Accessory tragus: report of two cases and review of the literature.

Abstract:

:Accessory tragus is a fairly common congenital malformation of the external ear. In the vast majority of cases it is an isolated developmental defect not associated with other abnormalities. However, the remote possibility exists that it could be associated with other abnormalities of the first and second branchial arch. Accessory tragus is a consistent feature of the oculoauriculovertebral syndrome (Goldenhar syndrome). When correctly identified, surgical excision of accessory tragus is quite simple and rarely results in any complications.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Jansen T,Romiti R,Altmeyer P

doi

10.1046/j.1525-1470.2000.017005391.x

subject

Has Abstract

pub_date

2000-09-01 00:00:00

pages

391-4

issue

5

eissn

0736-8046

issn

1525-1470

journal_volume

17

pub_type

杂志文章,评审
  • Hair casts: a clinical and electron microscopic study.

    abstract::Hair casts were seen in 22 girls ranging in age from 4 to 13 years. They were localized to the frontal, vertex, and temporal areas. The number of affected hairs varied from one-tenth to one-third. Twenty of the 22 girls styled their hair in ponytails or pigtails. Compound root sheath casts were present in six of nine ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1990.tb01023.x

    authors: Zhu WY,Xia MY,Wu JH,Do DA

    更新日期:1990-12-01 00:00:00

  • Meyerson phenomenon in children: observation in five cases of congenital melanocytic nevi.

    abstract::To describe the characteristics of five pediatric patients with the Meyerson phenomenon associated with congenital melanocytic nevi, five cases were reviewed to retrieve information relating to clinical presentation, treatment and evolution of the eczematous phenomenon and of the nevi. Three of five patients were male...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00931.x

    authors: Rolland S,Kokta V,Marcoux D

    更新日期:2009-05-01 00:00:00

  • Subcutaneous fat necrosis of the newborn: a review of 11 cases.

    abstract::Subcutaneous fat necrosis (SFN) of the newborn is uncommon and usually occurs in the first weeks of life following a complicated delivery. The frequency with which hypercalcemia develops as a complication is uncertain. We report the clinical features of SFN in 11 patients seen between 1991 and 1998. Ten were born by c...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.1999.00101.x

    authors: Burden AD,Krafchik BR

    更新日期:1999-09-01 00:00:00

  • Tongue granulomatous lesion caused by mandibular primary incisors eruption.

    abstract::The aim of this report was to present a case of granulomatous lesion on the ventral surface of the tongue in a 9-month-old, healthy, infant girl, caused by the habit of scraping the tongue on mandibular central incisors. Clinical treatment consisted of manual smoothing of the sharp edges of both incisors and excision ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.01009.x

    authors: Inagaki LT,Sullcahuamán JA,Hernandez Lara SM,Dezan CC,Walter LR

    更新日期:2009-09-01 00:00:00

  • Two cases of isolated anterior cervical hypertrichosis.

    abstract::Two unrelated Hispanic females, ages 4 and 3 years, respectively, each presented with a solitary patch of excessive terminal hair growth in the midline of the neck. This rare form of congenital localized hypertrichosis, known as anterior cervical hypertrichosis, is reported here as an isolated defect with no other und...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01269.x

    authors: Reddy S 4th,Antaya RJ

    更新日期:2010-09-01 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

  • The Fanny Pack: No Ifs, Ands, or Buts.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.13090

    authors: Habeshian K,Kirkorian AY,Marathe K

    更新日期:2017-05-01 00:00:00

  • Epidemiology of atopic dermatitis in primary schoolchildren in Turkey.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00697.x

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

    更新日期:2008-05-01 00:00:00

  • Henoch-Schönlein purpura associated with Helicobacter pylori infection in a child.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00786.x

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

    更新日期:2008-11-01 00:00:00

  • Acrodynia and hypertension in a young girl secondary to elemental mercury toxicity acquired in the home.

