Hodgkin's disease manifesting as prurigo nodularis.

Abstract:

:Prurigo nodularis is an uncommon pediatric cutaneous disorder that is associated with intense pruritus. We report a teenager with prurigo nodularis as the presenting sign of stage IIA Hodgkin's disease, primarily in the mediastinum. The pruritus and associated cutaneous lesions resolved with combination chemotherapy directed at the malignancy. In patients with prurigo nodularis and pruritus of unclear etiology, the possibility of underlying Hodgkin's disease must be considered.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Shelnitz LS,Paller AS

doi

10.1111/j.1525-1470.1990.tb00670.x

subject

Has Abstract

pub_date

1990-06-01 00:00:00

pages

136-9

issue

2

eissn

0736-8046

issn

1525-1470

journal_volume

7

pub_type

杂志文章
  • Pediatric teledermatology--a survey of current use.

    abstract::Demand for pediatric dermatologic care far exceeds the supply of pediatric dermatologists. Teledermatology has been proposed as a solution to improve access to care, however, data regarding teledermatology use for pediatric patients are lacking. Surveys assessing use and experience with teledermatology were administer...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00624.x

    authors: Fieleke DR,Edison K,Dyer JA

    更新日期:2008-03-01 00:00:00

  • Ischemic ulcers of the toes secondary to Raynaud's phenomenon in a child successfully treated with botulinum toxin.

    abstract::Raynaud's phenomenon (RP) is an episodic vasospastic response to cold or emotional stress causing color changes and pain. These attacks can lead to digital ischemia, ulcers, and gangrene. Severe and refractory RP in children is a therapeutic challenge for clinicians because there are no standardized treatment protocol...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.14160

    authors: Quintana Castanedo L,Feito Rodríguez M,Maseda Pedrero R,Chiloeches Fernández C,de Lucas Laguna R

    更新日期:2020-07-01 00:00:00

  • Bascule syndrome associated with syncopal episodes.

    abstract::Bascule syndrome is a recently described benign vasomotor dermatosis characterized by Bier anemic spots, cyanosis, and urticaria-like eruption. We report a case of a 13-year-old girl with cutaneous lesions consistent with Bascule syndrome who had had three exercise-related syncopal episodes. It would be recommended to...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13425

    authors: Martín JM,Torres C,Cordero P,Sánchez S,Terradez L,Ramón D

    更新日期:2018-03-01 00:00:00

  • Radiofrequency ablation-induced thermal cutaneous injury in a neonate: A potential complication after intrauterine radiofrequency ablation.

    abstract::Over the years, the application and complications of radiofrequency ablation (RFA) in selective fetal reduction for complex pregnancies have been increasingly documented. Despite its rising use in the field of obstetrics and gynecology, the cutaneous complications of RFA have not been commonly reported. Here, we prese...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14350

    authors: Law JY,Choi EC,Chandran NS

    更新日期:2020-11-01 00:00:00

  • Cervical occult spinal dysraphism: MRI findings and the value of a vascular birthmark.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1995.tb00172.x

    authors: Enjolras O,Boukobza M,Jdid R

    更新日期:1995-09-01 00:00:00

  • Focal preauricular dermal dysplasia: report of two cases and a review of literature.

    abstract::We report two cases of focal preauricular dermal dysplasia and review the available literature. Focal preauricular dermal dysplasia is a form of aplasia cutis congenita in which atrophic skin lesions occur in a stereotypical bilateral distribution in the preauricular region. Although focal preauricular dermal dysplasi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2008.00679.x

    authors: Krathen MS,Rosenbach M,Yan AC,Crawford GH

    更新日期:2008-05-01 00:00:00

  • Angioedema After Squaric Acid Treatment in a 6-Year-Old Girl.

    abstract::Alopecia areata (AA) involves the immune-related destruction of hair follicles, resulting in patches of complete hair loss, most often on the scalp. The topical sensitizer squaric acid dibutylester (SADBE) is a popular treatment option given its low side-effect profile, hair regrowth potential, and lack of cross-react...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.12993

    authors: Chen CA,Carlberg V,Kroshinsky D

    更新日期:2017-01-01 00:00:00

  • Epidermolysis bullosa simplex with mottled pigmentation due to a rare keratin 5 mutation: cutaneous findings in infancy.

