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Aneurysm

MedGen UID:
8076
Concept ID:
C0002940
Pathologic Function
Synonyms: Aneurysmal dilatation; Aneurysmal disease; Aneurysms; Vascular dilatation
SNOMED CT: Aneurysm (85659009); Aneurysmal dilatation (85659009); Aneurysm (432119003)
 
HPO: HP:0002617

Definition

Abnormal outpouching or sac-like dilatation in the wall of an atery, vein or the heart. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • Aneurysm

Conditions with this feature

Gastric mucosal hypertrophy
MedGen UID:
4844
Concept ID:
C0017155
Disease or Syndrome
Ménétrier disease (MD) is a rare premalignant hyperproliferative gastropathy characterized by massive overgrowth of foveolar cells in the gastric lining, resulting in large gastric folds, and manifesting with epigastric pain, nausea, vomiting, peripheral edema and, less commonly, anorexia and weight loss.
Caroli disease
MedGen UID:
57924
Concept ID:
C0162510
Congenital Abnormality
A rare congenital disorder characterised by multifocal, segmental dilatation of the large intrahepatic bile ducts. It may present at any age and predominantly affects females. Less than 250 cases have been described worldwide. Caroli disease is characterised by bile ductal ectasia without other apparent hepatic abnormalities. It presents with recurrent bacterial cholangitis, biliary stones causing biliary pain or episodes of pancreatitis. The more common variant of this disease, named Caroli syndrome, is characterised by dilatations of the large bile duct associated with congenital hepatic fibrosis. The aetiology of Caroli disease is unknown and its occurrence is sporadic, whereas Caroli syndrome is generally inherited in an autosomal recessive manner.
Johanson-Blizzard syndrome
MedGen UID:
59798
Concept ID:
C0175692
Disease or Syndrome
Johanson-Blizzard syndrome is an autosomal recessive disorder characterized by poor growth, mental retardation, and variable dysmorphic features, including aplasia or hypoplasia of the nasal alae, abnormal hair patterns or scalp defects, and oligodontia. Other features include hypothyroidism, sensorineural hearing loss, imperforate anus, and pancreatic exocrine insufficiency (summary by Al-Dosari et al., 2008).
Cheilitis glandularis
MedGen UID:
75626
Concept ID:
C0267034
Disease or Syndrome
Cheilitis glandularis (CG) is an uncommon chronic inflammatory disease of unknown origin characterized by macrocheilia and secretions of thick saliva from swollen labial minor salivary glands.
Primary familial dilated cardiomyopathy
MedGen UID:
90951
Concept ID:
C0340427
Disease or Syndrome
A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.
Hereditary benign telangiectasia
MedGen UID:
140803
Concept ID:
C0406502
Disease or Syndrome
#64258;uent. Recurrent bleeding from the skin and mucous membranes is not a common feature. Likewise, co-existing epidermal or dermal abnormalities, like atrophy, depigmentation, or purpura, are absent. The condition is non-hereditary, and to establish the diagnosis, other primary and secondary telangiectases must be excluded.
Aneurysm of interventricular septum
MedGen UID:
234648
Concept ID:
C1387721
Disease or Syndrome
Interventricular septum aneurysm is a rare, non-syndromic, congenital heart malformation characterized by the presence of a congenital aneurysm of the membranous portion of the interventricular septum. Patients may be asymptomatic or may present with ventricular or supraventricular tachycardia, fatigue, exertional dyspnea, palpitations, and cardiac murmur. Ventricular septal defects and conduction defects, such as first-degree atrio-ventricular block or incomplete right bundle branch block, may also be also associated.
Orofaciodigital syndrome I
MedGen UID:
307142
Concept ID:
C1510460
Disease or Syndrome
Oral-facial-digital syndrome type I (OFD1) is usually male lethal during gestation and predominantly affects females. OFD1 is characterized by the following features: Oral (lobulated tongue, tongue nodules, cleft of the hard or soft palate, accessory gingival frenulae, hypodontia, and other dental abnormalities). Facial (widely spaced eyes or telecanthus, hypoplasia of the alae nasi, median cleft or pseudocleft upper lip, micrognathia). Digital (brachydactyly, syndactyly, clinodactyly of the fifth finger; duplicated hallux [great toe]). Kidney (polycystic kidney disease). Brain (e.g., intracerebral cysts, agenesis of the corpus callosum, cerebellar agenesis with or without Dandy-Walker malformation). Intellectual disability (in ~50% of individuals).
Currarino triad
MedGen UID:
323460
Concept ID:
C1531773
Disease or Syndrome
