-
Something wrong with this record ?
Temporomandibular joint disc perforation: a retrospective study
V. Machon, J. Levorova, D. Hirjak, M. Drahos, R. Foltan,
Language English Country Denmark
Document type Journal Article
- MeSH
- Arthroscopy MeSH
- Temporomandibular Joint Disc pathology surgery MeSH
- Adult MeSH
- Therapeutic Irrigation MeSH
- Middle Aged MeSH
- Humans MeSH
- Pain Measurement MeSH
- Temporomandibular Joint Disorders diagnosis etiology pathology surgery MeSH
- Retrospective Studies MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
The aim of this study was to evaluate disc perforation diagnosed in patients undergoing arthroscopy of the temporomandibular joint (TMJ). A retrospective analysis of 33 patients with disc perforation (35 joints) was performed. Patients and joints were divided into two groups: those with distal perforation (DP; perforation of the retrodiscal tissue, or the distal area of the disc at the site of ligament insertion into the retrodiscal tissue) and those with central perforation (CP; central and anterior part of the disc). The retrospective evaluation included aetiological factors, clinical symptoms, arthroscopic findings, and the effects of arthroscopic lavage. The most frequent aetiological factors in patients with disc perforation were stress and related parafunctional activities. The most frequent arthroscopic finding in both groups was hyperaemia of the bilaminar zone and synovial tissue. Other predominant arthroscopic findings were the presence of adhesions and anterior disc dislocation in the DP group and synovial hyperplasia in the CP group. Better outcomes of arthroscopic lysis and lavage were found in the CP group than in the DP group. At 12 months after arthroscopic lavage, the results showed that the therapy was satisfactory for 72% of the joints. The most common cause of distal perforation is anterior disc dislocation, whilst chronic inflammatory changes account for central perforation.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19035548
- 003
- CZ-PrNML
- 005
- 20191014112115.0
- 007
- ta
- 008
- 191007s2017 dk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.ijom.2017.05.008 $2 doi
- 035 __
- $a (PubMed)30954090
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a dk
- 100 1_
- $a Machon, V $u Department of Oral and Maxillofacial Surgery, First Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.
- 245 10
- $a Temporomandibular joint disc perforation: a retrospective study / $c V. Machon, J. Levorova, D. Hirjak, M. Drahos, R. Foltan,
- 520 9_
- $a The aim of this study was to evaluate disc perforation diagnosed in patients undergoing arthroscopy of the temporomandibular joint (TMJ). A retrospective analysis of 33 patients with disc perforation (35 joints) was performed. Patients and joints were divided into two groups: those with distal perforation (DP; perforation of the retrodiscal tissue, or the distal area of the disc at the site of ligament insertion into the retrodiscal tissue) and those with central perforation (CP; central and anterior part of the disc). The retrospective evaluation included aetiological factors, clinical symptoms, arthroscopic findings, and the effects of arthroscopic lavage. The most frequent aetiological factors in patients with disc perforation were stress and related parafunctional activities. The most frequent arthroscopic finding in both groups was hyperaemia of the bilaminar zone and synovial tissue. Other predominant arthroscopic findings were the presence of adhesions and anterior disc dislocation in the DP group and synovial hyperplasia in the CP group. Better outcomes of arthroscopic lysis and lavage were found in the CP group than in the DP group. At 12 months after arthroscopic lavage, the results showed that the therapy was satisfactory for 72% of the joints. The most common cause of distal perforation is anterior disc dislocation, whilst chronic inflammatory changes account for central perforation.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a artroskopie $7 D001182
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a měření bolesti $7 D010147
- 650 _2
- $a retrospektivní studie $7 D012189
- 650 _2
- $a discus articularis čelistního kloubu $x patologie $x chirurgie $7 D019224
- 650 _2
- $a nemoci temporomandibulárního kloubu $x diagnóza $x etiologie $x patologie $x chirurgie $7 D013705
- 650 _2
- $a léčebná irigace $7 D007507
- 650 _2
- $a výsledek terapie $7 D016896
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Levorova, J $u Department of Oral and Maxillofacial Surgery, First Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic. Electronic address: jitka.levorova@gmail.com.
- 700 1_
- $a Hirjak, D $u Department of Oral and Maxillofacial Surgery, Ruzinov University Hospital, Bratislava, Slovakia.
- 700 1_
- $a Drahos, M $u Department of Oral and Maxillofacial Surgery, First Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.
- 700 1_
- $a Foltan, R $u Department of Oral and Maxillofacial Surgery, First Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic.
- 773 0_
- $w MED00009905 $t International journal of oral and maxillofacial surgery $x 1399-0020 $g Roč. 46, č. 11 (2017), s. 1411-1416
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30954090 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20191007 $b ABA008
- 991 __
- $a 20191014112539 $b ABA008
- 999 __
- $a ok $b bmc $g 1452208 $s 1074098
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 46 $c 11 $d 1411-1416 $e 20170620 $i 1399-0020 $m International journal of oral and maxillofacial surgery $n Int J Oral Maxillofac Surg $x MED00009905
- LZP __
- $a Pubmed-20191007