A Pediatric Case of Sclerodermatous Graft-Versus-Host Disease Responsive to Ultraviolet A1 Phototherapy.

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 deposition of collagen in the skin and other soft tissues and resulting in loss of range of motion and functional capabilities. Treatment of sGVHD is challenging and largely limited by systemic side effects. Ultraviolet A1 phototherapy has been reported to be effective in connective tissue disorders, including sGVHD. We report a case of sGVHD in a 15-year-old girl that was resistant to traditional therapy but showed improvement in cutaneous symptoms with ultraviolet A1 phototherapy three times a week for 6 weeks (10 J/cm(2) single dose, 180 J/cm(2) cumulative dose).

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

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

doi

10.1111/pde.12794

subject

Has Abstract

pub_date

2016-03-01 00:00:00

pages

e99-102

issue

2

eissn

0736-8046

issn

1525-1470

journal_volume

33

pub_type

杂志文章
  • Cutaneous manifestations and massive genital involvement in Hennekam syndrome.

    abstract::We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous p...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00225.x

    authors: Musumeci ML,Nasca MR,De Pasquale R,Schwartz RA,Micali G

    更新日期:2006-05-01 00:00:00

  • S100-protein-containing dendritic cells in fetal and newborn epidermis and thymus.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1986.tb00518.x

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

    更新日期:1986-06-01 00:00:00

  • Tinea capitis in a newborn caused by two organisms.

    abstract::Tinea capitis is a common infection of childhood. There have been several reports of tinea capitis in newborns. Our patient presented at 19 days of age to the emergency room with a scalp lesion of 5 days duration. The fungal culture grew both Trichophyton rubrum and Trichophyton mentagrophytes. The patient was success...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1997.tb00245.x

    authors: Ungar SL,Laude TA

    更新日期:1997-05-01 00:00:00

  • Accessory tragus: report of two cases and review of the literature.

    abstract::Accessory tragus is a fairly common congenital malformation of the external ear. In the vast majority of cases it is an isolated developmental defect not associated with other abnormalities. However, the remote possibility exists that it could be associated with other abnormalities of the first and second branchial ar...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.2000.017005391.x

    authors: Jansen T,Romiti R,Altmeyer P

    更新日期:2000-09-01 00:00:00

  • Bronchiolitis obliterans: a rare chronic pulmonary complication associated with Stevens-Johnson syndrome.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00433.x

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

    更新日期:2007-07-01 00:00:00

  • Complementary and alternative therapy for pediatric acne: A review of botanical extracts, dietary interventions, and oral supplements.

    abstract::Many supplements and products containing botanical extracts are marketed to patients for the treatment of acne vulgaris. Additionally, increasing attention has been paid to the role of diet in acne vulgaris. Studies on this topic including pediatric patients are limited, with variable efficacy data. Despite these limi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13904

    authors: Gurnee EA,Kamath S,Kruse L

    更新日期:2019-09-01 00:00:00

  • Congenital cutaneous hemangioma causing cardiac failure: a case report and review of the literature.

    abstract::We present a case of a large congenital hemangioma (CH) on the neck causing cardiac failure and thrombocytopenia in a female neonate. A trial of medical therapy with corticosteroids and propranolol was attempted, but the patient ultimately underwent definitive treatment with embolization and surgical resection with a ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2012.01875.x

    authors: Weitz NA,Lauren CT,Starc TJ,Kandel JJ,Bateman DA,Morel KD,Meyers PM,Kadenhe-Chiweshe A,Wu JK,Garzon MC

    更新日期:2013-11-01 00:00:00

  • Postvaccination morphea profunda in a child.

    abstract::We report a new case of postvaccination morphea profunda (MP) in a child and discuss its different clinical presentations, prognosis, and therapy and its relationship with "solitary morphea profunda." A 2-year-old healthy girl presented with an induration of the anterior aspect of the left thigh of 9 months duration. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01548.x

    authors: Khaled A,Kharfi M,Zaouek A,Rameh S,Zermani R,Fazaa B,Kamoun MR

    更新日期:2012-07-01 00:00:00

  • Subacute cutaneous lupus erythematosus presenting in childhood: a case report and review of the literature.

    abstract::A 2-year-old African American, Hispanic boy presented with well-defined, violaceous, annular dermal plaques without scale over the upper extremities, face, lower extremities, and buttocks. The clinical presentation and laboratory studies were consistent with a diagnosis of subacute cutaneous lupus erythematous (SCLE)....

