Urticating Hashimoto-Pritzker Langerhans cell histiocytosis.

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：:Proteus syndrome is an extremely rare mosaic condition characterized by progressive overgrowth of tissues due to a somatic activating mutation of the AKT1 gene. Distinct cutaneous features, including cerebriform connective tissue nevi, epidermal nevi, vascular malformations, and adipose abnormalities, can alert the de...

journal_title：Pediatric dermatology

authors： Rodenbeck DL,Greyling LA,Anderson JH,Davis LS

更新日期：2016-09-01 00:00:00

abstract：:Superficial granulomatous pyoderma is a rare entity thought to be a variant of pyoderma gangrenosum and is often mistaken for classic pyoderma gangrenosum. Superficial granulomatous pyoderma has mainly been described in adults. We describe a case of Superficial granulomatous pyoderma in an 11-year-old girl and present...

journal_title：Pediatric dermatology

authors： Tollefson MM,Cook-Norris RH,Theos A,Davis DM

更新日期：2010-09-01 00:00:00

abstract：:This is a follow-up report on a boy with phacomatosis pigmentokeratotica. At the age of 10 years he had, in addition to a sebaceous nevus and a speckled lentiginous nevus, multiple lesions of a collagen nevus localized on the chin and in the lumbar area. On the left shoulder, a small telangiectatic spot was present wi...

journal_title：Pediatric dermatology

authors： Boente Mdel C,Asial RA,Happle R

更新日期：2008-01-01 00:00:00

abstract：:Acquired progressive lymphangioma (APL), or benign lymphangioendothelioma, is an unusual entity derived from vascular structures. Clinically and histopathologically it may resemble Kaposi's sarcoma and well-differentiated angiosarcoma, causing a diagnostic problem. We report an individual with APL initially diagnosed ...

journal_title：Pediatric dermatology

authors： Salman A,Sarac G,Can Kuru B,Cinel L,Yucelten AD,Ergun T

更新日期：2017-11-01 00:00:00

abstract：:Although papulonecrotic tuberculid is an uncommon cutaneous manifestation of tuberculosis (TB) associated with Mycobacterium tuberculosis infection, the simultaneous occurrence of papulonecrotic tuberculid and erythema induratum is even rarer. Papulonecrotic tuberculid occurs predominantly in young adults and is chara...

journal_title：Pediatric dermatology

authors： Kim GW,Park HJ,Kim HS,Chin HW,Kim SH,Ko HC,Kim MB,Kim BS

更新日期：2013-03-01 00:00:00

abstract：:Aplasia cutis congenita (ACC) is characterized by the complete or partial absence of skin at birth, with 85% of cases of ACC involving the scalp vertex. The etiology of ACC is unclear and appears to be multifactorial. We present the case of a 3-month-old boy who presented with a diagnosis of non-scalp ACC affecting ap...

journal_title：Pediatric dermatology

authors： Davis MJ,Voller LM,Gonzalez SR,Abu-Ghname A,Davies LW,Bedwell JR,Lee GL,Hunt RD,Phung TL,Buchanan EP

更新日期：2021-01-22 00:00:00

abstract：:Striated muscle hamartoma is a rare entity which was described only recently. It is a congenital malformation characterized by the presence of striated, mature muscle fibers in the reticular dermis and hypodermis. We describe a striated muscle hamartoma of the perianal region in a female infant associated with an hema...

journal_title：Pediatric dermatology

authors： Scrivener Y,Petiau P,Rodier-Bruant C,Cribier B,Heid E,Grosshans E

更新日期：1998-07-01 00:00:00

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

authors： Price HN,O'Haver J,Marghoob A,Badger K,Etchevers H,Krengel S

更新日期：2015-01-01 00:00:00

abstract：:Identification of melanoma or worrisome moles is often taught as an important part of routine skin checks. We sought to evaluate the efficacy of gamified education vs. traditional ABCDEs education on melanoma identification and self-confidence in identifying worrisome moles. We report that in our cohort (n = 271), par...

journal_title：Pediatric dermatology

authors： Jia JL,Shen A,Tabata MM,Sarin KY

更新日期：2020-07-01 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：: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

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

更新日期：1993-03-01 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：: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：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

authors： Polat Ekinci A,Kiliç S,Baykal C

更新日期：2016-05-01 00:00:00

abstract：:Diaper dermatitis, an acute inflammation of the skin in the diaper area, is the most common dermatologic disorder of infancy. This placebo-controlled, randomized, double-blind, parallel-group trial compared the efficacy and safety of miconazole nitrate 0.25% in a zinc oxide/petrolatum base with that of the ointment ba...

journal_title：Pediatric dermatology

authors： Concannon P,Gisoldi E,Phillips S,Grossman R

更新日期：2001-03-01 00:00:00

abstract：:Familial cold auto-inflammatory syndrome, Muckle-Wells syndrome and chronic infantile neurologic, cutaneous, articular syndrome are related disorders associated with mutations in the CIAS1 gene. They appear to represent a continuum of one disease characterized by IL-1-mediated inflammation. Until recently, these condi...

