Fibromatosis colli with hypertrichosis: a rare case of cutaneous manifestation of a muscular disorder.

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：: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：:Circumscribed juvenile pityriasis rubra pilaris (PRP) is an uncommon dermatosis. We describe the unusual clustering of circumscribed juvenile PRP cases in our pediatric dermatology clinic in 2011. A retrospective chart review was done of patients presenting during the summer of 2011 with classic findings of circumscri...

journal_title：Pediatric dermatology

authors： Martin KL,Holland KE,Lyon V,Chiu YE

更新日期：2014-03-01 00:00:00

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：:Prurigo pigmentosa (PP) is a rare inflammatory skin disease. Neutrophil-mediated inflammation is considered to be responsible for the etiopathogenesis of PP. We consider that colchicine may be an effective agent in the treatment of PP since it exerts an antiinflammatory effect by inhibiting neutrophil chemotaxis. Furt...

journal_title：Pediatric dermatology

authors： An I,Ucmak D,Ibiloglu I,Demir V,Akdeniz S

更新日期：2018-05-01 00:00:00

abstract：:Microgeodic disease, similar to chilblains (pernio), is characterized by painful, erythematous swelling, as well as small, punched-out erosions found in affected phalanges. Although they share a similar appearance and proposed pathogenesis, chilblains has rarely been diagnosed in children with microgeodic disease, and...

journal_title：Pediatric dermatology

authors： Prindaville B,Antaya RJ

更新日期：2013-03-01 00:00:00

abstract：BACKGROUND:Kindler syndrome is a rare genodermatosis. Major clinical criteria include acral blistering in infancy and childhood, progressive poikiloderma, skin atrophy, abnormal photosensitivity, and gingival fragility. METHODS:FERMT1 gene was sequenced in 5 patients with a clinical diagnosis of Kindler syndrome. RES...

journal_title：Pediatric dermatology

authors： Valinotto LE,Natale MI,Lusso SB,Cella E,Gutiérrez O,Sebastiani F,Manzur GB

更新日期：2020-03-01 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：:Onychomycosis is widespread in the adult population, but considered to be rare in children. A number of studies in recent years show a rise in the prevalence of toenail onychomycosis in children. Of these, only a few were population-based. Here, we present a comprehensive cross-sectional population-based survey of toe...

journal_title：Pediatric dermatology

authors： Leibovici V,Evron R,Dunchin M,Westerman M,Ingber A

更新日期：2009-01-01 00:00:00

abstract：:A 2-year-old boy had hundreds of discrete, small, flat yellow to brown colored papules distributed over the face, neck, and trunk. Biopsy revealed a well-demarcated infiltrate within the papillary dermis composed of histiocytes and some Touton giant cells and eosinophils. The cells were negative for protein S-100 and ...

journal_title：Pediatric dermatology

authors： Torrelo A,Juarez A,Hernández A,Colmenero I

更新日期：2009-03-01 00:00:00

abstract：:Pigmented purpuric dermatoses (PPDs) are a group of idiopathic, chronic, and self-resolving conditions easily recognizable in adults but extremely uncommon in infants. We present the youngest patient with PPD reported to date. ...

journal_title：Pediatric dermatology

authors： Martos-Cabrera L,López-Balboa P,Ramírez-Lluch M,Colmenero I,Mateos-Mayo A,Torrelo A,Hernández-Martin Á

更新日期：2021-01-06 00:00:00

abstract：:Leukemia cutis and facial nerve palsy are rare presenting symptoms of leukemia. This report describes a case of acute T-cell lymphoblastic leukemia (ALL) presenting with only these two symptoms, a presentation of ALL that, to our knowledge, has not been previously described. It serves to alert physicians to look for u...

journal_title：Pediatric dermatology

authors： Gold HL,Grynspan D,Kanigsberg N

更新日期：2014-05-01 00:00:00

abstract：:An 11-year-old girl with a history of diabetes mellitus type I and celiac disease presented with multiple, depressed patches of purple-brown skin on the right lower extremity and central back, with histopathologic features of early morphea. Though morphea may coexist with other autoimmune diseases, its presentation wi...

journal_title：Pediatric dermatology

authors： Firoz EF,Kamino H,Lehman TJ,Orlow SJ

更新日期：2010-01-01 00:00:00

abstract：:Mutations in the keratinocyte lipid transporter adenosine triphosphate-binding cassette A12 (ABCA12) are known to cause harlequin ichthyosis. More recently, mutations in this gene have been demonstrated to cause other phenotypes within the spectrum of recessive congenital ichthyosis. We report the case of an infant wi...

