Childhood pemphigus vulgaris treated with dapsone: a case report.

abstract：:Connective tissue nevi of collagen type are now classified in four major subtypes. In addition to the clinicopathological features of papulolinear collagenoma, which is considered as a variant of isolated collagen harmatoma, the case we present has a unique arborizing pattern. ...

journal_title：Pediatric dermatology

authors： Lo LK,Tsai TF,Chen YF,Hung CM,Ko WC

更新日期：2009-01-01 00:00:00

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

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

更新日期：2003-07-01 00:00:00

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

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

更新日期：2011-07-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Sun protection starting in childhood is an important means of skin cancer prevention. Factors associated with sunscreen use have been previously described. However, less is known about factors associated with children's utilization of non-sunscreen sun protection strategies. We sought to examine p...

journal_title：Pediatric dermatology

authors： Schlarbaum JP,Lazovich D,Dodd E,Hanson B,Polcari IC

更新日期：2020-09-01 00:00:00

abstract：:Cranioectodermal dysplasia is a rare syndrome characterized by craniofacial and skeletal anomalies and ectodermal dysplasia. Life-threatening associated conditions (i.e., kidney failure and abnormal regulation of the parathyroid-bone axis) can also develop. We report a patient whose features are suggestive of an inapp...

journal_title：Pediatric dermatology

authors： Zannolli R,Mostardini R,Carpentieri ML,Gatti MG,Galluzzi P,Terrosi Vagnoli P,Giorgetti R,Calvieri S,Morgese G

更新日期：2001-07-01 00:00:00

abstract：:Pulmonary manifestations are well recognized during the acute phase of Stevens-Johnson syndrome but persistent pulmonary sequela is rarely reported. We report two boys with bronchiolitis obliterans following the acute phase of Stevens-Johnson syndrome and discuss the clinical picture and treatment of persistent pulmon...

journal_title：Pediatric dermatology

authors： Bakirtas A,Harmanci K,Toyran M,Razi CH,Turktas I

更新日期：2007-07-01 00:00:00

abstract：BACKGROUND/OBJECTIVES:Palmar hyperlinearity is a typical clinical feature of Filaggrin gene (FLG) null mutations. There are reports of FLG mutations and allergic sensitization; however, reports on the relationship between palmar hyperlinearity to sensitization are limited. This study aimed to examine the association be...

journal_title：Pediatric dermatology

authors： Fukuie T,Yasuoka R,Fujiyama T,Sakabe JI,Taguchi T,Tokura Y

更新日期：2019-03-01 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：:Rothmund-Thomson syndrome (RTS) is a rare autosomal recessive disorder that is caused by a DNA repair defect. It is characterized mainly by skin, eye, and skeletal abnormalities. Cutaneous changes appear at between 3 and 6 months of age and include poikiloderma, photosensitivity, scaling, hyperkeratosis, and disturban...

journal_title：Pediatric dermatology

authors： Narayan S,Fleming C,Trainer AH,Craig JA

更新日期：2001-05-01 00:00:00

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

authors： Chateau A,Makhubele J,Dlova N

更新日期：2020-09-06 00:00:00

abstract：:Hypertrichosis cubiti, also named hairy elbows syndrome (HES), is an uncommon variety of congenital, circumscribed hypertrichosis in which a remarkable amount of long vellus hair is localized on the extensor surfaces of the upper extremities. Usually, this condition appears in infancy, increases during early childhood...

journal_title：Pediatric dermatology

authors： Escalonilla P,Aguilar A,Gallego M,Piqué E,Fariña MC,Requena L

更新日期：1996-07-01 00:00:00

abstract：:Ataxia telangiectasia (AT) is a rare autosomal recessive neurodegenerative disorder caused by a mutation in the ATM gene. An impaired immune response due to the gene mutation leads to an increased risk of infection and malignancy. We present a rare case of dermatofibrosarcoma protuberans arising in a patient with AT. ...

journal_title：Pediatric dermatology

authors： Duffy R,Liaqat M,Lawrence N,Manders S

更新日期：2019-05-01 00:00:00

abstract：:Skin diseases are common in children. However, only a very few prospective epidemiologic surveys are available in the literature. The present survey was directed at determining the spectrum and pattern of skin diseases of children in Kuwait. A total of 10,000 consecutive new patients were studied; 96% were children of...

journal_title：Pediatric dermatology

authors： Nanda A,Al-Hasawi F,Alsaleh QA

更新日期：1999-01-01 00:00:00

abstract：:Eccrine angiomatous hamartoma (EAH) is a rare, benign cutaneous lesion histologically defined as a proliferation of eccrine glands within a closely associated vascular stroma. Typically EAH presents as a solitary flesh-colored, hyperhidrotic, painful papule or plaque appearing at birth or during childhood. Only two pr...

journal_title：Pediatric dermatology

authors： Morrell DS,Ghali FE,Stahr BJ,McCauliffe DP

更新日期：2001-03-01 00:00:00

abstract：:Childhood lichen sclerosus (LS) is a rare and often misdiagnosed inflammatory dermatitis with an unpredictable course. The complications of LS are architectural changes of the vulva; malignant transformation is possible. The objective of our study was to define the background and the long-term course of childhood LS. ...

journal_title：Pediatric dermatology

authors： Lagerstedt M,Karvinen K,Joki-Erkkilä M,Huotari-Orava R,Snellman E,Laasanen SL

更新日期：2013-07-01 00:00:00

abstract：BACKGROUND:Children with congenital melanocytic nevi (CMN) were historically managed with surgical removal to lower the risk of malignant transformation. The evolving literature over the last decade has indicated a significantly lower risk than previously estimated. Indications for excision currently revolve around aes...

