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

abstract：:Depigmentation after the use of topical immune modulators is a rare but reported event. Herein we present what is to our knowledge the first case of vitiligo at a site of Candida antigen injection. ...

journal_title：Pediatric dermatology

authors： Wilmer EN,Burkhart CN,Morrell DS

更新日期：2013-11-01 00:00:00

abstract：:Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive malignancy of the skin and hematopoietic system. There are few pediatric cases reported in the literature. Management of primary cutaneous BPDCN is challenging because, despite an apparently indolent clinical presentation, rapid disseminatio...

journal_title：Pediatric dermatology

authors： Rivas-Calderón MK,Cheirif-Wolosky O,Rosas-Romero ME,Toussaint-Caire S,Duran-Mckinster C,González-Pedroza ML,López-Santiago NC,García-Romero MT

更新日期：2020-12-04 00:00:00

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

authors： Zeng R,Li M,Jiang Y,Liu W

更新日期：2014-11-01 00:00:00

abstract：:Phrynoderma is a distinctive form of follicular hyperkeratosis associated with nutritional deficiency. Although originally thought to represent vitamin A deficiency, several studies have demonstrated multiple etiologies. Characteristic skin lesions are hyperkeratotic papules that first appear on the extensor surfaces ...

journal_title：Pediatric dermatology

authors： Maronn M,Allen DM,Esterly NB

更新日期：2005-01-01 00:00:00

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 ar...

journal_title：Pediatric dermatology

authors： Jansen T,Romiti R,Altmeyer P

更新日期：2000-09-01 00:00:00

abstract：:Cutaneous tuberculosis is a rare form of extrapulmonary tuberculosis that accounts for 1% to 2% of cases. Childhood skin tuberculosis represents 18% to 82% of all cutaneous tuberculosis cases. Scrofuloderma and lupus vulgaris are the two most common clinical forms in children. An increase in the number of tuberculids,...

journal_title：Pediatric dermatology

authors： Sethuraman G,Ramesh V

更新日期：2013-01-01 00:00:00

abstract：:Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a variety of underlying abnormalities. The phenotype includes parchment-like hyperkeratosis, pseudocontractures, ectropion, eclabium, absence of eyebrows, and sparse hair. Asymmetric crying facies is caused by congenital hyp...

journal_title：Pediatric dermatology

authors： Akcakus M,Gunes T,Kurtoglu S,Ozturk A

更新日期：2003-03-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Recent technological advances and diagnostic and therapeutic innovations have resulted in an impressive improvement in the survival of newborn infants requiring intensive care. Consequently, with the use of modern invasive diagnostic and therapeutic procedures, the incidence of iatrogenic events h...

journal_title：Pediatric dermatology

authors： Csoma ZR,Meszes A,Ábrahám R,Kemény L,Tálosi G,Doró P

更新日期：2016-09-01 00:00:00

abstract：:Two native Yanomami children from the Venezuelan Amazonia with erythroderma were hospitalized on our service. Clinical, histologic, and immunofluorescence studies diagnosed endemic pemphigus foliaceous. Human leukocyte antigen class II showed DRB1*04 subtype *0411, which has not been previously associated with this di...

journal_title：Pediatric dermatology

authors： González F,Sáenz AM,Cirocco A,Tacaronte IM,Fajardo JE,Calebotta A

更新日期：2006-03-01 00:00:00

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

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

更新日期：2002-11-01 00:00:00

abstract：:A boy with junctional epidermolysis bullosa died from acute laryngeal obstruction at the age of 29 months, having been hoarse since early infancy. Post mortem studies showed gross narrowing of the laryngeal airway by cystic dilatations of the ducts of the seromucinous glands, and replacement of the laryngeal epitheliu...

journal_title：Pediatric dermatology

authors： Davies H,Atherton DJ

更新日期：1987-08-01 00:00:00

abstract：:The objective of the study was to determine the prevalence of pediatric human immunodeficiency virus 1 (HIV-1) mucocutaneous manifestations in the era of highly active antiretroviral therapy (HAART). We conducted population-based, prospective, multicenter pediatric HIV-1 surveillance in 276 children with perinatally a...

journal_title：Pediatric dermatology

authors： Sturt AS,Anglemyer A,Berk DR,Maldonado YA

更新日期：2013-07-01 00:00:00

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

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

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

authors： Butler DF,Ranatunge BD,Rapini RP

更新日期：2001-01-01 00:00:00

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

authors： Burden AD,Krafchik BR

更新日期：1999-09-01 00:00:00

abstract：:Follicular mucinosis (FM) is an uncommon reaction pattern in which the accumulation of mucin in the follicular epithelium is the main pathologic finding. FM may be idiopathic (primary follicular mucinosis [PFM]), in association with mycosis fungoides or cutaneous T-cell lymphoma, or in association with other neoplasti...

journal_title：Pediatric dermatology

authors： Santos-Briz A,Cañueto J,García-Dorado J,Alonso MT,Balanzategui A,González-Díaz M

更新日期：2013-11-01 00:00:00

abstract：BACKGROUND:In recent years propranolol has become the treatment of choice for infantile hemangiomas (IHs). There is broad variation in the approach to propranolol initiation in clinical practice. This retrospective study explored the effectiveness of routine pre-treatment ECG in screening infants being considered for s...

