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1.
Cardiovasc Pathol ; 71: 107628, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38453103

RESUMO

A case of a 40-year-old male patient with a right subclavian artery aneurysm of fibromuscular dysplasia origin is reported. The patient presented with thoracic outlet-like symptoms and underwent aneurysm resection. Microscopic examination revealed intimal and medial fibroplasia. Additional cases of fibromuscular dysplasia at this rare location are reviewed, indicating a male and right-sided predominance. The most frequent clinicopathological manifestation was an aneurysm, with the histopathological pattern characterized by medial fibroplasia. Treatment modalities included the use of either graft prosthesis or end-to-end anastomosis.


Assuntos
Aneurisma , Displasia Fibromuscular , Artéria Subclávia , Humanos , Displasia Fibromuscular/patologia , Displasia Fibromuscular/complicações , Displasia Fibromuscular/cirurgia , Masculino , Artéria Subclávia/patologia , Artéria Subclávia/cirurgia , Artéria Subclávia/diagnóstico por imagem , Adulto , Aneurisma/patologia , Aneurisma/cirurgia , Aneurisma/diagnóstico por imagem , Resultado do Tratamento , Implante de Prótese Vascular
2.
Eur J Cardiothorac Surg ; 65(1)2024 Jan 02.
Artigo em Inglês | MEDLINE | ID: mdl-38218722

RESUMO

The transmanubrial musculoskeletal sparing approach (TMA) is commonly used for resecting apical lung tumours with vascular involvement. Non-neoplastic conditions which might require surgical exploration of the thoracic outlet include the 'cervical rib', a clinical condition consisting of an additional rib forming above the first rib and growing from the base of the neck just above the clavicle. Type 1 cervical rib-when a complete cervical rib articulates with the first rib or manubrium of the sternum-is the most challenging scenario where the subclavian artery can be damaged by continuous compression due to the narrow space between clavicle, first rib and supernumerary cervical rib, requiring prosthetic reconstruction of the involved tract. Here, we describe a modified TMA in which the incision in the neck is conducted posteriorly to the sternocleidomastoid muscle, thus allowing safe dissection of the superior and middle trunk of the brachial plexus.


Assuntos
Costela Cervical , Neoplasias Pulmonares , Procedimentos de Cirurgia Plástica , Síndrome do Desfiladeiro Torácico , Humanos , Artéria Subclávia/diagnóstico por imagem , Artéria Subclávia/cirurgia , Artéria Subclávia/patologia , Costela Cervical/patologia , Costela Cervical/cirurgia , Neoplasias Pulmonares/patologia , Costelas/cirurgia , Costelas/patologia , Síndrome do Desfiladeiro Torácico/etiologia , Síndrome do Desfiladeiro Torácico/patologia , Síndrome do Desfiladeiro Torácico/cirurgia
3.
Rom J Morphol Embryol ; 63(1): 181-189, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36074682

RESUMO

INTRODUCTION: Tuberous sclerosis complex (TSC) is a rare autosomal dominant condition characterized by cutaneous, cerebral, and other multiorgan involvement. Aneurysms due to TSC pathogenic mechanism are rarely present, mainly aortic, renal, or intracranial and very few associated with peripheral circulation. A TSC patient, aged 31 years, who developed brachial and subclavian arteries aneurysms is presented. The question of a random association of the aneurysms with TSC versus aneurysms within pathogenic released mammalian target of rapamycin (mTOR) pathway effect was raised. CASE PRESENTATION: Patient's file, available from the age of six months, was analyzed for demonstration of the TSC diagnosis. Patient was examined, and cerebral magnetic resonance imaging (MRI) was repeated. Surgery and angiographic reports and images were reviewed. Pathology of the aneurysmal wall available from surgery was reexamined and special stainings and immunohistochemistry markers were applied. Genetic characterization of the patient was performed. Definite TSC was diagnosed based on major criteria [ungual fibromas, shagreen patch, cortical tubers, subependymal nodules (SENs), subependymal giant cell astrocytoma (SEGA)], minor criteria (confetti skin lesions, dental enamel pits, gingival fibromas), genetic result showing heterozygous variant in exon 8 of TSC1 gene (c.733C>T-p.Arg245*). Pathology analysis revealed markedly thickened aneurysmal wall due to smooth muscle cells (SMCs) proliferation in media and neoformation vessels with similar characteristics in the aneurysmal wall. DISCUSSIONS AND CONCLUSIONS: This is a rare case with aneurysms related to TSC, with an exceptional peripheral localization. Pathology exam is the key investigation in demonstrating the TSC-related pathogenic mechanism. A literature review showed 73 TSC cases presenting aneurysms published until now.


