Management of congenital melanocytic nevi in the plastic surgery clinic: Families' expectations and their persistent concern about malignancy.

abstract：:Cutaneous histiocytosis may take two principal forms. It is either a benign proliferative process or a relentless, progressive process with a poor prognosis. In histiocytic medullary reticulosis, histiocytes demonstrate nuclear atypia and the outcome is uniformly fatal. Benign cephalic histiocytosis X causes lesions s...

journal_title：Pediatric dermatology

authors： Roper SS,Spraker MK

更新日期：1985-11-01 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：:Tetracycline is well known to cause pigmentation of various body tissues, such as teeth, bone, lunulae, conjunctivae, and lymph nodes. It has not been reported to cause discoloration of the skin, unlike its semisynthetic derivative, minocycline. We report an 18-year-old girl who developed lower extremity pigmentation ...

journal_title：Pediatric dermatology

authors： Hawfield W,Goodrich R,Warren S,Morrell D

更新日期：2004-03-01 00:00:00

abstract：:Epidermolysis bullosa-associated nevi are recently described dysplastic nevi found in patients with epidermolysis bullosa. These lesions display clinical features of unusual nevi suggestive of malignancy but thus far cases with malignant transformation have not been reported. We describe a case of epidermolysis bullos...

journal_title：Pediatric dermatology

authors： Mollet T,Henderson FW,Groben PA,Burkhart CN,Morrell DS

更新日期：2011-01-01 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：:We report a family affected to the fourth generation by uncombable hair syndrome. This syndrome is characterized by unruly, dry, blond hair with a tangled appearance. The family pedigree strongly supports the hypothesis of autosomal dominant inheritance; some members of the family had, apart from uncombable hair, mino...

journal_title：Pediatric dermatology

authors： Boccaletti V,Zendri E,Giordano G,Gnetti L,De Panfilis G

更新日期：2007-05-01 00:00:00

abstract：:Familial hyperpigmentation, or melanosis universalis hereditaria, is a rare hyperpigmentary disorder with onset in infancy. Here, we describe monozygotic twins with similar pattern of progressive hyperpigmentation with onset in early neonatal period without any family history. Histopathological examination showed incr...

journal_title：Pediatric dermatology

authors： Gupta N,Sharma MC,Ramam M,Kabra M

更新日期：2011-01-01 00:00:00

abstract：:Although lentigines are usually benign, they can be associated with a number of genetic syndromes in which neoplasms and other multi-system pathological processes occur. Here, we report the case of a 6-year-old girl who presented with atypical lentiginosis and hyperpigmentation caused by a de novo genetic variant in t...

journal_title：Pediatric dermatology

authors： Tran AK,Pearce A,López-Sánchez M,Pérez-Jurado LA,Barnett C

更新日期：2019-11-01 00:00:00

abstract：:Demodex mites are commensal inhabitants of the pilosebaceous unit that are typically absent or at low numbers in childhood. When they are present, they can cause a primary eruption or exacerbate an underlying facial dermatosis. Here we report five cases of demodicosis occurring in childhood, the clinical presentations...

journal_title：Pediatric dermatology

authors： Douglas A,Zaenglein AL

更新日期：2019-09-01 00:00:00

abstract：:Congenital erythropoietic porphyria is a rare form of porphyria, presenting during the neonatal period or during infancy. Clinical features include photosensitive blistering and severe anemia. Wood's lamp fluorescence of the diaper is a useful screening test. We describe a severely affected neonate with systemic invol...

journal_title：Pediatric dermatology

authors： Hogeling M,Nakano T,Dvorak CC,Maguiness S,Frieden IJ

更新日期：2011-07-01 00:00:00

abstract：:Spitz nevi are benign melanocytic lesions with many histologic similarities to malignant melanoma. A case of agminated Spitz nevi on a 2-year-old boy's left cheek is reported and 41 other cases of agminated Spitz nevi are reviewed. In this case, two biopsies were performed on two different-appearing lesions and the re...

journal_title：Pediatric dermatology

authors： Zeng MH,Kong QT,Sang H,Deng DQ,Xie QM

更新日期：2013-09-01 00:00:00

abstract：:We report a girl with lipophagic lobular panniculitis of unknown origin located on her ankles leading to circumferential fat atrophy of the ankles, a condition usually referred to as "annular lipoatrophy of the ankles." According to our patient's features and five additional cases reported so far, we conclude that thi...

journal_title：Pediatric dermatology

authors： Corredera C,Iglesias M,Hernández-Martín A,Colmenero I,Dilme E,Torrelo A

更新日期：2011-03-01 00:00:00

abstract：:Epidermolysis bullosa acquisita (EBA) is a rare, acquired, subepidermal blistering disease characterized by autoantibodies directed against type VII collagen, the major component of anchoring fibrils. We report a 5-year-old Chinese boy who presented with extensive lesions consisting of disseminated pruritic vesicles a...

