology, treatment options, and prognosis of this entity in the infantile population compared to that in the adult and pediatric literat...

journal_title：Pediatric dermatology

authors： Nassim JS,Karim SA,Grenier PO,Schmidt B,Jones KM

更新日期：2020-10-30 00:00:00

abstract：:Scurvy, or hypovitaminosis C, is an uncommon condition that exists today primarily within certain unique populations-particularly the elderly subjects, patients with neurodevelopmental disabilities or psychiatric illnesses, or others with unusual dietary habits. Vitamin C is an essential nutrient in the human body, an...

journal_title：Pediatric dermatology

authors： Cole JA,Warthan MM,Hirano SA,Gowen CW Jr,Williams JV

更新日期：2011-07-01 00:00:00

abstract：:Amniotic band syndrome is one of the many causes of aplasia cutis congenita. It is usually seen as a constriction band surrounding a limb or as a membrane that adheres to some part of the body. This syndrome can be associated with various malformations. An infant with amniotic adhesions producing aplasia cutis, radial...

journal_title：Pediatric dermatology

authors： Nagore E,Sánchez-Motilla JM,Febrer MI,Cremades B,Aleu M,Aliaga A

更新日期：1999-05-01 00:00:00

abstract：:We examined a father and son affected by Ehlers-Danlos syndrome type II. Both patients had micrognathia together with ligament and skin hyperlaxity. The son exhibited complete cleft palate. Ultrastructural studies revealed abnormal collagen fibrils in the dermis of both patients. In the child the most striking alterat...

journal_title：Pediatric dermatology

authors： Rizzo R,Contri MB,Micali G,Quaglino D,Pavone L,Ronchetti IP

更新日期：1987-11-01 00:00:00

abstract：:A case of childhood granulomatous periorificial dermatitis is described. This disorder occurs predominantly in prepubertal black children and is characterized by a monomorphous, papular eruption occurring around the mouth, nose, and eyes. It is benign and self-limited. Treatment may include topical metronidazole in yo...

journal_title：Pediatric dermatology

authors： Knautz MA,Lesher JL Jr

更新日期：1996-03-01 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：:Henoch-Schönlein purpura is an acute leukocytoclastic vasculitis that primarily affects children. Henoch-Schönlein purpura is often associated with an infection, and a wide variety of infectious agents have been implicated in the pathogenesis. We report a child with Henoch-Schönlein purpura associated with Helicobacte...

journal_title：Pediatric dermatology

authors： Mytinger JR,Patterson JW,Thibault ES,Webb J,Saulsbury FT

更新日期：2008-11-01 00:00:00

abstract：:Lichen planus (LP) in children is a rare entity. We report 23 cases of childhood LP seen over a period of 7 years. Ninety-six percent of the children were of Arab ancestry. There were 52% boys and 48% girls. Classic LP was the most common clinical variant (70%), followed by eruptive generalized LP (13%). A majority of...

journal_title：Pediatric dermatology

authors： Nanda A,Al-Ajmi HS,Al-Sabah H,Al-Hasawi F,Alsaleh QA

更新日期：2001-01-01 00:00:00

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

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

更新日期：2007-09-01 00:00:00

abstract：:Preschool sarcoidosis is characterized by the triad of skin, joint, and eye disease without pulmonary involvement. Arthritis and uveitis are also frequently seen together in juvenile rheumatoid arthritis. We report two patients with preschool sarcoidosis, both of whom were initially diagnosed and treated as having juv...

journal_title：Pediatric dermatology

authors： Sahn EE,Hampton MT,Garen PD,Warrick J,Smith D,Silver RM

更新日期：1990-09-01 00:00:00

abstract：:Pigmented purpuric dermatoses (PPDs) are a group of idiopathic, chronic, and self-resolving conditions easily recognizable in adults but extremely uncommon in infants. We present the youngest patient with PPD reported to date. ...

journal_title：Pediatric dermatology

authors： Martos-Cabrera L,López-Balboa P,Ramírez-Lluch M,Colmenero I,Mateos-Mayo A,Torrelo A,Hernández-Martin Á

更新日期：2021-01-06 00:00:00

abstract：:We report a rare presentation of vulvar lymphangiectasia that developed secondary to gastrointestinal tuberculosis in a teenager, and its spontaneous resolution after anti-tuberculous treatment was completed. ...

journal_title：Pediatric dermatology

authors： Ho VPY,Koh MJA

更新日期：2020-01-01 00:00:00

abstract：:We aimed to better understand the pathogenesis, clinical features, prognosis, and treatment of neonatal autoimmune blistering diseases (AIBDs). We searched Medline, Embase, PubMed, Latin American and Caribbean Health Sciences Literature, and reference lists of identified articles. Inclusion criteria were articles publ...

journal_title：Pediatric dermatology

authors： Zhao CY,Chiang YZ,Murrell DF

更新日期：2016-07-01 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：:We present a special case of an 8-year-old girl diagnosed with severe drug reaction with eosinophilia and systemic symptoms due to trimethoprim-sulfamethoxazole for urinary tract infection prophylaxis for congenital vesicoureteral reflux. The patient is believed to have developed drug reaction with eosinophilia and sy...

journal_title：Pediatric dermatology

authors： Maarouf M,Wickenheiser M,Krase JM,Wolter S,Shi VY

更新日期：2018-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Chromhidrosis is a rare condition of which there are only a few case reports in the literature. The aim of this study was to evaluate clinical, laboratory, and possible environmental factors in 13 patients with chromhidrosis to elucidate causative agents. METHODS:Data were obtained from the medic...

journal_title：Pediatric dermatology

authors： Erdol S,Karakaya S,Saglam H,Tarim O

更新日期：2018-07-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are medical emergencies. Mainstays of treatment include removal of the offending agent, supportive care, and wound care. The use of immunosuppressive agents such as corticosteroids and intravenous immunoglobulin (IVIg) is controve...

journal_title：Pediatric dermatology

authors： St John J,Ratushny V,Liu KJ,Bach DQ,Badri O,Gracey LE,Ho AW,Raff AB,Sugai DY,Schalock P,Kroshinsky D

更新日期：2017-09-01 00:00:00

abstract：:Metastatic Crohn's disease (MCD) is a rare extraintestinal manifestation of Crohn's disease characterized by the histologic finding of granulomatous dermatitis at a site noncontiguous to the gastrointestinal tract. An adolescent had MCD of the face that was initially mistaken for severe, treatment-resistant acne. Hist...

journal_title：Pediatric dermatology

authors： Cummins RE,Mullins D,Smith LJ,Ford MJ

更新日期：1996-01-01 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

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：: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

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

更新日期：2012-05-01 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