Acute genital ulcers in nonsexually active young girls: case series, review of the literature, and evaluation and management recommendations.

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：:Acquired ichythosis has been described in adult hematopoietic stem cell transplant recipients. While some authors have suggested the association of acquired ichythosis with cutaneous graft-versus-host disease, the evidence to support this association is rare. We describe a patient who developed enteritis secondary to ...

journal_title：Pediatric dermatology

authors： Huang J,Pol-Rodriguez M,Silvers D,Garzon MC

更新日期：2007-01-01 00:00:00

abstract：BACKGROUND:Spiny hyperkeratosis refers to a rare clinical phenotype characterized by nonfollicular keratotic projections and sometimes associated with other acquired and inherited conditions. We describe a case of congenital patterned spiny hyperkeratosis. METHODS:To identify the cause of this disorder, we used a comb...

journal_title：Pediatric dermatology

authors： Eskin-Schwartz M,Metzger Y,Peled A,Weissglas-Volkov D,Malchin N,Gat A,Vodo D,Mevorah B,Shomron N,Sprecher E,Sarig O

更新日期：2016-05-01 00:00:00

abstract：:Rapidly involuting congenital hemangioma is a subtype of congenital hemangioma. Ulceration and bleeding are rarely reported in rapidly involuting congenital hemangioma, with only four cases reported in the literature to our knowledge. We describe a case of a newborn girl who presented with rapidly involuting congenita...

journal_title：Pediatric dermatology

authors： Al Malki A,Al Bluwi S,Malloizel-Delaunay J,Mazereeuw-Hautier J

更新日期：2018-05-01 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：:Although papulonecrotic tuberculid is an uncommon cutaneous manifestation of tuberculosis (TB) associated with Mycobacterium tuberculosis infection, the simultaneous occurrence of papulonecrotic tuberculid and erythema induratum is even rarer. Papulonecrotic tuberculid occurs predominantly in young adults and is chara...

journal_title：Pediatric dermatology

authors： Kim GW,Park HJ,Kim HS,Chin HW,Kim SH,Ko HC,Kim MB,Kim BS

更新日期：2013-03-01 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：: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：:Dyshidrotic eczema is one of the rare cutaneous adverse effects of intravenous immunoglobulin therapy, usually seen in adults. We herein report the first pediatric case of severe dyshidrotic eczema occurring after intravenous immunoglobulin therapy for Kawasaki syndrome. ...

journal_title：Pediatric dermatology

authors： Shiraishi T,Yamamoto T

更新日期：2013-05-01 00:00:00

abstract：:Benign fibrous histiocytoma is a common soft tissue tumor that usually occurs in adults and is relatively rare in childhood. This report describes a 7-month-old Caucasian boy with an enlarging firm congenital nodule on his occipital scalp. Histologic analysis revealed a benign fibrous histiocytoma with osteoclast-like...

journal_title：Pediatric dermatology

authors： Stinehelfer SE,Woosley JT,Losken HW,Morrell DS

更新日期：2007-09-01 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：:The most common cause of death in blue rubber bleb nevus syndrome is gastrointestinal bleeding. Here we present a case of central nervous system bleeding that resulted in death. ...

journal_title：Pediatric dermatology

authors： Ocampo-Garza J,Salas-Alanís JC,Ponce-Camacho MA,Rosales-Solis GM,Miranda Maldonado I,Elizondo-Riojas G,Villanueva-Nava D,Barbosa-Quintana O,Gonzalez Colunga K,Ocampo-Candiani J

更新日期：2016-01-01 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：:Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report a 13-year-old girl with extensive lupus panniculitis since the age of 8 months and no e...

journal_title：Pediatric dermatology

authors： Nousari HC,Kimyai-Asadi A,Santana HM,Diglio GM,Tausk FA,Cohen BA

更新日期：1999-07-01 00:00:00

abstract：:A new type of organoid epidermal nevus, characterized by the presence of multiple trichilemmal cysts disposed in a linear arrangement, was recently recognized and named nevus trichilemmocysticus. We report a 10-year-old girl with a congenital linear dermatosis affecting the head, neck, trunk, limbs, palms, and soles. ...

