Hypopigmented mycosis fungoides associated with atopy in two children.

abstract：:Bullous pemphigoid (BP) is the most common autoimmune blistering disease affecting the elderly but is quite rare in childhood. The majority of pediatric cases have been reported during early childhood. Adolescence is divided into three phases: early (10-13 years), middle (14-17), and late (18-21). This review aimed to...

journal_title：Pediatric dermatology

authors： Patsatsi A,Kyriakou A,Werth VP

更新日期：2019-03-01 00:00:00

abstract：:The common manifestations of atopic dermatitis (AD) appear sequentially with involvement of the cheeks in infancy, flexural extremities in childhood, and hands in adulthood. Although less common clinical manifestations are well described, they have not been the subject of epidemiologic studies to describe their preval...

journal_title：Pediatric dermatology

authors： Julián-Gónzalez RE,Orozco-Covarrubias L,Durán-McKinster C,Palacios-Lopez C,Ruiz-Maldonado R,Sáez-de-Ocariz M

更新日期：2012-09-01 00:00:00

abstract：:Melanonychia striata in childhood is primarily due to congenital nevi, but melanoma should be excluded. We report a case in which dermoscopy was used in an attempt to avoid incisional biopsy. ...

journal_title：Pediatric dermatology

authors： Lazaridou E,Giannopoulou C,Fotiadou C,Demiri E,Ioannides D

更新日期：2013-11-01 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：:Throughout history, individuals have had a myriad of dermatologic conditions characterized as chronic pruritic dermatoses. The term atopic dermatitis was not coined until the early 20th century. Many diseases typical of this condition were reported using a variety of eponyms and descriptive terms. Even as the incidenc...

journal_title：Pediatric dermatology

authors： Bhattacharya T,Strom MA,Lio PA

更新日期：2016-07-01 00:00:00

abstract：:PHACE syndrome is characterized by posterior fossa malformations (P), large facial hemangiomas (H), arterial anomalies (A), cardiac anomalies or coarctation of aorta (C), and eye anomalies (E) and has striking female predominance. Endocrine abnormalities have recently been described in these patients, involving the th...

journal_title：Pediatric dermatology

authors： Altin H,Alp H,Sap F,Karataş Z,Baysal T,Karaaslan S

更新日期：2012-05-01 00:00:00

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

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

更新日期：2013-01-01 00:00:00

abstract：:Poikiloderma with neutropenia (PN), Clericuzio type (OMIM #604173) is a new, unique genodermatosis first described by Clericuzio et al (Am J Med Genet A, 2011, 155, 337) in Navajo Indian population. This disease is characterized by poikiloderma that usually develops in the first year of life and is associated with nai...

journal_title：Pediatric dermatology

authors： Chantorn R,Shwayder T

更新日期：2012-07-01 00:00:00

abstract：:Stevens-Johnson syndrome is a potentially fatal condition that manifests mainly on the skin and mucosal surfaces but also affects other vital organs. There are no report of Stevens-Johnson syndrome caused by brucella infection in the literature. In this article, a previously healthy boy, diagnosed as Stevens-Johnson s...

journal_title：Pediatric dermatology

authors： Babayigit A,Olmez D,Uzuner N,Caglayan S,Kumral A,Asilsoy SK,Ozer E,Karaman O

更新日期：2007-07-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Emollients are part of the standard treatment for atopic dermatitis (AD), although there is limited evidence that regular use of emollients as management therapy reduces the frequency of flares and corticosteroid consumption. The objective of this study was to evaluate the benefit of emollient use...

journal_title：Pediatric dermatology

authors： Tiplica GS,Kaszuba A,Malinauskienė L,Konno P,Boralevi F,Garrigue E,Saint-Aroman M,Delarue A

更新日期：2017-05-01 00:00:00

abstract：:A 3-year-old girl presented with longer hair on the left side of her scalp, coarse hair of abnormal length on her extremities, and a tuft of hair in the lumbosacral region, with all hair distributed on normally pigmented skin. Neither similar or relevant family history nor associated extracutaneous abnormalities was d...

journal_title：Pediatric dermatology

authors： Sotiriadis D,Patsatsi A,Lazaridou E,Sotiriou E,Devliotou-Panagiotidou D

更新日期：2009-07-01 00:00:00

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

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

更新日期：2016-09-01 00:00:00

abstract：:Recently an unusual chronic dermatosis, considered a new clinical entity and closely resembling psoriasis, has been described in the literature under the term psoriasiform acral dermatitis (PAD). It is characterized by cutaneous involvement of the digits without nail dystrophy. We describe three young patients, ages 6...

journal_title：Pediatric dermatology

authors： Patrizi A,Bardazzi F,Neri I,Fanti PA

更新日期：1999-11-01 00:00:00

abstract：:Acne fulminans is a severe form of acne characterized by painful, inflammatory nodules that progress into ulcers and concurrent systemic symptoms. Treatment of acne with isotretinoin can precipitate a syndrome called isotretinoin-induced acne fulminans without systemic symptoms. An exuberant granulation tissue respons...

