Scalp infestation by Phthirus pubis in a 6-week-old infant.

abstract：:We report a 12-year-old Japanese boy with a 3-year history of skin lesions that had been unsuccessfully treated with topical steroids. We initiated two different topical treatments with adapalene gel 0.1% (Differin(®) Gel 0.1%) and high-concentration vitamin D3 (tacalcitol) ointment; the lesions treated with adapalene...

journal_title：Pediatric dermatology

authors： Abe M,Inoue C,Yokoyama Y,Ishikawa O

更新日期：2011-03-01 00:00:00

abstract：:Graft-versus-host disease (GVHD) is one of the major complications after hematopoietic stem cell transplantation and is responsible for post-therapeutic morbidity, mortality, and poor quality of life of recipients. Sclerodermatous graft-versus-host disease (sGVHD) is a rare variant of chronic GVHD characterized by dep...

journal_title：Pediatric dermatology

authors： Lazzeri L,Tripo L,Pescitelli L,Ricceri F,Prignano F

更新日期：2016-03-01 00:00:00

abstract：:Dermal mucinosis occurred in a 3-month-old and persisted for six years. The features suggest is represents a novel type of childhood mucinosis. ...

journal_title：Pediatric dermatology

authors： Calza AM,Masouyé I,Saurat JH

更新日期：1994-09-01 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：:An 8-month-old male infant had fever, polymorphonuclear leukocytosis, and tender, firm, elevated erythematous plaques on his face, trunk, and extremities. Histologic examination revealed a dense, perivascular, polymorphonuclear, inflammatory cell infiltrate with nuclear dust in the dermis and intrafollicular abscesses...

journal_title：Pediatric dermatology

authors： Kibbi AG,Zaynoun ST,Kurban AK,Najjar SS

更新日期：1985-11-01 00:00:00

abstract：:Congenital fibrous hamartoma of the tip of the tongue, a peculiar and novel entity, consists of one or two asymptomatic pearly or yellowish nodules, not exceeding 0.5 cm in maximum diameter, at the tip of the tongue, ventrally or dorsally. Unlike other localizations, congenital fibrous hamartoma of the tip of the tong...

journal_title：Pediatric dermatology

authors： Di Altobrando A,Patrizi A,Misciali C,Virdi A,Tarsitano A,Vara G,Baraldi C,Neri I

更新日期：2020-11-11 00:00:00

abstract：:Diaper dermatitis is the most common contact eczema present in early childhood. The main cause is an irritant reaction to urine and feces, which is facilitated by the occlusive conditions under the diaper, leading to hyperhydration of the stratum corneum (diaper dermatitis). In addition, diaper pressure and friction c...

journal_title：Pediatric dermatology

authors： Fölster-Holst R

更新日期：2018-03-01 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：BACKGROUND/OBJECTIVES:Drug reaction with eosinophilia and systemic symptoms (DRESS) is rare but potentially fatal in children. Fever and rash, which are salient features of DRESS, may mimic other commonly encountered pediatric conditions. We profiled the DRESS cases in a tertiary children's hospital in Singapore. METH...

journal_title：Pediatric dermatology

authors： Han XD,Koh MJ,Wong SMY

更新日期：2019-05-01 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：: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：:Juvenile xanthogranuloma is a benign, self-healing disorder with characteristic lesions mainly involving the skin. Although most patients with juvenile xanthogranuloma have only cutaneous symptoms, recent articles have documented extracutaneous manifestations: systemic involvement of many organs has been reported and ...

journal_title：Pediatric dermatology

authors： Aparicio G,Mollet J,Bartralot R,Bodet D,Heras C,Bassas P,Virós A,García-Patos V

更新日期：2008-07-01 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：: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：:Spinal dysraphism is easily recognized in the overt form as a meningocele or myelomeningocele. The closed form or occult spinal dysraphism (OSD) can be overlooked. It occurs predominantly at the lumbosacral level, but OSD at the cervical level, although very rare, also occurs. The value of magnetic resonance imaging i...