journal_title：Pediatric dermatology

authors： Larralde M,Boggio P,Abad ME,Corbella C,Happle R

更新日期：2011-05-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Drug reaction with eosinophilia and systemic symptoms (DRESS) is rare but potentially fatal in children. Fever and rash, which are salient features of DRESS, may mimic other commonly encountered pediatric conditions. We profiled the DRESS cases in a tertiary children's hospital in Singapore. METH...

journal_title：Pediatric dermatology

authors： Han XD,Koh MJ,Wong SMY

更新日期：2019-05-01 00:00:00

abstract：:Eosinophilic pustular folliculitis of infancy is a rare inflammatory disease characterized by recurrent, itchy sterile pustules mainly located on the scalp. Topical agents are mostly effective to suppress the symptoms in the majority of cases. However, systemic agents that are safe for long-term use are required for p...

journal_title：Pediatric dermatology

authors： Odyakmaz Demirsoy E,Demirsoy U,Ozod U,Kiran R

更新日期：2019-05-01 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：: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：:Cutaneous tuberculosis is a rare form of extrapulmonary tuberculosis that accounts for 1% to 2% of cases. Childhood skin tuberculosis represents 18% to 82% of all cutaneous tuberculosis cases. Scrofuloderma and lupus vulgaris are the two most common clinical forms in children. An increase in the number of tuberculids,...

journal_title：Pediatric dermatology

authors： Sethuraman G,Ramesh V

更新日期：2013-01-01 00:00:00

abstract：:Clinical and pathologic features of five cases of epidermolysis bullosa simplex, Dowling-Meara type (EBS-DM), are described. Four patients were children, and two were related (father and daughter). Clinical history revealed blistering at birth in three patients; in all of them the signs and symptoms improved with age....

journal_title：Pediatric dermatology

authors： Puddu P,Angelo C,Faraggiana T,Onetti Muda A,Colonna L,Paradisi M

更新日期：1996-05-01 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：:Langerhans cell histiocytosis (LCH) is a rare disorder characterized by clonal proliferation of Langerhans cells in the skin. A molluscum-like presentation of cutaneous LCH is rare but important to consider for examination and management. We present an atypical molluscum-like LCH case and review the literature for com...

journal_title：Pediatric dermatology

authors： Karpman MS,AlJasser MI,Lam JM

更新日期：2017-09-01 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：: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：: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：:Infantile hemangiomas are the most common benign vascular tumors in childhood. Propranolol is the first-line treatment for infantile hemangiomas, but failures may occur. Sirolimus, an mTOR inhibitor, is a promising drug for the treatment of vascular malformations and vascular tumors. We present the case of a child wit...

journal_title：Pediatric dermatology

authors： Dávila-Osorio VL,Iznardo H,Roé E,Puig L,Baselga E

更新日期：2020-07-01 00:00:00

abstract：:The reported data on the association of kidney and urinary tract malformations with supernumerary nipples are contradictory. We examined 200 children, ages 1 month-16 years, who were being followed because of recurrent urinary tract infection for supernumerary nipples. The patients were divided into two groups: those ...

journal_title：Pediatric dermatology

authors： Grotto I,Browner-Elhanan K,Mimouni D,Varsano I,Cohen HA,Mimouni M

更新日期：2001-07-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Bullous impetigo (BI) is a common dermatologic condition, particularly in children, yet confusion regarding its diagnosis and treatment persists. This study measured pediatricians' ability to diagnose and appropriately treat BI and explored factors that might influence pediatricians' accuracy in m...

journal_title：Pediatric dermatology

authors： Simkin DJ,Grossberg AL,Cohen BA

更新日期：2016-11-01 00:00:00

abstract：:An unselected cohort of 4,641 newborns was ascertained prospectively for the purpose of detecting any cutaneous lesion. These were catalogued into pigmented lesions, vascular lesions, and miscellaneous lesions. Several important findings were elucidated: congenital nevocellular nevi are speckled at their borders; no w...

journal_title：Pediatric dermatology

authors： Alper JC,Holmes LB

更新日期：1983-07-01 00:00:00