journal_title：Pediatric dermatology

authors： Li AW,Antaya RJ

更新日期：2018-03-01 00:00:00

abstract：:Clinical and pathologic features of five cases of epidermolysis bullosa simplex, Dowling-Meara type (EBS-DM), are described. Four patients were children, and two were related (father and daughter). Clinical history revealed blistering at birth in three patients; in all of them the signs and symptoms improved with age....

journal_title：Pediatric dermatology

authors： Puddu P,Angelo C,Faraggiana T,Onetti Muda A,Colonna L,Paradisi M

更新日期：1996-05-01 00:00:00

abstract：:We report the exceptional case of 11-year-old identical male twins who both developed discoid lupus erythematosus lesions. Although systemic lupus erythematosus has often been reported in identical twins, discoid lupus erythematosus has only occasionally been described, with only one other case in twin children, as fa...

journal_title：Pediatric dermatology

authors： Del Boz J,Martín T,Samaniego E,Vera A,Sanz A,Crespo V

更新日期：2008-11-01 00:00:00

abstract：:Benign fibrous histiocytoma is a common soft tissue tumor that usually occurs in adults and is relatively rare in childhood. This report describes a 7-month-old Caucasian boy with an enlarging firm congenital nodule on his occipital scalp. Histologic analysis revealed a benign fibrous histiocytoma with osteoclast-like...

journal_title：Pediatric dermatology

authors： Stinehelfer SE,Woosley JT,Losken HW,Morrell DS

更新日期：2007-09-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Previous studies have demonstrated an increased prevalence of inflammatory bowel disease (IBD) in adults with hidradenitis suppurativa (HS). Whether the same association exists in pediatric patients is unknown. Fecal calprotectin (FC) is used to screen and monitor disease activity in IBD. There ar...

journal_title：Pediatric dermatology

authors： Lloyd-McLennan AM,Ali S,Kittler NW

更新日期：2020-10-25 00:00:00

abstract：:We report the rare instance of four family members with numerous cutaneous lesions of Leishmania major contracted while on holiday in Algeria. Treatment was successful with oral itraconazole for the children and intralesional sodium stibogluconate for the mother. Cutaneous leishmaniasis should be considered in those w...

journal_title：Pediatric dermatology

authors： White JM,Salisbury JR,Jones J,Higgins EM,Vega-Lopez F

更新日期：2006-01-01 00:00:00

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

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

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：: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

authors： Hill A,Metry D

更新日期：2003-11-01 00:00:00

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

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

更新日期：2013-07-01 00:00:00

abstract：BACKGROUND:Phosphodiesterase-4 (PDE4) is a promising target in atopic dermatitis (AD) treatment. The pharmacokinetics (PK), safety, and efficacy of crisaborole topical ointment, 2% (formerly AN2728) (Anacor Pharmaceuticals, Palo Alto, CA), a boron-based benzoxaborole PDE4 inhibitor, were evaluated in children with mild...

journal_title：Pediatric dermatology

authors： Zane LT,Kircik L,Call R,Tschen E,Draelos ZD,Chanda S,Van Syoc M,Hebert AA

更新日期：2016-07-01 00:00:00

abstract：:We present a 16-year-old girl with a 4-year history of chronic persistent erythema nodosum. Recurrently low serum iron values suggested the possibility of a malabsorption syndrome. The presence of antitransglutaminase and antiendomysium antibodies and the jejunal biopsy specimen findings showed an underlying celiac di...

journal_title：Pediatric dermatology

authors： Bartyik K,Várkonyi A,Kirschner A,Endreffy E,Túri S,Karg E

更新日期：2004-05-01 00:00:00

abstract：:Lichen striatus is a common childhood eruption, but only rare reports link cutaneous manifestations and onychodystrophy. We report a case of lichen striatus and onychodystrophy in a 12-year-old girl, only the eighth such patient in the dermatologic literature. Nail changes may precede the rash of lichen striatus and s...

journal_title：Pediatric dermatology

authors： Karp DL,Cohen BA

更新日期：1993-12-01 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：:Loose anagen hair syndrome (LAHS) is a condition of sparse, short hair that is easily and painlessly extracted from the scalp. Since it was first described in the 1980s, it is considered a rare, sporadic condition found predominantly in females. Since then, there have been multiple reports of LAHS occurring in familie...

journal_title：Pediatric dermatology

authors： Pham CM,Krejci-Manwaring J

更新日期：2010-07-01 00:00:00

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

authors： Wieser I,Wohlmuth C,Duvic M

更新日期：2016-09-01 00:00:00

abstract：:We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous p...

journal_title：Pediatric dermatology

authors： Musumeci ML,Nasca MR,De Pasquale R,Schwartz RA,Micali G

更新日期：2006-05-01 00:00:00