Hypomelanosis of ito-whorled hyperpigmentation combination: a mirror image presentation.

abstract：:The epidermal nevus syndrome is a disease complex consisting of the association of an epidermal nevus with various developmental abnormalities of the skin, eyes, nervous, skeletal, cardiovascular, and urogenital systems. The epidermal nevi are classified according to their predominant component; nevus sebaceus (sebace...

journal_title：Pediatric dermatology

authors： Demerdjieva Z,Kavaklieva S,Tsankov N

更新日期：2007-09-01 00:00:00

abstract：:Polycystic ovary syndrome (PCOS) is an endocrine syndrome with variable phenotypic expression and important systemic associations and sequelae, including obesity, insulin resistance, infertility, risk of endometrial cancer, and possible risk of cardiovascular events. PCOS is recognized as a condition influenced by gen...

journal_title：Pediatric dermatology

authors： Kamangar F,Okhovat JP,Schmidt T,Beshay A,Pasch L,Cedars MI,Huddleston H,Shinkai K

更新日期：2015-09-01 00:00:00

abstract：:Psychologic factors may play a significant role in acne in at least three ways. First, as many patients readily report, emotional stress can exacerbate acne. Second, it is common for patients to develop psychiatric problems as a consequence of the conditions, such as those related to low self-esteem, social phobias, o...

journal_title：Pediatric dermatology

authors： Koo JY,Smith LL

更新日期：1991-09-01 00:00:00

abstract：:This article reviews skin changes occurring in diabetic children. Skin changes may be related to metabolic alterations associated with diabetes. Others may be manifestations of macro or microvascular disease. Insulin injections, required for management of most diabetes in the pediatric age group, may also cause cutane...

journal_title：Pediatric dermatology

authors： Edidin DV

更新日期：1985-03-01 00:00:00

abstract：:Aplasia cutis congenita (ACC) is a congenital defect consisting of a circumscribed absence of skin that usually involves the scalp. The etiology is uncertain, and several teratogenic agents such as methimazole have been involved. We report two cases of ACC and other anomalies in newborns exposed to methimazole during ...

journal_title：Pediatric dermatology

authors： Rodríguez-García C,González-Hernández S,Hernández-Martín A,Pérez-Robayna N,Sánchez R,Torrelo A

更新日期：2011-11-01 00:00:00

abstract：:A newborn male Thai infant had numerous brownish red nodules of various sizes scattered over both palms and soles, left thigh, abdomen, chin, and left upper eyelid. An extremely large tumor mass was present on the right sole. Many lesions showed spontaneous ulceration. No extracutaneous involvement was found. All lesi...

journal_title：Pediatric dermatology

authors： Timpatanapong P,Rochanawutanon M,Siripoonya P,Nitidandhaprabhas P

更新日期：1989-03-01 00:00:00

abstract：:Corticosteroids and photochemotherapy, using a combination of psoralen and ultraviolet A (PUVA) exposure, are the most widely prescribed therapies for vitiligo. These treatments are not uniformly effective and many patients have inadequate responses. Calcipotriene has been shown to be effective in adults and children ...

journal_title：Pediatric dermatology

authors： Travis LB,Silverberg NB

更新日期：2004-07-01 00:00:00

abstract：:Acute genital ulcers rarely occur in nonsexually active young girls. When present, they can cause significant physical and emotional distress for the patient and her parents, and prompt an evaluation for sexual abuse and sexually transmitted diseases. With this review, we aim to further characterize acute genital ulce...

journal_title：Pediatric dermatology

authors： Rosman IS,Berk DR,Bayliss SJ,White AJ,Merritt DF

更新日期：2012-03-01 00:00:00

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：:Rat bite fever is a rare but potentially fatal Gram-negative infection that predominantly affects populations with exposure to rats, notably children. The clinical presentation is nonspecific and requires a high threshold of suspicion to elicit a history of rat exposure. We report here a case of a child whose diagnosi...

journal_title：Pediatric dermatology

authors： Lewis BK,Vanderhooft S

更新日期：2012-11-01 00:00:00

abstract：:Microcomedonal lesions can be aesthetically and psychologically displeasing. The burden of comedones increases when considering their frequency and demand for time-consuming attention. The objective of the current study was to describe a novel technique to facilitate open microcomedone extraction. The instrumentation ...

journal_title：Pediatric dermatology

authors： Naimer SA

更新日期：2016-11-01 00:00:00

abstract：:Transient reactive papulotranslucent acrokeratoderma is a rare palmoplantar keratoderma seen predominantly in adolescent and young adult women. Clinically it is characterized by translucent white papules generally involving the palmar surfaces after exposure to water. The typical "hands-in-the-bucket" sign, which is n...

