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 without systemic symptoms. He had a protracted course of multiple erythematous subcutaneous nodules for 1 year and underwent biopsy of lesional skin for histology and T-cell receptor (TCR) gene analysis. Histopathology showed infiltration of medium to large atypical pleomorphic cells involving the subcutis with characteristic rimming of fat spaces. TCR gene rearrangement shows monoclonal rearrangements of the TCR β and γ chains. Immunophenotypic studies showed that CD3, CD4, and CD8 were strongly and diffusely positive in lesional cells and that CD56 was focally positive. In contrast, these cells were negative for CD20, CD30, and CD68. The combined morphology, characteristic histologic features, and positive T-CR gene rearrangement supported a diagnosis of SPTCL. He is being treated with combination chemotherapy of cyclophosphamide, doxorubicin, vincristine, and prednisolone.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Hu ZL,Sang H,Deng L,Li Z

doi

10.1111/pde.12452

subject

Has Abstract

pub_date

2015-07-01 00:00:00

pages

526-32

issue

4

eissn

0736-8046

issn

1525-1470

journal_volume

32

pub_type

杂志文章,评审
  • Xanthomas and the inherited hyperlipoproteinemias in children and adolescents.

    abstract::Early recognition of the hyperlipoproteinemias is a crucial element in preventing premature coronary artery disease. Xanthomas provide a cutaneous marker of the silent, underlying pathology. Identifying them, and understanding their relation to the inherited hyperlipoproteinemias may facilitate early diagnosis of hype...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1990.tb00275.x

    authors: Maher-Wiese VL,Marmer EL,Grant-Kels JM

    更新日期:1990-09-01 00:00:00

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

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1990.tb00284.x

    authors: Silburt BS,Parsons WL

    更新日期:1990-09-01 00:00:00

  • Simultaneous occurrence of papulonecrotic tuberculid and erythema induratum in a patient with pulmonary tuberculosis.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2012.01744.x

    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

  • Preschool sarcoidosis masquerading as juvenile rheumatoid arthritis: two case reports and a review of the literature.

    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

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.1990.tb00285.x

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

    更新日期:1990-09-01 00:00:00

  • Henoch-Schönlein purpura associated with Helicobacter pylori infection in a child.

    abstract::Henoch-Schönlein purpura is an acute leukocytoclastic vasculitis that primarily affects children. Henoch-Schönlein purpura is often associated with an infection, and a wide variety of infectious agents have been implicated in the pathogenesis. We report a child with Henoch-Schönlein purpura associated with Helicobacte...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00786.x

    authors: Mytinger JR,Patterson JW,Thibault ES,Webb J,Saulsbury FT

    更新日期:2008-11-01 00:00:00

  • Guidelines for the management of tinea capitis in children.

    abstract::Practice guidelines for the treatment of tinea capitis (TC) from the European Society for Pediatric Dermatology are presented. Tinea capitis always requires systemic treatment because topical antifungal agents do not penetrate the hair follicle. Topical treatment is only used as adjuvant therapy to systemic antifungal...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,实务指引

    doi:10.1111/j.1525-1470.2010.01137.x

    authors: Kakourou T,Uksal U,European Society for Pediatric Dermatology.

    更新日期:2010-05-01 00:00:00

  • Granular cell tumor of the vulva.

    abstract::Granular cell tumors are uncommon in the vulva. We cared for a child who had a solitary vulvar tumor since infancy. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1993.tb00044.x

    authors: Guenther L,Shum D

    更新日期:1993-06-01 00:00:00

  • Less common clinical manifestations of atopic dermatitis: prevalence by age.

    abstract::The common manifestations of atopic dermatitis (AD) appear sequentially with involvement of the cheeks in infancy, flexural extremities in childhood, and hands in adulthood. Although less common clinical manifestations are well described, they have not been the subject of epidemiologic studies to describe their preval...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2012.01739.x

    authors: Julián-Gónzalez RE,Orozco-Covarrubias L,Durán-McKinster C,Palacios-Lopez C,Ruiz-Maldonado R,Sáez-de-Ocariz M

    更新日期:2012-09-01 00:00:00

  • Early Recognition of Proteus Syndrome.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12900

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

    更新日期:2016-09-01 00:00:00

  • Leukemia cutis and facial nerve palsy as presenting symptoms of acute lymphoblastic leukemia.

