Giant condyloma acuminatum in an infant.

Abstract:

:We report a 10-month-old boy who presented with a giant perianal condyloma acuminatum, and a similar lesion on the neck. These lesions were treated by surgical excision with satisfactory results. This size, extent, and early age of appearance make this case highly unusual.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Tinsa F,Gharbi A,Essid A,Driss M,Bousnina S

doi

10.1111/j.1525-1470.2009.00968.x

subject

Has Abstract

pub_date

2009-07-01 00:00:00

pages

488-9

issue

4

eissn

0736-8046

issn

1525-1470

pii

PDE968

journal_volume

26

pub_type

杂志文章
  • Colchicine may be of therapeutic benefit in prurigo pigmentosa.

    abstract::Prurigo pigmentosa (PP) is a rare inflammatory skin disease. Neutrophil-mediated inflammation is considered to be responsible for the etiopathogenesis of PP. We consider that colchicine may be an effective agent in the treatment of PP since it exerts an antiinflammatory effect by inhibiting neutrophil chemotaxis. Furt...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13480

    authors: An I,Ucmak D,Ibiloglu I,Demir V,Akdeniz S

    更新日期:2018-05-01 00:00:00

  • Cutaneous ultrasound and its utility in Pediatric Dermatology: Part II-Developmental anomalies and vascular lesions.

    abstract::High-frequency ultrasonography represents a promising tool for pediatric dermatologists. It is a noninvasive and harmless diagnostic technique that is especially appealing when working with children. It can be easily performed at the patient's bedside, avoiding diagnostic delays, sedation, or multiple visits. It repre...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13897

    authors: Rodríguez Bandera AI,Sebaratnam DF,Feito Rodríguez M,de Lucas Laguna R

    更新日期:2020-01-01 00:00:00

  • Cutaneous involvement of polymorphic post-transplant lymphoproliferative disorder in a child after liver transplantation.

    abstract::Post-transplantation lymphoproliferative disorder (PTLD) is one of the most common de novo malignancies in patients who receive immunosuppressive therapy after solid organ transplantation. We report a case of a 5-year-old girl who presented with indurated violaceous skin nodules 3.5 years post-liver transplantation, d...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13903

    authors: Chen KY,Lin CY,Kuo TT,Shih LY,Chang CH,Chen WT,Yang CY

    更新日期:2019-09-01 00:00:00

  • Recalcitrant scrofuloderma due to rib tuberculosis.

    abstract::Tuberculosis (TB) of the ribs is extremely rare and its diagnosis is often delayed due to the late appearance of radiologic signs. Although antituberculous drugs are the mainstay of treatment, surgery has a definite therapeutic role in recalcitrant or recurrent cases. A 5-year-old boy with scrofuloderma of the chest w...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.20406.x

    authors: Kaur S,Thami GP,Gupta PN,Kanwar AJ

    更新日期:2003-07-01 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

  • Ischemic ulcers of the toes secondary to Raynaud's phenomenon in a child successfully treated with botulinum toxin.

    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

    pub_type:

    doi:10.1111/pde.14160

    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

  • Ulcerated congenital plexiform fibrohistiocytic tumor: Case report and literature review.

    abstract::A newborn boy presented with a progressively infiltrating and painful congenital ulcerated plaque on the back of his left foot. A partial excision was performed and histopathologic examination confirmed a diagnosis of a plexiform fibrohistiocytic tumor. This rare tumor usually appears in children and adolescents, with...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13652

    authors: Nieto D,Feito M,Rueda JM,Rodríguez A,Berjón A,López JC,de Lucas R

    更新日期:2018-11-01 00:00:00

  • Acute febrile neutrophilic dermatosis (Sweet's syndrome): case report and review of the literature.

    abstract::An 8-month-old male infant had fever, polymorphonuclear leukocytosis, and tender, firm, elevated erythematous plaques on his face, trunk, and extremities. Histologic examination revealed a dense, perivascular, polymorphonuclear, inflammatory cell infiltrate with nuclear dust in the dermis and intrafollicular abscesses...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1985.tb00484.x

    authors: Kibbi AG,Zaynoun ST,Kurban AK,Najjar SS

    更新日期:1985-11-01 00:00:00

  • Juvenile xanthogranuloma: a congenital giant form leading to a wide atrophic sequela.

    abstract::Juvenile xanthogranuloma is the most common non-Langerhans cell histiocytosis of infancy and childhood. It is a benign disorder that usually regresses spontaneously, more often without or with limited skin changes. The clinical features are very pleomorphic and recognition of the atypical presentations should facilita...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21206.x

    authors: Imiela A,Carpentier O,Segard-Drouard M,Martin de Lassalle E,Piette F

    更新日期:2004-03-01 00:00:00

  • Xanthoma disseminatum with hepatic involvement in a child.

