-
Je něco špatně v tomto záznamu ?
A contemporary approach to a young female patient with Loeys-Dietz syndrome and an uncomplicated type B aortic dissection: a case report
P. Prodanov, H. Linkova, R. Petr, R. Fojt, Z. Motovska, J. Knot, F. Rohac, B. Koznar, M. Majid, P. Widimsky, P. Kacer,
Jazyk angličtina Země Velká Británie
Typ dokumentu kazuistiky, časopisecké články
NLK
BioMedCentral
od 2006-01-12
BioMedCentral Open Access
od 2006
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
PubMed Central
od 2006
Europe PubMed Central
od 2006
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2006-01-01
Medline Complete (EBSCOhost)
od 2007-01-04
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2006
Springer Nature OA/Free Journals
od 2006-12-01
- MeSH
- antihypertenziva terapeutické užití MeSH
- aorta thoracica diagnostické zobrazování patologie chirurgie MeSH
- chirurgické síťky * MeSH
- CT angiografie MeSH
- dilatace patologická prevence a kontrola MeSH
- disekce aorty diagnostické zobrazování farmakoterapie etiologie chirurgie MeSH
- dospělí MeSH
- lidé MeSH
- Loeysův-Dietzův syndrom komplikace diagnostické zobrazování farmakoterapie chirurgie MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
BACKGROUND: Aortic dissection is a relatively uncommon, but often catastrophic disease that requires early and accurate diagnosis. It often presents in patients with congenital connective tissue disorders. The current aortic surgical techniques are related with serious early and late complications. This case report emphasizes the importance of early diagnosis of aortic root dilatation and the risk of dissection, especially in patients with congenital connective tissue disorders. We present an alternative, contemporary and multidisciplinary approach based on the present state of knowledge. CASE PRESENTATION: We present a rare case of a young female patient with Loeys-Dietz syndrome who was admitted with an uncomplicated aortic dissection (Stanford type B / DeBakey type III) and a dilated aortic root. After a period of close surveillance and extensive vascular imaging, thoracic endovascular aortic repair was deemed to be technically not possible. Medical treatment was optimized and our patient successfully underwent a personalised external aortic root support procedure (PEARS) as a contemporary alternative to existing aortic root surgical techniques. CONCLUSIONS: This case highlights the importance of interdisciplinary approach, close follow-up and multimodality imaging. The decision to intervene in a chronic type B aortic dissection is still challenging and should be made in experienced centers by an interdisciplinary team. However, if an acute complication occurs, thoracic endovascular aortic repair TEVAR is the method of choice. In all cases optimal medical treatment is important. There is increasing evidence that personalized external aortic root support procedure PEARS is effective in stabilizing the aortic root and preventing its dilatation and dissection not only in patients with Marfan syndrome, but also in other cases of aortic root dilation of other etiologies. Moreover, many publications have reported the additional benefit of reduction or even eradication of aortic regurgitation by improving coaptation of the aortic valve leaflets in dilated aortas.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20027913
- 003
- CZ-PrNML
- 005
- 20210114152609.0
- 007
- ta
- 008
- 210105s2020 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1186/s13019-020-01274-0 $2 doi
- 035 __
- $a (PubMed)32867844
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Prodanov, Petko $u Department of Cardiac surgery, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic. petko.prodanov@fnkv.cz.
- 245 12
- $a A contemporary approach to a young female patient with Loeys-Dietz syndrome and an uncomplicated type B aortic dissection: a case report / $c P. Prodanov, H. Linkova, R. Petr, R. Fojt, Z. Motovska, J. Knot, F. Rohac, B. Koznar, M. Majid, P. Widimsky, P. Kacer,
- 520 9_
- $a BACKGROUND: Aortic dissection is a relatively uncommon, but often catastrophic disease that requires early and accurate diagnosis. It often presents in patients with congenital connective tissue disorders. The current aortic surgical techniques are related with serious early and late complications. This case report emphasizes the importance of early diagnosis of aortic root dilatation and the risk of dissection, especially in patients with congenital connective tissue disorders. We present an alternative, contemporary and multidisciplinary approach based on the present state of knowledge. CASE PRESENTATION: We present a rare case of a young female patient with Loeys-Dietz syndrome who was admitted with an uncomplicated aortic dissection (Stanford type B / DeBakey type III) and a dilated aortic root. After a period of close surveillance and extensive vascular imaging, thoracic endovascular aortic repair was deemed to be technically not possible. Medical treatment was optimized and our patient successfully underwent a personalised external aortic root support procedure (PEARS) as a contemporary alternative to existing aortic root surgical techniques. CONCLUSIONS: This case highlights the importance of interdisciplinary approach, close follow-up and multimodality imaging. The decision to intervene in a chronic type B aortic dissection is still challenging and should be made in experienced centers by an interdisciplinary team. However, if an acute complication occurs, thoracic endovascular aortic repair TEVAR is the method of choice. In all cases optimal medical treatment is important. There is increasing evidence that personalized external aortic root support procedure PEARS is effective in stabilizing the aortic root and preventing its dilatation and dissection not only in patients with Marfan syndrome, but also in other cases of aortic root dilation of other etiologies. Moreover, many publications have reported the additional benefit of reduction or even eradication of aortic regurgitation by improving coaptation of the aortic valve leaflets in dilated aortas.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a disekce aorty $x diagnostické zobrazování $x farmakoterapie $x etiologie $x chirurgie $7 D000784
- 650 _2
- $a antihypertenziva $x terapeutické užití $7 D000959
- 650 _2
- $a aorta thoracica $x diagnostické zobrazování $x patologie $x chirurgie $7 D001013
- 650 _2
- $a CT angiografie $7 D000072226
- 650 _2
- $a dilatace patologická $x prevence a kontrola $7 D004108
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a Loeysův-Dietzův syndrom $x komplikace $x diagnostické zobrazování $x farmakoterapie $x chirurgie $7 D055947
- 650 12
- $a chirurgické síťky $7 D013526
- 650 _2
- $a výsledek terapie $7 D016896
- 655 _2
- $a kazuistiky $7 D002363
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Linkova, Hana $u 3rd Department of Internal Medicine - Cardiology, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Petr, Robert $u 3rd Department of Internal Medicine - Cardiology, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Fojt, Richard $u Department of Cardiac surgery, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Motovska, Zuzana $u 3rd Department of Internal Medicine - Cardiology, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Knot, Jiri $u 3rd Department of Internal Medicine - Cardiology, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Rohac, Filip $u 3rd Department of Internal Medicine - Cardiology, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Koznar, Boris $u 3rd Department of Internal Medicine - Cardiology, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Majid, Mariwan $u Department of Cardiac surgery, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Widimsky, Petr $u 3rd Department of Internal Medicine - Cardiology, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 700 1_
- $a Kacer, Petr $u Department of Cardiac surgery, Faculty Hospital Královské Vinohrady, Srobarova 50, 10034, Praha, Czech Republic.
- 773 0_
- $w MED00163181 $t Journal of cardiothoracic surgery $x 1749-8090 $g Roč. 15, č. 1 (2020), s. 231
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32867844 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20210105 $b ABA008
- 991 __
- $a 20210114152607 $b ABA008
- 999 __
- $a ok $b bmc $g 1608248 $s 1119093
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 15 $c 1 $d 231 $e 20200831 $i 1749-8090 $m Journal of cardiothoracic surgery $n J Cardiothorac Surg $x MED00163181
- LZP __
- $a Pubmed-20210105