    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

    pub_type: 杂志文章

    doi:10.1111/pde.12314

    authors: Gold HL,Grynspan D,Kanigsberg N

    更新日期:2014-05-01 00:00:00

  • Epidermolysis bullosa of the Dowling-Meara type: clinical and ultrastructural findings in five patients.

    abstract::Clinical and pathologic features of five cases of epidermolysis bullosa simplex, Dowling-Meara type (EBS-DM), are described. Four patients were children, and two were related (father and daughter). Clinical history revealed blistering at birth in three patients; in all of them the signs and symptoms improved with age....

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1996.tb01204.x

    authors: Puddu P,Angelo C,Faraggiana T,Onetti Muda A,Colonna L,Paradisi M

    更新日期:1996-05-01 00:00:00

  • Autosomal recessive congenital ichthyosis due to homozygous variants in NIPAL4 with a dramatic response to ustekinumab.

    abstract::Autosomal recessive congenital ichthyosis is a genetically and phenotypically heterogenous group of scaling skin disorders. We describe a patient with ARCI caused by homozygous variants in NIPAL4, in whom the dermatologic phenotype and an associated arthropathy, markedly improved with ustekinumab. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13995

    authors: Poulton C,Gration D,Murray K,Baynam G,Halbert A

    更新日期:2019-11-01 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

  • Unnecessary milk elimination diets in children with atopic dermatitis.

    abstract::Milk elimination diets are frequently adopted in the treatment of atopic dermatitis, although the real prevalence of clinically relevant food allergy remains unclear and reports from different authors are often in disagreement. We investigated the percentage of children allergic to cow's milk compared with the rate of...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00323.x

    authors: Sinagra JL,Bordignon V,Ferraro C,Cristaudo A,Di Rocco M,Amorosi B,Capitanio B

    更新日期:2007-01-01 00:00:00

  • Inner thigh friction as a cause of acne mechanica.

    abstract::Acne mechanica is defined as being any acneiform eruption in areas of friction, pressure, stretching, rubbing, pinching, or occlusion of the skin in any individual, regardless of preexisting acne. Various causes have been reported, including prolonged back rest against a chair or bed, occlusive clothing, pressure from...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13817

    authors: Mazhar M,Simpson M,Marathe K

    更新日期:2019-07-01 00:00:00

  • Endemic pemphigus foliaceus in Venezuela: report of two children.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00197.x

    authors: González F,Sáenz AM,Cirocco A,Tacaronte IM,Fajardo JE,Calebotta A

    更新日期:2006-03-01 00:00:00

  • Use of self-adherent silicone sheets in a pediatric burn patient: A case report and instructions for use.

    abstract::Burns and scalds are relatively common injuries in children. Formation of hypertrophic scars or keloids is feared complications. A 2-year-old girl who spilled a cup of hot coffee onto herself developed widespread hypertrophic scars and beginning keloids on her upper chest, despite application of pressure garments and ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14017

    authors: Eisendle K,Pichler M,De Luca J,Thuile T

    更新日期:2020-01-01 00:00:00

  • Reversible neurotoxicity after an overdose of topical lindane in an infant.

    abstract::Lindane (gamma benzene hexachloride) is a widely prescribed topical scabicide because of its efficacy and cost-effectiveness. Although toxicity from a single proper application of lindane is generally not observed, the hazards of repeated applications, industrial exposure, and accidental ingestion have been well docum...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21515.x

    authors: Bhalla M,Thami GP

    更新日期:2004-09-01 00:00:00

  • Familial progressive hypermelanosis in Indian monozygotic twins.

    abstract::Familial hyperpigmentation, or melanosis universalis hereditaria, is a rare hyperpigmentary disorder with onset in infancy. Here, we describe monozygotic twins with similar pattern of progressive hyperpigmentation with onset in early neonatal period without any family history. Histopathological examination showed incr...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01361.x

    authors: Gupta N,Sharma MC,Ramam M,Kabra M

    更新日期:2011-01-01 00:00:00

  • PHACE syndrome with growth hormone deficiency and absence of bilateral internal carotid arteries: a case report.

