Prosthetic temporomandibular joint reconstruction in a cohort of adolescent females with juvenile idiopathic arthritis.

Abstract:

BACKGROUND:Temporomandibular joint (TMJ) arthritis and involvement is commonly seen in Juvenile Idiopathic Arthritis (JIA). Therapy includes conservative measures, but also includes intraarticular corticosteroid injections (IASI) and systemic immunosuppressive therapy. Despite aggressive medical therapy, some patients develop arthritic changes and frank TMJ ankylosis that can result in persistent pain and limitation in range of motion (ROM). A surgical option is prosthetic TMJ replacement with concurrent correction of dentofacial deformities, which can be performed simultaneously. The objective of this study was to evaluate the outcomes of prosthetic TMJ replacement in a cohort of adolescent females with JIA and severe TMJ involvement. METHODS:This is a retrospective case series that took place at one tertiary care center. Patients with a diagnosis of JIA who also underwent alloplastic TMJ replacement were identified through electronic medical record system (EMR) and reviewed. Chart review included analysis of all documents in the EMR, including demographic data, JIA history, surgical complications, ROM of TMJ measured by maximal incisal opening in millimeters (mm) and TMJ pain scores (4-point Likert scale: none, mild, moderate, severe) obtained pre- and postoperatively. RESULTS:Five female patients, ages 15-17 year when TMJ replacement was performed, had nine total joints replaced with a post-operative follow-up period of 12-30 months. All patients had polyarticular, seronegative JIA and were treated with IASI and multiple immunosuppressive therapies without resolution of TMJ symptoms. One patient had bilateral TMJ ankylosis. Three of the five patients demonstrated significant dentofacial deformities, and all underwent simultaneous or staged orthognathic surgery. All patients had improvement in TMJ pain with most (80%) reporting no pain, and all had similar or improved ROM of their TMJ postoperatively. There was one delayed postoperative infection with Cutibacterium Acnes that presented 15 months after surgery and required removal and reimplantation of prosthesis. CONCLUSION:The sequelae of TMJ arthritis and involvement from JIA in the adolescent population can be difficult to treat. Current medical therapy can be successful, however, in select cases that develop chronic changes in the TMJ despite extensive medical therapy, early results show that prosthetic joint replacement maybe a reasonable surgical option. With prosthetic joint replacement pain levels were reduced and range of motion was maintained or improved for all patients.

authors

Lypka M,Shah K,Jones J

doi

10.1186/s12969-020-00453-6

subject

Has Abstract

pub_date

2020-09-04 00:00:00

pages

68

issue

1

issn

1546-0096

pii

10.1186/s12969-020-00453-6

journal_volume

18

pub_type

杂志文章
  • MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura.

    abstract:BACKGROUND:Due to an increased frequency of vasculitis in FMF patients, many investigators have studied MEFV mutations in patients with HSP. The aim of the study is to investigate the frequency and clinical significance of MEFV mutations in Egyptian children with Henoch-Schonlein purpura (HSP). Investigating MEFV mutat...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-12-41

    authors: Salah S,Rizk S,Lotfy HM,El Houchi S,Marzouk H,Farag Y

    更新日期:2014-09-09 00:00:00

  • A case of Henoch-Schonlein Purpura with dilated coronary arteries.

    abstract:BACKGROUND:Henoch-Schonlein Purpura (HSP) is one of the most common vasculitides of childhood, with 10-20 cases per 100,000 children. It frequently occurs following an infectious trigger and involves IgA and C3 deposition in small vessel walls. HSP is characterized by palpable purpura plus IgA deposition on biopsy, art...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-018-0270-9

    authors: Bloom JL,Darst JR,Prok L,Soep JB

    更新日期:2018-09-04 00:00:00

  • Choroidal vascularity index as a biomarker of systemic inflammation in childhood Polyarteritis Nodosa and adenosine deaminase-2 deficiency.

    abstract:BACKGROUND/PURPOSE:To assess EDI-OCT (enhanced depth imaging optical coherence tomography) of choroid for inflammatory signs in children with polyarteritis nodosa (PAN) and adenosine deaminase-2 deficiency (DADA-2). METHODS:In this cross-sectional study conducted between June 2017 and September 2018, we evaluated chil...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-020-0417-3

    authors: Baytaroğlu A,Kadayifçilar S,Ağin A,Deliktaş Ö,Demir S,Bilginer Y,Karakaya J,Özen S,Eldem B

