Handy Hints About Raynaud's Phenomenon in Children: A Critical Review.

abstract：:A 2-year-old boy had hundreds of discrete, small, flat yellow to brown colored papules distributed over the face, neck, and trunk. Biopsy revealed a well-demarcated infiltrate within the papillary dermis composed of histiocytes and some Touton giant cells and eosinophils. The cells were negative for protein S-100 and ...

journal_title：Pediatric dermatology

authors： Torrelo A,Juarez A,Hernández A,Colmenero I

更新日期：2009-03-01 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：:Lymphangioma circumscriptum is a lymphatic malformation that involves the skin and may extend to subcutaneous tissue and muscle. Treatment of these lesions is challenging. Surgical excision may be performed but recurrence is common. Herein we report a child with a symptomatic lymphangioma circumscriptum that was treat...

journal_title：Pediatric dermatology

authors： Lai CH,Hanson SG,Mallory SB

更新日期：2001-11-01 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：: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：: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：:The proband in this study was a 4-year-old Mexican girl with Blau syndrome. She and her affected family members had skin rash and arthritis but no uveitis. Exome sequencing and DNA direct sequencing from blood samples revealed a novel nucleotide-binding oligomerization domain-containing protein 2 gene mutation in the ...

journal_title：Pediatric dermatology

authors： Toral-López J,González-Huerta LM,Martín-Del Campo M,Messina-Baas O,Cuevas-Covarrubias SA

更新日期：2018-05-01 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：: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：: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：:Although the prognosis of maculopapular cutaneous mastocytosis (MPCM), also referred to as urticaria pigmentosa, is often benign, clinicians lack evidence to reliably predict those at risk of associated systemic manifestations. We sought to elucidate clinical markers of disease severity to provide better treatment and...

journal_title：Pediatric dermatology

authors： Barnes M,Van L,DeLong L,Lawley LP

更新日期：2014-05-01 00:00:00

abstract：:Juvenile xanthogranuloma is a benign, self-healing disorder with characteristic lesions mainly involving the skin. Although most patients with juvenile xanthogranuloma have only cutaneous symptoms, recent articles have documented extracutaneous manifestations: systemic involvement of many organs has been reported and ...

journal_title：Pediatric dermatology

authors： Aparicio G,Mollet J,Bartralot R,Bodet D,Heras C,Bassas P,Virós A,García-Patos V

更新日期：2008-07-01 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：:We report a 5-month-old girl diagnosed with bullous pemphigoid who initially did not respond to systemic corticosteroids and dapsone but rapidly improved after the addition of intravenous immunoglobulin (IVIG) infusions. A literature search revealed anecdotal cases of infantile bullous pemphigoid treated with IVIG, al...

journal_title：Pediatric dermatology

authors： Tekin B,Yücelten AD

更新日期：2015-09-01 00:00:00

abstract：:Red-brown papules developing during the neonatal period may present a diagnostic dilemma. The Darier sign has been a reliable feature in the diagnosis of mastocytosis. However, the cutaneous infiltrate of Hashimoto-Pritzker Langerhans cell histiocytosis (LCH) may contain a large number of mast cells, leading to confus...

journal_title：Pediatric dermatology

authors： Butler DF,Ranatunge BD,Rapini RP

更新日期：2001-01-01 00:00:00

abstract：:The first report of spinous follicular lichen nitidus with perifollicular granulomas was by Madhok and Winkelmann in 1988. Since this report, a few cases of follicular or periappendageal lichen nitidus have been described, in a more localized form or without perifollicular granulomas. We describe a 5-year-old girl wit...

journal_title：Pediatric dermatology

authors： Summe HS,Greenlaw SM,Deng A,Magro C,Wiss K

更新日期：2013-05-01 00:00:00

abstract：:Skin prick tests were performed in 12 children with atopic eczema before and after 2 weeks of treatment with topical mometasone furoate and tacrolimus. Both treatments significantly suppressed the allergen wheal size. Mometasone furoate reduced the histamine wheal size as well. Skin prick testing in children treated w...