    abstract::Acrodynia, also known as pink disease, erythredema polyneuropathy, Feer syndrome, and raw-beef hands and feet, is thought to be a toxic reaction to elemental mercury and less commonly to organic and inorganic forms. Occurring commonly in the early 20th century, acrodynia is now a seemingly extinct disease in the moder...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2012.01737.x

    authors: Mercer JJ,Bercovitch L,Muglia JJ

    更新日期:2012-03-01 00:00:00

  • Lymphangioma associated with Becker's nevus: a report of coincident hamartomas in a child.

    abstract::Lymphangiomas are hamartomas which often occur during childhood. Their classification is primarily size dependent and predicts their clinical course. Larger lesions can be life threatening, but for many patients with lymphangiomas, cosmetic disfigurement is the primary concern. Treatment options are limited and have s...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1997.tb00986.x

    authors: Oyler RM,Davis DA,Woosley JT

    更新日期:1997-09-01 00:00:00

  • Follicular Mucinosis in a Male Adolescent with a History of Acute Myelogenous Leukemia and Graft-versus-Host Disease.

    abstract::Although many cases of follicular mucinosis are idiopathic, numerous others are associated with mycosis fungoides or, rarely, other neoplastic or inflammatory disorders. There are only three reported cases, all in adults, of follicular mucinosis arising in association with acute myelogenous leukemia, two of which invo...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12724

    authors: Jefferson J,Taube J,Grossberg A

    更新日期:2016-01-01 00:00:00

  • A case of cutaneous mastocytosis in a child with prominent Langerhans cell infiltration.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01205.x

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

    更新日期:2011-07-01 00:00:00

  • Granulomatous Mycosis Fungoides in an Adolescent-A Rare Encounter and Review of the Literature.

    abstract::Granulomatous mycosis fungoides (GMF) is a rare form of mycosis fungoides (MF) characterized by an infiltrate of atypical lymphocytes, histiocytes, and multinucleated giant cells. Clinically, GMF has a slowly progressing course with a worse prognosis than other forms of MF. With its peak incidence being in the fifth t...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12959

    authors: Wieser I,Wohlmuth C,Duvic M

    更新日期:2016-09-01 00:00:00

  • Childhood Pemphigus Foliaceus with Exclusive Immunoglobulin G Autoantibodies to Desmocollins.

    abstract::Pemphigus refers to a group of potentially fatal blistering skin diseases that are often due to the deleterious effects of autoantibodies directed against desmosomal antigens. Although desmogleins have been mainly implicated as autoantigens in pemphigus, a steadily growing body of evidence suggests that other desmosom...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12729

    authors: Geller S,Gat A,Harel A,Mashiah J,Zeeli T,Eming R,Ishii N,Hertl M,Hashimoto T,Sprecher E

    更新日期:2016-01-01 00:00:00

  • Congenital hemangioma with milialike structures: a case report.

    abstract::A 4-month-old infant had two 3 cm x 4 cm hemangiomatous lesions on the scalp and back, present since birth, which contained peculiar white-yellowish small nodules. Histologically the lesions proved to have a hemangiomatous (capillary-type) component together with small keratin-containing epidermal cysts (milia-like) w...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.1998.1998015307.x

    authors: Rositto A,Avila S,Carames C,Drut R

    更新日期:1998-07-01 00:00:00

  • Benign cephalic histiocytosis with diabetes insipidus.

    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

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2000.01779.x

    authors: Weston WL,Travers SH,Mierau GW,Heasley D,Fitzpatrick J

    更新日期:2000-07-01 00:00:00

  • Multiple Café au Lait Spots in a Group of Fair-Skinned Children without Signs or Symptoms of Neurofibromatosis Type 1.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12936

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

    更新日期:2016-09-01 00:00:00

  • Novel dermoscopic features of pityriasis versicolor-like macules in epidermodysplasia verruciformis.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.14031

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

    更新日期:2020-01-01 00:00:00

  • A patient with trisomy 13 mosaicism with an unusual skin pigmentary pattern and prolonged survival.

    abstract::Trisomy 13, or Patau syndrome, is a chromosomal disorder that can occur in complete, partial, or mosaic forms. Mosaicism is observed in 6% of individuals with trisomy 13 and, in contrast to the complete form, has wide phenotypic variability, longer survival, and in some patients an unusual skin pigmentary pattern simi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12339

    authors: González-del Angel A,Estandia-Ortega B,Gaviño-Vergara A,Sáez-de-Ocariz M,Velasco-Hernández Mde L,Salas-Labadía C

