Aplasia cutis congenita and other anomalies associated with methimazole exposure during pregnancy.

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 pregnancy.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

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

doi

10.1111/j.1525-1470.2011.01572.x

subject

Has Abstract

pub_date

2011-11-01 00:00:00

pages

743-5

issue

6

eissn

0736-8046

issn

1525-1470

journal_volume

28

pub_type

杂志文章
  • Phacomatosis pigmentovascularis type 2b (phacomatosis cesioflammea) with double superior vena cava, abdominal varicosities, and natal tooth: Novel associations.

    abstract::Phacomatosis pigmentovascularis is characterized by coexistent extensive cutaneous vascular (capillary) and pigmentary anomalies. We describe a 2-month-old infant presenting with classic features of phacomatosis pigmentovascularis 2b (phacomatosis cesioflammea). He was also found to have hitherto unreported associatio...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13427

    authors: Singal A,Mittal H,Aggarwal A,Das S,Manchanda S

    更新日期:2018-05-01 00:00:00

  • Skin cancer prevention counseling and clinical practices of pediatricians.

    abstract::Little is known about pediatricians' counseling and clinical practices to reduce skin cancer risk among their patients. Thus our objectives were to characterize skin cancer preventive counseling and clinical practices in a sample of pediatricians and identify correlates of these practices. Physicians practicing genera...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.03004.x

    authors: Gritz ER,Tripp MK,de Moor CA,Eicher SA,Mueller NH,Spedale JH

    更新日期:2003-01-01 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

  • Corticosteroid wraps as monotherapy in a child with extensive idiopathic pyoderma gangrenosum.

    abstract::Pyoderma gangrenosum (PG) is an inflammatory neutrophilic dermatosis that may present with limited to severe disease, posing a therapeutic challenge. A 7-year-old African female who presented with extensive PG showed a remarkable response to corticosteroid wrap monotherapy. ...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.14348

    authors: Chateau A,Makhubele J,Dlova N

    更新日期:2020-09-06 00:00:00

  • Diffuse capillary malformation in association with fetal pleural effusion: report of five patients.

    abstract::Capillary malformation (CM) can be a "red flag" for several syndromic vascular anomalies. We identified a subset of patients with diffuse CM and fetal pleural effusion and documented the type of CM, the etiology of the pleural effusion, the potential syndromic diagnosis, and outcome. Patients with a history of CM and ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12401

    authors: Rork JF,Alomari AI,Mulliken JB,Fishman SJ,Liang MG

    更新日期:2015-01-01 00:00:00

  • FOXN1 Duplication and Congenital Hypertrichosis.

    abstract::We report a case of congenital hypertrichosis and FOXN1 duplication. FOXN1 is a member of the forkhead box gene family, located on chromosome 17. Its function includes differentiation of epithelial cells and regulation of keratinocytes, especially hair keratins. Loss of function of these transcription factors leads to...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13078

    authors: Gilhooley E,Gormally S,Irvine A,Lynch SA,Collins S

    更新日期:2017-03-01 00:00:00

  • Head-and-neck dermatitis: Diagnostic difficulties and management pearls.

    abstract::Head-and-neck dermatitis is a variant of atopic dermatitis (AD) often seen in children and is challenging to diagnose, as it frequently overlaps with other eczematous dermatoses. Successful head-and-neck dermatitis (HND) treatment requires identification of common triggers and clinical mimickers, such as airborne derm...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13642

    authors: Maarouf M,Saberian C,Lio PA,Shi VY

    更新日期:2018-11-01 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

  • Transient Porphyrinemia in a Neonate: A Case Report.

    abstract::We describe a neonate with anemia, thrombocytopenia, and hyperbilirubinemia secondary to hemolytic disease of the newborn. After phototherapy for hyperbilirubinemia, the neonate developed a photodistributed eruption with high serum and urine porphyrin levels. This transient porphyrinemia resolved at 1 month. ...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.12963

    authors: Boer B,Tisack A,Shwayder T

    更新日期:2016-11-01 00:00:00

  • Statistical survey of skin changes in Japanese neonates.

