Sacral hemangioma with sinus tract in an infant.

abstract：:Orofacial granulomatosis, a rare disease in childhood, is characterized by orofacial swelling in the absence of systemic disease. We report the case of a 12-year-old girl with asymptomatic erythematous infiltration of her upper lip, cheeks, and chin that had persisted for more than 2 years; biopsy confirmed granuloma ...

journal_title：Pediatric dermatology

authors： Lalosevic J,Gajic-Veljic M,Nikolic M

更新日期：2017-11-01 00:00:00

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

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

更新日期：2014-09-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Drug reaction with eosinophilia and systemic symptoms (DRESS) is rare but potentially fatal in children. Fever and rash, which are salient features of DRESS, may mimic other commonly encountered pediatric conditions. We profiled the DRESS cases in a tertiary children's hospital in Singapore. METH...

journal_title：Pediatric dermatology

authors： Han XD,Koh MJ,Wong SMY

更新日期：2019-05-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Despite rising skin cancer rates in children, multiple studies reveal inadequate youth sun-protective behavior (eg, sunscreen use). Using Healthy Passages data for fifth-graders, we set out to determine sunscreen adherence in these children and investigated factors related to sunscreen performance...

journal_title：Pediatric dermatology

authors： Correnti CM,Klein DJ,Elliott MN,Veledar E,Saraiya M,Chien AT,Schwebel DC,Mrug S,Tortolero SR,Cuccaro PM,Schuster MA,Chen SC

更新日期：2018-09-01 00:00:00

abstract：:Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is a rare, autosomal dominant syndrome that is known to have variable expressivity in multiple organ systems. We describe the case of a young male child with nevoid basal cell carcinoma syndrome and scalp lesions, including a branchial cleft cyst with respiratory ...

journal_title：Pediatric dermatology

authors： Findley AB,Pride H

更新日期：2010-03-01 00:00:00

abstract：:Acne fulminans is a severe form of acne characterized by painful, inflammatory nodules that progress into ulcers and concurrent systemic symptoms. Treatment of acne with isotretinoin can precipitate a syndrome called isotretinoin-induced acne fulminans without systemic symptoms. An exuberant granulation tissue respons...

journal_title：Pediatric dermatology

authors： Li AW,Antaya RJ

更新日期：2018-03-01 00:00:00

abstract：:Rothmund-Thomson syndrome, a rare autosomal recessive disorder, is characterized by photosensitivity; specific skin changes including poikiloderma, atrophy, and telangiectases; juvenile cataracts; short stature; and bone defects. We describe two siblings with this syndrome. ...

journal_title：Pediatric dermatology

authors： Nanda A,Kanwar AJ,Kapoor MM,Thappa DM,Radotra BD,Vaishnavi C,Kaur S

更新日期：1989-12-01 00:00:00

abstract：:Highly active antiretroviral therapy can restore specific immune responses and control of microorganism infections in human immunodeficiency virus-positive patients. This immune recovery may cause an inflammatory reaction to microbial and autoimmune antigens known as immune reconstitution inflammatory syndrome. We des...

journal_title：Pediatric dermatology

authors： de Carvalho VO,Cruz CR,Noronha L,Abagge KT,Lima HC

更新日期：2010-11-01 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：:We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous p...

journal_title：Pediatric dermatology

authors： Musumeci ML,Nasca MR,De Pasquale R,Schwartz RA,Micali G

更新日期：2006-05-01 00:00:00

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

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

更新日期：2019-05-01 00:00:00

abstract：:Graft-versus-host disease (GVHD) is one of the major complications after hematopoietic stem cell transplantation and is responsible for post-therapeutic morbidity, mortality, and poor quality of life of recipients. Sclerodermatous graft-versus-host disease (sGVHD) is a rare variant of chronic GVHD characterized by dep...

journal_title：Pediatric dermatology

authors： Lazzeri L,Tripo L,Pescitelli L,Ricceri F,Prignano F

更新日期：2016-03-01 00:00:00

abstract：:We evaluated the prevalence of acanthosis nigricans among urban youth. Youth (7-17 years) at nine pediatric practices completed surveys on demographics and family history of diabetes and had weight and height measured. Acanthosis nigricans was scored and digital photography of the neck performed. A total of 618 youth ...

journal_title：Pediatric dermatology

authors： Brickman WJ,Binns HJ,Jovanovic BD,Kolesky S,Mancini AJ,Metzger BE,Pediatric Practice Research Group.

