Fibro-Osseous Pseudotumor of the Digits Mimicking Pyogenic Granuloma.

Abstract:

:Fibro-osseous pseudotumor of the digits is a benign neoplasm that originates in the soft tissue adjacent to the short bones of the hands and feet. We present a case in a 13-year-old girl that was initially misdiagnosed as pyogenic granuloma. Familiarity with this entity and imaging and histologic studies are necessary to avoid incorrect diagnoses and aggressive surgical interventions.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Gómez-Zubiaur A,Pericet-Fernández L,Vélez-Velázquez MD,Cabrera-Hernández A,Piteiro-Bermejo AB,Beá-Ardebol S,Medina-Montalvo S,Trasobares-Marugán L

doi

10.1111/pde.13087

subject

Has Abstract

pub_date

2017-05-01 00:00:00

pages

e126-e127

issue

3

eissn

0736-8046

issn

1525-1470

journal_volume

34

pub_type

杂志文章
  • Cutaneous manifestations of diabetes mellitus in children.

    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

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1985.tb01047.x

    authors: Edidin DV

    更新日期:1985-03-01 00:00:00

  • Midline congenital cervical cleft mimicking linear scleroderma.

    abstract::Midline congenital cervical cleft is an extremely uncommon anomaly of the neck. Fewer than 100 cases have been reported. It is usually described as a cervical scar-like skin defect. We present a case of midline cervical cleft mimicking linear morphea and treated with topical steroids for 2 years. This is an unusual pr...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12021

    authors: Méndez-Gallart R,Martinez EE,Rodríguez-Barca P,Nallib IA,Bautista-Casasnovas A

    更新日期:2013-07-01 00:00:00

  • Early morphea mimicking acquired port-wine stain.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12116

    authors: Pickert AJ,Carpentieri D,Price H,Hansen RC

    更新日期:2014-09-01 00:00:00

  • CLOVE syndrome with nevus unis lateris: report of a case.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01149.x

    authors: Harit D,Aggarwal A

    更新日期:2010-05-01 00:00:00

  • An audit of the activities of the pediatric dermatology nurse specialist (PDNS).

    abstract::In the current financial climate where resources in the National Health Service are becoming increasingly limited, it is essential that the role of the pediatric dermatology nurse specialist remains appreciated and supported. Our pediatric dermatology nurse specialist was first employed in September 2002 having had 6 ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00886.x

    authors: Usmani N,Teasdale J,Clark SM

    更新日期:2009-03-01 00:00:00

  • Diaper dermatitis: a therapeutic dilemma. Results of a double-blind placebo controlled trial of miconazole nitrate 0.25%.

    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

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1046/j.1525-1470.2001.018002149.x

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

    更新日期:2001-03-01 00:00:00

  • A barrier to care: Distance traveled affects adherence to treatment and follow-up plans for patients with infantile hemangioma.

    abstract::A chart review was performed of all patients diagnosed with infantile hemangioma in the pediatric dermatology clinic to determine whether distance traveled by the patient affected adherence to follow-up and treatment plans. An increase in distance was associated with an increase in likelihood of nonadherence to treatm...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13788

    authors: Desrosiers AS,Ibrahim JM,Jacks SK

    更新日期:2019-05-01 00:00:00

  • Vesicular erythema multiforme-like reaction to para-phenylenediamine in a henna tattoo.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00634.x

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

    更新日期:2008-03-01 00:00:00

  • A Pediatric Case of Sclerodermatous Graft-Versus-Host Disease Responsive to Ultraviolet A1 Phototherapy.

    abstract::Graft-versus-host disease (GVHD) is one of the major complications after hematopoietic stem cell transplantation and is responsible for post-therapeutic morbidity, mortality, and poor quality of life of recipients. Sclerodermatous graft-versus-host disease (sGVHD) is a rare variant of chronic GVHD characterized by dep...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12794

    authors: Lazzeri L,Tripo L,Pescitelli L,Ricceri F,Prignano F

    更新日期:2016-03-01 00:00:00

  • Sacral hemangioma with sinus tract in an infant.

    abstract::Congenital midline cutaneous lesions should always alert the clinician to the possibility of spinal dysraphism. These lesions can take many different forms. The physician should be cognizant of such lesions in order to avoid potential neurologic complications. We present a patient with a midline sacral hemangioma asso...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.20307.x

    authors: Winstanley D,Graham B,Blair M,Linfesty R,Tomita S,Matthews J

    更新日期:2003-05-01 00:00:00

  • Congenital insensitivity to pain in four related Saudi families.