Currarino syndrome (CS) is a rare congenital disease characterized by the triad of anorectal malformations (ARMs) (usually anal stenosis), presacral mass (commonly anterior sacral meningocele (ASM) or teratoma) and sacral anomalies (i.e. total or partial agenesis of the sacrum and coccyx or deformity of the sacral vertebrae).
Duane-radial ray syndrome
MedGen UID:
301647
Concept ID:
C1623209
Disease or Syndrome
SALL4-related disorders include Duane-radial ray syndrome (DRRS, Okihiro syndrome), acro-renal-ocular syndrome (AROS), and SALL4-related Holt-Oram syndrome (HOS), three phenotypes previously thought to be distinct entities: DRRS is characterized by uni- or bilateral Duane anomaly and radial ray malformation that can include thenar hypoplasia and/or hypoplasia or aplasia of the thumbs, hypoplasia or aplasia of the radii, shortening and radial deviation of the forearms, triphalangeal thumbs, and duplication of the thumb (preaxial polydactyly). AROS is characterized by radial ray malformations, renal abnormalities (mild malrotation, ectopia, horseshoe kidney, renal hypoplasia, vesico-ureteral reflux, bladder diverticula), ocular coloboma, and Duane anomaly. Rarely, pathogenic variants in SALL4 may cause clinically typical HOS (i.e., radial ray malformations and cardiac malformations without additional features).
Arrhythmogenic right ventricular dysplasia 9
MedGen UID:
373205
Concept ID:
C1836906
Disease or Syndrome
Arrhythmogenic right ventricular cardiomyopathy (ARVC) – previously referred to as arrhythmogenic right ventricular dysplasia (ARVD) – is characterized by progressive fibrofatty replacement of the myocardium that predisposes to ventricular tachycardia and sudden death in young individuals and athletes. It primarily affects the right ventricle, and it may also involve the left ventricle. The presentation of disease is highly variable even within families, and some affected individuals may not meet established clinical criteria. The mean age at diagnosis is 31 years (±13; range: 4-64 years).
PHACE syndrome
MedGen UID:
376231
Concept ID:
C1847874
Disease or Syndrome
PHACE is an acronym for a neurocutaneous syndrome encompassing the following features: posterior fossa brain malformations, hemangiomas of the face (large or complex), arterial anomalies, cardiac anomalies, and eye abnormalities. The association is referred to as PHACES when ventral developmental defects, such as sternal clefting or supraumbilical raphe, are present (summary by Bracken et al., 2011).
Visceral myopathy familial with external ophthalmoplegia
MedGen UID:
336376
Concept ID:
C1848586
Disease or Syndrome
An extremely rare autosomal recessively inherited neuromuscular disease characterised by ocular manifestations such as ptosis and diplopia followed by chronic diarrhoea, malnutrition and intestinal pseudo-obstruction.
Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome
MedGen UID:
376398
Concept ID:
C1848590
Disease or Syndrome
A rare systemic disease characterized by progressive hyalinosis involving capillaries, arterioles and small veins of the digestive tract, kidneys, and retina, associated with idiopathic cerebral calcifications, manifesting with severe diarrhea (with rectal bleeding and malabsorption), nephropathy (with renal failure and systemic hypertension), chorioretinal scarring, and subarachnoid hemorrhage. Poikiloderma and premature greying of the hair may be additionally observed.
Encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration
MedGen UID:
346482
Concept ID:
C1856973
Disease or Syndrome
Bonnemann-Meinecke-Reich syndrome is a syndrome of multiple congenital anomalies characterized by an encephalopathy which predominantly occurs in the first year of life and presenting as psychomotor delay. Additional features of the disease include moderate dysmorphia, craniosynostosis, dwarfism (due to growth hormone deficiency), intellectual disability, spasticity, ataxia, retinal degeneration, and adrenal and uterine hypoplasia. The disease has been described in only two families, with each family having two affected siblings. An autosomal recessive inheritance has been suggested. There have been no further descriptions in the literature since 1991.
Dandy-Walker malformation-postaxial polydactyly syndrome
MedGen UID:
341751
Concept ID:
C1857351
Disease or Syndrome
A syndromic disorder with the association between Dandy-Walker malformation and postaxial polydactyly as a major feature. The Dandy-Walker malformation has a variable expression and characteristics of a posterior fossa cyst communicating with the fourth ventricle, the partial or complete absence of the cerebellar vermis, and facultative hydrocephalus. Postaxial polydactyly includes tetramelic postaxial polydactyly of hands and feet with possible enlargement of the fifth metacarpal and metatarsal bones, as well as bifid fifth metacarpals.