更新日期：2007-11-01 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：:Two unrelated Hispanic females, ages 4 and 3 years, respectively, each presented with a solitary patch of excessive terminal hair growth in the midline of the neck. This rare form of congenital localized hypertrichosis, known as anterior cervical hypertrichosis, is reported here as an isolated defect with no other und...

journal_title：Pediatric dermatology

authors： Reddy S 4th,Antaya RJ

更新日期：2010-09-01 00:00:00

abstract：OBJECTIVES:To compare prevalence and severity of diaper dermatitis (DD) in infants and toddlers (babies) across three countries (China, USA, and Germany), including diapered skin measures and caregiver practices. METHODS:A cross-sectional study of 1791 babies (~600 from each country) was recruited at each clinical sit...

journal_title：Pediatric dermatology

authors： Carr AN,DeWitt T,Cork MJ,Eichenfield LF,Fölster-Holst R,Hohl D,Lane AT,Paller A,Pickering L,Taieb A,Cui TY,Xu ZG,Wang X,Brink S,Niu Y,Ogle J,Odio M,Gibb RD

更新日期：2020-01-01 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：: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：: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：:We report a 12-year-old Japanese boy with a 3-year history of skin lesions that had been unsuccessfully treated with topical steroids. We initiated two different topical treatments with adapalene gel 0.1% (Differin(®) Gel 0.1%) and high-concentration vitamin D3 (tacalcitol) ointment; the lesions treated with adapalene...

journal_title：Pediatric dermatology

authors： Abe M,Inoue C,Yokoyama Y,Ishikawa O

更新日期：2011-03-01 00:00:00

abstract：:Alopecia areata (AA) involves the immune-related destruction of hair follicles, resulting in patches of complete hair loss, most often on the scalp. The topical sensitizer squaric acid dibutylester (SADBE) is a popular treatment option given its low side-effect profile, hair regrowth potential, and lack of cross-react...

journal_title：Pediatric dermatology

authors： Chen CA,Carlberg V,Kroshinsky D

更新日期：2017-01-01 00:00:00

abstract：:Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report a 13-year-old girl with extensive lupus panniculitis since the age of 8 months and no e...

journal_title：Pediatric dermatology

authors： Nousari HC,Kimyai-Asadi A,Santana HM,Diglio GM,Tausk FA,Cohen BA

更新日期：1999-07-01 00:00:00

abstract：:Pemphigus refers to a group of potentially fatal blistering skin diseases that are often due to the deleterious effects of autoantibodies directed against desmosomal antigens. Although desmogleins have been mainly implicated as autoantigens in pemphigus, a steadily growing body of evidence suggests that other desmosom...

journal_title：Pediatric dermatology

authors： Geller S,Gat A,Harel A,Mashiah J,Zeeli T,Eming R,Ishii N,Hertl M,Hashimoto T,Sprecher E

更新日期：2016-01-01 00:00:00

abstract：BACKGROUND AND OBJECTIVES:Melanonychia striata is common in children of darker-skinned Asian races, while subungual melanoma is extremely rare and it is difficult to make a diagnosis clinically. However, performing nail unit biopsies in children is particularly challenging and can result in permanent nail dystrophy. Th...

journal_title：Pediatric dermatology

authors： Colin Tan W,Wang DY,Seghers AC,Koh MJA,Nicholas Goh SG,Joyce Lee SS

更新日期：2019-11-01 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：:Infantile myofibromatosis is a rare benign tumor of infancy and childhood that occurs in solitary, multiple, and generalized forms with similar histology but different clinicopathologic and prognostic implications. Even solitary tumors need follow-up, as the type of presentation will be determined over time. It is nec...

journal_title：Pediatric dermatology

authors： Jurcić V,Perković T,Pohar-Marinsek Z,Hvala A,Lazar I

更新日期：2003-07-01 00:00:00

abstract：:Eccrine angiomatous hamartoma (EAH) is a rare, benign cutaneous lesion histologically defined as a proliferation of eccrine glands within a closely associated vascular stroma. Typically EAH presents as a solitary flesh-colored, hyperhidrotic, painful papule or plaque appearing at birth or during childhood. Only two pr...

journal_title：Pediatric dermatology

authors： Morrell DS,Ghali FE,Stahr BJ,McCauliffe DP

更新日期：2001-03-01 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：:Several dermatologic abnormalities have been described in anorexia nervosa, but only rare associations have been made with perniosis. We recently saw two teenage girls and one woman with anorexia nervosa who had symptoms of perniosis. We suggest that altered thermoregulation and a hyperreactive peripheral vascular res...

journal_title：Pediatric dermatology

authors： White KP,Rothe MJ,Milanese A,Grant-Kels JM

更新日期：1994-03-01 00:00:00

abstract：:Children's and teens' frequent use of inexpensive "costume" jewelry exposes them to a variety of contact allergens. Greater use heightens the risk of developing allergic contact dermatitis, especially in the setting of body piercings. Several clinical pearls, prevention strategies, and avoidance alternatives are provi...

journal_title：Pediatric dermatology

authors： Ivey LA,Limone BA,Jacob SE

更新日期：2018-03-01 00:00:00