Vitamin a deficiency phrynoderma associated with chronic giardiasis.

abstract：:Computerized tomography (CT) of the brain was performed in 10 of 11 consecutive infants with neonatal lupus erythematosus (NLE) (five boys and six girls). Ten of the 11 infants had brain neurosonography. Nine of 10 infants had abnormal CT scans. There was diffuse, markedly reduced attenuation of the cerebral white mat...

journal_title：Pediatric dermatology

authors： Prendiville JS,Cabral DA,Poskitt KJ,Au S,Sargent MA

更新日期：2003-01-01 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：:Although the white coat is central to the practice of adult medicine, pediatricians often shed it to avoid creating negative associations and provoking fear in children. In our pediatric dermatology practice, the fanny pack (FP) has replaced many of the functional elements of the white coat. The FP is a kid-friendly w...

journal_title：Pediatric dermatology

authors： Habeshian K,Kirkorian AY,Marathe K

更新日期：2017-05-01 00:00:00

abstract：:Nipple adenoma is an uncommon proliferative process of the breast and predominantly occurs in women aged 40-50. Its incidence is extremely low in men, and it has not been reported in a boy. Although nipple adenoma is rare and benign, being familiar with it is important because it clinically resembles Paget disease and...

journal_title：Pediatric dermatology

authors： Fujisawa K,Kato M,Kono T,Utsunomiya H,Watanabe A,Watanabe S

更新日期：2018-05-01 00:00:00

abstract：:Trichothiodystrophy is characterized by sparse, short, sulfur-deficient hair. Numerous symptom complexes have been described in which the hair abnormality represents a constant feature. We report a boy with trichothiodystrophy, ichthyotic skin changes, onychodystrophy, chronic neutropenia, osteosclerosis, hypothyroidi...

journal_title：Pediatric dermatology

authors： Hersh JH,Klein LR,Joyce MR,Hordinsky MK,Tsai MY,Paller A,Hyzer R,Zax RH

更新日期：1993-06-01 00:00:00

abstract：:Diaper dermatitis is the most common contact eczema present in early childhood. The main cause is an irritant reaction to urine and feces, which is facilitated by the occlusive conditions under the diaper, leading to hyperhydration of the stratum corneum (diaper dermatitis). In addition, diaper pressure and friction c...

journal_title：Pediatric dermatology

authors： Fölster-Holst R

更新日期：2018-03-01 00:00:00

abstract：:Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder that is caused by a DNA repair defect. It is characterized mainly by skin, eye, and skeletal abnormalities. Cutaneous changes appear at between 3 and 6 months of age and include poikiloderma, photosensitivity, scaling, hyperkeratosis, and disturban...

journal_title：Pediatric dermatology

authors： Narayan S,Fleming C,Trainer AH,Craig JA

更新日期：2001-05-01 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：:Vitiligo is a common acquired progressive depigmenting condition that can have devastating psychological effects in dark-skinned patients. We performed a retrospective review of patients younger than 16 years of age with a clinical diagnosis of vitiligo treated using phototherapy at the National Skin Center, Singapore...

journal_title：Pediatric dermatology

authors： Koh MJ,Mok ZR,Chong WS

更新日期：2015-03-01 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：:Henoch-Schönlein purpura (HSP) is an acute systemic vasculitis with unknown etiology, although several studies have found HSP to be related to cytokines such as tumor necrosis factor α, interleukin (IL)-1, and adhesion molecules. In the present study we determined the levels of cytokines such as IL-18 and endothelin-1...

journal_title：Pediatric dermatology

authors： Mahajan N,Kapoor D,Bisht D,Singh S,Minz RW,Dhawan V

更新日期：2013-11-01 00:00:00

abstract：:X-linked chronic granulomatous disease (CGD), a defect of leukocyte bactericidal capacity, was seen in three generations of a large kindred. The association of discoid lupus erythematosus (DLE) with CGD was noted. Recurrent antigenic stimulation leading to autoantibody formation may explain the apparently increased fr...

journal_title：Pediatric dermatology

authors： Barton LL,Johnson CR

更新日期：1986-11-01 00:00:00

abstract：:Acne fulminans is a severe form of acne vulgaris accompanied by systemic symptoms. A 17-year-old Chinese boy presented with an outbreak of necrotic lesions on his face eight days after the onset of palpable purpura, arthralgia, fever, abdominal pain, and proteinuria. He was successfully treated with oral prednisolone ...

journal_title：Pediatric dermatology

authors： Xu X,Li X,Pradhan S,Li W

更新日期：2020-11-01 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：:An 8-month-old Caucasian infant with neurofibromatosis type 1 presented with a congenital plexiform neurofibroma and multiple café au lait spots. A pale area surrounded one of the café au lait spots located on the left gluteus in the area of dermal melanocytosis. This halolike phenomenon results from the disappearance...