Ventriculomegaly with cystic kidney disease
MedGen UID:
346584
Concept ID:
C1857423
Disease or Syndrome
Ventriculomegaly with cystic kidney disease is a severe autosomal recessive developmental disorder characterized by onset in utero of dilated cerebral ventricles and microscopic renal tubular cysts. The pregnancies of affected individuals are associated with increased alpha-fetoprotein (AFP). Most affected pregnancies have been terminated (summary by Slavotinek et al., 2015). See also 602200 for a disorder characterized by ventriculomegaly and defects of the radius and kidney.
Arteritis, familial granulomatous, with juvenile polyarthritis
MedGen UID:
349529
Concept ID:
C1862510
Disease or Syndrome
Ventriculomegaly with defects of the radius and kidney
MedGen UID:
400843
Concept ID:
C1865780
Disease or Syndrome
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps
MedGen UID:
382033
Concept ID:
C2673195
Disease or Syndrome
The spectrum of COL4A1-related disorders includes: small-vessel brain disease of varying severity including porencephaly, variably associated with eye defects (retinal arterial tortuosity, Axenfeld-Rieger anomaly, cataract) and systemic findings (kidney involvement, muscle cramps, cerebral aneurysms, Raynaud phenomenon, cardiac arrhythmia, and hemolytic anemia). On imaging studies, small-vessel brain disease is manifest as diffuse periventricular leukoencephalopathy, lacunar infarcts, microhemorrhage, dilated perivascular spaces, and deep intracerebral hemorrhages. Clinically, small-vessel brain disease manifests as infantile hemiparesis, seizures, single or recurrent hemorrhagic stroke, ischemic stroke, and isolated migraine with aura. Porencephaly (fluid-filled cavities in the brain detected by CT or MRI) is typically manifest as infantile hemiparesis, seizures, and intellectual disability; however, on occasion it can be an incidental finding. HANAC (hereditary angiopathy with nephropathy, aneurysms, and muscle cramps) syndrome usually associates asymptomatic small-vessel brain disease, cerebral large vessel involvement (i.e., aneurysms), and systemic findings involving the kidney, muscle, and small vessels of the eye. Two additional phenotypes include isolated retinal artery tortuosity and nonsyndromic autosomal dominant congenital cataract.
Waardenburg syndrome type 2E
MedGen UID:
398476
Concept ID:
C2700405
Disease or Syndrome
Waardenburg syndrome type 2 is an auditory-pigmentary syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes; congenital sensorineural hearing loss; and the absence of 'dystopia canthorum,' the lateral displacement of the inner canthus of each eye, which is seen in some other forms of WS (review by Read and Newton, 1997). Individuals with WS type 2E, which is caused by mutation in the SOX10 gene (602229), may have neurologic abnormalities, including mental impairment, myelination defects, and ataxia. Waardenburg syndrome type 2 is genetically heterogeneous (see WS2A; 193510). For a description of other clinical variants of Waardenburg syndrome, see WS1 (193500), WS3 (148820), and WS4 (277580).
Lipodystrophy, congenital generalized, type 4
MedGen UID:
412871
Concept ID:
C2750069
Disease or Syndrome
Congenital generalized lipodystrophy type 4 combines the phenotype of classic Berardinelli-Seip lipodystrophy (608594) with muscular dystrophy and cardiac conduction anomalies (Hayashi et al., 2009). For a general description and a discussion of genetic heterogeneity of congenital generalized lipodystrophy, see CGL1 (608594).
Spondylometaphyseal dysplasia, megarbane-dagher-melki type
MedGen UID:
413221
Concept ID:
C2750075
Disease or Syndrome
Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type is a rare, primary bone dysplasia characterized by intrauterine growth retardation, pre- and postnatal disproportionate short stature with short, rhizomelic limbs, facial dysmorphism, a short neck and small thorax. Hypotonia, cardiomegaly and global developmetal delay have also been associated. Several radiographic findings have been reported, including ribs with cupped ends, platyspondyly, square iliac bones, horizontal and trident acetabula, hypoplastic ischia, and delayed epiphyseal ossification.
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities
MedGen UID:
442566
Concept ID:
C2750804
Disease or Syndrome