journal_title：Pediatric dermatology

authors： Peterson H,Lofgren S,Bremmer S,Krol A

更新日期：2013-11-01 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：:Acne fulminans is a severe form of acne vulgaris accompanied by systemic symptoms. A 17-year-old Chinese boy presented with an outbreak of necrotic lesions on his face eight days after the onset of palpable purpura, arthralgia, fever, abdominal pain, and proteinuria. He was successfully treated with oral prednisolone ...

journal_title：Pediatric dermatology

authors： Xu X,Li X,Pradhan S,Li W

更新日期：2020-11-01 00:00:00

abstract：:We report the case of a 2.5-year-old girl with linear morphea initially diagnosed as an acquired port-wine stain (PWS). She underwent three treatments to the right face using the pulsed dye laser (PDL) before sclerotic changes were observed and the correct diagnosis was confirmed with histopathology. Treatment using t...

journal_title：Pediatric dermatology

authors： Pickert AJ,Carpentieri D,Price H,Hansen RC

更新日期：2014-09-01 00:00:00

abstract：:Granular parakeratosis has only recently been described and typically occurs in adults. We report the first instance of this condition affecting a child. ...

journal_title：Pediatric dermatology

authors： Trowers AB,Assaf R,Jaworsky C

更新日期：2002-03-01 00:00:00

abstract：:Impetigo is a common cutaneous infection that is especially prevalent in children. The prevalence of colonization and infection with resistant strains is continually increasing, forcing clinicians to reevaluate treatment strategies. Newer topical agents are effective in treating infections with resistant strains and m...

journal_title：Pediatric dermatology

authors： Bangert S,Levy M,Hebert AA

更新日期：2012-05-01 00:00:00

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：:Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is a rare, autosomal dominant syndrome that is known to have variable expressivity in multiple organ systems. We describe the case of a young male child with nevoid basal cell carcinoma syndrome and scalp lesions, including a branchial cleft cyst with respiratory ...

journal_title：Pediatric dermatology

authors： Findley AB,Pride H

更新日期：2010-03-01 00:00:00

abstract：:This case report describes a 6-week-old infant with a Phthirus pubis infestation of the scalp. It is believed this patient is the first reported case in this age group. Treatment is discussed, as are the family dynamics that put this infant at risk. The authors address the possible association between infestation and ...

journal_title：Pediatric dermatology

authors： Silburt BS,Parsons WL

更新日期：1990-09-01 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：: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：:Sixty novice Buddhist monks with tinea capitis confirmed according to clinical presentation and mycological laboratory finding were included in this study. Mixed-type clinical presentation was observed in approximately half of all cases, together with scarring alopecia (95%) and superficial fungal skin infection at lo...

journal_title：Pediatric dermatology

authors： Bunyaratavej S,Leeyaphan C,Rujitharanawong C,Muanprasat C,Matthapan L

更新日期：2017-05-01 00:00:00

abstract：:Demodex mites are commensal inhabitants of the pilosebaceous unit that are typically absent or at low numbers in childhood. When they are present, they can cause a primary eruption or exacerbate an underlying facial dermatosis. Here we report five cases of demodicosis occurring in childhood, the clinical presentations...

journal_title：Pediatric dermatology

authors： Douglas A,Zaenglein AL

更新日期：2019-09-01 00:00:00

abstract：:Multisystem inflammatory syndrome in children (MIS-C) is a syndrome associated with coronavirus disease 2019. Various phenotypes of MIS-C have been described including Kawasaki disease (KD). Although perineal desquamation is a known early sign of KD, to our knowledge, this rash has not yet been described in the KD phe...

journal_title：Pediatric dermatology

authors： Mazori DR,Derrick KM,Kapoor U,Haribhai M,Gist RE,Glick SA

更新日期：2020-11-22 00:00:00

abstract：:We report a girl with lipophagic lobular panniculitis of unknown origin located on her ankles leading to circumferential fat atrophy of the ankles, a condition usually referred to as "annular lipoatrophy of the ankles." According to our patient's features and five additional cases reported so far, we conclude that thi...

journal_title：Pediatric dermatology

authors： Corredera C,Iglesias M,Hernández-Martín A,Colmenero I,Dilme E,Torrelo A

更新日期：2011-03-01 00:00:00

abstract：:Amniotic band syndrome is one of the many causes of aplasia cutis congenita. It is usually seen as a constriction band surrounding a limb or as a membrane that adheres to some part of the body. This syndrome can be associated with various malformations. An infant with amniotic adhesions producing aplasia cutis, radial...

journal_title：Pediatric dermatology

authors： Nagore E,Sánchez-Motilla JM,Febrer MI,Cremades B,Aleu M,Aliaga A

更新日期：1999-05-01 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