    更新日期:2020-04-03 00:00:00

  • Towards a new set of classification criteria for PFAPA syndrome.

    abstract:BACKGROUND:Diagnosis of Periodic Fever, Aphthous stomatitis, Pharyngitis and Cervical Adenitis (PFAPA) syndrome is currently based on the modified Marshall's criteria, but no validated evidence based classification criteria for PFAPA has been established so far. METHODS:A multistep process, based on the Delphi and Nom...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-018-0277-2

    authors: Vanoni F,Caorsi R,Aeby S,Cochard M,Antón J,Berg S,Brik R,Dolezalova P,Koné-Paut I,Neven B,Ozen S,Pillet P,Stojanov S,Wouters C,Gattorno M,Hofer M

    更新日期:2018-09-21 00:00:00

  • Autoimmune thyroiditis in antinuclear antibody positive children without rheumatologic disease.

    abstract:BACKGROUND:Children are commonly referred to a pediatric rheumatology center for the laboratory finding of an Anti-nuclear antibody (ANA) of undetermined significance. Previous studies regarding adult rheumatology patients have supported an association between ANA and anti-thyroid antibodies, with the prevalence of thy...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-8-15

    authors: Torok KS,Arkachaisri T

    更新日期:2010-05-05 00:00:00

  • Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia.

    abstract:PURPOSE:To present the case of a 14-year-old boy with clinical and radiographic features of pseudorheumatoid chondrodyspalsia with additional, potentially serious, cervical malformations. METHODS:Detailed clinical and radiological examinations were undertaken with emphasis on the usefulness of 3D-CT scanning. RESULTS...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-5-19

    authors: Al Kaissi A,Ben Chehida F,Ben Ghachem M,Grill F,Klaushofer K

    更新日期:2007-09-27 00:00:00

  • Pain hypersensitivity in juvenile idiopathic arthritis: a quantitative sensory testing study.

    abstract:BACKGROUND:Juvenile Idiopathic Arthritis (JIA) is the most common cause of non-infectious joint inflammation in children. Synovial inflammation results in pain, swelling and stiffness. Animal and adult human studies indicate that localized joint-associated inflammation may produce generalized changes in pain sensitivit...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章,多中心研究

    doi:10.1186/1546-0096-12-39

    authors: Cornelissen L,Donado C,Kim J,Chiel L,Zurakowski D,Logan DE,Meier P,Sethna NF,Blankenburg M,Zernikow B,Sundel RP,Berde CB

    更新日期:2014-09-06 00:00:00

  • Predictors for intravenous immunoglobulin resistance and coronary artery lesions in Kawasaki disease.

    abstract:BACKGROUND:To assess the predictors for intravenous immunoglobulin (IVIG) resistance and coronary artery lesions (CALs) in Kawasaki disease (KD). METHODS:A total of 560 KD patients were reviewed retrospectively, including 410 complete KD (cKD) and 150 incomplete KD (iKD) patients. The laboratory data were compared bet...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-017-0149-1

    authors: Xie T,Wang Y,Fu S,Wang W,Xie C,Zhang Y,Gong F

    更新日期:2017-03-21 00:00:00

  • Disease course and treatment effects of a JAK inhibitor in a patient with CANDLE syndrome.

    abstract:BACKGROUND:CANDLE syndrome (an acronym for Chronic Atypical Neutrophilic Dermatosis with Lipodystrophy and Elevated Temperature) is a recently described rare autosomal recessive disorder charaterized by systemic autoinflammation. Clinical manifestations include presentation in the first year of life, episodes of fever ...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-019-0322-9

    authors: Boyadzhiev M,Marinov L,Boyadzhiev V,Iotova V,Aksentijevich I,Hambleton S

    更新日期:2019-05-02 00:00:00

  • Development of practice and consensus-based strategies including a treat-to-target approach for the management of moderate and severe juvenile dermatomyositis in Germany and Austria.

    abstract:BACKGROUND:Juvenile dermatomyositis (JDM) is the most common inflammatory myopathy in childhood and a major cause of morbidity among children with pediatric rheumatic diseases. The management of JDM is very heterogeneous. The JDM working group of the Society for Pediatric Rheumatology (GKJR) aims to define consensus- a...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-018-0257-6

    authors: Hinze CH,Oommen PT,Dressler F,Urban A,Weller-Heinemann F,Speth F,Lainka E,Brunner J,Fesq H,Foell D,Müller-Felber W,Neudorf U,Rietschel C,Schwarz T,Schara U,Haas JP

