Sequestrated meningocele of the scalp: diagnostic value of hair anomalies.

abstract：:We describe the clinicopathologic features of an unusual case of fibromatosis colli. The lesion was rock hard, lateral, tightly affixed to the clavicle, and with overlying hypertrichosis. ...

journal_title：Pediatric dermatology

authors： Amin A,Loftis B,Shwayder TA

更新日期：2010-09-01 00:00:00

abstract：:Henoch-Schönlein purpura is an acute leukocytoclastic vasculitis that primarily affects children. Henoch-Schönlein purpura is often associated with an infection, and a wide variety of infectious agents have been implicated in the pathogenesis. We report a child with Henoch-Schönlein purpura associated with Helicobacte...

journal_title：Pediatric dermatology

authors： Mytinger JR,Patterson JW,Thibault ES,Webb J,Saulsbury FT

更新日期：2008-11-01 00:00:00

abstract：:Lamotrigine is an anticonvulsant with a broad spectrum of activity that has been approved in the United States for use in adults with either partial or generalized seizures. This drug is being widely prescribed by pediatricians and neurologists because it is effective in children with idiopathic, resistant, generalize...

journal_title：Pediatric dermatology

authors： Brown TS,Appel JE,Kasteler JS,Callen JP

更新日期：1999-01-01 00:00:00

abstract：:Intralesional injection of bleomycin (BLM) for the treatment of warts resistant to all conventional therapies is of certain interest because of the drug's low toxicity and its efficacy. However, delayed side effects may appear, particularly Raynaud phenomenon. Accordingly, some precautions must be taken in patients wi...

journal_title：Pediatric dermatology

authors： Vanhooteghem O,Richert B,de la Brassinne M

更新日期：2001-05-01 00:00:00

abstract：:Multisystem inflammatory syndrome in children (MIS-C) is a syndrome associated with coronavirus disease 2019. Various phenotypes of MIS-C have been described including Kawasaki disease (KD). Although perineal desquamation is a known early sign of KD, to our knowledge, this rash has not yet been described in the KD phe...

journal_title：Pediatric dermatology

authors： Mazori DR,Derrick KM,Kapoor U,Haribhai M,Gist RE,Glick SA

更新日期：2020-11-22 00:00:00

abstract：BACKGROUND:The presence of six or more café au lait (CAL) spots is a criterion for the diagnosis of neurofibromatosis type 1 (NF-1). Children with multiple CAL spots are often referred to dermatologists for NF-1 screening. The objective of this case series is to characterize a subset of fair-complected children with re...

journal_title：Pediatric dermatology

authors： St John J,Summe H,Csikesz C,Wiss K,Hay B,Belazarian L

更新日期：2016-09-01 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：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：: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：:Microvenular hemangioma (MVH) is a rare, benign, acquired vascular tumor. We report a case that shows the characteristic histopathologic features of this disorder in a boy with acute myelogenous leukemia (AML), suggesting an association with systemic immunosuppression. ...

journal_title：Pediatric dermatology

authors： Chang SE,Roh KH,Lee MW,Choi JH,Sung KJ,Moon KC,Koh JK,Yoon GS

更新日期：2003-05-01 00:00:00

abstract：:Diaper dermatitis, an acute inflammation of the skin in the diaper area, is the most common dermatologic disorder of infancy. This placebo-controlled, randomized, double-blind, parallel-group trial compared the efficacy and safety of miconazole nitrate 0.25% in a zinc oxide/petrolatum base with that of the ointment ba...

journal_title：Pediatric dermatology

authors： Concannon P,Gisoldi E,Phillips S,Grossman R

更新日期：2001-03-01 00:00:00

abstract：:We describe a premature neonate who was born with pancytopenia and a single subcutaneous nodule on her right lower extremity. A biopsy specimen from the nodule demonstrated a dense infiltrate of pleomorphic mononuclear cells that extended throughout the dermis and into the subcutaneous tissue. Immunohistochemical stai...

journal_title：Pediatric dermatology

authors： Fender AB,Gust A,Wang N,Scott GA,Mercurio MG

更新日期：2008-01-01 00:00:00

abstract：BACKGROUND:Understanding the importance of the barrier function of the skin of preterm and term neonates is crucial in effective neonatal skin and diaper care. This literature search aimed to review the development of different practices in neonatal care to maintain skin barrier function, in turn preventing diaper derm...

journal_title：Pediatric dermatology

authors： Burdall O,Willgress L,Goad N

更新日期：2019-01-01 00:00:00

abstract：:We evaluated the prevalence of acanthosis nigricans among urban youth. Youth (7-17 years) at nine pediatric practices completed surveys on demographics and family history of diabetes and had weight and height measured. Acanthosis nigricans was scored and digital photography of the neck performed. A total of 618 youth ...

journal_title：Pediatric dermatology

authors： Brickman WJ,Binns HJ,Jovanovic BD,Kolesky S,Mancini AJ,Metzger BE,Pediatric Practice Research Group.