    abstract::We observed 5387 infants over 10 years in weekly visits to a neonatal ward and obtained the following frequency data on these skin changes: erythema toxicum neonatorum, 40.8%; perianal dermatitis, 18.9%; scrotal pigmentation, 15.2%; miliaria, 8.5%; and adnexal polyp of neonatal skin, 4.1%. The frequencies of the types...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1986.tb00505.x

    authors: Hidano A,Purwoko R,Jitsukawa K

    更新日期:1986-02-01 00:00:00

  • Perforating folliculitis in a patient with cystic fibrosis.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01329.x

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

    更新日期:2010-11-01 00:00:00

  • Trichothiodystrophy associated with urologic malformation and primary hypercalciuria.

    abstract::Trichothiodystrophy (TTD) is a hair abnormality that may be associated with a large number of alterations affecting the skin phenotype and skin appendages, nervous system, eyes, bones, and immune, gonadal, and endocrine systems. We report the first case of TTD associated with a urologic malformation and primary hyperc...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1997.tb00685.x

    authors: Malvehy J,Ferrando J,Soler J,Tuneu A,Ballesta F,Estrach T

    更新日期:1997-11-01 00:00:00

  • Nodular lichen myxedematosus during childhood: a case report.

    abstract::Nodular lichen myxedematosus (LM) is a rare disease and is one of the five subtypes of localized LM. It is distinctly characterized by multiple nodules on the trunk and limbs with or without papular lesions. A healthy 6-year-old boy presented with complaints of "knots" on his right chest, upper limb, and thigh for 4 m...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12376

    authors: Zeng R,Li M,Jiang Y,Liu W

    更新日期:2014-11-01 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

  • Streptococcal exanthem in a blaschkolinear pattern: clinical evidence for genetic mosaicism in hypomelanosis of ito.

    abstract::Due to the presence of two different clones of cells in early embryogenesis, numerous congenital and acquired dermatoses have a linear distribution following the lines of Blaschko. Acquired inflammatory skin diseases are rarely observed in linear patterns. Our patient was born with macrocephaly, left eye glaucoma, and...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2002.00119.x

    authors: Durán-McKinster C,Moises C,Rodríguez-Jurado R,Tamayo-Sánchez L,Orozco-Covarrubias L,Ruiz-Maldonado R

    更新日期:2002-09-01 00:00:00

  • Metastatic Crohn's disease: a case report.

    abstract::Metastatic Crohn's disease (MCD) is a rare extraintestinal manifestation of Crohn's disease characterized by the histologic finding of granulomatous dermatitis at a site noncontiguous to the gastrointestinal tract. An adolescent had MCD of the face that was initially mistaken for severe, treatment-resistant acne. Hist...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1996.tb01182.x

    authors: Cummins RE,Mullins D,Smith LJ,Ford MJ

    更新日期:1996-01-01 00:00:00

  • Primary annular plaque-type psoriasis.

    abstract::We described two adolescent girls with untreated, consistently annular, plaque-type psoriasis without pustules, a presentation that is to our knowledge, not previously described. No typical confluent plaque-type lesions were present. The plaques in our patients resembled other entities such as tinea corporis and eryth...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22103.x

    authors: Guill CL,Hoang MP,Carder KR

    更新日期:2005-01-01 00:00:00

  • Xanthomas and the inherited hyperlipoproteinemias in children and adolescents.

    abstract::Early recognition of the hyperlipoproteinemias is a crucial element in preventing premature coronary artery disease. Xanthomas provide a cutaneous marker of the silent, underlying pathology. Identifying them, and understanding their relation to the inherited hyperlipoproteinemias may facilitate early diagnosis of hype...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1990.tb00275.x

    authors: Maher-Wiese VL,Marmer EL,Grant-Kels JM

    更新日期:1990-09-01 00:00:00

  • Scalp infestation by Phthirus pubis in a 6-week-old infant.

    abstract::This case report describes a 6-week-old infant with a Phthirus pubis infestation of the scalp. It is believed this patient is the first reported case in this age group. Treatment is discussed, as are the family dynamics that put this infant at risk. The authors address the possible association between infestation and ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1990.tb00284.x

    authors: Silburt BS,Parsons WL

    更新日期:1990-09-01 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

  • Polyurethane toilet seat contact dermatitis.

