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1.
Clin Anat ; 34(5): 685-709, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33078444

RESUMO

Myocardial bridges are anatomical entities characterized by myocardium covering segments of coronary arteries. In some patients, the presence of a myocardial bridge is benign and is only incidentally found on autopsy. In other patients, however, myocardial bridges can lead to compression of the coronary artery during systolic contraction and delayed diastolic relaxation, resulting in myocardial ischemia. This ischemia in turn can lead to myocardial infarction, ventricular arrhythmias and sudden cardiac death. Myocardial bridges have also been linked to an increased incidence of atherosclerosis, which has been attributed to increased shear stress and the presence of vasoactive factors. Other studies however, demonstrated the protective roles of myocardial bridges. In this study, using systematic review and a meta-analytical approach we investigate the prevalence and morphology of myocardial bridges in both clinical imaging and cadaveric dissections. We also discuss the pathophysiology, clinical significance, and management of these anatomical entities.


Assuntos
Ponte Miocárdica , Animais , Cadáver , Humanos , Ponte Miocárdica/complicações , Ponte Miocárdica/diagnóstico por imagem , Ponte Miocárdica/epidemiologia , Prevalência
2.
Cureus ; 10(10): e3441, 2018 Oct 11.
Artigo em Inglês | MEDLINE | ID: mdl-30555756

RESUMO

Pseudomonas luteola is a rare infective agent with a variable resistance-sensitivity panel. Clinical suspicion and appropriate empiric treatment is necessary for resolution of such infections. We report a case of post-surgical gangrene as a result of Pseudomonas luteola culminating in limb amputation.

3.
Clin Anat ; 31(6): 878-886, 2018 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-29732618

RESUMO

An estimated 1.4% of the population worldwide has been diagnosed with Gender Dysphoria, as defined by the Diagnostic and Statistical Manual of Mental Disorders. Gender reassignment, which holistically encompasses psychotherapy, hormonal therapy and genital and nongenital surgeries, is considered the most effective treatment for transgender nonconforming patients afflicted with gender dysphoria. Little research is currently available identifying the psychosocial needs of the transgender population and their access to preventative and primary care during this transitioning process. This article presents an overview of the evolution and current approaches to genital surgical procedures available for both male-to-female, as well as female-to-male gender-affirmation surgeries. Clin. Anat. 31:878-886, 2018. © 2018 Wiley Periodicals, Inc.


Assuntos
Disforia de Gênero/cirurgia , Procedimentos de Readequação Sexual/métodos , Atitude do Pessoal de Saúde , Manual Diagnóstico e Estatístico de Transtornos Mentais , Feminino , Disforia de Gênero/história , Disforia de Gênero/psicologia , História do Século XVI , História do Século XVII , História do Século XVIII , História do Século XIX , História do Século XX , Humanos , Masculino , Procedimentos de Readequação Sexual/história , Procedimentos de Readequação Sexual/tendências , Padrão de Cuidado , Pessoas Transgênero/história , Pessoas Transgênero/psicologia , Transexualidade/história
4.
Clin Anat ; 31(2): 160-168, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-29178184

RESUMO

Incidence of transexualism and request for neophalloplasty is increasing yielding a current prevalence of trans-male in the USA of 1:2500. Surgeons have explored various techniques to improve desirable outcomes of neophallic construction, decrease the length of surgery, and minimize stigmatizing scars. The anterolateral thigh (ALT) flap is an alternative to the traditional radial forearm flap for patients who do not want a forearm scar. Surgical text descriptions were enhanced by the creation of new anatomic illustrations. Anatomy of the donor and recipient sites as well as the surgical technique leading to creation of the neophallus are demonstrated in detail with new relevant illustrations. The ALT flap is a skin, fat and fascia flap that is usually supplied by the descending branch of the lateral circumflex femoral vessels and the lateral femoral cutaneous nerve. However, variability in neurovascular supply does exist with important clinical implications. In the pedicled surgical procedure, neurovascular supply is left partly attached to the donor site ("pedicle") and simply transposed to the perineum, keeping the pedicle intact as a conduit to supply the tissue with blood and innervation. ALT flap offers clinical advantages of less obvious donor site concealable with clothing, decreased surgical time, preservation of erogenous sensation and vascular supply of the flap without microsurgical anastomosis of nerves and vessels, and good potential for urethroplasty. This surgery may be difficult in patients with thicker skin and more subcutaneous thigh fat. Clin. Anat, 2017. © 2017 Wiley Periodicals, Inc. © 2017 Wiley Periodicals, Inc.


