Rat bite fever: fever, arthritis, and rash in a 4-year-old boy.

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：:A boy with junctional epidermolysis bullosa died from acute laryngeal obstruction at the age of 29 months, having been hoarse since early infancy. Post mortem studies showed gross narrowing of the laryngeal airway by cystic dilatations of the ducts of the seromucinous glands, and replacement of the laryngeal epitheliu...

journal_title：Pediatric dermatology

authors： Davies H,Atherton DJ

更新日期：1987-08-01 00:00:00

abstract：:In 1980 a syndrome was first described in two adult males, consisting of macrocephaly, pigmented macules on the glans and shaft of the penis, and hamartomatous intestinal polyps. Since then, 10 additional cases have been identified. Herein, we present two new cases and review the cutaneous manifestations as well as ad...

journal_title：Pediatric dermatology

authors： Gretzula JC,Hevia O,Schachner LS,DiLiberti JH,Ruvalcaba RH,Schimschock JR,Weleber RG,Halal F,Lipson MH,Blumberg B

更新日期：1988-02-01 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：: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：: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：BACKGROUND/OBJECTIVES:Recent technological advances and diagnostic and therapeutic innovations have resulted in an impressive improvement in the survival of newborn infants requiring intensive care. Consequently, with the use of modern invasive diagnostic and therapeutic procedures, the incidence of iatrogenic events h...

journal_title：Pediatric dermatology

authors： Csoma ZR,Meszes A,Ábrahám R,Kemény L,Tálosi G,Doró P

更新日期：2016-09-01 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：:We evaluated two patients with hereditary bullous poikiloderma. Both had acral bullae, generalized poikiloderma with prominent atrophy, and acral keratoses. One patient, with sporadic disease, had, in addition, urethral and subglottic stenoses, webbing of digits, and poor dentition. The other patient, whose disease wa...

journal_title：Pediatric dermatology

authors： Forman AB,Prendiville JS,Esterly NB,Hebert AA,Duvic M,Horiguchi Y,Fine JD

更新日期：1989-06-01 00:00:00

abstract：:Granular cell tumors are uncommon, usually benign tumors of neural origin. They are most often diagnosed in the third to sixth decades of life and are infrequently seen in the pediatric population. Although they can be found in a wide distribution throughout the body, more than half occur in the oral cavity and other ...

journal_title：Pediatric dermatology

authors： Abraham T,Jackson B,Davis L,Yu J,Peterson C

更新日期：2007-05-01 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

abstract：BACKGROUND/OBJECTIVES:Atypical and severe clinical manifestations of primary and recurrent herpes simplex virus (HSV) infections may present to a pediatric dermatologist for evaluation. The purpose of this study was to characterize the clinical features of the population diagnosed with HSV referred to a pediatric derma...

journal_title：Pediatric dermatology

authors： Gittler JK,Mu EW,Orlow SJ

更新日期：2017-07-01 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：:Capillary malformation-arteriovenous malformation syndrome (CM-AVM) is an autosomal dominant disorder caused by heterozygous mutations in RASA1 and EPHB4. Capillary stains in CM-AVM are compatible with Schöbinger's phase I AVMs. Vascular laser has been classically contraindicated for the treatment of AVMs, as there is...

journal_title：Pediatric dermatology

authors： Iznardo H,Roé E,Puig L,Vikula M,López-Sánchez C,Baselga E

更新日期：2020-03-01 00:00:00

abstract：:A 12-year-old girl presented for excision of a nevus sebaceous of the scalp. The surgery was complicated by unexpected difficult-to-control bleeding in the operating room. Numerous attempts to obtain hemostasis were unsuccessful including the use of local anesthetic containing epinephrine, direct pressure, wall suctio...

journal_title：Pediatric dermatology

authors： Bellet JS,Wagner AM

更新日期：2009-09-01 00:00:00

abstract：:Currently wound treatment options of amputation stumps due to purpura fulminans include healing by secondary intention from wound debridement, split-thickness skin grafting, tissue and muscle flaps, plantar skin free transfer, skin expansion, artificial skin, and hyperbaric oxygen therapy. We saw a 6-month-old girl wi...

journal_title：Pediatric dermatology

authors： Greenberg JE,Falabella AF,Bello YM,Schachner LA

更新日期：2003-03-01 00:00:00

abstract：:We report two cases of focal preauricular dermal dysplasia and review the available literature. Focal preauricular dermal dysplasia is a form of aplasia cutis congenita in which atrophic skin lesions occur in a stereotypical bilateral distribution in the preauricular region. Although focal preauricular dermal dysplasi...

journal_title：Pediatric dermatology

authors： Krathen MS,Rosenbach M,Yan AC,Crawford GH

更新日期：2008-05-01 00:00:00

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：BACKGROUND/OBJECTIVES:Sun protection starting in childhood is an important means of skin cancer prevention. Factors associated with sunscreen use have been previously described. However, less is known about factors associated with children's utilization of non-sunscreen sun protection strategies. We sought to examine p...

journal_title：Pediatric dermatology

authors： Schlarbaum JP,Lazovich D,Dodd E,Hanson B,Polcari IC

更新日期：2020-09-01 00:00:00

abstract：:This report documents a possible rabies vaccine-induced erythema multiforme manifestation in a 10-year-old boy. ...

journal_title：Pediatric dermatology

authors： Verma P

更新日期：2013-11-01 00:00:00

abstract：:Nickel allergic contact dermatitis is the most prevalent allergy in North America, with an incidence of 14.3%. It is on the rise from 10 years ago, when the incidence was 10%. This has been presumed to represent an increased exposure to nickel in the environment-especially in costume jewelry and belt buckles. We exami...

journal_title：Pediatric dermatology

authors： Silverberg NB,Licht J,Friedler S,Sethi S,Laude TA

更新日期：2002-03-01 00:00:00

abstract：:Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome is a recently described syndrome similar to Proteus syndrome but lacking the progressive or distorting bony overgrowth of Proteus syndrome. We describe a neonate with features of CLOVE syndrome and nevus unius lateris. ...

journal_title：Pediatric dermatology

authors： Harit D,Aggarwal A

更新日期：2010-05-01 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：: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：:Molluscum contagiosum is a common childhood condition, and although it is self-limited, treatments are often prescribed. Several medications are available, but there is no consensus regarding the optimal choice in the pediatric population. We report a child who underwent potassium hydroxide 5% treatment resulting in s...

journal_title：Pediatric dermatology

authors： Bresesti I,Ciolfi C,Rotatore G,Borisov AN,Zuccotti GV,Brazzelli V

更新日期：2020-01-01 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：: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：: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：: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：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