Congenital nevocytic nevi: follow-up of a Swedish birth register sample regarding etiologic factors, discomfort, and removal rate.

abstract：:Precalcaneal congenital fibrolipomatous hamartomas are uncommon, congenital, nontender papules located on the medial plantar aspects of the heel. We report the occurrence of this rare disorder in two half brothers, suggesting that it may occur in a familial pattern. ...

journal_title：Pediatric dermatology

authors： Fangman WL,Prose NS

更新日期：2004-11-01 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：: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：:When vulvar lichen sclerosus occurs in prepubertal children it is widely believed that it is likely to remit at puberty. However when it occurs in adult women it is accepted that remission is unlikely and that in addition untreated or inadequately treated disease may be complicated by significant disturbance of vulvar...

journal_title：Pediatric dermatology

authors： Smith SD,Fischer G

更新日期：2009-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Port-wine stains, also known as capillary malformations, are due to dermal vascular ectasia and dilation and are most commonly congenital; however, acquired port-wine stains (APWS) developing later in life have been noted in the literature, most commonly in the context of trauma. METHODS/RESULTS:...

journal_title：Pediatric dermatology

authors： Stephens MR,Putterman E,Yan AC,Castelo-Soccio L,Perman MJ

更新日期：2020-01-01 00:00:00

abstract：:Xanthoma disseminatum is a rare, usually self-healing dermatologic disease of unknown etiology. Involvement of other organs and tissues including bone marrow, bone, and brain may be seen rarely in children. However, to date, hepatic involvement has not been reported. We describe a child with xanthoma disseminatum who ...

journal_title：Pediatric dermatology

authors： Büyükavci M,Selimoglu A,Yildirim U,Ertekin V,Atasoy M

更新日期：2005-11-01 00:00:00

abstract：:A 3-year-old girl presented with longer hair on the left side of her scalp, coarse hair of abnormal length on her extremities, and a tuft of hair in the lumbosacral region, with all hair distributed on normally pigmented skin. Neither similar or relevant family history nor associated extracutaneous abnormalities was d...

journal_title：Pediatric dermatology

authors： Sotiriadis D,Patsatsi A,Lazaridou E,Sotiriou E,Devliotou-Panagiotidou D

更新日期：2009-07-01 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：:Infantile acne is a rare occurrence. It is more common in boys and predominately occurs on the cheeks in infants between the ages of 1 and 16 months. Clinically, the lesions range from comedones to inflammatory papulopustules to cysts. Successful therapies include topical tretinoin, benzoyl peroxide and topical and or...

journal_title：Pediatric dermatology

authors： Barnes CJ,Eichenfield LF,Lee J,Cunningham BB

更新日期：2005-03-01 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：: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：: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：:This is a follow-up report on a boy with phacomatosis pigmentokeratotica. At the age of 10 years he had, in addition to a sebaceous nevus and a speckled lentiginous nevus, multiple lesions of a collagen nevus localized on the chin and in the lumbar area. On the left shoulder, a small telangiectatic spot was present wi...

journal_title：Pediatric dermatology

authors： Boente Mdel C,Asial RA,Happle R

更新日期：2008-01-01 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：:Systemic sclerosis-polymyositis overlap syndrome is rare in children. Anti-PM/Scl is the most common autoantibody associated with this syndrome. We present a case of systemic sclerosis-polymyositis overlap syndrome in a child with isolated anti-Ku antibodies, an uncommon antibody associated with this rare syndrome. ...

journal_title：Pediatric dermatology

authors： Loo RJ,Nocton JJ,Harmelink MM,Chiu YE

更新日期：2020-09-01 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：:To describe the characteristics of five pediatric patients with the Meyerson phenomenon associated with congenital melanocytic nevi, five cases were reviewed to retrieve information relating to clinical presentation, treatment and evolution of the eczematous phenomenon and of the nevi. Three of five patients were male...

journal_title：Pediatric dermatology

authors： Rolland S,Kokta V,Marcoux D

更新日期：2009-05-01 00:00:00

abstract：:Cutaneous myxomas are rare, benign, connective tissue tumors composed of stellate cells set in a loose mucoid stroma containing delicate reticulin fibers running in various directions. They are also called angiomyxomas to reinforce their vascular component. These lesions have been recognized as part of Carney complex....

journal_title：Pediatric dermatology

authors： Martí N,Jordá E,Monteagudo C,Gámez L,Reig I,Calduch L

更新日期：2011-07-01 00:00:00

abstract：:The present study aimed to investigate the prevalence of atopic dermatitis in primary schoolchildren in Denizli, Turkey, and to determine the possible risk factors for atopic dermatitis in home environment. A self-administered questionnaire was handled to the parents of 2,100 children aged 7 to 15 years, from three ra...