    更新日期:2018-06-25 00:00:00

  • Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies.

    abstract:BACKGROUND:Acquired complement deficiency can occur in the setting of autoimmune syndromes, such as systemic lupus erythematosus (SLE), with very low or, occasionally, undetectable C3 levels. Based on inherited complement defects, patients with transiently low complement may be at similar risk for serious bacterial inf...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-020-00467-0

    authors: Al-Shaikhly T,Hayward K,Basiaga ML,Allenspach EJ

    更新日期:2020-09-24 00:00:00

  • Monitoring change in volume of calcifications in juvenile idiopathic inflammatory myopathy: a pilot study using low dose computed tomography.

    abstract:BACKGROUND:Dystrophic calcifications may occur in patients with J uvenile Idiopathic Inflammatory Myopathy (JIIM) as well as other connective tissue and metabolic diseases, but a reliable method of measuring the volume of these calcifications has not been established. The purpose of this study is to determine the feasi...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-016-0123-3

    authors: Ibarra M,Rigsby C,Morgan GA,Sammet CL,Huang CC,Xu D,Targoff IN,Pachman LM

    更新日期:2016-11-29 00:00:00

  • Childhood Cogan syndrome with aortitis and anti-neutrophil cytoplasmic antibody-associated glomerulonephritis.

    abstract::Cogan syndrome is a systemic disease manifesting interstitial keratitis, sensorineural hearing loss, tinnitus, and rotatory vertigo. Renal complications of this syndrome are very rare. We encountered an adolescent with Cogan syndrome complicated by aortitis and anti-neutrophil cytoplasmic antibody (ANCA)-associated gl...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-12-15

    authors: Sugimoto K,Miyazawa T,Nishi H,Izu A,Enya T,Okada M,Takemura T

    更新日期:2014-04-25 00:00:00

  • Fatal myocarditis in a child with systemic onset juvenile idiopathic arthritis during treatment with an interleukin 1 receptor antagonist.

    abstract:BACKGROUND:The pathologic diagnosis of isolated myocarditis without pericardial involvement is uncommonly encountered in systemic onset Juvenile Idiopathic Arthritis (soJIA). CASE:An eleven year-old boy with soJIA died suddenly while being treated with the interleukin 1 (IL-1) receptor inhibitor, anakinra. His autopsy...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-10-8

    authors: Zeft AS,Menon SC,Miller D

    更新日期:2012-04-10 00:00:00

  • Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study.

    abstract:BACKGROUND:Periodic fever syndromes (PFS) are an emerging group of autoinflammatory disorders. Clinical overlap exists and multiple genetic analyses may be needed to assist diagnosis. We evaluated the diagnostic value of a 5-gene sequencing panel (5GP) in patients with undiagnosed PFS. METHODS:Simultaneous double stra...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-015-0006-z

    authors: De Pieri C,Vuch J,De Martino E,Bianco AM,Ronfani L,Athanasakis E,Bortot B,Crovella S,Taddio A,Severini GM,Tommasini A

    更新日期:2015-04-10 00:00:00

  • Telemedicine and other care models in pediatric rheumatology: an exploratory study of parents' perceptions of barriers to care and care preferences.

    abstract:BACKGROUND:The United States pediatric rheumatology workforce is committed to a mission of providing children access to pediatric rheumatology care. With a limited number and distribution of pediatric rheumatologists, telemedicine has been proposed as one way to meet this mission, yet the adoption of this modality has ...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-017-0184-y

    authors: Bullock DR,Vehe RK,Zhang L,Correll CK

    更新日期:2017-07-11 00:00:00

  • Calm in the midst of cytokine storm: a collaborative approach to the diagnosis and treatment of hemophagocytic lymphohistiocytosis and macrophage activation syndrome.