    abstract::Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is an autosomal dominant inherited blistering skin disease characterized by nonscarring blistering and reticulated hyperpigmentation. It is most commonly due to a heterozygous point mutation, P25L, in the nonhelical V1 domain of keratin 5 (KRT5). Here we...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12206

    authors: Geller L,Kristal L,Morel KD

    更新日期:2013-09-01 00:00:00

  • Evolution of congenital melanocytic nevi toward benignity: A case series.

    abstract::We report on four children born with medium to large congenital melanocytic nevi (CMN) with color heterogeneity and irregular surface rugosity. As these patients aged, their nevi evolved to become more homogeneous and lighter in color, and developed a smoother, more even texture. We propose that given this evolution t...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13745

    authors: Cotton CH,Goldberg GN

    更新日期:2019-03-01 00:00:00

  • Subcutaneous Panniculitis-Like T-Cell Lymphoma in Children: A Review of the Literature.

    abstract::Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a type of skin lymphoma. Pleomorphic T-cells infiltrate the subcutaneous tissue and mimic lobular panniculitis. We report a case occurring in a 12-year-old Chinese boy who presented with multiple indolent erythematous subcutaneous nodules on both extremities wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12452

    authors: Hu ZL,Sang H,Deng L,Li Z

    更新日期:2015-07-01 00:00:00

  • Transient myeloproliferative disorder causing a vesiculopustular eruption in a phenotypically normal neonate.

    abstract::We report an unusual congenital vesiculopustular eruption arising in a neonate as the result of the transient myeloproliferative disorder (TMD) associated with trisomy 21. In this instance, the neonate was phenotypically normal, making the diagnosis more elusive. Initially the lesions were clinically suspicious for he...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21505.x

    authors: Solky BA,Yang FC,Xu X,Levins P

    更新日期:2004-09-01 00:00:00

  • Central nervous system involvement in neonatal lupus erythematosus.

    abstract::Computerized tomography (CT) of the brain was performed in 10 of 11 consecutive infants with neonatal lupus erythematosus (NLE) (five boys and six girls). Ten of the 11 infants had brain neurosonography. Nine of 10 infants had abnormal CT scans. There was diffuse, markedly reduced attenuation of the cerebral white mat...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.2003.03014.x

    authors: Prendiville JS,Cabral DA,Poskitt KJ,Au S,Sargent MA

    更新日期:2003-01-01 00:00:00

  • A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.14076

    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

  • 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

  • Bacterial resistance and impetigo treatment trends: a review.

    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

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2011.01700.x

    authors: Bangert S,Levy M,Hebert AA

    更新日期:2012-05-01 00:00:00

  • Approach to the jewelry aficionado.

    abstract::Children's and teens' frequent use of inexpensive "costume" jewelry exposes them to a variety of contact allergens. Greater use heightens the risk of developing allergic contact dermatitis, especially in the setting of body piercings. Several clinical pearls, prevention strategies, and avoidance alternatives are provi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13379

    authors: Ivey LA,Limone BA,Jacob SE

    更新日期:2018-03-01 00:00:00

  • Hereditary Progressive Mucinous Histiocytosis: New Insights Into a Rare Disease.

    abstract::Hereditary progressive mucinous histiocytosis is a rare, benign, skin-limited form of non-Langerhans cell histiocytosis. We report on a 5-year-old boy who presented in infancy with self-resolving dermal nodules but later developed persistent and progressive erythematous papules on the face and scalp. Histologic evalua...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12694

    authors: Nguyen NV,Prok L,Burgos A,Bruckner AL

    更新日期:2015-11-01 00:00:00

  • Pediculosis capitis: why prefer a solution to shampoo or spray?

    abstract::Two hundred and sixty-eight children with pediculosis capitis took part in a comparative study to test the efficacy of five different pediculocides commonly used in Israel. The preparations used were pyrethrin shampoo, pyrethroid spray, malathion solution, carbaryl shampoo and carbaryl lotion. Carbaryl lotion and mala...

    journal_title:Pediatric dermatology

    pub_type: 临床试验,杂志文章

    doi:10.1111/j.1525-1470.1988.tb00903.x

    authors: Armoni M,Bibi H,Schlesinger M,Pollak S,Metzker A

    更新日期:1988-11-01 00:00:00

  • Molluscum Contagiosum-Like Presentation of Langerhans Cell Histiocytosis: A Case and Review.