LTBP4-related cutis laxa is characterized by cutis laxa, early childhood-onset pulmonary emphysema, peripheral pulmonary artery stenosis, and other evidence of a generalized connective tissue disorder such as inguinal hernias and hollow visceral diverticula (e.g., intestine, bladder). Other manifestations can include pyloric stenosis, diaphragmatic hernia, rectal prolapse, gastrointestinal elongation/tortuosity, cardiovascular abnormality, pulmonary hypertension, hypotonia and frequent pulmonary infections. Bladder diverticula and hydronephrosis are common. Early demise has been associated with pulmonary emphysema.
Multisystemic smooth muscle dysfunction syndrome
MedGen UID:
462551
Concept ID:
C3151201
Disease or Syndrome
Multisystemic smooth muscle dysfunction syndrome (MSMDS) presents with a recognizable pattern of complications, including congenital mydriasis, patent ductus arteriosus (PDA), pulmonary artery hypertension, aortic and other arterial aneurysms, moyamoya-like cerebrovascular disease, intestinal hypoperistalsis and malrotation, and hypotonic bladder. It is caused by heterozygous mutations of the ACTA2 gene altering the arginine-179 codon (summary by Regalado et al., 2018). See also familial thoracic aortic aneurysm (AAT6; 611788) and moyamoya disease-5 (MYMY5; 614042), which can also be caused by ACTA2 mutation.
Peroxisome biogenesis disorder 3A
MedGen UID:
766843
Concept ID:
C3553929
Disease or Syndrome
The peroxisomal biogenesis disorder (PBD) Zellweger syndrome (ZS) is an autosomal recessive multiple congenital anomaly syndrome resulting from disordered peroxisome biogenesis. Affected children present in the newborn period with profound hypotonia, seizures, and inability to feed. Characteristic craniofacial anomalies, eye abnormalities, neuronal migration defects, hepatomegaly, and chondrodysplasia punctata are present. Children with this condition do not show any significant development and usually die in the first year of life (summary by Steinberg et al., 2006). For a complete phenotypic description and a discussion of genetic heterogeneity of Zellweger syndrome, see 214100. Individuals with PBDs of complementation group 3 (CG3) have mutations in the PEX12 gene. For information on the history of PBD complementation groups, see 214100.
Meckel syndrome type 1
MedGen UID:
811346
Concept ID:
C3714506
Disease or Syndrome
Meckel syndrome, also known as Meckel-Gruber syndrome, is a severe pleiotropic autosomal recessive developmental disorder caused by dysfunction of primary cilia during early embryogenesis. There is extensive clinical variability and controversy as to the minimum diagnostic criteria. Early reports, including that of Opitz and Howe (1969) and Wright et al. (1994), stated that the classic triad of Meckel syndrome comprises (1) cystic renal disease; (2) a central nervous system malformation, most commonly occipital encephalocele; and (3) polydactyly, most often postaxial. However, based on a study of 67 patients, Salonen (1984) concluded that the minimum diagnostic criteria are (1) cystic renal disease; (2) CNS malformation, and (3) hepatic abnormalities, including portal fibrosis or ductal proliferation. In a review of Meckel syndrome, Logan et al. (2011) stated that the classic triad first described by Meckel (1822) included occipital encephalocele, cystic kidneys, and fibrotic changes to the liver. Genetic Heterogeneity of Meckel Syndrome See also MKS2 (603194), caused by mutation in the TMEM216 gene (613277) on chromosome 11q12; MKS3 (607361), caused by mutation in the TMEM67 gene (609884) on chromosome 8q; MKS4 (611134), caused by mutation in the CEP290 gene (610142) on chromosome 12q; MKS5 (611561), caused by mutation in the RPGRIP1L gene (610937) on chromosome 16q12; MKS6 (612284), caused by mutation in the CC2D2A gene (612013) on chromosome 4p15; MKS7 (267010), caused by mutation in the NPHP3 (608002) gene on chromosome 3q22; MKS8 (613885), caused by mutation in the TCTN2 gene (613846) on chromosome 12q24; MKS9 (614209), caused by mutation in the B9D1 gene (614144) on chromosome 17p11; MKS10 (614175), caused by mutation in the B9D2 gene (611951) on chromosome 19q13; MKS11 (615397), caused by mutation in the TMEM231 gene (614949) on chromosome 16q23; MKS12 (616258), caused by mutation in the KIF14 gene (611279) on chromosome 1q32; and MKS13 (617562), caused by mutation in the TMEM107 gene (616183) on chromosome 17p13.
Atrial standstill 2
MedGen UID:
816731
Concept ID:
C3810401
Disease or Syndrome
Atrial standstill (AS) is a rare condition characterized by the absence of electrical and mechanical activity in the atria. On surface ECG, AS is distinguished by bradycardia, junctional (usually narrow complex) escape rhythm, and absence of the P wave. Nearly 50% of patients with AS experience syncope. AS can be persistent or transient, and diffuse or partial (summary by Fazelifar et al., 2005).
Hyperphosphatasia with mental retardation syndrome 6
MedGen UID:
906509