Assuntos
Aneurisma , Astrocitoma , Fibroma , Esclerose Tuberosa , Aneurisma/complicações , Fibroma/complicações , Humanos , Artéria Subclávia/patologia , Esclerose Tuberosa/complicações , Esclerose Tuberosa/genética , Esclerose Tuberosa/patologia
5.
Eur J Vasc Endovasc Surg ; 61(6): 938-944, 2021 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-33773906

RESUMO

OBJECTIVE: Type I hybrid arch repair has become popular as a procedure that is less invasive than total arch replacement. The major advantage of this technique is that antegrade endograft implantation can be performed during the procedure, thereby avoiding the complications of introducing the endograft from the groin. The aim of this study was to assess the midterm outcomes of type I hybrid aortic arch repair with antegrade endograft implantation. METHODS: Thirty consecutive patients who underwent type I hybrid repair with antegrade endograft implantation from 2009 to 2015 were reviewed retrospectively. Patient demographics, and peri-operative and late results were collected from a prospective database and analysed. RESULTS: Four patients (13%) were female and the median age was 78 years. Median aneurysm size was 64 mm. Six patients (20%) developed stroke, and the 30 day mortality rate was 3%. Two patients suffered aortic dissection at the site of debranching anastomosis. The median follow up was 5.2 years. All aneurysms remained stable or had decreased in size at three years, and 82% were stable at five years. Overall survival was 79% at three years and 71% at five years. The rates of freedom from aorta related death were 86% at three and five years, respectively. During the follow up period, three additional left subclavian artery embolisations and one endograft relining due to type IIIb endoleak were required. CONCLUSION: Midterm outcomes of type I hybrid aortic arch repair with antegrade endograft implantation for aortic arch aneurysms are reported. Although the incidence of peri-operative stroke was high, late sac behaviour was acceptable.


Assuntos
Anastomose Cirúrgica , Aorta Torácica , Aneurisma da Aorta Torácica/cirurgia , Dissecção Aórtica/cirurgia , Implante de Prótese Vascular , Prótese Vascular , Endoleak , Procedimentos Endovasculares , Idoso , Anastomose Cirúrgica/efeitos adversos , Anastomose Cirúrgica/métodos , Aorta Torácica/patologia , Aorta Torácica/cirurgia , Implante de Prótese Vascular/efeitos adversos , Implante de Prótese Vascular/métodos , Endoleak/etiologia , Endoleak/cirurgia , Procedimentos Endovasculares/efeitos adversos , Procedimentos Endovasculares/métodos , Feminino , Virilha/irrigação sanguínea , Humanos , Japão/epidemiologia , Masculino , Mortalidade , Avaliação de Processos e Resultados em Cuidados de Saúde , Artéria Subclávia/patologia , Artéria Subclávia/cirurgia
7.
Clin Nucl Med ; 46(3): e173-e175, 2021 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-33181750

RESUMO

ABSTRACT: A 19-year-old woman presented with a primary mediastinal B-cell lymphoma invading the superior vena cava with associated thrombosis of the left brachiocephalic and subclavian vein. She underwent thrombolysis followed by chemotherapy. The midtreatment 18F-FDG PET/CT demonstrated important regression of the primary mediastinal B-cell lymphoma, but showed intense focal hepatic uptake in segment IV, without a corresponding lesion on ultrasonography, non-contrast-enhanced low-dose CT, and MRI. This focal uptake disappeared on a subsequent 18F-FDG PET/CT study when the radiotracer was injected in the foot, suggesting an anomalous venous return pathway that persisted despite thrombolysis.