journal_title：Pediatric dermatology

authors： Gradman J,Wolthers OD

更新日期：2008-03-01 00:00:00

abstract：:A newborn girl had typical "blueberry muffin" skin lesions, which showed histopathologic features of myelomonocytic leukemia cutis. We could not demonstrate leukemic infiltration of bone marrow in four aspirates. Her course was complicated with primary pulmonary hypertension, which led to death at 7 months of age. We ...

journal_title：Pediatric dermatology

authors： Torrelo A,Madero L,Mediero IG,Baño A,Zambrano A

更新日期：2004-07-01 00:00:00

abstract：:Stevens-Johnson syndrome is a potentially fatal condition that manifests mainly on the skin and mucosal surfaces but also affects other vital organs. There are no report of Stevens-Johnson syndrome caused by brucella infection in the literature. In this article, a previously healthy boy, diagnosed as Stevens-Johnson s...

journal_title：Pediatric dermatology

authors： Babayigit A,Olmez D,Uzuner N,Caglayan S,Kumral A,Asilsoy SK,Ozer E,Karaman O

更新日期：2007-07-01 00:00:00

abstract：:Skin diseases are common in children. However, only a very few prospective epidemiologic surveys are available in the literature. The present survey was directed at determining the spectrum and pattern of skin diseases of children in Kuwait. A total of 10,000 consecutive new patients were studied; 96% were children of...

journal_title：Pediatric dermatology

authors： Nanda A,Al-Hasawi F,Alsaleh QA

更新日期：1999-01-01 00:00:00

abstract：:A case of an accessory tragus located on the nasal vestibule is reported. This represents the third case of this entity located outside of a derivative of a branchial arch. All three of these cases were located in the nose/glabella region. ...

journal_title：Pediatric dermatology

authors： Moradi S,Castiglione C,Ehrig T

更新日期：2020-03-01 00:00:00

abstract：:We aimed to better understand the pathogenesis, clinical features, prognosis, and treatment of neonatal autoimmune blistering diseases (AIBDs). We searched Medline, Embase, PubMed, Latin American and Caribbean Health Sciences Literature, and reference lists of identified articles. Inclusion criteria were articles publ...

journal_title：Pediatric dermatology

authors： Zhao CY,Chiang YZ,Murrell DF

更新日期：2016-07-01 00:00:00

abstract：:We report a case of lichenoid sarcoidosis in a 3-year-old girl. She had numerous discrete skin-colored or erythematous, infiltrated follicular papules on the buttocks and extremities since 2 months of age. Histopathologic examination showed follicular plugging and an upper dermal granulomatous infiltrate of epithelioi...

journal_title：Pediatric dermatology

authors： Seo SK,Yeum JS,Suh JC,Na GY

更新日期：2001-09-01 00:00:00

abstract：:Scurvy, or hypovitaminosis C, is an uncommon condition that exists today primarily within certain unique populations-particularly the elderly subjects, patients with neurodevelopmental disabilities or psychiatric illnesses, or others with unusual dietary habits. Vitamin C is an essential nutrient in the human body, an...

journal_title：Pediatric dermatology

authors： Cole JA,Warthan MM,Hirano SA,Gowen CW Jr,Williams JV

更新日期：2011-07-01 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：:Post-transplantation lymphoproliferative disorder (PTLD) is one of the most common de novo malignancies in patients who receive immunosuppressive therapy after solid organ transplantation. We report a case of a 5-year-old girl who presented with indurated violaceous skin nodules 3.5 years post-liver transplantation, d...

journal_title：Pediatric dermatology

authors： Chen KY,Lin CY,Kuo TT,Shih LY,Chang CH,Chen WT,Yang CY

更新日期：2019-09-01 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

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：:Bullous pemphigoid (BP) is the most common autoimmune blistering disease affecting the elderly but is quite rare in childhood. The majority of pediatric cases have been reported during early childhood. Adolescence is divided into three phases: early (10-13 years), middle (14-17), and late (18-21). This review aimed to...

journal_title：Pediatric dermatology

authors： Patsatsi A,Kyriakou A,Werth VP

更新日期：2019-03-01 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