更新日期：2007-11-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Previous studies have demonstrated an increased prevalence of inflammatory bowel disease (IBD) in adults with hidradenitis suppurativa (HS). Whether the same association exists in pediatric patients is unknown. Fecal calprotectin (FC) is used to screen and monitor disease activity in IBD. There ar...

journal_title：Pediatric dermatology

authors： Lloyd-McLennan AM,Ali S,Kittler NW

更新日期：2020-10-25 00:00:00

abstract：:Lichen sclerosus is a T-lymphocyte mediated chronic cutaneous disorder with predilection for the vulva. In prepubertal girls, lichen sclerosus presents as vulvar discomfort, pruritus, bruising/bleeding, discharge, dysuria, or painful defecation. Diagnosis and treatment of lichen sclerosus is of utmost importance in th...

journal_title：Pediatric dermatology

authors： Yousefi M,Pride H,Elston D

更新日期：2009-05-01 00:00:00

abstract：:Raynaud's phenomenon (RP) is an episodic vasospastic response to cold or emotional stress causing color changes and pain. These attacks can lead to digital ischemia, ulcers, and gangrene. Severe and refractory RP in children is a therapeutic challenge for clinicians because there are no standardized treatment protocol...

journal_title：Pediatric dermatology

authors： Quintana Castanedo L,Feito Rodríguez M,Maseda Pedrero R,Chiloeches Fernández C,de Lucas Laguna R

更新日期：2020-07-01 00:00:00

abstract：:Congenital midline cervical cleft is a rare anomaly of the ventral neck that heretofore has not been reported in the dermatology literature. We present a case of a midline cervical cleft that was diagnosed and managed at an early age. We also review the literature and discuss its clinical and histologic features, trea...

journal_title：Pediatric dermatology

authors： Eastlack JP,Howard RM,Frieden IJ

更新日期：2000-03-01 00:00:00

abstract：:We evaluated two patients with hereditary bullous poikiloderma. Both had acral bullae, generalized poikiloderma with prominent atrophy, and acral keratoses. One patient, with sporadic disease, had, in addition, urethral and subglottic stenoses, webbing of digits, and poor dentition. The other patient, whose disease wa...

journal_title：Pediatric dermatology

authors： Forman AB,Prendiville JS,Esterly NB,Hebert AA,Duvic M,Horiguchi Y,Fine JD

更新日期：1989-06-01 00:00:00

abstract：:In order to assess the clinical characteristics and impact of group A streptococcal infection in children with atopic dermatitis, a retrospective review was performed in children diagnosed with atopic dermatitis who had a skin culture. Culture results and clinical characteristics of those with group A streptococcus we...

journal_title：Pediatric dermatology

authors： Sugarman JL,Hersh AL,Okamura T,Howard R,Frieden IJ

更新日期：2011-05-01 00:00:00

abstract：:Successful management of toxic epidermal necrolysis (TEN) with tumor necrosis factor-α inhibitors has been described in adults. We present a case of a 7-year-old boy with infection-associated TEN, diagnosed by typical clinical and histopathological features, most likely caused by Mycoplasma pneumoniae. Treatment with ...

journal_title：Pediatric dermatology

authors： Chafranska L,Saunte DM,Behrendt N,Nygaard U,Christensen RJ,Sand C,Jemec GB

更新日期：2019-05-01 00:00:00

abstract：:Four unrelated children with osteoma cutis and Albright hereditary osteodystrophy (pseudohypoparathyroidism and pseudopseudohypoparathyroidism) are described. All four patients were normocalcemic when they were first seen with cutaneous ossification. A diagnosis of Albright hereditary osteodystrophy was established on...

journal_title：Pediatric dermatology

authors： Prendiville JS,Lucky AW,Mallory SB,Mughal Z,Mimouni F,Langman CB

更新日期：1992-03-01 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：:This study sought to identify barriers to treatment in children with chronic inflammatory skin disease, particularly those with atopic dermatitis, psoriasis, and acne vulgaris. Caregivers of 101 patients seen in the Children's Specialty Group Division of Dermatology, Children's Hospital of The King's Daughters, Norfol...

journal_title：Pediatric dermatology

authors： Ellis RM,Koch LH,McGuire E,Williams JV

更新日期：2011-05-01 00:00:00

abstract：:Two infants experienced subcutaneous fat necrosis (SCFN) at a relatively late age after cardiac surgery with induced hypothermia. The condition resolved in both patients over four weeks without treatment. The appearance of SCFN after the newborn period is very unusual, and in these patients was probably related to the...

journal_title：Pediatric dermatology

authors： Glover MT,Catterall MD,Atherton DJ

更新日期：1991-09-01 00:00:00

abstract：:Cutis laxa is a rare disorder resulting from degradation and clumping of elastic fibers in dermis. Type II acquired cutis laxa, shows only cutaneous changes without any systemic involvement. We describe an infant with acquired cutis laxa type II following a generalized inflammatory dermatitis. ...

journal_title：Pediatric dermatology

authors： Haider M,Alfadley A,Kadry R,Almutawa A

更新日期：2010-01-01 00:00:00

abstract：:A 17-year-old woman with Cornelia de Lange syndrome had asymptomatic skin lesions since the age of 4 years. These were multiple, follicular, horny papules, present on both cheeks, and surrounded by erythematous skin. Similar lesions were present on the external aspect of the arms, but amidst skin of normal coloration....

journal_title：Pediatric dermatology

authors： Flórez A,Fernández-Redondo V,Toribio J

更新日期：2002-01-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Palmar hyperlinearity is a typical clinical feature of Filaggrin gene (FLG) null mutations. There are reports of FLG mutations and allergic sensitization; however, reports on the relationship between palmar hyperlinearity to sensitization are limited. This study aimed to examine the association be...

journal_title：Pediatric dermatology

authors： Fukuie T,Yasuoka R,Fujiyama T,Sakabe JI,Taguchi T,Tokura Y

更新日期：2019-03-01 00:00:00

abstract：:We report an unusual congenital vesiculopustular eruption arising in a neonate as the result of the transient myeloproliferative disorder (TMD) associated with trisomy 21. In this instance, the neonate was phenotypically normal, making the diagnosis more elusive. Initially the lesions were clinically suspicious for he...

journal_title：Pediatric dermatology

authors： Solky BA,Yang FC,Xu X,Levins P

更新日期：2004-09-01 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