Assuntos
Fluordesoxiglucose F18/metabolismo , Fígado/metabolismo , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Terapia Trombolítica , Trombose/tratamento farmacológico , Trombose/metabolismo , Transporte Biológico , Veias Braquiocefálicas/patologia , Feminino , Humanos , Fígado/diagnóstico por imagem , Linfoma/complicações , Neoplasias do Mediastino/complicações , Artéria Subclávia/patologia , Trombose/complicações , Trombose/diagnóstico por imagem , Adulto Jovem
11.
Vet Surg ; 49(2): 265-273, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31598999

RESUMO

OBJECTIVE: To report the clinical characteristics, types of vascular ring anomalies (VRA), operative findings, complications, and survival after surgical treatment of cats with VRA. STUDY DESIGN: Retrospective, multi-institutional case series. ANIMALS: Client- or shelter-owned cats presenting to academic, referral veterinary institutions. METHODS: Medical records of cats with VRA that underwent surgical treatment were reviewed. Signalment, relevant medical history, clinical signs, diagnostic imaging, surgical findings, complications, and survival were recorded. RESULTS: Twenty cats with VRA were included. Vascular ring anomalies were most commonly (75% [15/20]) diagnosed in cats less than 1 year old, with no breed or sex predilection. Regurgitation was the most common clinical sign, present in 18 of 20 (90%) cats. A persistent right aortic arch was diagnosed in 17 of 20 (85%) cats, with concurrent aberrant left subclavian artery in four of the cats. Surgical treatment was associated with survival to discharge in 18 of 20 (90%) cats. Persistent clinical signs were reported in nine of 13 (69%) cats, and radiographic evidence of megaesophagus persisted in four of 13 (31%) cats, with a median follow-up of 275 days after discharge. CONCLUSION: Persistent right aortic arch was the most commonly diagnosed VRA in cats in this series, although multiple anomalies were observed. Surgical treatment of VRA in cats was associated with a high survival to discharge, although persistence of clinical signs and megaesophagus was noted in 69% and 31% of the cats, respectively. CLINICAL SIGNIFICANCE: Surgical treatment of VRA in cats is associated with a high survival rate; however, persistence of clinical signs is an expected outcome.


Assuntos
Anormalidades Cardiovasculares/veterinária , Doenças do Gato/patologia , Artéria Subclávia/anormalidades , Anel Vascular/veterinária , Anormalidades Múltiplas , Animais , Anormalidades Cardiovasculares/patologia , Gatos , Feminino , Masculino , Estudos Retrospectivos , Artéria Subclávia/patologia , Anel Vascular/patologia , Anel Vascular/cirurgia
12.
Neuro Endocrinol Lett ; 40(3): 113-118, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31816217

RESUMO

We reported a case of carotid artery stenosis with stroke symptoms detected in a patient with lung cancer after radiotherapy. The patient was a 58-year-old male with a complaint of \"a single episode of temporary amaurosis in the right eye for 10 minutes". The clinical diagnosis at admission, after consideration of the patient's age, medical history, and auxiliary examination results, was as follows: lung cancer; right common carotid artery stenosis; left common carotid artery stenosis; left vertebral artery stenosis; and right subclavian artery occlusion with right subclavian steal syndrome (Grade 3). Carotid angioplasty and stenting (CAS) were subsequently performed. During the 6-month follow-up, we observed no episode of temporary vision loss or other signs of stroke. Clinicians should pay great attention to delayed radiation-induced carotid stenosis. It is recommended that patients with a history of radiotherapy should undergo regular color Doppler ultrasound examination of the cervical region to diagnose, prevent, and treat RICS in an expedient fashion. This approach should improve survival rate and quality of life.