    abstract::PHACE syndrome is characterized by posterior fossa malformations (P), large facial hemangiomas (H), arterial anomalies (A), cardiac anomalies or coarctation of aorta (C), and eye anomalies (E) and has striking female predominance. Endocrine abnormalities have recently been described in these patients, involving the th...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01540.x

    authors: Altin H,Alp H,Sap F,Karataş Z,Baysal T,Karaaslan S

    更新日期:2012-05-01 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

  • Childhood lichen planus: a report of fifty cases.

    abstract::Lichen planus is an uncommonly encountered dermatosis in children. In the present study of 50 children the limbs were the most common site of involvement (70.0%). A majority of the children (60.0%) presented with the classic form of the disease. Hypertrophic lesions were present in 26.0% of children while linear lesio...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.1999.00074.x

    authors: Sharma R,Maheshwari V

    更新日期:1999-09-01 00:00:00

  • Verruciform xanthoma in a patient with recessive dystrophic epidermolysis bullosa: Case report and literature review.

    abstract::Verruciform xanthoma (VX) is a rare finding thought to be caused by epidermal damage from trauma or inflammation and has been reported in a limited number of patients with recessive dystrophic epidermolysis bullosa (RDEB). Herein, we describe a 20-year-old woman with RDEB who developed a large, verrucous, pink plaque ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14079

    authors: Stephens M,Rubin AI,Perman MJ

    更新日期:2020-03-01 00:00:00

  • Anti-Ku antibody-positive systemic sclerosis-polymyositis overlap syndrome in an adolescent.

    abstract::Systemic sclerosis-polymyositis overlap syndrome is rare in children. Anti-PM/Scl is the most common autoantibody associated with this syndrome. We present a case of systemic sclerosis-polymyositis overlap syndrome in a child with isolated anti-Ku antibodies, an uncommon antibody associated with this rare syndrome. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14243

    authors: Loo RJ,Nocton JJ,Harmelink MM,Chiu YE

    更新日期:2020-09-01 00:00:00

  • Human papillomavirus (HPV) genotyping of cutaneous warts in Greek children.

    abstract::The human papillomavirus (HPV) infects the squamous epithelium of the skin and produces common warts, plantar warts, and flat warts, which occur commonly on the hands, face, and feet. The objective of this study was to determine the presence of HPV in warts in children in order to associate the virus with the disease....

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12113

    authors: Giannaki M,Kakourou T,Theodoridou M,Syriopoulou V,Kabouris M,Louizou E,Chrousos G

    更新日期:2013-11-01 00:00:00

  • A case of cutaneous mastocytosis in a child with prominent Langerhans cell infiltration.

    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

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01205.x

    authors: Mitsuya J,Hara H,Fukuda N,Terui T

    更新日期:2011-07-01 00:00:00

  • Acrodynia and hypertension in a young girl secondary to elemental mercury toxicity acquired in the home.

    abstract::Acrodynia, also known as pink disease, erythredema polyneuropathy, Feer syndrome, and raw-beef hands and feet, is thought to be a toxic reaction to elemental mercury and less commonly to organic and inorganic forms. Occurring commonly in the early 20th century, acrodynia is now a seemingly extinct disease in the moder...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2012.01737.x

    authors: Mercer JJ,Bercovitch L,Muglia JJ

    更新日期:2012-03-01 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

  • Pine tar callus: A mimicker of a melanocytic lesion.

    abstract::We report a case of acral pigmented lesions due to pine tar, a common compound used on baseball bats to improve grip, deposition. The patient presented with an acute concern for a new melanocytic lesion, and dermoscopy revealed large brown globules, not typical of melanocytic neoplasms. We propose that the coupling of...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13773

    authors: Donaldson M,Chamlin SL,Vivar KL

    更新日期:2019-05-01 00:00:00

  • Idiopathic infantile pyoderma gangrenosum with stridor responsive to infliximab.

    abstract::A 4-month-old female infant presented with widespread pyoderma gangrenosum associated with stridor, presumed secondary to tracheal involvement. No underlying cause was revealed despite extensive investigation. Treatment with immunosuppressive agents only partially suppressed disease activity. Complete resolution follo...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00825.x

    authors: Rajan N,Das S,Taylor A,Abinun M,Spencer D,Carmichael A

    更新日期:2009-01-01 00:00:00