    abstract::Xanthoma disseminatum is a rare, usually self-healing dermatologic disease of unknown etiology. Involvement of other organs and tissues including bone marrow, bone, and brain may be seen rarely in children. However, to date, hepatic involvement has not been reported. We describe a child with xanthoma disseminatum who ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.00138.x

    authors: Büyükavci M,Selimoglu A,Yildirim U,Ertekin V,Atasoy M

    更新日期:2005-11-01 00:00:00

  • Pediatric teledermatology--a survey of current use.

    abstract::Demand for pediatric dermatologic care far exceeds the supply of pediatric dermatologists. Teledermatology has been proposed as a solution to improve access to care, however, data regarding teledermatology use for pediatric patients are lacking. Surveys assessing use and experience with teledermatology were administer...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00624.x

    authors: Fieleke DR,Edison K,Dyer JA

    更新日期:2008-03-01 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

  • 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

  • Infantile Bullous Pemphigoid Treated Using Intravenous Immunoglobulin: Case Report and Review of the Literature.

    abstract::We report a 5-month-old girl diagnosed with bullous pemphigoid who initially did not respond to systemic corticosteroids and dapsone but rapidly improved after the addition of intravenous immunoglobulin (IVIG) infusions. A literature search revealed anecdotal cases of infantile bullous pemphigoid treated with IVIG, al...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12635

    authors: Tekin B,Yücelten AD

    更新日期:2015-09-01 00:00:00

  • Deep Granuloma Annulare Mimicking Inflamed Cysts in a Teenager.

    abstract::We describe deep granuloma annulare (DGA) of the forehead mimicking inflamed cysts. Reactive inflammation and sterile purulent drainage may be an underrecognized feature of DGA. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13137

    authors: Guo EL,Degesys CA,Jahan-Tigh R,Chan A

    更新日期:2017-07-01 00:00:00

  • Cutaneous histiocytosis syndromes.

    abstract::Cutaneous histiocytosis may take two principal forms. It is either a benign proliferative process or a relentless, progressive process with a poor prognosis. In histiocytic medullary reticulosis, histiocytes demonstrate nuclear atypia and the outcome is uniformly fatal. Benign cephalic histiocytosis X causes lesions s...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1985.tb00480.x

    authors: Roper SS,Spraker MK

    更新日期:1985-11-01 00:00:00

  • Eosinophilic pustular folliculitis of infancy suppressed with cetirizine.

    abstract::Eosinophilic pustular folliculitis of infancy is a rare inflammatory disease characterized by recurrent, itchy sterile pustules mainly located on the scalp. Topical agents are mostly effective to suppress the symptoms in the majority of cases. However, systemic agents that are safe for long-term use are required for p...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13764

    authors: Odyakmaz Demirsoy E,Demirsoy U,Ozod U,Kiran R

    更新日期:2019-05-01 00:00:00

  • Dermatologic findings of vitamin B12 deficiency in infants.

    abstract:BACKGROUND/OBJECTIVES:Vitamin B12 deficiency in infants is uncommonly reported from developed countries and generally lacks dermatologic manifestations. On the contrary, infantile vitamin B12 deficiency is common in India and cutaneous manifestations are a constant feature, although often overshadowed by neurologic and...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13679

    authors: Kaur S,Goraya JS

    更新日期:2018-11-01 00:00:00

  • Melanocytic nevi in Turner syndrome.

    abstract::One morphologic feature of Turner syndrome is increased numbers of melanocytic nevi; however, little attention has been given to their characterization. The development of a melanoma in one of our patients with Turner syndrome prompted this study. We prospectively examined 10 patients with the disease, confirmed by ka...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1994.tb00564.x

    authors: Becker B,Jospe N,Goldsmith LA

    更新日期:1994-06-01 00:00:00

  • Retrospective Study of Rocky Mountain Spotted Fever in Children.

    abstract:BACKGROUND/OBJECTIVES:Rocky Mountain spotted fever (RMSF), a lethal tick-borne illness, is prevalent in the south central United States. Children younger than 10 years old have the greatest risk of fatal outcome from RMSF. The objective of the current study was to review pediatric cases of RMSF seen in the dermatology ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13053

    authors: Tull R,Ahn C,Daniel A,Yosipovitch G,Strowd LC

    更新日期:2017-03-01 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

  • Gamification improves melanoma visual identification among high school students: Results from a randomized study.