Assuntos
Estenose das Carótidas/etiologia , Neoplasias Pulmonares/radioterapia , Radioterapia/efeitos adversos , Síndrome do Roubo Subclávio/etiologia , Artéria Carótida Primitiva/patologia , Artéria Carótida Primitiva/efeitos da radiação , Artéria Carótida Primitiva/cirurgia , Estenose das Carótidas/diagnóstico , Estenose das Carótidas/patologia , Estenose das Carótidas/cirurgia , Humanos , Neoplasias Pulmonares/diagnóstico , Neoplasias Pulmonares/patologia , Masculino , Pessoa de Meia-Idade , Lesões por Radiação/diagnóstico , Lesões por Radiação/etiologia , Lesões por Radiação/patologia , Lesões por Radiação/cirurgia , Stents , Artéria Subclávia/patologia , Artéria Subclávia/efeitos da radiação , Artéria Subclávia/cirurgia , Síndrome do Roubo Subclávio/diagnóstico , Síndrome do Roubo Subclávio/patologia , Síndrome do Roubo Subclávio/cirurgia , Ultrassonografia Doppler em Cores , Artéria Vertebral/patologia , Artéria Vertebral/efeitos da radiação , Artéria Vertebral/cirurgia
13.
J Forensic Sci ; 64(6): 1926-1928, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31162649

RESUMO

A 53-year-old woman was admitted to the hospital due to unexpected dizziness and died the following morning. To investigate the cause of death, a forensic autopsy along with histological examination was performed 3 days after her death. The major findings of the autopsy were that a fish bone had pierced the left subclavian artery after perforating the esophagus with 680 mL of blood in the stomach and bloody and tarry contents were present in the intestines, and the cause of death was confirmed to be subsequent hemorrhagic shock. Unfortunately, none of her family realized that she had eaten a fish 4 days before the tragedy until the fish bone was found. The present case is rare and instructive. The histopathological findings of left subclavian artery-esophageal fistula induced by a fish bone can be used as a reference in forensic practice.


Assuntos
Morte Súbita/etiologia , Fístula Esofágica/patologia , Perfuração Esofágica/patologia , Corpos Estranhos/patologia , Artéria Subclávia/patologia , Fístula Vascular/patologia , Animais , Fístula Esofágica/etiologia , Perfuração Esofágica/etiologia , Feminino , Peixes , Corpos Estranhos/complicações , Humanos , Pessoa de Meia-Idade , Artéria Subclávia/lesões , Fístula Vascular/etiologia
15.
Clin Exp Hypertens ; 41(4): 323-329, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-29902063

RESUMO

BACKGROUND AND AIMS: Genetic factors play an important role in the cervico-cerebral large-artery atherosclerotic stenosis (LAS), and ATP2B1 gene has been associated with the process of atherosclerosis disorders, such as coronary artery disease and arterial stiffness. But there is little information about the relationship between ATP2B1 gene and atherosclerosis in the intracranial arteries. We hereby investigated the association of common variants in ATP2B1 gene with LAS in asymptomatic Chinese hypertension patients. METHODS: The stenosis of intracranial and extracranial arteries were evaluated in 899 subjects through computerized tomography angiography from the aortic arch to the skull base. A total of 11 ATP2B1 common variants were genotyped. Multivariate logistic regression was carried out in a dominant model with confounding factors adjusted. RESULTS: rs17249754-A (OR = 0.43, p = 0.0002) and rs1401982-G (OR = 0.47, p = 0.0007) were associated with decreased susceptibility of concurrent extra and intracranial stenosis even after Bonferroni correction. These two minor alleles were also significantly associated with less stenotic arteries and moderate-to-severe stenosis. CONCLUSION: rs17249754 and rs1401982 were associated with asymptomatic LAS in stroke-free Chinese hypertension patients and might benefit early recognition of LAS patients in clinical practice.


Assuntos
Artérias/diagnóstico por imagem , Aterosclerose/genética , Hipertensão/complicações , ATPases Transportadoras de Cálcio da Membrana Plasmática/genética , Idoso , Artérias/patologia , Doenças Assintomáticas , Aterosclerose/complicações , Aterosclerose/diagnóstico por imagem , Artéria Basilar/diagnóstico por imagem , Artéria Basilar/patologia , Artérias Carótidas/diagnóstico por imagem , Artérias Carótidas/patologia , Artérias Cerebrais/diagnóstico por imagem , Artérias Cerebrais/patologia , Angiografia por Tomografia Computadorizada , Constrição Patológica/diagnóstico por imagem , Constrição Patológica/genética , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Artéria Subclávia/diagnóstico por imagem , Artéria Subclávia/patologia , Rigidez Vascular/genética , Artéria Vertebral/diagnóstico por imagem , Artéria Vertebral/patologia
18.
Eur J Cardiothorac Surg ; 55(6): 1228-1230, 2019 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-30364973