journal_title：Pediatric dermatology

authors： Ergin S,Ozşahin A,Erdoğan BS,Aktan S,Zencir M

更新日期：2008-05-01 00:00:00

abstract：:We report a child with bilateral congenital triangular alopecia. Shaving the scalp and inserting intravenous cannulas into scalp vessels during the neonatal period was misconstrued by the parents as the cause of hair loss, and resulted in medicolegal implications. ...

journal_title：Pediatric dermatology

authors： Armstrong DK,Burrows D

更新日期：1996-09-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Vitamin B12 deficiency in infants is uncommonly reported from developed countries and generally lacks dermatologic manifestations. On the contrary, infantile vitamin B12 deficiency is common in India and cutaneous manifestations are a constant feature, although often overshadowed by neurologic and...

journal_title：Pediatric dermatology

authors： Kaur S,Goraya JS

更新日期：2018-11-01 00:00:00

abstract：BACKGROUND:Treatment of palmar and axillary primary focal hyperhidrosis (PFH) in children up to 16 years using thoracoscopic sympathicotomy is supported by scarce evidence. Therefore, this study aimed to summarize the results of our standardized bilateral, one-stage, single-port sympathicotomy (BOSS) in children up to ...

journal_title：Pediatric dermatology

authors： Verhaegh AJFP,Kuijpers M,Boon M,DeJongste MJL,Bouma W,Mariani MA,Klinkenberg TJ

更新日期：2020-09-01 00:00:00

abstract：:Our objective was to establish the aerobic and anaerobic microbiology of nonbullous impetigo (NI) in children. We used a retrospective review of clinical microbiology laboratory and patients' records. Specimens were obtained from 40 patients with NI lesions and showed bacterial growth. Aerobic or facultative anaerobic...

journal_title：Pediatric dermatology

authors： Brook I,Frazier EH,Yeager JK

更新日期：1997-05-01 00:00:00

abstract：:Early recognition of the hyperlipoproteinemias is a crucial element in preventing premature coronary artery disease. Xanthomas provide a cutaneous marker of the silent, underlying pathology. Identifying them, and understanding their relation to the inherited hyperlipoproteinemias may facilitate early diagnosis of hype...

journal_title：Pediatric dermatology

authors： Maher-Wiese VL,Marmer EL,Grant-Kels JM

更新日期：1990-09-01 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：:We report the first case of lupus-like lesions in an infant with chronic granulomatous disease during the treatment with voriconazole for chronic invasive aspergillosis. The lesions disappeared with termination of the treatment. ...

journal_title：Pediatric dermatology

authors： Gomez-Moyano E,Vera-Casaño A,Moreno-Perez D,Sanz-Trelles A,Crespo-Erchiga V

更新日期：2010-01-01 00:00:00

abstract：:Henoch-Schönlein purpura (HSP) is an acute systemic vasculitis with unknown etiology, although several studies have found HSP to be related to cytokines such as tumor necrosis factor α, interleukin (IL)-1, and adhesion molecules. In the present study we determined the levels of cytokines such as IL-18 and endothelin-1...

journal_title：Pediatric dermatology

authors： Mahajan N,Kapoor D,Bisht D,Singh S,Minz RW,Dhawan V

更新日期：2013-11-01 00:00:00

abstract：:An 8-month-old male infant had fever, polymorphonuclear leukocytosis, and tender, firm, elevated erythematous plaques on his face, trunk, and extremities. Histologic examination revealed a dense, perivascular, polymorphonuclear, inflammatory cell infiltrate with nuclear dust in the dermis and intrafollicular abscesses...

journal_title：Pediatric dermatology

authors： Kibbi AG,Zaynoun ST,Kurban AK,Najjar SS

更新日期：1985-11-01 00:00:00

abstract：:Acne fulminans is a severe form of acne vulgaris accompanied by systemic symptoms. A 17-year-old Chinese boy presented with an outbreak of necrotic lesions on his face eight days after the onset of palpable purpura, arthralgia, fever, abdominal pain, and proteinuria. He was successfully treated with oral prednisolone ...

journal_title：Pediatric dermatology

authors： Xu X,Li X,Pradhan S,Li W

更新日期：2020-11-01 00:00:00

abstract：:We report a new case of postvaccination morphea profunda (MP) in a child and discuss its different clinical presentations, prognosis, and therapy and its relationship with "solitary morphea profunda." A 2-year-old healthy girl presented with an induration of the anterior aspect of the left thigh of 9 months duration. ...

journal_title：Pediatric dermatology

authors： Khaled A,Kharfi M,Zaouek A,Rameh S,Zermani R,Fazaa B,Kamoun MR

更新日期：2012-07-01 00:00:00