Large multifocal cutaneous hemangioma along lines of Blaschko with cardiac failure treated with propranolol.

abstract：:A 6-year-old Hispanic boy presented to the ophthalmology department with complaints of pain, photophobia, and blurry vision of both eyes. He was found to have bilateral granulomatous panuveitis, cataracts, and high intraocular pressures. He later developed multiple asymptomatic, ovoid, hypopigmented patches over the m...

journal_title：Pediatric dermatology

authors： Hernandez C,LePoole C,Tessler HH

更新日期：2012-03-01 00:00:00

abstract：:Langerhans cell histiocytosis (LCH) is a rare disorder characterized by clonal proliferation of Langerhans cells in the skin. A molluscum-like presentation of cutaneous LCH is rare but important to consider for examination and management. We present an atypical molluscum-like LCH case and review the literature for com...

journal_title：Pediatric dermatology

authors： Karpman MS,AlJasser MI,Lam JM

更新日期：2017-09-01 00:00:00

abstract：:This article reviews skin changes occurring in diabetic children. Skin changes may be related to metabolic alterations associated with diabetes. Others may be manifestations of macro or microvascular disease. Insulin injections, required for management of most diabetes in the pediatric age group, may also cause cutane...

journal_title：Pediatric dermatology

authors： Edidin DV

更新日期：1985-03-01 00:00:00

abstract：:We describe the clinicopathologic features of an unusual case of fibromatosis colli. The lesion was rock hard, lateral, tightly affixed to the clavicle, and with overlying hypertrichosis. ...

journal_title：Pediatric dermatology

authors： Amin A,Loftis B,Shwayder TA

更新日期：2010-09-01 00:00:00

abstract：:Pustular psoriasis (PP) is rare in children. The small number of reported cases makes deciding on treatment and follow-up challenging. The current study was an evaluation of treatment approaches and courses of PP in 18 children diagnosed and followed over a 20-year period. From 1992 to 2011 we treated 1,447 children w...

journal_title：Pediatric dermatology

authors： Popadic S,Nikolic M

更新日期：2014-09-01 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：: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: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：:Lindane (gamma benzene hexachloride) is a widely prescribed topical scabicide because of its efficacy and cost-effectiveness. Although toxicity from a single proper application of lindane is generally not observed, the hazards of repeated applications, industrial exposure, and accidental ingestion have been well docum...

journal_title：Pediatric dermatology

authors： Bhalla M,Thami GP

更新日期：2004-09-01 00:00:00

abstract：:Treatment of verruca plana is often challenging, and multiple treatment modalities, both pharmacologic and destructive, are frequently necessary to clear lesions. We report a case of a 16-year-old girl with a 2-year history of extensive verruca plana of the forehead, temples, and upper periorbital skin, recalcitrant t...

journal_title：Pediatric dermatology

authors： Johnson NM,Pickard CM

更新日期：2020-10-08 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：:Two unrelated Hispanic females, ages 4 and 3 years, respectively, each presented with a solitary patch of excessive terminal hair growth in the midline of the neck. This rare form of congenital localized hypertrichosis, known as anterior cervical hypertrichosis, is reported here as an isolated defect with no other und...

journal_title：Pediatric dermatology

authors： Reddy S 4th,Antaya RJ

更新日期：2010-09-01 00:00:00

abstract：:Childhood granulomatous periorificial dermatitis (CGPD) is a condition included in the spectrum of rosacea and perioral dermatitis that affects prepubescent children. It is characterized by papular eruptions located around the mouth, nose, and eyes that histopathologically show a granulomatous pattern. We report a 9-y...

journal_title：Pediatric dermatology

authors： Rodriguez-Caruncho C,Bielsa I,Fernandez-Figueras MT,Ferrándiz C

更新日期：2013-09-01 00:00:00

abstract：:Anogenital (AG) warts in 31 prepubertal children were HPV typed by nonisotopic in situ hybridization (NISH) using digoxigenin-labeled probes for human papilloma virus (HPV) types 1-5, 6, 11, 16, 18, 31, and 33. Mode of transmission was determined from historical, clinical, and laboratory data independent of HPV typing...

journal_title：Pediatric dermatology

authors： Handley J,Hanks E,Armstrong K,Bingham A,Dinsmore W,Swann A,Evans MF,McGee JO,O'Leary J

更新日期：1997-09-01 00:00:00

abstract：:Subcutaneous fat necrosis is an inflammatory disorder of adipose tissue. Although patients need long-term follow-up to prevent hypercalcemia, the prognosis is generally favorable. We herein present a case of a newborn who developed subcutaneous fat necrosis-related hypercalcemia after hypothermia treatment for hypoxic...