    abstract::Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy [HSAN] type V) is a rare disorder of pain perception in which pain sensation is absent from birth, with no other neurologic deficits. We report five Saudi patients (three male and two female) age 10 months to 23 years who lacked pain sensati...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2002.00095.x

    authors: Karkashan EM,Joharji HS,Al-Harbi NN

    更新日期:2002-07-01 00:00:00

  • Successful Use of Cyclosporin A for Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Three Children.

    abstract:BACKGROUND/OBJECTIVES:Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are medical emergencies. Mainstays of treatment include removal of the offending agent, supportive care, and wound care. The use of immunosuppressive agents such as corticosteroids and intravenous immunoglobulin (IVIg) is controve...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13236

    authors: St John J,Ratushny V,Liu KJ,Bach DQ,Badri O,Gracey LE,Ho AW,Raff AB,Sugai DY,Schalock P,Kroshinsky D

    更新日期:2017-09-01 00:00:00

  • Successful treatment of Darier's disease with adapalene gel.

    abstract::We report a 12-year-old Japanese boy with a 3-year history of skin lesions that had been unsuccessfully treated with topical steroids. We initiated two different topical treatments with adapalene gel 0.1% (Differin(®) Gel 0.1%) and high-concentration vitamin D3 (tacalcitol) ointment; the lesions treated with adapalene...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.01077.x

    authors: Abe M,Inoue C,Yokoyama Y,Ishikawa O

    更新日期:2011-03-01 00:00:00

  • Treating protruding infantile hemangiomas with topical imiquimod 5% cream caused severe local reactions and disfiguring scars.

    abstract::Infantile hemangiomas (IHs) are the most common tumors of infancy. Imiquimod, an immune-response modifier, has been proven effective and safe in the treatment of superficial and mixed hemangiomas, but severe local reactions caused by imiquimod have been reported sporadically. To evaluate the safety of imiquimod 5% cre...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12002

    authors: Qiu Y,Ma G,Lin X,Jin Y,Chen H,Hu X

    更新日期:2013-05-01 00:00:00

  • Chromhidrosis due to exogenous oxidizing heavy metals: Clinical and laboratory findings.

    abstract:BACKGROUND/OBJECTIVES:Chromhidrosis is a rare condition of which there are only a few case reports in the literature. The aim of this study was to evaluate clinical, laboratory, and possible environmental factors in 13 patients with chromhidrosis to elucidate causative agents. METHODS:Data were obtained from the medic...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13491

    authors: Erdol S,Karakaya S,Saglam H,Tarim O

    更新日期:2018-07-01 00:00:00

  • Congenital curved nail of the fourth toe--three different clinical presentations.

    abstract::A congenital curved nail of the fourth toe (NIM 219070) is a rare nail deformity with no other associated abnormalities. Three patients with this congenital anomaly are reported here. Radiologic examination in all three revealed distal symphalangism of the fourth toes bilaterally. The clinical manifestations in these ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00454.x

    authors: Lin YC,Wu YH,Scher RK

    更新日期:2007-07-01 00:00:00

  • Varied Presentations of Pediatric Lipoblastoma: Case Series and Review of the Literature.

    abstract::Lipoblastoma is a rare neoplasm of embryonal adipose tissue most often encountered on the trunk and extremities of children. It commonly presents as a painless subcutaneous soft tissue mass, but there are other unique clinical presentations that are important to recognize. The differential is broad and includes sarcom...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13071

    authors: Shen LY,Amin SM,Chamlin SL,Mancini AJ

    更新日期:2017-03-01 00:00:00

  • Two cases of spontaneous stellate scars.

    abstract::Scar formation is a physiologic reaction to dermal injury. We describe a 11-year-old girl and her 15-year-old cousin, who both presented with stellate scarlike lesions primarily located on the hands. Histopathologic examination confirmed scar tissue formation. There was no history of initiating trauma or other possibl...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00644.x

    authors: van Montfrans C,Lagendijk J,Hayes D,Bousema M

    更新日期:2008-03-01 00:00:00

  • S100-protein-containing dendritic cells in fetal and newborn epidermis and thymus.