    abstract:BACKGROUND:Hemophagocytic lymphohistiocytosis (HLH) and macrophage activation syndrome (MAS) were historically thought to be distinct entities, often managed in isolation. In fact, these conditions are closely related. A collaborative approach, which incorporates expertise from subspecialties that previously treated HL...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-019-0309-6

    authors: Halyabar O,Chang MH,Schoettler ML,Schwartz MA,Baris EH,Benson LA,Biggs CM,Gorman M,Lehmann L,Lo MS,Nigrovic PA,Platt CD,Priebe GP,Rowe J,Sundel RP,Surana NK,Weinacht KG,Mann A,Yuen JC,Meleedy-Rey P,Starmer A,Ban

    更新日期:2019-02-14 00:00:00

  • Nonsteroidal Anti-Inflammatory Drugs: A survey of practices and concerns of pediatric medical and surgical specialists and a summary of available safety data.

    abstract:OBJECTIVES:To examine the prescribing habits of NSAIDs among pediatric medical and surgical practitioners, and to examine concerns and barriers to their use. METHODS:A sample of 1289 pediatricians, pediatric rheumatologists, sports medicine physicians, pediatric surgeons and pediatric orthopedic surgeons in the United...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-8-7

    authors: Levy DM,Imundo LF

    更新日期:2010-02-04 00:00:00

  • Development of neoplasms in pediatric patients with rheumatic disease exposed to anti-tumor necrosis factor therapies: a single Centre retrospective study.

    abstract:BACKGROUND:Anti-TNF (Tumor necrosis factor) therapy is effective in treating pediatric patients with refractory rheumatic disease. There is however a concern that anti-TNF usage may increase the risk of malignancy. Reports on specific types of malignancy in this patient population have been emerging over the past decad...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-018-0233-1

    authors: Okihiro A,Hasija R,Fung L,Cameron B,Feldman BM,Laxer R,Schneider R,Silverman E,Spiegel L,Yeung RSM,Tse SML

    更新日期:2018-03-14 00:00:00

  • Amendment of the OMERACT ultrasound definitions of joints' features in healthy children when using the DOPPLER technique.

    abstract:BACKGROUND:Recently preliminary ultrasonography (US) definitions, in B mode, for normal components of pediatric joints have been developed by the OMERACT US group. The aim of the current study was to include Doppler findings in the evaluation and definition of normal joint features that can be visualized in healthy chi...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-018-0240-2

    authors: Collado P,Windschall D,Vojinovic J,Magni-Manzoni S,Balint P,Bruyn GAW,Hernandez-Diaz C,Nieto JC,Ravagnani V,Tzaribachev N,Iagnocco A,D'Agostino MA,Naredo E,OMERACT ultrasound subtask force on pediatric.

    更新日期:2018-04-10 00:00:00

  • Relapsing periodic arthritis, palindromic rheumatism and MEFV gene-related variants alleles in children.

    abstract:BACKGROUND:Relapsing periodic arthritis is a general term used for a group of diseases with recurring and periodic nature, in which the joints are intermittently involved. The aim of this study is to evaluation of the possible relationship between MEFV gene mutations in intermittent arthritis of children which has recu...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-019-0329-2

    authors: Salehzadeh F,Barak M,Nematdoust Haghi R

    更新日期:2019-06-06 00:00:00

  • Long-term follow-up of autologous hematopoietic stem cell transplantation for refractory juvenile dermatomyositis: a case-series study.

    abstract:OBJECTIVE:To follow up the refractory juvenile dermatomyositis (JDM) with autologous hematopoietic stem cell transplantation (AHSCT) in a long time and to investigate whether AHSCT is effective and safe to treat refractory JDM. METHODS:We collected the AHSCT and follow-up data of three patients with refractory JDM who...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-018-0284-3

    authors: Zhu J,Su G,Lai J,Dong B,Kang M,Li S,Zhou Z,Wu F

    更新日期:2018-11-20 00:00:00

  • Proposal for a definition for response to treatment, inactive disease and damage for JIA associated uveitis based on the validation of a uveitis related JIA outcome measures from the Multinational Interdisciplinary Working Group for Uveitis in Childhood (

    abstract:BACKGROUND:JIA-associated uveitis (JIAU) is a serious, sight-threatening disease with significant long-term complications and risk of blindness, even with improved contemporary treatments. The MIWGUC was set up in order to propose specific JIAU activity and response items and to validate their applicability for clinica...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-019-0345-2

    authors: Foeldvari I,Klotsche J,Simonini G,Edelsten C,Angeles-Han ST,Bangsgaard R,de Boer J,Brumm G,Torrent RB,Constantin T,DeLibero C,Diaz J,Gerloni VM,Guedes M,Heiligenhaus A,Kotaniemi K,Leinonen S,Minden K,Miranda V,Miser

