Leukemia cutis and facial nerve palsy as presenting symptoms of acute lymphoblastic leukemia.

abstract：:Dermal mucinosis occurred in a 3-month-old and persisted for six years. The features suggest is represents a novel type of childhood mucinosis. ...

journal_title：Pediatric dermatology

authors： Calza AM,Masouyé I,Saurat JH

更新日期：1994-09-01 00:00:00

abstract：:Pemphigus herpetiformis (PH) is a rare autoimmune bullous condition usually seen in adults and likely underrecognized in children. We describe a 2-year-old girl who presented with a chronic, generalized, blistering rash consistent with pediatric PH based on histology and immunohistochemistry and review the literature....

journal_title：Pediatric dermatology

authors： Peterman CM,Vadeboncoeur S,Schmidt BA,Gellis SE

更新日期：2017-05-01 00:00:00

abstract：:Epidermodysplasia verruciformis (EV) manifests early in childhood as pityriasis versicolor (PV)-like macules on sun-exposed sites such as the face. These hypopigmented lesions closely resemble commoner pediatric dermatoses such as PV or pityriasis alba. In this report of two cases, we describe the distinguishing dermo...

journal_title：Pediatric dermatology

authors： Afra TP,Vinay K,Razmi T M,Khader A,Hafi NAB

更新日期：2020-01-01 00:00:00

abstract：:Fixed drug eruption (FDE) is manifested as localized, circumscribed, round or oval plaques that characteristically recur in the same site with each use of the offending drug. The drugs most commonly implicated are phenolphthalein, barbiturates, antibiotics, salicylates, contraceptives, and anticonvulsants. FDE can app...

journal_title：Pediatric dermatology

authors： Nussinovitch M,Prais D,Ben-Amitai D,Amir J,Volovitz B

更新日期：2002-05-01 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：:Halo dermatitis is a pruritic, eczematous eruption on pigmented nevi and halo nevi in young adults. It may be mistaken for nummular eczema, psoriasis, or fungal skin infection. Awareness of halo dermatitis will possibly reveal more cases in children, which have been reported only rarely. ...

journal_title：Pediatric dermatology

authors： Shifer O,Tchetchik R,Glazer O,Metzker A

更新日期：1992-09-01 00:00:00

abstract：:We report a case of congenital hypertrichosis and FOXN1 duplication. FOXN1 is a member of the forkhead box gene family, located on chromosome 17. Its function includes differentiation of epithelial cells and regulation of keratinocytes, especially hair keratins. Loss of function of these transcription factors leads to...

journal_title：Pediatric dermatology

authors： Gilhooley E,Gormally S,Irvine A,Lynch SA,Collins S

更新日期：2017-03-01 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：: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：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：: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：: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：: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：:A 5-year-old boy developed hemorrhagic mucocutaneous blisters on various parts of the body leading to fetor, dysphagia, dysuria, anal pruritus, pain on defecation, and weight loss. The histopathology showed the classic features of pemphigus vulgaris, and direct immunofluorescence showed intercellular deposition of IgG...

journal_title：Pediatric dermatology

authors： Bjarnason B,Skoglund C,Flosadóttir E

更新日期：1998-09-01 00:00:00

abstract：:We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous p...

journal_title：Pediatric dermatology

authors： Musumeci ML,Nasca MR,De Pasquale R,Schwartz RA,Micali G

更新日期：2006-05-01 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：:The Goeckerman regimen (GR) represents a local treatment of psoriasis and includes topical dermal application of crude coal tar (containing polycyclic aromatic hydrocarbons) and exposure to UV-irradiation. The aim of the study was to evaluate contribution of GR to genotoxic risk and cellular stress in pediatric patien...

journal_title：Pediatric dermatology

authors： Borska L,Andrys C,Krejsek J,Hamakova K,Kremlacek J,Ettler K,Vellappally S,Vimal J,Fiala Z

更新日期：2009-01-01 00:00:00

abstract：:Allergic contact dermatitis reaction to topical "black henna" tattoo is usually described secondary to the organic dye para-phenylenediamine, a derivative of analine. Allergic contact dermatitis reactions to para-phenylenediamine are well recognized and most commonly involve an eczematous reaction that may become gene...

journal_title：Pediatric dermatology

authors： Sidwell RU,Francis ND,Basarab T,Morar N

更新日期：2008-03-01 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：: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：:Hair loss and thinning are possible complications in those undergoing endocrine therapies with aromatase inhibitors. Alopecia in pediatric patients undergoing endocrine therapy has not been previously reported. We describe two adolescents, 14 and 16 years of age, who developed androgenetic alopecia following treatment...

journal_title：Pediatric dermatology

authors： Perper M,Herskovitz I,Tosti A

更新日期：2020-11-01 00:00:00

abstract：:Lichen planus is an uncommonly encountered dermatosis in children. In the present study of 50 children the limbs were the most common site of involvement (70.0%). A majority of the children (60.0%) presented with the classic form of the disease. Hypertrophic lesions were present in 26.0% of children while linear lesio...

journal_title：Pediatric dermatology

authors： Sharma R,Maheshwari V

更新日期：1999-09-01 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：:Early recognition of the hyperlipoproteinemias is a crucial element in preventing premature coronary artery disease. Xanthomas provide a cutaneous marker of the silent, underlying pathology. Identifying them, and understanding their relation to the inherited hyperlipoproteinemias may facilitate early diagnosis of hype...

journal_title：Pediatric dermatology

authors： Maher-Wiese VL,Marmer EL,Grant-Kels JM

更新日期：1990-09-01 00:00:00

abstract：INTRODUCTION:Extravasation injuries are a common and challenging problem in hospitalized newborns. Accidental infusion leakage into the surrounding tissues in immature infants may frequently result in skin necrosis, with significant risk of functional and cosmetic impairment. MATERIAL AND METHODS:In the present study ...

journal_title：Pediatric dermatology

authors： Kostogloudis N,Demiri E,Tsimponis A,Dionyssiou D,Ioannidis S,Chatziioannidis I,Nikolaidis N

更新日期：2015-11-01 00:00:00

abstract：:We recently encountered a 2-year-old boy with slightly infiltrative brown papules on the face, trunk, and extremities. Stroking of one of the papules produced an urticarial wheal (positive Darier's sign). Histopathologic tests revealed a dense infiltration of mast cells containing numerous granules and showing metachr...

journal_title：Pediatric dermatology

authors： Mitsuya J,Hara H,Fukuda N,Terui T

更新日期：2011-07-01 00:00:00

abstract：:Cranioectodermal dysplasia is a rare syndrome characterized by craniofacial and skeletal anomalies and ectodermal dysplasia. Life-threatening associated conditions (i.e., kidney failure and abnormal regulation of the parathyroid-bone axis) can also develop. We report a patient whose features are suggestive of an inapp...

journal_title：Pediatric dermatology

authors： Zannolli R,Mostardini R,Carpentieri ML,Gatti MG,Galluzzi P,Terrosi Vagnoli P,Giorgetti R,Calvieri S,Morgese G

更新日期：2001-07-01 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 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：BACKGROUND:Topical occlusive agents, such as petroleum jelly and silicone oils, kill head lice by coating and blocking its excretory system and are unlikely to induce treatment resistance. Although a popular alternative to neurotoxic pediculicides, their efficacy and safety remain unclear. METHODS:We searched CENTRAL,...

journal_title：Pediatric dermatology

authors： Flores-Genuino RNS,Gnilo CMS,Dofitas BL

更新日期：2020-01-01 00:00:00