Concept ID:
C4225201
Disease or Syndrome
Hyperphosphatasia with mental retardation syndrome-6 (HPMRS6) is an autosomal recessive multisystem disorder characterized by global developmental delay, dysmorphic features, seizures, and congenital cataracts. Severity is variable, and the disorder may show a range of phenotypic and biochemical abnormalities, including increased serum alkaline phosphatase levels (summary by Ilkovski et al., 2015). The disorder is caused by a defect in glycosylphosphatidylinositol (GPI) biosynthesis. For a discussion of genetic heterogeneity of HPMRS, see HPMRS1 (239300). For a discussion of genetic heterogeneity of GPI biosynthesis defects, see GPIBD1 (610293).
Combined oxidative phosphorylation deficiency 25
MedGen UID:
896555
Concept ID:
C4225329
Disease or Syndrome
Combined oxidative phosphorylation defect type 25 is a rare mitochondrial oxidative phosphorylation disorder with decreased respiratory complex I and IV enzyme activities, characterized by hypotonia, global developmental delay, neonatal onset of progressive pectus carinatum without other skeletal abnormalities, poor growth, sensorineural hearing loss, dysmorphic features and brain abnormalities such as cerebral atrophy, quadriventricular dilatation and thin corpus callosum posteriorly.
Senior-Loken syndrome 8
MedGen UID:
905171
Concept ID:
C4225376
Disease or Syndrome
Hyperuricemic nephropathy, familial juvenile, 4
MedGen UID:
934708
Concept ID:
C4310741
Disease or Syndrome
Autosomal dominant tubulointerstitial kidney disease-5 (ADTKD5) is characterized by the onset of progressive chronic renal disease in the first decades of life. Mild hyperuricemia may be present, but gout, hypertension, and proteinuria are usually absent. The disease may be associated with anemia or neutropenia. Some patients may have additional findings, including poor overall growth and impaired cognitive function. Renal biopsy shows tubulointerstitial abnormalities with atrophic tubules and fibrosis; secondary glomerular abnormalities and simple cysts may also be present (summary by Bolar et al., 2016). For a discussion of genetic heterogeneity and revised nomenclature of ADTKD, see ADTKD1 (162000).
Chromosome 19q13.11 deletion syndrome, proximal
MedGen UID:
935013
Concept ID:
C4311046
Disease or Syndrome
Proximal chromosome 19q13.11 deletion syndrome is an autosomal dominant neurodevelopmental disorder characterized by delayed development, intellectual disability with poor speech, feeding difficulties, and autistic features. Some patients may have additional features, including renal tract anomalies (summary by Caubit et al., 2016).
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay
MedGen UID:
1612119
Concept ID:
C4539968
Disease or Syndrome
CAKUTHED is an autosomal dominant highly pleiotropic developmental disorder characterized mainly by variable congenital anomalies of the kidney and urinary tract, sometimes resulting in renal dysfunction or failure, dysmorphic facial features, and abnormalities of the outer ear, often with hearing loss. Most patients have global developmental delay (summary by Heidet et al., 2017 and Slavotinek et al., 2017).
Polymicrogyria with or without vascular-type ehlers-danlos syndrome
MedGen UID:
1675672
Concept ID:
C5193040
Disease or Syndrome
Polymicrogyria with or without vascular-type Ehlers-Danlos syndrome is an autosomal recessive disorder with a highly variable phenotype. Although all patients have polymicrogyria and other variable structural brain anomalies on imaging, only some show developmental delay and/or seizures. Similarly, only some patients have connective tissue defects that particularly affect the vascular system and can result in early death (summary by Vandervore et al., 2017).
Joubert syndrome with hepatic defect
MedGen UID:
1769861
Concept ID:
C5435651
Disease or Syndrome
COACH syndrome is an autosomal recessive disorder characterized by impaired intellectual development, ataxia due to cerebellar hypoplasia, and hepatic fibrosis. Other features, such as coloboma and renal cysts, may be variable. COACH syndrome is considered by some to be a subtype of Joubert syndrome (JBTS; see 213300) with congenital hepatic fibrosis. Identification of liver disease in these patients is critical because some may develop complications such as portal hypertension with fatal variceal bleeding (Brancati et al., 2009; Doherty et al., 2010). Genetic Heterogeneity of COACH Syndrome Also see COACH syndrome-2 (COACH2; 619111), caused by mutation in in the CC2D2A gene (612013), and COACH syndrome-3 (COACH3; 619113), caused by mutation the RPGRIP1L gene (610937). Most cases of COACH syndrome are caused by mutation in the TMEM67 gene.

