Congenital leukemia cutis.

abstract：:Familial cold auto-inflammatory syndrome, Muckle-Wells syndrome and chronic infantile neurologic, cutaneous, articular syndrome are related disorders associated with mutations in the CIAS1 gene. They appear to represent a continuum of one disease characterized by IL-1-mediated inflammation. Until recently, these condi...

journal_title：Pediatric dermatology

authors： O'Connell SM,O'Regan GM,Bolger T,Hoffman HM,Cant A,Irvine AD,Watson RM

更新日期：2007-01-01 00:00:00

abstract：:Two infants experienced subcutaneous fat necrosis (SCFN) at a relatively late age after cardiac surgery with induced hypothermia. The condition resolved in both patients over four weeks without treatment. The appearance of SCFN after the newborn period is very unusual, and in these patients was probably related to the...

journal_title：Pediatric dermatology

authors： Glover MT,Catterall MD,Atherton DJ

更新日期：1991-09-01 00:00:00

abstract：BACKGROUND:Fibroblastic connective tissue nevi (FCTN) are benign skin conditions characterized by bland spindle cells infiltrating the reticular dermis and the upper subcutis with preservation of adnexal structures. A subset of FCTN expresses CD34, which may cause difficulties in the differential diagnosis, in particul...

journal_title：Pediatric dermatology

authors： Bouaoud J,Fraitag S,Soupre V,Mitrofanoff M,Boccara O,Galliot C,Bodemer C,Picard A,Khonsari RH

更新日期：2018-09-01 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：:Ataxia telangiectasia (AT) is a rare autosomal recessive neurodegenerative disorder caused by a mutation in the ATM gene. An impaired immune response due to the gene mutation leads to an increased risk of infection and malignancy. We present a rare case of dermatofibrosarcoma protuberans arising in a patient with AT. ...

journal_title：Pediatric dermatology

authors： Duffy R,Liaqat M,Lawrence N,Manders S

更新日期：2019-05-01 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：:Two brothers demonstrated a severe variant of trichothiodystrophy. Both had brittle hair, developmental delay with severe failure to thrive, recurrent infections, cataracts, and angioendotheliomas of the liver at autopsy. The elder died at 12 weeks, the younger at 6 months. The younger had the typical appearance of ba...

journal_title：Pediatric dermatology

authors： Petrin JH,Meckler KA,Sybert VP

更新日期：1998-01-01 00:00:00

abstract：:Identification of melanoma or worrisome moles is often taught as an important part of routine skin checks. We sought to evaluate the efficacy of gamified education vs. traditional ABCDEs education on melanoma identification and self-confidence in identifying worrisome moles. We report that in our cohort (n = 271), par...

journal_title：Pediatric dermatology

authors： Jia JL,Shen A,Tabata MM,Sarin KY

更新日期：2020-07-01 00:00:00

abstract：:Hemangiomas, common proliferative vascular tumors, can grow rapidly in the first months of life. Although therapy with high-dose oral glucocorticoids is standard for lesions that threaten vital functions or are disfiguring, little is known about the endocrine consequences of this treatment. Using retrospective data, w...

journal_title：Pediatric dermatology

authors： Lomenick JP,Backeljauw PF,Lucky AW

更新日期：2006-03-01 00:00:00

abstract：:Childhood granulomatous periorificial dermatitis (CGPD) is a condition included in the spectrum of rosacea and perioral dermatitis that affects prepubescent children. It is characterized by papular eruptions located around the mouth, nose, and eyes that histopathologically show a granulomatous pattern. We report a 9-y...

journal_title：Pediatric dermatology

authors： Rodriguez-Caruncho C,Bielsa I,Fernandez-Figueras MT,Ferrándiz C

更新日期：2013-09-01 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：:Superficial granulomatous pyoderma is a rare entity thought to be a variant of pyoderma gangrenosum and is often mistaken for classic pyoderma gangrenosum. Superficial granulomatous pyoderma has mainly been described in adults. We describe a case of Superficial granulomatous pyoderma in an 11-year-old girl and present...

journal_title：Pediatric dermatology

authors： Tollefson MM,Cook-Norris RH,Theos A,Davis DM

更新日期：2010-09-01 00:00:00

abstract：:Trisomy 13, or Patau syndrome, is a chromosomal disorder that can occur in complete, partial, or mosaic forms. Mosaicism is observed in 6% of individuals with trisomy 13 and, in contrast to the complete form, has wide phenotypic variability, longer survival, and in some patients an unusual skin pigmentary pattern simi...

journal_title：Pediatric dermatology

authors： González-del Angel A,Estandia-Ortega B,Gaviño-Vergara A,Sáez-de-Ocariz M,Velasco-Hernández Mde L,Salas-Labadía C