journal_title：Pediatric dermatology

authors： Enjolras O,Boukobza M,Jdid R

更新日期：1995-09-01 00:00:00

abstract：:Traumatic tattoos induced by pencil point puncture in children may result in persistent disfigurement if left untreated. The Q-switched ruby laser effectively removes darkly colored cutaneous chromophores with minimal disruption of unaffected skin. We present a young patient with pencil point induced traumatic tattooi...

journal_title：Pediatric dermatology

authors： Knoell KA,Schreiber AJ,Kutenplon M,Milgraum SS

更新日期：1997-07-01 00:00:00

abstract：:We report a 5-month-old girl diagnosed with bullous pemphigoid who initially did not respond to systemic corticosteroids and dapsone but rapidly improved after the addition of intravenous immunoglobulin (IVIG) infusions. A literature search revealed anecdotal cases of infantile bullous pemphigoid treated with IVIG, al...

journal_title：Pediatric dermatology

authors： Tekin B,Yücelten AD

更新日期：2015-09-01 00:00:00

abstract：:Metastatic Crohn's disease (MCD) is a rare extraintestinal manifestation of Crohn's disease characterized by the histologic finding of granulomatous dermatitis at a site noncontiguous to the gastrointestinal tract. An adolescent had MCD of the face that was initially mistaken for severe, treatment-resistant acne. Hist...

journal_title：Pediatric dermatology

authors： Cummins RE,Mullins D,Smith LJ,Ford MJ

更新日期：1996-01-01 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：:The term Mycoplasma pneumoniae-induced rash and mucositis (MIRM) was recently proposed to identify the mucocutaneous condition secondary to M. pneumoniae infection that had historically been regarded among the more confusing pathologies of erythema multiforme and Stevens-Johnson syndrome. Based on a number of previous...

journal_title：Pediatric dermatology

authors： Mayor-Ibarguren A,Feito-Rodriguez M,González-Ramos J,Del Rosal-Rabes T,González-Sainz FJ,Sánchez-Orta A,de Lucas-Laguna R

更新日期：2017-07-01 00:00:00

abstract：:Bloom syndrome (congenital telangiectatic erythema) is a rare autosomal recessive disorder characterized by telangiectasias and photosensitivity, growth deficiency of prenatal onset, variable degrees of immunodeficiency, and increased susceptibility to neoplasms of many sites and types. We are reporting Bloom syndrome...

journal_title：Pediatric dermatology

authors： Sultan SJ,Sultan ST

更新日期：2010-03-01 00:00:00

abstract：:Microvenular hemangioma (MVH) is a rare, benign, acquired vascular tumor. We report a case that shows the characteristic histopathologic features of this disorder in a boy with acute myelogenous leukemia (AML), suggesting an association with systemic immunosuppression. ...

journal_title：Pediatric dermatology

authors： Chang SE,Roh KH,Lee MW,Choi JH,Sung KJ,Moon KC,Koh JK,Yoon GS

更新日期：2003-05-01 00:00:00

abstract：:Preschool sarcoidosis is characterized by the triad of skin, joint, and eye disease without pulmonary involvement. Arthritis and uveitis are also frequently seen together in juvenile rheumatoid arthritis. We report two patients with preschool sarcoidosis, both of whom were initially diagnosed and treated as having juv...

journal_title：Pediatric dermatology

authors： Sahn EE,Hampton MT,Garen PD,Warrick J,Smith D,Silver RM

更新日期：1990-09-01 00:00:00

abstract：:Hereditary mucoepithelial dysplasia (HMD) is a rare genodermatosis characterized by nonscarring alopecia, fiery red gums, perineal erythema, and visual impairment. Histologically, dyskeratotic keratinocytes and a small number of desmosomes are the hallmark of the disease. We report on two unrelated patients who presen...

journal_title：Pediatric dermatology

authors： Hernández-Martín A,Colmenero I,Torrelo A

更新日期：2012-05-01 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：:An 8-month-old Caucasian infant with neurofibromatosis type 1 presented with a congenital plexiform neurofibroma and multiple café au lait spots. A pale area surrounded one of the café au lait spots located on the left gluteus in the area of dermal melanocytosis. This halolike phenomenon results from the disappearance...

journal_title：Pediatric dermatology

authors： Neri I,Lambertini M,Tengattini V,Rivalta B,Patrizi A

更新日期：2017-05-01 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：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：: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 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