journal_title：Pediatric dermatology

authors： Mosa A,Ho ES,Heinelt M,Wong K,Neuhaus K

更新日期：2019-11-01 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：:Four unrelated children with osteoma cutis and Albright hereditary osteodystrophy (pseudohypoparathyroidism and pseudopseudohypoparathyroidism) are described. All four patients were normocalcemic when they were first seen with cutaneous ossification. A diagnosis of Albright hereditary osteodystrophy was established on...

journal_title：Pediatric dermatology

authors： Prendiville JS,Lucky AW,Mallory SB,Mughal Z,Mimouni F,Langman CB

更新日期：1992-03-01 00:00:00

abstract：:Congenital midline cervical cleft is a rare anomaly of the ventral neck that heretofore has not been reported in the dermatology literature. We present a case of a midline cervical cleft that was diagnosed and managed at an early age. We also review the literature and discuss its clinical and histologic features, trea...

journal_title：Pediatric dermatology

authors： Eastlack JP,Howard RM,Frieden IJ

更新日期：2000-03-01 00:00:00

abstract：:Spitz nevi are benign melanocytic lesions with many histologic similarities to malignant melanoma. A case of agminated Spitz nevi on a 2-year-old boy's left cheek is reported and 41 other cases of agminated Spitz nevi are reviewed. In this case, two biopsies were performed on two different-appearing lesions and the re...

journal_title：Pediatric dermatology

authors： Zeng MH,Kong QT,Sang H,Deng DQ,Xie QM

更新日期：2013-09-01 00:00:00

abstract：:Nickel allergic contact dermatitis is the most prevalent allergy in North America, with an incidence of 14.3%. It is on the rise from 10 years ago, when the incidence was 10%. This has been presumed to represent an increased exposure to nickel in the environment-especially in costume jewelry and belt buckles. We exami...

journal_title：Pediatric dermatology

authors： Silverberg NB,Licht J,Friedler S,Sethi S,Laude TA

更新日期：2002-03-01 00:00:00

abstract：:Verruciform xanthoma (VX) is a rare finding thought to be caused by epidermal damage from trauma or inflammation and has been reported in a limited number of patients with recessive dystrophic epidermolysis bullosa (RDEB). Herein, we describe a 20-year-old woman with RDEB who developed a large, verrucous, pink plaque ...

journal_title：Pediatric dermatology

authors： Stephens M,Rubin AI,Perman MJ

更新日期：2020-03-01 00:00:00

abstract：:An 8-year-old girl had Crohn's disease of the vulva 16 months before the onset of intestinal symptoms. At the time of diagnosis she had no evidence of systemic disease. Cutaneous and intestinal lesions responded rapidly to corticosteroids and metronidazole. Crohn's disease must be considered in the differential diagno...

journal_title：Pediatric dermatology

authors： Lally MR,Orenstein SR,Cohen BA

更新日期：1988-05-01 00:00:00

abstract：:Pediatric dermatologists may care for patients with percutaneous enteral feeding tubes. Although ostomy complications such as allergic contact and irritant dermatitis are common, psoriasis may be misdiagnosed. We report three novel cases of childhood psoriasis first presenting around an enteral feeding tube site. Loca...

journal_title：Pediatric dermatology

authors： Zitelli KB,Lucky AW

更新日期：2014-01-01 00:00:00

abstract：:Hair loss and thinning are possible complications in those undergoing endocrine therapies with aromatase inhibitors. Alopecia in pediatric patients undergoing endocrine therapy has not been previously reported. We describe two adolescents, 14 and 16 years of age, who developed androgenetic alopecia following treatment...

journal_title：Pediatric dermatology

authors： Perper M,Herskovitz I,Tosti A

更新日期：2020-11-01 00:00:00

abstract：:Successful management of toxic epidermal necrolysis (TEN) with tumor necrosis factor-α inhibitors has been described in adults. We present a case of a 7-year-old boy with infection-associated TEN, diagnosed by typical clinical and histopathological features, most likely caused by Mycoplasma pneumoniae. Treatment with ...

journal_title：Pediatric dermatology

authors： Chafranska L,Saunte DM,Behrendt N,Nygaard U,Christensen RJ,Sand C,Jemec GB

更新日期：2019-05-01 00:00:00

abstract：:In 1980 a syndrome was first described in two adult males, consisting of macrocephaly, pigmented macules on the glans and shaft of the penis, and hamartomatous intestinal polyps. Since then, 10 additional cases have been identified. Herein, we present two new cases and review the cutaneous manifestations as well as ad...

journal_title：Pediatric dermatology

authors： Gretzula JC,Hevia O,Schachner LS,DiLiberti JH,Ruvalcaba RH,Schimschock JR,Weleber RG,Halal F,Lipson MH,Blumberg B

更新日期：1988-02-01 00:00:00

abstract：:Tuberous sclerosis complex is an autosomal dominant disorder that often manifests early in life with cutaneous features, and it is important that dermatologists who care for children remain up to date on its diagnosis and management. This article provides an update regarding the most recent guidelines for diagnosis pu...

journal_title：Pediatric dermatology

authors： Jacks SK,Witman PM

更新日期：2015-09-01 00:00:00

abstract：:We examined a father and son affected by Ehlers-Danlos syndrome type II. Both patients had micrognathia together with ligament and skin hyperlaxity. The son exhibited complete cleft palate. Ultrastructural studies revealed abnormal collagen fibrils in the dermis of both patients. In the child the most striking alterat...

journal_title：Pediatric dermatology

authors： Rizzo R,Contri MB,Micali G,Quaglino D,Pavone L,Ronchetti IP

更新日期：1987-11-01 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