    abstract::Skin and thymus were obtained from abortuses of varying ages and from neonatal autopsies to determine if S100-protein-containing dendritic cells were present. Using an unlabeled antibody peroxidase-antiperoxidase method, we could not detect these dendritic cells in epidermis prior to live birth, but did detect them at...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1986.tb00518.x

    authors: Penneys NS,Kott-Blumenkranz R,Buck BE,Nadji M,Gould E,Ibe M

    更新日期:1986-06-01 00:00:00

  • Accessory tragus: Report of a case in a rare location on the nasal vestibule.

    abstract::A case of an accessory tragus located on the nasal vestibule is reported. This represents the third case of this entity located outside of a derivative of a branchial arch. All three of these cases were located in the nose/glabella region. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14090

    authors: Moradi S,Castiglione C,Ehrig T

    更新日期:2020-03-01 00:00:00

  • An unusual cluster of circumscribed juvenile pityriasis rubra pilaris cases.

    abstract::Circumscribed juvenile pityriasis rubra pilaris (PRP) is an uncommon dermatosis. We describe the unusual clustering of circumscribed juvenile PRP cases in our pediatric dermatology clinic in 2011. A retrospective chart review was done of patients presenting during the summer of 2011 with classic findings of circumscri...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12260

    authors: Martin KL,Holland KE,Lyon V,Chiu YE

    更新日期:2014-03-01 00:00:00

  • Occurrence of supernumerary nipples in children with kidney and urinary tract malformations.

    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

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2001.01930.x

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

    更新日期:2001-07-01 00:00:00

  • Novel ABCA-12 mutations leading to recessive congenital ichthyosis.

    abstract::Mutations in the keratinocyte lipid transporter adenosine triphosphate-binding cassette A12 (ABCA12) are known to cause harlequin ichthyosis. More recently, mutations in this gene have been demonstrated to cause other phenotypes within the spectrum of recessive congenital ichthyosis. We report the case of an infant wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01695.x

    authors: Peterson H,Lofgren S,Bremmer S,Krol A

    更新日期:2013-11-01 00:00:00

  • Urticating Hashimoto-Pritzker Langerhans cell histiocytosis.

    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

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2001.018001041.x

    authors: Butler DF,Ranatunge BD,Rapini RP

    更新日期:2001-01-01 00:00:00

  • Crohn's disease of the vulva in an 8-year-old girl.

    abstract::An 8-year-old girl had Crohn's disease of the vulva 16 months before the onset of intestinal symptoms. At the time of diagnosis she had no evidence of systemic disease. Cutaneous and intestinal lesions responded rapidly to corticosteroids and metronidazole. Crohn's disease must be considered in the differential diagno...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1988.tb01148.x

    authors: Lally MR,Orenstein SR,Cohen BA

    更新日期:1988-05-01 00:00:00

  • Acquired progressive lymphangioma: Case report with partial response to imiquimod 5% cream.

    abstract::Acquired progressive lymphangioma (APL), or benign lymphangioendothelioma, is an unusual entity derived from vascular structures. Clinically and histopathologically it may resemble Kaposi's sarcoma and well-differentiated angiosarcoma, causing a diagnostic problem. We report an individual with APL initially diagnosed ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13283

    authors: Salman A,Sarac G,Can Kuru B,Cinel L,Yucelten AD,Ergun T

    更新日期:2017-11-01 00:00:00

  • Wet-wrap treatment in children with atopic dermatitis: a practical guideline.

    abstract::Treatment of children with severe atopic dermatitis (AD) can be especially challenging because several possible intervention treatments have (relative) contraindications in childhood. In recent years, wet-wrap treatment (WWT) has been advocated as a relatively safe and efficacious intervention in children with severe ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2011.01691.x

    authors: Devillers AC,Oranje AP

    更新日期:2012-01-01 00:00:00

  • Early Recognition of Proteus Syndrome.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12900

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

    更新日期:2016-09-01 00:00:00

  • Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement.

    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

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12848

    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

  • Lichen planus in the lines of Blaschko.

    abstract::We describe three adolescents with eruptive linear lesions of the back, abdomen, and extremities distributed along the lines of Blaschko. Clinically one of these lesions resembled an epidermal nevus in its morphology and distribution. A biopsy specimen demonstrated the typical histology of lichen planus (LP). There ha...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.2002.00229.x

    authors: Kabbash C,Laude TA,Weinberg JM,Silverberg NB

    更新日期:2002-11-01 00:00:00