更新日期：2014-09-01 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/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：:Oral-facial-digital syndrome type 1 (OMIM #311200) is an X-linked dominant, developmental disorder. Among the 13 described clinical variants of oral-facial-digital syndrome, oral-facial-digital syndrome type 1 is of significance to dermatologists due to presence of congenital milia and hypotrichosis, not described in ...

journal_title：Pediatric dermatology

authors： Nanda A,Sharaf A,Alsaleh QA

更新日期：2010-11-01 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 report the exceptional case of 11-year-old identical male twins who both developed discoid lupus erythematosus lesions. Although systemic lupus erythematosus has often been reported in identical twins, discoid lupus erythematosus has only occasionally been described, with only one other case in twin children, as fa...

journal_title：Pediatric dermatology

authors： Del Boz J,Martín T,Samaniego E,Vera A,Sanz A,Crespo V

更新日期：2008-11-01 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：:Subcutaneous granuloma annulare is a benign inflammatory disorder that primarily affects healthy children and manifests as a rapidly growing, painless, nonmobile mass, most commonly located in the leg. The current case highlights the sonographic appearance of subcutaneous granuloma annulare. Ultrasound color Doppler i...

journal_title：Pediatric dermatology

authors： Vázquez-Osorio I,Quevedo A,Rodríguez-Vidal A,Rodríguez-Díaz E

更新日期：2018-05-01 00:00:00

abstract：:The epidermal nevus syndrome is a disease complex consisting of the association of an epidermal nevus with various developmental abnormalities of the skin, eyes, nervous, skeletal, cardiovascular, and urogenital systems. The epidermal nevi are classified according to their predominant component; nevus sebaceus (sebace...

journal_title：Pediatric dermatology

authors： Demerdjieva Z,Kavaklieva S,Tsankov N

更新日期：2007-09-01 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：: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：:A congenital curved nail of the fourth toe (NIM 219070) is a rare nail deformity with no other associated abnormalities. Three patients with this congenital anomaly are reported here. Radiologic examination in all three revealed distal symphalangism of the fourth toes bilaterally. The clinical manifestations in these ...

journal_title：Pediatric dermatology

authors： Lin YC,Wu YH,Scher RK

更新日期：2007-07-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Rocky Mountain spotted fever (RMSF), a lethal tick-borne illness, is prevalent in the south central United States. Children younger than 10 years old have the greatest risk of fatal outcome from RMSF. The objective of the current study was to review pediatric cases of RMSF seen in the dermatology ...

journal_title：Pediatric dermatology

authors： Tull R,Ahn C,Daniel A,Yosipovitch G,Strowd LC

更新日期：2017-03-01 00:00:00

abstract：:We describe a new case of a rare syndrome characterized by ocular abnormalities and pathognomonic linear skin defects. This syndrome is the result of an unbalanced translocation resulting in a deletion of the distal end of the short arm of the X chromosome. We report the thirteenth case and review the clinical and cyt...

journal_title：Pediatric dermatology

authors： Paulger BR,Kraus EW,Pulitzer DR,Moore CM

更新日期：1997-01-01 00:00:00

abstract：:We treated a 5-year-old boy with clear-cell hidradenoma of the forearm. Our literature search found only one previous report of this disease occurring during the first decade of life, and the present patient is the first with involvement of the limbs. This presentation demonstrates that clear-cell hidradenoma needs to...

journal_title：Pediatric dermatology

authors： Ozawa T,Fujiwara M,Nose K,Muraoka M

更新日期：2005-09-01 00:00:00

abstract：:Case of an 18-month-old child with congenital lymphedema subsequently diagnosed with tuberous sclerosis and Hirschsprung disease. ...

journal_title：Pediatric dermatology

authors： Lucas M,Andrade Y

更新日期：2011-03-01 00:00:00

abstract：:Lichen planus is a dermatosis of unknown origin with a very limited frequency in children. Over a period of one and a half years we observed 17 cases of childhood lichen planus. The classic form of the disease as seen in adults was the most common in these children; unlike adults, however, mucosal and nail involvement...

journal_title：Pediatric dermatology

authors： Kanwar AJ,Handa S,Ghosh S,Kaur S

更新日期：1991-12-01 00:00:00

abstract：:A 6-year-old Hispanic boy presented to the ophthalmology department with complaints of pain, photophobia, and blurry vision of both eyes. He was found to have bilateral granulomatous panuveitis, cataracts, and high intraocular pressures. He later developed multiple asymptomatic, ovoid, hypopigmented patches over the m...

journal_title：Pediatric dermatology

authors： Hernandez C,LePoole C,Tessler HH

更新日期：2012-03-01 00:00:00