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12007

    authors: Berry T,Walsh E,Berry R,DeSantis E,Smidt AC

    更新日期:2014-05-01 00:00:00

  • Benzoate Allergy in Children--From Foods to Personal Hygiene Products.

    abstract::Benzoate allergy may be an overlooked allergen in children and one that may be of increasing importance with its increasing role as a preservative in pediatric personal hygiene formulations. The cases herein report an association with cola and benzoate allergy and discusses the implications of replacement of formaldeh...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12759

    authors: Jacob SE,Hill H,Lucero H,Nedorost S

    更新日期:2016-03-01 00:00:00

  • Trauma-induced cutaneous pigmentation from tetracycline: a case report.

    abstract::Tetracycline is well known to cause pigmentation of various body tissues, such as teeth, bone, lunulae, conjunctivae, and lymph nodes. It has not been reported to cause discoloration of the skin, unlike its semisynthetic derivative, minocycline. We report an 18-year-old girl who developed lower extremity pigmentation ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21216.x

    authors: Hawfield W,Goodrich R,Warren S,Morrell D

    更新日期:2004-03-01 00:00:00

  • Novel ABCA-12 mutations leading to recessive congenital ichthyosis.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01695.x

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

    更新日期:2013-11-01 00:00:00

  • Arborescent vascular dilatation mimicking Lichtenberg figures from lightning.

    abstract::The clinical presentation of arborizing vascular dilatation can resemble Lichtenberg figures from lightning. Both have a feather-like or ferning pattern. We report an interesting case of pressure-induced vasodilatation (PIV) caused by temporary vascular occlusion from jeans buttons. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12350

    authors: Tempark T,Iwasaki J,Shwayder T

    更新日期:2014-07-01 00:00:00

  • Congenital self-healing reticulohistiocytosis: report of a patient with a strikingly large tumor mass.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1989.tb00263.x

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

    更新日期:1989-03-01 00:00:00

  • Ulerythema ophryogenes in Cornelia de Lange syndrome.

    abstract::A 17-year-old woman with Cornelia de Lange syndrome had asymptomatic skin lesions since the age of 4 years. These were multiple, follicular, horny papules, present on both cheeks, and surrounded by erythematous skin. Similar lesions were present on the external aspect of the arms, but amidst skin of normal coloration....

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2002.00003.x

    authors: Flórez A,Fernández-Redondo V,Toribio J

    更新日期:2002-01-01 00:00:00

  • Infantile acropustulosis revisited: history of scabies and response to topical corticosteroids.

    abstract::Infantile acropustulosis (IA) is a condition of young children characterized by recurrent episodes of pruritic vesicles and pustules in an acral distribution. Several reports describe patients with scabies infestation prior to the diagnosis of IA, although the relationship between the two remains unclear. Furthermore,...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.1998.1998015337.x

    authors: Mancini AJ,Frieden IJ,Paller AS

    更新日期:1998-09-01 00:00:00

  • Neonatal linear immunoglobulin a bullous dermatosis: a rare presentation.

    abstract::Linear immunoglobulin A bullous dermatosis (LABD) is an autoimmune blistering disease that most commonly presents in preschool-aged children. There have been few neonatal reports, all of which had life-threatening aerodigestive complications requiring mechanical intervention and systemic therapy. We present a case of ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01507.x

    authors: Julapalli MR,Brandon KL,Rosales CM,Grover RK,Plunkett RW,Metry DW

    更新日期:2012-09-01 00:00:00

  • Management of infantile hemangiomas during the COVID pandemic.

    abstract::The COVID-19 pandemic has caused significant shifts in patient care including a steep decline in ambulatory visits and a marked increase in the use of telemedicine. Infantile hemangiomas (IH) can require urgent evaluation and risk stratification to determine which infants need treatment and which can be managed with c...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14196

    authors: Frieden IJ,Püttgen KB,Drolet BA,Garzon MC,Chamlin SL,Pope E,Mancini AJ,Lauren CT,Mathes EF,Siegel DH,Gupta D,Haggstrom AN,Tollefson MM,Baselga E,Morel KD,Shah SD,Holland KE,Adams DM,Horii KA,Newell BD,Powell J,M

    更新日期:2020-05-01 00:00:00

  • Aromatase inhibitor-induced hair loss in two adolescents.