journal_title：Pediatric dermatology

authors： Yarbrough KB,Tollefson MM,Krol AL,Leitenberger SL,Mann JA,MacArthur CJ

更新日期：2016-11-01 00:00:00

abstract：:Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a type of skin lymphoma. Pleomorphic T-cells infiltrate the subcutaneous tissue and mimic lobular panniculitis. We report a case occurring in a 12-year-old Chinese boy who presented with multiple indolent erythematous subcutaneous nodules on both extremities wi...

journal_title：Pediatric dermatology

authors： Hu ZL,Sang H,Deng L,Li Z

更新日期：2015-07-01 00:00:00

abstract：:We report an unusual occurrence of spontaneous pigmentary regression with a desmoplastic reaction in a neonatally eroded giant congenital melanocytic nevus. This process has been documented with photographs and skin biopsy specimens. Neonatal histology demonstrated connective tissue proliferation. Histology at age 5 y...

journal_title：Pediatric dermatology

authors： Gass JK,Grant JW,Hall PN,Atherton DJ,Burrows NP

更新日期：2006-11-01 00:00:00

abstract：:Although lentigines are usually benign, they can be associated with a number of genetic syndromes in which neoplasms and other multi-system pathological processes occur. Here, we report the case of a 6-year-old girl who presented with atypical lentiginosis and hyperpigmentation caused by a de novo genetic variant in t...

journal_title：Pediatric dermatology

authors： Tran AK,Pearce A,López-Sánchez M,Pérez-Jurado LA,Barnett C

更新日期：2019-11-01 00:00:00

abstract：:A wide spectrum of histopathologic changes has been reported to occur within epidermal nevi. We saw two patients with warty nevoid lesions in which histopathologic features of incontinentia pigmenti, verrucous phase, were present. The diagnosis of incontinentia pigmenti was excluded because both patients were male, la...

journal_title：Pediatric dermatology

authors： Fletcher V,Williams ML,Lane AT

更新日期：1985-11-01 00:00:00

abstract：:Although acne vulgaris is common in preadolescents (<13 yrs), few acne treatments are currently approved for children. This study assessed the safety and efficacy of tretinoin microsphere gel (TMG) 0.04% pump in children aged 9-11 with acne vulgaris. In this multicenter, randomized, double-blind, vehicle-controlled pi...

journal_title：Pediatric dermatology

authors： Eichenfield LF,Hebert AA,Schachner L,Paller AS,Rossi AB,Lucky AW

更新日期：2012-09-01 00:00:00

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

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

更新日期：2002-07-01 00:00:00

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

authors： Silburt BS,Parsons WL

更新日期：1990-09-01 00:00:00

abstract：:Acute genital ulcers rarely occur in nonsexually active young girls. When present, they can cause significant physical and emotional distress for the patient and her parents, and prompt an evaluation for sexual abuse and sexually transmitted diseases. With this review, we aim to further characterize acute genital ulce...

journal_title：Pediatric dermatology

authors： Rosman IS,Berk DR,Bayliss SJ,White AJ,Merritt DF

更新日期：2012-03-01 00:00:00

abstract：:Infantile myofibromatosis is a rare benign tumor of infancy and childhood that occurs in solitary, multiple, and generalized forms with similar histology but different clinicopathologic and prognostic implications. Even solitary tumors need follow-up, as the type of presentation will be determined over time. It is nec...

journal_title：Pediatric dermatology

authors： Jurcić V,Perković T,Pohar-Marinsek Z,Hvala A,Lazar I

更新日期：2003-07-01 00:00:00

abstract：:Oral-facial-digital syndrome type 1 (OMIM #311200) is an X-linked dominant, developmental disorder. Among the 13 described clinical variants of oral-facial-digital syndrome, oral-facial-digital syndrome type 1 is of significance to dermatologists due to presence of congenital milia and hypotrichosis, not described in ...

journal_title：Pediatric dermatology

authors： Nanda A,Sharaf A,Alsaleh QA

更新日期：2010-11-01 00:00:00

abstract：:Orofacial granulomatosis, a rare disease in childhood, is characterized by orofacial swelling in the absence of systemic disease. We report the case of a 12-year-old girl with asymptomatic erythematous infiltration of her upper lip, cheeks, and chin that had persisted for more than 2 years; biopsy confirmed granuloma ...

journal_title：Pediatric dermatology

authors： Lalosevic J,Gajic-Veljic M,Nikolic M

更新日期：2017-11-01 00:00:00

abstract：:Over the years, the application and complications of radiofrequency ablation (RFA) in selective fetal reduction for complex pregnancies have been increasingly documented. Despite its rising use in the field of obstetrics and gynecology, the cutaneous complications of RFA have not been commonly reported. Here, we prese...

journal_title：Pediatric dermatology

authors： Law JY,Choi EC,Chandran NS

更新日期：2020-11-01 00:00:00

abstract：:A 40-year-old man and his 6-year-old only son had numerous, firm papulonodular lesions on their faces. Their medical histories were unremarkable and no family consanguinity was recorded. Surgical excision of several lesions was performed on each patient. All the lesions were solid tumors with the characteristic histop...

journal_title：Pediatric dermatology

authors： Pujol RM,Casanova JM,Egido R,Pujol J,de Moragas JM

更新日期：1995-12-01 00:00:00