Recent clinical studies

Etiology

Góra R, Bojakowski K, Piasecki A, Kasprzak D, Kaźmierczak S, Andziak P
Vasc Endovascular Surg 2021 Apr;55(3):216-220. Epub 2020 Dec 7 doi: 10.1177/1538574420976723. PMID: 33280544
Dráč P, Utíkal P, Černá M, Bachleda P
Rozhl Chir 2020 Summer;99(8):356-360. doi: 10.33699/PIS.2020.99.8.356-360. PMID: 33032440
Spanos K, Kölbel T, Scheerbaum M, Donas KP, Austermann M, Rohlffs F, Verzini F, Tsilimparis N; pELVIS Collaborators.
J Endovasc Ther 2020 Dec;27(6):910-916. Epub 2020 Aug 4 doi: 10.1177/1526602820944611. PMID: 32748727
Góra R, Bojakowski K, Foroncewicz B, Kaźmierczak S, Andziak P
Vascular 2020 Dec;28(6):775-783. Epub 2020 Jun 11 doi: 10.1177/1708538120931626. PMID: 32522136
Illuminati G, Pizzardi G, Pasqua R, Nardi P, Calio' FG, Ricco JB
J Vasc Surg 2020 Oct;72(4):1413-1420. Epub 2020 Feb 5 doi: 10.1016/j.jvs.2019.11.054. PMID: 32035773

Diagnosis

Obikane H, Kaneko M, Kasao M, Kumagai H, Tanino T, Yokoyama M
Int Heart J 2021 Jul 30;62(4):938-943. Epub 2021 Jul 6 doi: 10.1536/ihj.20-572. PMID: 34234071
Takamori S, Oizumi H, Utsunomiya A, Suzuki J
Gen Thorac Cardiovasc Surg 2021 Sep;69(9):1335-1337. Epub 2021 May 26 doi: 10.1007/s11748-021-01652-y. PMID: 34037949
Jaswal V, Kumar V, Thingnam SKS, Puri GD
J Card Surg 2021 Apr;36(4):1264-1269. Epub 2021 Jan 21 doi: 10.1111/jocs.15358. PMID: 33476446
Dwivedi A, Wayne E, Sangroula D, Sigdel A
Vasc Endovascular Surg 2021 May;55(4):398-401. Epub 2020 Nov 26 doi: 10.1177/1538574420975906. PMID: 33243094
Dráč P, Utíkal P, Černá M, Bachleda P
Rozhl Chir 2020 Summer;99(8):356-360. doi: 10.33699/PIS.2020.99.8.356-360. PMID: 33032440