    abstract::Identification of melanoma or worrisome moles is often taught as an important part of routine skin checks. We sought to evaluate the efficacy of gamified education vs. traditional ABCDEs education on melanoma identification and self-confidence in identifying worrisome moles. We report that in our cohort (n = 271), par...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14158

    authors: Jia JL,Shen A,Tabata MM,Sarin KY

    更新日期:2020-07-01 00:00:00

  • Urticarial lesions in a child with acute lymphoblastic leukemia and eosinophilia.

    abstract::The hypereosinophilic syndrome (HES) is defined by a longer than 6-month history of peripheral blood hypereosinophilia (greater than 1.5 x 10(9)/L), with signs and symptoms of internal organ involvement, in the absence of an identifiable cause. HES is therefore a diagnosis of exclusion. Patients have been reported who...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2003.20610.x

    authors: Hill A,Metry D

    更新日期:2003-11-01 00:00:00

  • Preschool sarcoidosis masquerading as juvenile rheumatoid arthritis: two case reports and a review of the literature.

    abstract::Preschool sarcoidosis is characterized by the triad of skin, joint, and eye disease without pulmonary involvement. Arthritis and uveitis are also frequently seen together in juvenile rheumatoid arthritis. We report two patients with preschool sarcoidosis, both of whom were initially diagnosed and treated as having juv...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1990.tb00285.x

    authors: Sahn EE,Hampton MT,Garen PD,Warrick J,Smith D,Silver RM

    更新日期:1990-09-01 00:00:00

  • Precalcaneal congenital fibrolipomatous hamartomas: report of occurrence in half brothers.

    abstract::Precalcaneal congenital fibrolipomatous hamartomas are uncommon, congenital, nontender papules located on the medial plantar aspects of the heel. We report the occurrence of this rare disorder in two half brothers, suggesting that it may occur in a familial pattern. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21608.x

    authors: Fangman WL,Prose NS

    更新日期:2004-11-01 00:00:00

  • Practical application of the new classification scheme for congenital melanocytic nevi.

    abstract::A new consensus-based classification of congenital melanocytic nevi (CMN) has recently been proposed. It includes categories for projected adult size (PAS) and location, satellite nevi counts, and morphologic characteristics (color heterogeneity, rugosity, nodularity, and hypertrichosis). The objective of the current ...

    journal_title:Pediatric dermatology

    pub_type: 指南,杂志文章

    doi:10.1111/pde.12428

    authors: Price HN,O'Haver J,Marghoob A,Badger K,Etchevers H,Krengel S

    更新日期:2015-01-01 00:00:00

  • Langerhans cell histiocytosis: clinical experience with 124 patients.

    abstract::We cared for 124 pediatric patients with a histologic diagnosis of Langerhans' cell histiocytosis (histiocytosis X) over a period of 14 years. Clinical, laboratory, and radiographic findings were analyzed. The most frequent manifestations were bone lesions, lymph node involvement, and skin infiltration. Liver disease ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1988.tb01160.x

    authors: Rivera-Luna R,Martinez-Guerra G,Altamirano-Alvarez E,Martinez-Avalos A,Cardenas-Cardoz R,Ayon-Cardenas A,Ruiz-Maldonado R,Lopez-Corella E

    更新日期:1988-08-01 00:00:00

  • Congenital triangular alopecia.

    abstract::We report a child with bilateral congenital triangular alopecia. Shaving the scalp and inserting intravenous cannulas into scalp vessels during the neonatal period was misconstrued by the parents as the cause of hair loss, and resulted in medicolegal implications. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1996.tb00708.x

    authors: Armstrong DK,Burrows D

    更新日期:1996-09-01 00:00:00

  • Tuberous sclerosis with macrodactyly.

    abstract::Tuberous sclerosis with macrodactyly is a very uncommon presentation. We report a 15-year-old girl with a thick, loose hyperpigmented area on the dorsum of the left hand with macrodactyly. A skin biopsy specimen from the dorsum of the left hand revealed dense collagenization in the dermis. Radiographs showed marked ir...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2000.01821.x

    authors: Sahoo B,Handa S,Kumar B

    更新日期:2000-11-01 00:00:00

  • Infantile toxic epidermal necrolysis: Successful treatment of an 8-week-old with intravenous immunoglobulin and amniotic membrane transplant.

    abstract::Stevens-Johnson syndrome and toxic epidermal necrolysis comprise a spectrum of severe mucocutaneous hypersensitivity reactions. A paucity of data limits current understanding of the etiology, treatment options, and prognosis of this entity in the infantile population compared to that in the adult and pediatric literat...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.14376

    authors: Nassim JS,Karim SA,Grenier PO,Schmidt B,Jones KM

    更新日期:2020-10-30 00:00:00