RESUMO

Endograft placement is a minimally invasive procedure used to repair thoracic aortic aneurysms. This technique is used for treating aneurysms and aortic dissections or ruptures, but it can also be applied for the resection of malignant tumours with vascular invasion. We describe the successful use of the thoracic endovascular aortic repair technique to remove a malignant tumour infiltrating the left subclavian artery in a 50-year-old man. The resection of the left subclavian artery infiltrated by thoracic malignant tumours may require temporary cardiopulmonary bypass, direct clamping of the aorta or extracorporeal circulation techniques. However, the off-label use of thoracic endovascular aortic repair avoids the need for these high-risk surgical techniques. After the surgical removal of the mass and combined aortic resection without complications, the patient was eligible to undergo chemotherapy/radiotherapy, thus improving his prognosis.


Assuntos
Aorta Torácica/cirurgia , Dissecção Aórtica/cirurgia , Implante de Prótese Vascular/métodos , Procedimentos Endovasculares/métodos , Neoplasias/complicações , Stents , Artéria Subclávia/patologia , Dissecção Aórtica/complicações , Dissecção Aórtica/diagnóstico , Aorta Torácica/diagnóstico por imagem , Aortografia/métodos , Humanos , Masculino , Pessoa de Meia-Idade , Invasividade Neoplásica , Neoplasias/diagnóstico , Prognóstico , Desenho de Prótese , Artéria Subclávia/cirurgia
19.
J Thorac Cardiovasc Surg ; 157(6): 2150-2156, 2019 06.
Artigo em Inglês | MEDLINE | ID: mdl-30578062

RESUMO

OBJECTIVES: The aim of this study was to investigate the fate of nonaortic arterial segments in patients with Marfan syndrome (MFS). METHODS: This was a retrospective analysis of 100 consecutive patients with MFS fulfilling Ghent criteria who underwent 192 interventions on any segment of the arterial tree and were followed over the past 20 years. A review of the available imaging regarding 9 defined regions of interest of the carotid, innominate, subclavian, iliac, and femoral arteries was performed. RESULTS: Mean follow-up interval was 11.6 ± 7.7 years. Of 600 measurements that were performed, 414 (69%) arterial segments showed dilatation above the upper range of normal. There were no significant sex differences. In 100 patients, 66 dissections in nonaortic arterial segments in 33 patients were identified. Nineteen patients with or without previous dissection underwent 34 interventions. Most interventions were performed on the iliac arteries (56%), followed by the subclavian arteries (21%), the intercostal arteries (9%), the carotid arteries (6%), the visceral arteries (6%), and the innominate artery (3%). Most iliac artery interventions (88%) were caused by dilatations due to previous dissections, whereas this was only the case in 17% of interventions on the subclavian arteries. CONCLUSIONS: Most patients with MFS presented with at least 2 dilated nonaortic arterial segments. The current data suggest that 20% of MFS patients will need some form of intervention on nonaortic arterial segments 5 to 6 years after their first aortic intervention, referring to the first aortic dissection of the patient if the patient had a history of dissection. Routine long-term follow-up imaging should include the iliac arteries as well as the supra-aortic branches.


Assuntos
Aneurisma/etiologia , Artérias/patologia , Síndrome de Marfan/complicações , Fatores Etários , Aneurisma/cirurgia , Dissecção Aórtica/etiologia , Dissecção Aórtica/cirurgia , Artérias/cirurgia , Artérias Carótidas/patologia , Artéria Femoral/patologia , Humanos , Artéria Ilíaca/patologia , Masculino , Síndrome de Marfan/patologia , Síndrome de Marfan/cirurgia , Pessoa de Meia-Idade , Estudos Retrospectivos , Artéria Subclávia/patologia , Procedimentos Cirúrgicos Vasculares/estatística & dados numéricos
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