journal_title：Pediatric dermatology

authors： Yang B,Wang C,Wang N,Pan F,Chen S,Zhou G,Yu M,Zhang F

更新日期：2012-09-01 00:00:00

abstract：:A wide spectrum of histopathologic changes has been reported to occur within epidermal nevi. We saw two patients with warty nevoid lesions in which histopathologic features of incontinentia pigmenti, verrucous phase, were present. The diagnosis of incontinentia pigmenti was excluded because both patients were male, la...

journal_title：Pediatric dermatology

authors： Fletcher V,Williams ML,Lane AT

更新日期：1985-11-01 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：:Raynaud's phenomenon (RP) is a vasospastic disorder characterized by recurrent self-limited episodes of skin pallor, cyanosis, and hyperemia caused by paroxysmal spasms in the small arteries of the fingers and toes and can occur in any age group. Hands, feet, nose, ears, and nipples can be affected. The diagnosis is m...

journal_title：Pediatric dermatology

authors： Rigante D,Fastiggi M,Ricci F,D'Errico F,Bracci B,Guerriero C

更新日期：2017-05-01 00:00:00

abstract：:Intralesional injection of bleomycin (BLM) for the treatment of warts resistant to all conventional therapies is of certain interest because of the drug's low toxicity and its efficacy. However, delayed side effects may appear, particularly Raynaud phenomenon. Accordingly, some precautions must be taken in patients wi...

journal_title：Pediatric dermatology

authors： Vanhooteghem O,Richert B,de la Brassinne M

更新日期：2001-05-01 00:00:00

abstract：:Burns and scalds are relatively common injuries in children. Formation of hypertrophic scars or keloids is feared complications. A 2-year-old girl who spilled a cup of hot coffee onto herself developed widespread hypertrophic scars and beginning keloids on her upper chest, despite application of pressure garments and ...

journal_title：Pediatric dermatology

authors： Eisendle K,Pichler M,De Luca J,Thuile T

更新日期：2020-01-01 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：: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：:Although acne vulgaris is common in preadolescents (<13 yrs), few acne treatments are currently approved for children. This study assessed the safety and efficacy of tretinoin microsphere gel (TMG) 0.04% pump in children aged 9-11 with acne vulgaris. In this multicenter, randomized, double-blind, vehicle-controlled pi...

journal_title：Pediatric dermatology

authors： Eichenfield LF,Hebert AA,Schachner L,Paller AS,Rossi AB,Lucky AW

更新日期：2012-09-01 00:00:00

abstract：:Infantile acropustulosis (IA) is a condition of young children characterized by recurrent episodes of pruritic vesicles and pustules in an acral distribution. Several reports describe patients with scabies infestation prior to the diagnosis of IA, although the relationship between the two remains unclear. Furthermore,...

journal_title：Pediatric dermatology

authors： Mancini AJ,Frieden IJ,Paller AS

更新日期：1998-09-01 00:00:00

abstract：:We present a case of an infant with severe atopic dermatitis infected with Streptococcus pyogenes who presented with pustules, honey-colored crusts, and punched-out erosions with scalloped borders mimicking eczema herpeticum or eczema coxsackium. We draw attention to this case to highlight the similar clinical appeara...

journal_title：Pediatric dermatology

authors： Shayegan LH,Richards LE,Morel KD,Levin LE

更新日期：2019-11-01 00:00:00

abstract：:Acrodynia, also known as pink disease, erythredema polyneuropathy, Feer syndrome, and raw-beef hands and feet, is thought to be a toxic reaction to elemental mercury and less commonly to organic and inorganic forms. Occurring commonly in the early 20th century, acrodynia is now a seemingly extinct disease in the moder...

journal_title：Pediatric dermatology

authors： Mercer JJ,Bercovitch L,Muglia JJ

更新日期：2012-03-01 00:00:00

abstract：:Condylomata acuminata (CA), or anogenital warts, are typically benign lesions caused by human papillomavirus infection. Although they are rare, immunocompromised individuals are at a higher risk of CA undergoing transformation into invasive anal squamous cell carcinoma (SCC). These patients need aggressive evaluation ...

journal_title：Pediatric dermatology

authors： Paul S,Cheng CE,Kroshinsky D

更新日期：2015-07-01 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：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：:A 13-year-old Korean girl presented with a 7-year history of a pruritic, light-brown patch containing multiple 0.2- to 0.5-cm brownish-to-reddish maculopapules on the left anterior chest. When her skin was rubbed, the lesion became itchy and red. Histopathologic evaluation demonstrated marked dense dermal infiltration...

journal_title：Pediatric dermatology

authors： Ahn HJ,Park HJ,Jeong KH,Park YK,Lee MH

更新日期：2018-09-01 00:00:00

abstract：:We report an unusual congenital vesiculopustular eruption arising in a neonate as the result of the transient myeloproliferative disorder (TMD) associated with trisomy 21. In this instance, the neonate was phenotypically normal, making the diagnosis more elusive. Initially the lesions were clinically suspicious for he...

journal_title：Pediatric dermatology

authors： Solky BA,Yang FC,Xu X,Levins P

更新日期：2004-09-01 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