    更新日期:2014-09-01 00:00:00

  • Aeromonas hydrophila folliculitis associated with an inflatable swimming pool: mimicking Pseudomonas aeruginosa infection.

    abstract::Aeromonas species are ubiquitous, facultative, anaerobic, gram-negative flagellated rods, mainly found in aquatic ecosystems worldwide. Skin and soft-tissue infections, including cellulitis and wound infections, are the second most frequent location of isolations of Aeromonas spp. in clinical samples, after the gastro...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00993.x

    authors: Julià Manresa M,Vicente Villa A,Gené Giralt A,González-Enseñat MA

    更新日期:2009-09-01 00:00:00

  • Human papillomavirus (HPV) genotyping of cutaneous warts in Greek children.

    abstract::The human papillomavirus (HPV) infects the squamous epithelium of the skin and produces common warts, plantar warts, and flat warts, which occur commonly on the hands, face, and feet. The objective of this study was to determine the presence of HPV in warts in children in order to associate the virus with the disease....

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12113

    authors: Giannaki M,Kakourou T,Theodoridou M,Syriopoulou V,Kabouris M,Louizou E,Chrousos G

    更新日期:2013-11-01 00:00:00

  • A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina.

    abstract:BACKGROUND:Kindler syndrome is a rare genodermatosis. Major clinical criteria include acral blistering in infancy and childhood, progressive poikiloderma, skin atrophy, abnormal photosensitivity, and gingival fragility. METHODS:FERMT1 gene was sequenced in 5 patients with a clinical diagnosis of Kindler syndrome. RES...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14076

    authors: Valinotto LE,Natale MI,Lusso SB,Cella E,Gutiérrez O,Sebastiani F,Manzur GB

    更新日期:2020-03-01 00:00:00

  • Acanthosis nigricans: a common finding in overweight youth.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00547.x

    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

  • Telangiectasia macularis eruptiva perstans.

    abstract::Telangiectasia macularis eruptiva perstans (TMEP) is a form of mastocytosis. It is an uncommon condition, particularly in children. The disorder is characterized by telangiectatic macules and generally has a good prognosis, with little tendency to urticate or cause constitutional symptoms. We report a girl who present...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2000.01750.x

    authors: Gibbs NF,Friedlander SF,Harpster EF

    更新日期:2000-05-01 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

  • Dramatic improvement of pyoderma gangrenosum with infliximab in a patient with PAPA syndrome.

    abstract::Infliximab, a chimeric antitumor necrosis factor alpha monoclonal antibody (anti-TNF alpha), has been recently shown to have a beneficial effect on pyoderma gangrenosum associated with inflammatory bowel disease. Patients with the syndromic triad of pyogenic sterile arthritis, pyoderma gangrenosum, and acne, an autoin...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22320.x

    authors: Stichweh DS,Punaro M,Pascual V

    更新日期:2005-05-01 00:00:00

  • Hodgkin's disease manifesting as prurigo nodularis.

    abstract::Prurigo nodularis is an uncommon pediatric cutaneous disorder that is associated with intense pruritus. We report a teenager with prurigo nodularis as the presenting sign of stage IIA Hodgkin's disease, primarily in the mediastinum. The pruritus and associated cutaneous lesions resolved with combination chemotherapy d...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1990.tb00670.x

    authors: Shelnitz LS,Paller AS

    更新日期:1990-06-01 00:00:00

  • Pigmented purpuric dermatosis in an infant.

    abstract::Pigmented purpuric dermatoses (PPDs) are a group of idiopathic, chronic, and self-resolving conditions easily recognizable in adults but extremely uncommon in infants. We present the youngest patient with PPD reported to date. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14500

    authors: Martos-Cabrera L,López-Balboa P,Ramírez-Lluch M,Colmenero I,Mateos-Mayo A,Torrelo A,Hernández-Martin Á

    更新日期:2021-01-06 00:00:00

  • Genotoxic hazard and cellular stress in pediatric patients treated for psoriasis with the Goeckerman regimen.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00774.x

    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