Assuntos
Fascia Lata/anatomia & histologia , Artéria Femoral/anatomia & histologia , Nervo Femoral/anatomia & histologia , Pênis/anatomia & histologia , Cirurgia de Readequação Sexual/métodos , Retalhos Cirúrgicos , Sítio Doador de Transplante , Cicatriz/psicologia , Fascia Lata/transplante , Feminino , Humanos , Masculino , Pênis/cirurgia , Cirurgia de Readequação Sexual/efeitos adversos , Retalhos Cirúrgicos/irrigação sanguínea , Retalhos Cirúrgicos/inervação , Retalhos Cirúrgicos/transplante , Coxa da Perna/anatomia & histologia , Coxa da Perna/cirurgia , Coleta de Tecidos e Órgãos/métodos , Sítio Doador de Transplante/irrigação sanguínea , Sítio Doador de Transplante/inervação , Uretra/anatomia & histologia , Uretra/cirurgia , Micção
5.
Clin Anat ; 29(5): 633-7, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27087350

RESUMO

Trisomy 12 is a rare aneuploidy and fetuses with this defect tend to spontaneously abort. However, mosaicism allows this anomaly to manifest itself in live births. Due to the fact that mosaicism represents a common genetic abnormality, trisomy 12 is encountered more frequently than expected at a rate of 1 in 500 live births. Thus, it is imperative that medical practitioners are aware of this aneuploidy. Moreover, this genetic disorder may result from a complete or partial duplication of chromosome 12. A partial duplication may refer to a specific segment on the chromosome, or one of the arms. On the other hand, a complete duplication refers to duplication of both arms of chromosome 12. The combination of mosaicism and the variable duplication sites has led to variable phenotypes ranging from normal phenotype to Potter sequence to gross physical defects of the various organ systems. This article provides a review of the common anatomical variation of the different types of trisomy 12. This review revealed that further documentation is needed for trisomy 12q and complete trisomy 12 to clearly delineate the constellation of anomalies that characterize each genetic defect. Clin. Anat. 29:633-637, 2016. © 2016 Wiley Periodicals, Inc.


Assuntos
Trissomia/patologia , Cromossomos Humanos Par 12 , Humanos , Mosaicismo
6.
Clin Anat ; 29(5): 628-32, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27087248

RESUMO

Trisomy 18 is the second most common aneuploidy after trisomy 21. Due to its multi-systemic defects, it has a poor prognosis with a 50% chance of survival beyond one week and a <10% chance of survival beyond one year of life. However, this prognosis has been challenged by the introduction of aggressive interventional therapies for patients born with trisomy 18. As a result, a review of the anatomy associated with this defect is imperative. While any of the systems can be affected by trisomy 18, the following areas are the most likely to be affected: craniofacial, musculoskeletal system, cardiac system, abdominal, and nervous system. More specifically, the following features are considered characteristic of trisomy 18: low-set ears, rocker bottom feet, clenched fists, and ventricular septal defect. Of particular interest is the associated cardiac defect, as surgical repairs of these defects have shown an improved survivability. In this article, the anatomical defects associated with each system are reviewed. Clin. Anat. 29:628-632, 2016. © 2016 Wiley Periodicals, Inc.


Assuntos
Trissomia/patologia , Cromossomos Humanos Par 18/genética , Diagnóstico Pré-Natal , Trissomia/diagnóstico , Trissomia/genética , Síndrome da Trissomía do Cromossomo 18
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