    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

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13223

    authors: Karpman MS,AlJasser MI,Lam JM

    更新日期:2017-09-01 00:00:00

  • Harlequin baby treated with etretinate.

    abstract::A child born with the harlequin fetus abnormality survived and showed a surprising degree of spontaneous improvement in the first six weeks of life. At this age etretinate was instituted, producing considerable further resolution. The child is now over 2 years old. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1989.tb00821.x

    authors: Rogers M,Scraf C

    更新日期:1989-09-01 00:00:00

  • Improvement of atopic dermatitis and reduction of skin allergic responses by oral intake of konjac ceramide.

    abstract::Although topical application of ceramide is effective in the treatment of atopic dermatitis, its effect is transient. Thus, the effect of oral intake of ceramide on atopic dermatitis was studied. Two groups of 25 children with moderate atopic dermatitis, who were allergic to house dust mite took either milk sugar (con...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00268.x

    authors: Kimata H

    更新日期:2006-07-01 00:00:00

  • Hidradenitis suppurativa (acne inversa): management of a recalcitrant disease.

    abstract::Hidradenitis suppurativa is a chronic relapsing disorder of follicular occlusion that is often recalcitrant to therapy. Topical and systemic antibiotics, hormonal therapies, oral retinoids, immunosuppressant agents, and surgical treatment are some of the therapeutic alternatives used for this often recalcitrant and fr...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2007.00544.x

    authors: Lam J,Krakowski AC,Friedlander SF

    更新日期:2007-09-01 00:00:00

  • Rapp-Hodgkin syndrome with pili canaliculi.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1993.tb00015.x

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

    更新日期:1993-03-01 00:00:00

  • Febrile ulceronecrotic Mucha-Habermann disease with central nervous system vasculitis.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01669.x

    authors: Rosman IS,Liang LC,Patil S,Bayliss SJ,White AJ

    更新日期:2013-01-01 00:00:00

  • Scurvy in a 10-year-old boy.

    abstract::Scurvy, or hypovitaminosis C, is an uncommon condition that exists today primarily within certain unique populations-particularly the elderly subjects, patients with neurodevelopmental disabilities or psychiatric illnesses, or others with unusual dietary habits. Vitamin C is an essential nutrient in the human body, an...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01095.x

    authors: Cole JA,Warthan MM,Hirano SA,Gowen CW Jr,Williams JV

    更新日期:2011-07-01 00:00:00

  • Eruptive juvenile xanthogranuloma associated with relapsing acute lymphoblastic leukemia.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00721.x

    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

  • Sacral hemangioma with sinus tract in an infant.

    abstract::Congenital midline cutaneous lesions should always alert the clinician to the possibility of spinal dysraphism. These lesions can take many different forms. The physician should be cognizant of such lesions in order to avoid potential neurologic complications. We present a patient with a midline sacral hemangioma asso...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.20307.x

    authors: Winstanley D,Graham B,Blair M,Linfesty R,Tomita S,Matthews J

    更新日期:2003-05-01 00:00:00

  • Spectrum of phenotypic manifestations from a single point mutation of the p63 gene, including new cutaneous and immunologic findings.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.00105.x

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

    更新日期:2005-09-01 00:00:00

  • Annular lipoatrophic panniculitis of the ankles.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01208.x

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

    更新日期:2011-03-01 00:00:00

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

    abstract::Hemangiomas are classified as focal or segmental according to the morphology and distribution of lesions. Congestive cardiac failure is frequently encountered in diffuse hepatic hemangiomas due to high-volume shunting and rarely in hemangiomas confined to the skin. We report here the case of a large multifocal hemangi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12476

    authors: Khanna D,Chakravarty P,Arora P,Jain R,Mittal M

    更新日期:2015-01-01 00:00:00