    abstract::Polyurethane chemicals are produced by the reaction of isocyanates and they may cause allergic contact dermatitis or precipitate asthma attacks. Contact dermatitis to polyurethane toilet seat has not been reported before. Herein we present a case of allergic contact dermatitis to polyurethane toilet seat. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01482.x

    authors: Turan H,Saricaoğlu H,Turan A,Tunali S

    更新日期:2011-11-01 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

  • Rapp-Hodgkin syndrome with pili canaliculi.

    abstract::A 20-year-old woman and her 12-year-old brother had hypohidrotic ectodermal dysplasia, cleft lip and palate, midfacial hypoplasia with narrow nose from the nasal bridge to the tip, narrow dysplastic nails, and conical teeth and hypodontia, and hypospadias and hypoplastic uvula in the boy. The woman had major underdeve...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1993.tb00015.x

    authors: Camacho F,Ferrando J,Pichardo AR,Sotillo I,Jorquera E

    更新日期:1993-03-01 00:00:00

  • Hypopigmented mycosis fungoides associated with atopy in two children.

    abstract::Mycosis fungoides is very rare in children. Hypopigmented lesions of this disease are usually observed in dark-skinned individuals and often show a T supressor CD8(+) phenotype. Two Caucasian children with predominantly hypopigmented lesions of mycosis fungoides are presented here. Atopy was a concomitant feature in b...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00291.x

    authors: Onsun N,Kural Y,Su O,Demirkesen C,Büyükbabani N

    更新日期:2006-09-01 00:00:00

  • Lichenoid sarcoidosis in a 3-year-old girl.

    abstract::We report a case of lichenoid sarcoidosis in a 3-year-old girl. She had numerous discrete skin-colored or erythematous, infiltrated follicular papules on the buttocks and extremities since 2 months of age. Histopathologic examination showed follicular plugging and an upper dermal granulomatous infiltrate of epithelioi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2001.01958.x

    authors: Seo SK,Yeum JS,Suh JC,Na GY

    更新日期:2001-09-01 00:00:00

  • Febrile ulceronecrotic Mucha-Habermann disease with central nervous system vasculitis.

    abstract::Febrile ulceronecrotic Mucha-Habermann disease (FUMHD) is a severe variant of pityriasis lichenoides et varioliformis acuta (PLEVA). We report a case of FUMHD in an 11-year-old boy who subsequently developed neurologic symptoms and was found to have necrotizing vasculitis on brain biopsy. Over 5 years of follow-up, he...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01669.x

    authors: Rosman IS,Liang LC,Patil S,Bayliss SJ,White AJ

    更新日期:2013-01-01 00:00:00

  • Pigment Loss in Patients with Large Congenital Melanocytic Nevi: Various Clinical Presentations Documented in a Large Series.

    abstract:BACKGROUND/OBJECTIVES:The association between vitiligo and congenital melanocytic nevi remains incompletely understood. The objective of this study was to investigate the frequency of depigmentation, including vitiligo, in patients with a large congenital melanocytic nevus (LCMN), which is a rare melanocytic tumor vari...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12823

    authors: Polat Ekinci A,Kiliç S,Baykal C

    更新日期:2016-05-01 00:00:00

  • Increased melanocytic nevi and lentigines in two patients with harlequin ichthyosis.

    abstract::An increased number of melanocytic nevi and lentigines have been reported in patients with two types of autosomal recessive congenital ichthyosis (ARCI): lamellar ichthyosis and nonbullous congenital ichthyosiform erythroderma. These melanocytic lesions may have clinical and dermoscopic features of atypia, necessitati...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.14066

    authors: McKenzie S,Arzeno J,Lonowski S,Cheng CE,Hogeling M

    更新日期:2020-01-01 00:00:00

  • Case report: vulvar lichen sclerosus in a premenarchal girl with a complicated biopsy.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00922.x

    authors: Yousefi M,Pride H,Elston D

    更新日期:2009-05-01 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