journal_title：Pediatric dermatology

authors： Neri I,Lambertini M,Tengattini V,Rivalta B,Patrizi A

更新日期：2017-05-01 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 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：: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：:Accessory scrotum is an extremely rare congenital scrotal anomaly defined as the occurrence of scrotal skin outside of its proper location with no testicular tissue. We report a preterm twin male infant who had an accessory scrotum located on the right inguinal and proximal femoral region. ...

journal_title：Pediatric dermatology

authors： Korkmaz A,Tekinalp G,Aygün C,Sahin S

更新日期：1999-03-01 00:00:00

abstract：:Onychomycosis is widespread in the adult population, but considered to be rare in children. A number of studies in recent years show a rise in the prevalence of toenail onychomycosis in children. Of these, only a few were population-based. Here, we present a comprehensive cross-sectional population-based survey of toe...

journal_title：Pediatric dermatology

authors： Leibovici V,Evron R,Dunchin M,Westerman M,Ingber A

更新日期：2009-01-01 00:00:00

abstract：:Hidradenitis suppurativa is a chronic relapsing disorder of follicular occlusion that is often recalcitrant to therapy. Topical and systemic antibiotics, hormonal therapies, oral retinoids, immunosuppressant agents, and surgical treatment are some of the therapeutic alternatives used for this often recalcitrant and fr...

journal_title：Pediatric dermatology

authors： Lam J,Krakowski AC,Friedlander SF

更新日期：2007-09-01 00:00:00

abstract：BACKGROUND:In recent years propranolol has become the treatment of choice for infantile hemangiomas (IHs). There is broad variation in the approach to propranolol initiation in clinical practice. This retrospective study explored the effectiveness of routine pre-treatment ECG in screening infants being considered for s...

journal_title：Pediatric dermatology

authors： Yarbrough KB,Tollefson MM,Krol AL,Leitenberger SL,Mann JA,MacArthur CJ

更新日期：2016-11-01 00:00:00

abstract：:The keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of the ectoderm characterized by diffuse hyperkeratotic erythroderma, keratitis with neovascularization of the cornea, and severe neurosensory hearing loss. A familial occurrence of this syndrome has been mentioned in four reports inc...

journal_title：Pediatric dermatology

authors： Koné-Paut I,Hesse S,Palix C,Rey R,Rémédiani K,Garnier JM,Berbis P

更新日期：1998-05-01 00:00:00

abstract：:Knowledge of the molecular underpinnings of many epidermal nevi and epidermal nevus syndrome has expanded rapidly in recent years. In this review and update on epidermal nevus syndrome, we will cover recent genetic discoveries involving epidermal nevi, including nevus sebaceus, keratinocytic epidermal nevus, nevus com...

journal_title：Pediatric dermatology

authors： Asch S,Sugarman JL

更新日期：2018-01-01 00:00:00

abstract：:Verruciform xanthoma (VX) is a rare finding thought to be caused by epidermal damage from trauma or inflammation and has been reported in a limited number of patients with recessive dystrophic epidermolysis bullosa (RDEB). Herein, we describe a 20-year-old woman with RDEB who developed a large, verrucous, pink plaque ...

journal_title：Pediatric dermatology

authors： Stephens M,Rubin AI,Perman MJ

更新日期：2020-03-01 00:00:00

abstract：BACKGROUND:Acrodermatitis acidemica is a recently proposed term for the rash that is similar to acrodermatitis enteropathica, which is encountered in organic acidemias. However, acrodermatitis enteropathica-like eruption may be seen in metabolic disorders other than organic acidemias. OBJECTIVE:The aim of this study w...

journal_title：Pediatric dermatology

authors： Tabanlioğlu D,Ersoy-Evans S,Karaduman A

更新日期：2009-03-01 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：:The present study aimed to investigate the prevalence of atopic dermatitis in primary schoolchildren in Denizli, Turkey, and to determine the possible risk factors for atopic dermatitis in home environment. A self-administered questionnaire was handled to the parents of 2,100 children aged 7 to 15 years, from three ra...

journal_title：Pediatric dermatology

authors： Ergin S,Ozşahin A,Erdoğan BS,Aktan S,Zencir M

更新日期：2008-05-01 00:00:00

abstract：:An adolescent boy whose initial presentation consisted of an asymmetric, nonvesicular rash was eventually diagnosed with dermatitis herpetiformis (DH). Certain factors, including lesions limited to the genitals, an initial biopsy revealing nonspecific findings on microscopy studies, and the absence of characteristic d...

journal_title：Pediatric dermatology

authors： Clark K,Powers R,Kovach R

更新日期：2014-07-01 00:00:00

abstract：:Phacomatosis pigmentovascularis is characterized by coexistent extensive cutaneous vascular (capillary) and pigmentary anomalies. We describe a 2-month-old infant presenting with classic features of phacomatosis pigmentovascularis 2b (phacomatosis cesioflammea). He was also found to have hitherto unreported associatio...

journal_title：Pediatric dermatology

authors： Singal A,Mittal H,Aggarwal A,Das S,Manchanda S

更新日期：2018-05-01 00:00:00