journal_title：Pediatric dermatology

authors： Akcay A,Akar M,Oncel MY,Kızılelma A,Erdeve O,Oguz SS,Uras N,Dılmen U

更新日期：2013-01-01 00:00:00

abstract：:To describe the characteristics of five pediatric patients with the Meyerson phenomenon associated with congenital melanocytic nevi, five cases were reviewed to retrieve information relating to clinical presentation, treatment and evolution of the eczematous phenomenon and of the nevi. Three of five patients were male...

journal_title：Pediatric dermatology

authors： Rolland S,Kokta V,Marcoux D

更新日期：2009-05-01 00:00:00

abstract：:Radiation recall dermatitis (RRD) is an uncommon reaction typically triggered by the use of chemotherapeutic agents in the months after treatment with radiation therapy. It usually presents as dermatitis in the irradiated field with prominent intertriginous involvement, and because internal involvement occurs in up to...

journal_title：Pediatric dermatology

authors： Prindaville B,Horii KA,Canty KM

更新日期：2016-09-01 00:00:00

abstract：:Keratitis ichthyosis deafness syndrome is a rare congenital ectodermal disorder. It appears to be genetically heterogeneous and may be caused by mutations in the connexin 26 (Cx26) gene (GJB2) or in the connexin 30 gene. It is characterized by the association of ichthyosis-like skin lesions, hearing loss, and vascular...

journal_title：Pediatric dermatology

authors： De Raeve L,Bonduelle M,Deconinck H,Roseeuw D,Stene JJ

更新日期：2008-07-01 00:00:00

abstract：:We describe a new case of a rare syndrome characterized by ocular abnormalities and pathognomonic linear skin defects. This syndrome is the result of an unbalanced translocation resulting in a deletion of the distal end of the short arm of the X chromosome. We report the thirteenth case and review the clinical and cyt...

journal_title：Pediatric dermatology

authors： Paulger BR,Kraus EW,Pulitzer DR,Moore CM

更新日期：1997-01-01 00:00:00

abstract：:Menkes's syndrome (trichopoliodystrophy) is an x-linked, recessive genodermatosis characterized by hair defects, severe retardation, convulsions, progressive neurologic deterioration, and early death. Recent studies in copper metabolism suggest that Menkes's syndrome may be a storage disease in which copper is irrever...

journal_title：Pediatric dermatology

authors： Maddox JL Jr,Odom RB,Goette DK

更新日期：1984-04-01 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：: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

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

更新日期：1990-09-01 00:00:00

abstract：:An unselected cohort of 4,641 newborns was ascertained prospectively for the purpose of detecting any cutaneous lesion. These were catalogued into pigmented lesions, vascular lesions, and miscellaneous lesions. Several important findings were elucidated: congenital nevocellular nevi are speckled at their borders; no w...

journal_title：Pediatric dermatology

authors： Alper JC,Holmes LB

更新日期：1983-07-01 00:00:00

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

authors： Penneys NS,Kott-Blumenkranz R,Buck BE,Nadji M,Gould E,Ibe M

更新日期：1986-06-01 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：: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：:A newborn male Thai infant had numerous brownish red nodules of various sizes scattered over both palms and soles, left thigh, abdomen, chin, and left upper eyelid. An extremely large tumor mass was present on the right sole. Many lesions showed spontaneous ulceration. No extracutaneous involvement was found. All lesi...

journal_title：Pediatric dermatology

authors： Timpatanapong P,Rochanawutanon M,Siripoonya P,Nitidandhaprabhas P

更新日期：1989-03-01 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：:The keratitis, ichthyosis, and deafness (KID) syndrome is a rare congenital disorder of the ectoderm characterized by diffuse hyperkeratotic erythroderma, keratitis with neovascularization of the cornea, and severe neurosensory hearing loss. A familial occurrence of this syndrome has been mentioned in four reports inc...

journal_title：Pediatric dermatology

authors： Koné-Paut I,Hesse S,Palix C,Rey R,Rémédiani K,Garnier JM,Berbis P

更新日期：1998-05-01 00:00:00

abstract：:The proband in this study was a 4-year-old Mexican girl with Blau syndrome. She and her affected family members had skin rash and arthritis but no uveitis. Exome sequencing and DNA direct sequencing from blood samples revealed a novel nucleotide-binding oligomerization domain-containing protein 2 gene mutation in the ...

journal_title：Pediatric dermatology

authors： Toral-López J,González-Huerta LM,Martín-Del Campo M,Messina-Baas O,Cuevas-Covarrubias SA

更新日期：2018-05-01 00:00:00