journal_title：Pediatric dermatology

authors： Neri I,Bianchi F,Patrizi A

更新日期：2006-01-01 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：:Aplasia cutis congenita (ACC) is characterized by the complete or partial absence of skin at birth, with 85% of cases of ACC involving the scalp vertex. The etiology of ACC is unclear and appears to be multifactorial. We present the case of a 3-month-old boy who presented with a diagnosis of non-scalp ACC affecting ap...

journal_title：Pediatric dermatology

authors： Davis MJ,Voller LM,Gonzalez SR,Abu-Ghname A,Davies LW,Bedwell JR,Lee GL,Hunt RD,Phung TL,Buchanan EP

更新日期：2021-01-22 00:00:00

abstract：:Striated muscle hamartoma is a rare entity which was described only recently. It is a congenital malformation characterized by the presence of striated, mature muscle fibers in the reticular dermis and hypodermis. We describe a striated muscle hamartoma of the perianal region in a female infant associated with an hema...

journal_title：Pediatric dermatology

authors： Scrivener Y,Petiau P,Rodier-Bruant C,Cribier B,Heid E,Grosshans E

更新日期：1998-07-01 00:00:00

abstract：:Although lentigines are usually benign, they can be associated with a number of genetic syndromes in which neoplasms and other multi-system pathological processes occur. Here, we report the case of a 6-year-old girl who presented with atypical lentiginosis and hyperpigmentation caused by a de novo genetic variant in t...

journal_title：Pediatric dermatology

authors： Tran AK,Pearce A,López-Sánchez M,Pérez-Jurado LA,Barnett C

更新日期：2019-11-01 00:00:00

abstract：:Herpes zoster is rare in otherwise healthy children, but it is more common in association with immunosuppression. Maternal varicella infection during pregnancy and varicella occurring in the newborn represent risk factors for childhood herpes zoster. However, some controversies persist about risk factors, diagnosis, a...

journal_title：Pediatric dermatology

authors： Nikkels AF,Nikkels-Tassoudji N,Piérard GE

更新日期：2004-01-01 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：:Molluscum contagiosum is a common viral infection of the skin that frequently affects children. Lesions take between 6 and 18 months to resolve spontaneously and are a source of great embarrassment to both caretakers and children, often affecting attendance at school and limiting social activity. Treatment options to ...

journal_title：Pediatric dermatology

authors： Short KA,Fuller LC,Higgins EM

更新日期：2006-05-01 00:00:00

abstract：:Proteus syndrome is an extremely rare mosaic condition characterized by progressive overgrowth of tissues due to a somatic activating mutation of the AKT1 gene. Distinct cutaneous features, including cerebriform connective tissue nevi, epidermal nevi, vascular malformations, and adipose abnormalities, can alert the de...

journal_title：Pediatric dermatology

authors： Rodenbeck DL,Greyling LA,Anderson JH,Davis LS

更新日期：2016-09-01 00:00:00

abstract：:Pulmonary manifestations are well recognized during the acute phase of Stevens-Johnson syndrome but persistent pulmonary sequela is rarely reported. We report two boys with bronchiolitis obliterans following the acute phase of Stevens-Johnson syndrome and discuss the clinical picture and treatment of persistent pulmon...

journal_title：Pediatric dermatology

authors： Bakirtas A,Harmanci K,Toyran M,Razi CH,Turktas I

更新日期：2007-07-01 00:00:00

abstract：:Two native Yanomami children from the Venezuelan Amazonia with erythroderma were hospitalized on our service. Clinical, histologic, and immunofluorescence studies diagnosed endemic pemphigus foliaceous. Human leukocyte antigen class II showed DRB1*04 subtype *0411, which has not been previously associated with this di...

journal_title：Pediatric dermatology

authors： González F,Sáenz AM,Cirocco A,Tacaronte IM,Fajardo JE,Calebotta A

更新日期：2006-03-01 00:00:00

abstract：:A child born with the harlequin fetus abnormality survived and showed a surprising degree of spontaneous improvement in the first six weeks of life. At this age etretinate was instituted, producing considerable further resolution. The child is now over 2 years old. ...

journal_title：Pediatric dermatology

authors： Rogers M,Scraf C

更新日期：1989-09-01 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 case of a young man with perforating folliculitis and cystic fibrosis with complications including chronic obstructive pulmonary disease, insulin dependent diabetes mellitus, and liver cirrhosis. We demonstrate increased TGF-β1 immunohistochemical staining in the perforating folliculitis lesions of our pat...

journal_title：Pediatric dermatology

authors： Tuttle MS,Kwon EJ,Tamburro J,Honda K

更新日期：2010-11-01 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

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：:Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant inherited blistering skin disease characterized by nonscarring blistering and reticulated hyperpigmentation. It is most commonly due to a heterozygous point mutation, P25L, in the nonhelical V1 domain of keratin 5 (KRT5). Here we...

journal_title：Pediatric dermatology

authors： Geller L,Kristal L,Morel KD

更新日期：2013-09-01 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：: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