    更新日期:2019-10-01 00:00:00

  • Post-streptococcal reactive arthritis in children: a distinct entity from acute rheumatic fever.

    abstract:: There is a debate whether post-streptococcal reactive arthritis (PSRA) is a separate entity or a condition on the spectrum of acute rheumatic fever (ARF). We believe that PSRA is a distinct entity and in this paper we review the substantial differences between PSRA and ARF. We show how the demographic, clinical, gene...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-9-32

    authors: Uziel Y,Perl L,Barash J,Hashkes PJ

    更新日期:2011-10-20 00:00:00

  • Idiopathic juvenile osteoporosis: a cross-sectional single-centre experience with bone histomorphometry and quantitative computed tomography.

    abstract:BACKGROUND:Idiopathic juvenile osteoporosis (IJO) is a rare condition of poorly understood etiology and pathophysiology that affects otherwise healthy children. This condition is characterized clinically by bone pain and vertebral fractures; spontaneous recovery is observed after puberty in the majority of cases. Altho...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-11-6

    authors: Bacchetta J,Wesseling-Perry K,Gilsanz V,Gales B,Pereira RC,Salusky IB

    更新日期:2013-02-19 00:00:00

  • Being on the juvenile dermatomyositis rollercoaster: a qualitative study.

    abstract:BACKGROUND:Juvenile Dermatomyositis is a rare, potentially life-threatening condition with no known cure. There is no published literature capturing how children and young people feel about their condition, from their perspective. This study was therefore unique in that it asked children and young people what is it lik...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-019-0332-7

    authors: Livermore P,Gray S,Mulligan K,Stinson JN,Wedderburn LR,Gibson F

    更新日期:2019-06-18 00:00:00

  • Is fibrodysplasia ossificans progressiva an interleukin-1 driven auto-inflammatory syndrome?

    abstract:BACKGROUND:Fibrodysplasia ossificans progressiva (FOP) is the most catastrophic form of heterotopic ossification, due to ongoing intracellular signaling through the bone morphogenic protein pathway. The paroxysmal appearance of inflammatory lumps and elevated inflammatory markers during flares, suggest that FOP is an a...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/s12969-019-0386-6

    authors: Haviv R,Moshe V,De Benedetti F,Prencipe G,Rabinowicz N,Uziel Y

    更新日期:2019-12-21 00:00:00

  • Musculoskeletal ultrasound in pediatric rheumatology.

    abstract:: Although musculoskeletal ultrasound (MSUS) has emerged as an indispensible tool among physicians involved in musculoskeletal medicine in the last two decades, only recently has it become more attractive to pediatric rheumatologists. Thereafter, the use of MSUS in pediatric rheumatology has started to increase. Yet, a...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章

    doi:10.1186/1546-0096-9-25

    authors: Tok F,Demirkaya E,Ozçakar L

    更新日期:2011-09-12 00:00:00

  • The safety of live-attenuated vaccines in patients using IL-1 or IL-6 blockade: an international survey.

    abstract:BACKGROUND:Withholding live-attenuated vaccines in patients using interleukin (IL)-1 or IL-6 blocking agents is recommended by guidelines for both pediatric and adult rheumatic diseases, since there is a risk of infection in an immune suppressed host. However, this has never been studied. This retrospective, multicente...

    journal_title:Pediatric rheumatology online journal

    pub_type: 杂志文章,多中心研究

    doi:10.1186/s12969-018-0235-z

    authors: Jeyaratnam J,Ter Haar NM,Lachmann HJ,Kasapcopur O,Ombrello AK,Rigante D,Dedeoglu F,Baris EH,Vastert SJ,Wulffraat NM,Frenkel J

    更新日期:2018-03-21 00:00:00

  • Time to share.

    abstract::In the following a brief commentary is given on a new European project that aims to provide the European countries with recommendations for the care of children and yound adults with rheumatic diseases. These recommendations will be based on surveys sent to PRINTO members and systematic literature reviews. Surveys on ...

    journal_title:Pediatric rheumatology online journal

    pub_type: 社论

    doi:10.1186/1546-0096-11-5

    authors: Wulffraat NM,Vastert B,SHARE consortium.

    更新日期:2013-02-15 00:00:00