journal_title：Pediatric dermatology

authors： O'Connell SM,O'Regan GM,Bolger T,Hoffman HM,Cant A,Irvine AD,Watson RM

更新日期：2007-01-01 00:00:00

abstract：:Several dermatologic abnormalities have been described in anorexia nervosa, but only rare associations have been made with perniosis. We recently saw two teenage girls and one woman with anorexia nervosa who had symptoms of perniosis. We suggest that altered thermoregulation and a hyperreactive peripheral vascular res...

journal_title：Pediatric dermatology

authors： White KP,Rothe MJ,Milanese A,Grant-Kels JM

更新日期：1994-03-01 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：:A 3 year-old boy presented to our clinic with a 3-day history of itchy rash involving the face and limbs and recent contact with a caterpillar. A diagnosis of caterpillar dermatitis was suspected. This condition has rarely been reported and may be underestimated in the pediatric population who may suffer more systemic...

journal_title：Pediatric dermatology

authors： Jadoo AS,Treat JR

更新日期：2020-05-01 00:00:00

abstract：:We evaluated two patients with hereditary bullous poikiloderma. Both had acral bullae, generalized poikiloderma with prominent atrophy, and acral keratoses. One patient, with sporadic disease, had, in addition, urethral and subglottic stenoses, webbing of digits, and poor dentition. The other patient, whose disease wa...

journal_title：Pediatric dermatology

authors： Forman AB,Prendiville JS,Esterly NB,Hebert AA,Duvic M,Horiguchi Y,Fine JD

更新日期：1989-06-01 00:00:00

abstract：:Our objective was to establish the aerobic and anaerobic microbiology of nonbullous impetigo (NI) in children. We used a retrospective review of clinical microbiology laboratory and patients' records. Specimens were obtained from 40 patients with NI lesions and showed bacterial growth. Aerobic or facultative anaerobic...

journal_title：Pediatric dermatology

authors： Brook I,Frazier EH,Yeager JK

更新日期：1997-05-01 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：:The most common cause of death in blue rubber bleb nevus syndrome is gastrointestinal bleeding. Here we present a case of central nervous system bleeding that resulted in death. ...

journal_title：Pediatric dermatology

authors： Ocampo-Garza J,Salas-Alanís JC,Ponce-Camacho MA,Rosales-Solis GM,Miranda Maldonado I,Elizondo-Riojas G,Villanueva-Nava D,Barbosa-Quintana O,Gonzalez Colunga K,Ocampo-Candiani J

更新日期：2016-01-01 00:00:00

abstract：:We hereby report a 2-year-old boy who presented with a peculiar combination of hyperpigmented and hypopigmented skin lesions along the lines of Blaschko, sharply demarcated at the midline, both on the anterior and posterior trunk. Although combinations of hyperpigmented and hypopigmented skin lesions distributed along...

journal_title：Pediatric dermatology

authors： Thapa R,Dhar S,Malakar R,Chakrabartty S

更新日期：2007-09-01 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：:PLACK syndrome (OMIM 616295) is a form of generalized peeling skin syndrome (GPSS; OMIM 270300). It is an autosomal recessive genodermatosis caused by pathogenic mutations in CAST, which encodes calpastatin, an endogenous specific inhibitor of calpain, a calcium-dependent cysteine protease. We present a 5-year-old gir...

journal_title：Pediatric dermatology

authors： Boggs JME,Irvine AD

更新日期：2020-10-03 00:00:00

abstract：:Mutations in the p63 gene have been identified in five human disorders characterized by varying degrees of limb anomalies, ectodermal dysplasia, and facial clefts. We report a new point mutation in the p63 gene in a family in which the mother was initially diagnosed with Rapp-Hodgkin syndrome and her two offspring man...

journal_title：Pediatric dermatology

authors： Steele JA,Hansen H,Arn P,Kwong PC

更新日期：2005-09-01 00:00:00

abstract：:Congenital nevi both small and large are frequently removed. We attempted to study the removal rate and etiologic aspects of congenital nevi as well as their psychosocial effects through the use of a quality test. A questionnaire sent to a sample population of individuals with congenital nevocytic nevi (n=192) collect...

journal_title：Pediatric dermatology

authors： Berg P,Lindelöf B

更新日期：2002-07-01 00:00:00

abstract：:Cutis laxa is a rare disorder resulting from degradation and clumping of elastic fibers in dermis. Type II acquired cutis laxa, shows only cutaneous changes without any systemic involvement. We describe an infant with acquired cutis laxa type II following a generalized inflammatory dermatitis. ...

journal_title：Pediatric dermatology

authors： Haider M,Alfadley A,Kadry R,Almutawa A

更新日期：2010-01-01 00:00:00