    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

    pub_type:

    doi:10.1111/pde.14339

    authors: Perper M,Herskovitz I,Tosti A

    更新日期:2020-11-01 00:00:00

  • Rapid response to treatment with thalidomide in an adolescent with generalized discoid lupus erythematosus.

    abstract::Discoid lupus erythematosus (DLE) is the most common variant of cutaneous chronic lupus erythematosus (CLE). Sun protection, topical corticosteroids, and antimalarials constitute the first-line options for treatment. In refractory cases, alternative antimalarials, methotrexate, retinoids, and thalidomide have been uti...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14067

    authors: Tran B,Yazdani Abyaneh MA,Wu J

    更新日期:2020-01-01 00:00:00

  • Multiple lichenoid juvenile xanthogranuloma.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00896.x

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

    更新日期:2009-03-01 00:00:00

  • Hoyeraal-Hreidarsson Syndrome: An Extremely Rare Dyskeratosis Congenita Phenotype.

    abstract::Hoyeraal-Hreidarsson syndrome is a rare telomere biology disorder that is recognized as a severe variant of dyskeratosis congenita. We present a Libyan boy with hematologic and neurologic abnormalities with typical dermatologic manifestations of dyskeratosis congenita. Death usually occurs before the age of 4 years as...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12693

    authors: Bakar Ö,Işik U,Canpolat C,Alanay Y

    更新日期:2015-11-01 00:00:00

  • Apocrine chromhidrosis involving the areolae in a 15-year-old amateur figure skater.

    abstract::Apocrine chromhidrosis is a rare disease frequently localized to the face or axillae, and rarely has been reported to occur around the breasts. We report a 15-year-old amateur figure skater who displayed localized chromhidrosis around her areolae. The most common precipitating event was exercise. She was treated topic...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1995.tb00124.x

    authors: Saff DM,Owens R,Kahn TA

    更新日期:1995-03-01 00:00:00

  • Response to IL-1-receptor antagonist in a child with familial cold autoinflammatory syndrome.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00343.x

    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

  • Rat bite fever: fever, arthritis, and rash in a 4-year-old boy.

    abstract::Rat bite fever is a rare but potentially fatal Gram-negative infection that predominantly affects populations with exposure to rats, notably children. The clinical presentation is nonspecific and requires a high threshold of suspicion to elicit a history of rat exposure. We report here a case of a child whose diagnosi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01561.x

    authors: Lewis BK,Vanderhooft S

    更新日期:2012-11-01 00:00:00

  • Erythema nodosum in association with celiac disease.

    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

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21307.x

    authors: Bartyik K,Várkonyi A,Kirschner A,Endreffy E,Túri S,Karg E

    更新日期:2004-05-01 00:00:00

  • Granular parakeratosis in a child.

    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

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2002.00044.x

    authors: Trowers AB,Assaf R,Jaworsky C

    更新日期:2002-03-01 00:00:00

  • Hereditary mucoepithelial dysplasia: report of two sporadic cases.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01649.x

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

    更新日期:2012-05-01 00:00:00

  • Diffuse normolipemic plane xanthoma in a 9-year-old boy.

    abstract::Normolipemic plane xanthoma normally occurs in adults. We report the atypical instance of a 9-year-old boy who developed disseminated, flat, yellow-brown plaques up to 2 to 3 cm without any complaints. The histology showed the hallmarks of xanthoma, including the presence of CD68+ foam cells and Touton giant cells. No...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22207.x

    authors: Hofmann M,Zappel K,Trefzer U,Audring H,Albrecht-Nebe H,Sterry W,Blume-Peytavi U

    更新日期:2005-03-01 00:00:00

  • Midline congenital cervical cleft mimicking linear scleroderma.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12021

    authors: Méndez-Gallart R,Martinez EE,Rodríguez-Barca P,Nallib IA,Bautista-Casasnovas A

    更新日期:2013-07-01 00:00:00