Therapy

Góra R, Bojakowski K, Piasecki A, Kasprzak D, Kaźmierczak S, Andziak P
Vasc Endovascular Surg 2021 Apr;55(3):216-220. Epub 2020 Dec 7 doi: 10.1177/1538574420976723. PMID: 33280544
Lu JJ, Cuff RF, Chambers CM
Ann Vasc Surg 2021 Apr;72:665.e9-665.e13. Epub 2020 Nov 21 doi: 10.1016/j.avsg.2020.10.018. PMID: 33227480
Spanos K, Kölbel T, Scheerbaum M, Donas KP, Austermann M, Rohlffs F, Verzini F, Tsilimparis N; pELVIS Collaborators.
J Endovasc Ther 2020 Dec;27(6):910-916. Epub 2020 Aug 4 doi: 10.1177/1526602820944611. PMID: 32748727
Góra R, Bojakowski K, Foroncewicz B, Kaźmierczak S, Andziak P
Vascular 2020 Dec;28(6):775-783. Epub 2020 Jun 11 doi: 10.1177/1708538120931626. PMID: 32522136
Illuminati G, Pizzardi G, Pasqua R, Nardi P, Calio' FG, Ricco JB
J Vasc Surg 2020 Oct;72(4):1413-1420. Epub 2020 Feb 5 doi: 10.1016/j.jvs.2019.11.054. PMID: 32035773

Prognosis

Jaswal V, Kumar V, Thingnam SKS, Puri GD
J Card Surg 2021 Apr;36(4):1264-1269. Epub 2021 Jan 21 doi: 10.1111/jocs.15358. PMID: 33476446
Shetty GS, K S Bhat P, Balaji G, Ravindra BS, Udgire SP
Ann Vasc Surg 2021 Apr;72:666.e1-666.e6. Epub 2020 Nov 21 doi: 10.1016/j.avsg.2020.10.015. PMID: 33227466
Jayet J, Davaine JM, Tresson P, Verscheure D, Lawton J, Kashi M, Couture T, Gaudric J, Chiche L, Koskas F
Eur J Vasc Endovasc Surg 2020 Aug;60(2):211-218. Epub 2020 May 10 doi: 10.1016/j.ejvs.2020.04.016. PMID: 32402807
Fang C, Pan H, Li Z, Ma L, Han W
BMC Surg 2020 May 5;20(1):88. doi: 10.1186/s12893-020-00749-0. PMID: 32370775Free PMC Article
Illuminati G, Pizzardi G, Pasqua R, Nardi P, Calio' FG, Ricco JB
J Vasc Surg 2020 Oct;72(4):1413-1420. Epub 2020 Feb 5 doi: 10.1016/j.jvs.2019.11.054. PMID: 32035773

Clinical prediction guides

Mikami T, Naraoka S, Hashimoto A, Doi H, Nakanishi K, Shibata T, Nakajima T, Harada R, Kamada T, Kawaharada N
Gen Thorac Cardiovasc Surg 2021 Sep;69(9):1338-1343. Epub 2021 Jun 5 doi: 10.1007/s11748-021-01653-x. PMID: 34091872
Wolk S, Distler M, Radosa C, Ehehalt F, Bergert H, Weitz J, Reeps C, Ludwig S
Langenbecks Arch Surg 2021 May;406(3):623-630. Epub 2021 Mar 23 doi: 10.1007/s00423-021-02149-1. PMID: 33755764Free PMC Article
Góra R, Bojakowski K, Piasecki A, Kasprzak D, Kaźmierczak S, Andziak P
Vasc Endovascular Surg 2021 Apr;55(3):216-220. Epub 2020 Dec 7 doi: 10.1177/1538574420976723. PMID: 33280544
Góra R, Bojakowski K, Foroncewicz B, Kaźmierczak S, Andziak P
Vascular 2020 Dec;28(6):775-783. Epub 2020 Jun 11 doi: 10.1177/1708538120931626. PMID: 32522136
Illuminati G, Pizzardi G, Pasqua R, Nardi P, Calio' FG, Ricco JB
J Vasc Surg 2020 Oct;72(4):1413-1420. Epub 2020 Feb 5 doi: 10.1016/j.jvs.2019.11.054. PMID: 32035773

Recent systematic reviews

Murai Y, Shirokane K, Kitamura T, Tateyama K, Matano F, Mizunari T, Morita A
J Nippon Med Sch 2020 Sep 9;87(4):172-183. Epub 2020 Mar 31 doi: 10.1272/jnms.JNMS.2020_87-407. PMID: 32238731
Kibrik P, Arustamyan M, Stern JR, Dua A
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