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    <link>http://hdl.handle.net/11422/25220</link>
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    <pubDate>Wed, 22 Apr 2026 05:19:26 GMT</pubDate>
    <dc:date>2026-04-22T05:19:26Z</dc:date>
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      <title>Hipertensão refratária em paciente com aorta em recife de coral: um relato de caso</title>
      <link>http://hdl.handle.net/11422/26140</link>
      <description>Title: Hipertensão refratária em paciente com aorta em recife de coral: um relato de caso
Author(s)/Inventor(s): Menezes, Rubens Thadeu Mangilli de
Advisor: Silva, Luciana Moura Farjoun da
Abstract: Introduction: Coral reef aorta (ARC) is a relatively uncommon vascular pathology, with the formation of coarse atherosclerotic plaques and irregular calcification that grow towards the lumen of the aorta and cause stenosis with a reduction in the overall caliber of the vessel, which may have repercussions hemodynamics. Case Report: Patient female, 73 years old, with hypertensive encephalopathy refractory to sodium nitroprusside and nitroglycerin in full doses. Presents a history of previous lameness, without trophic lesions, monitored by the clinical cardiology team. Presents only reduced bilateral femoral pulses. There is an upper and lower blood pressure discrepancy, without neurological changes. The aorto-iliac tomography angiography showed diffuse atherosclerotic disease of irregular calcified plaques,&#xD;
with a diffusely reduced caliber of the aorta throughout its entire length, presenting two points of significant stenosis - with a presumed diagnosis of coral-like aorta as the trigger for renovascular hypertension. She had undergone balloon angioplasty of the descending thoracic aorta and had a self-expanding stent placed; Angioplasty of the abdominal aorta was then performed with a balloon and balloon-expanding stent implantation. She was discharged on the eighth postoperative day, with controlled SBP below 140mmHg and outpatient follow-up. Conclusion: Coral reef aorta is an&#xD;
uncommon pathology, which can present life-threatening symptoms, is still underdiagnosed and requires further studies.
Publisher: Universidade Federal do Rio de Janeiro
Type: Trabalho de conclusão de especialização</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/11422/26140</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Paraganglioma de carótida direita: tratamento cirúrgico de Glomus carotídeo em Hospital Público Universitário do Rio de Janeiro</title>
      <link>http://hdl.handle.net/11422/26139</link>
      <description>Title: Paraganglioma de carótida direita: tratamento cirúrgico de Glomus carotídeo em Hospital Público Universitário do Rio de Janeiro
Author(s)/Inventor(s): Knoploch, Brunno Bastos
Advisor: Silva, Luciana Moura Farjoun da
Abstract: Paragangliomas are rare neuroendocrine tumors that originate from extra-adrenal autonomic paraganglia, small structures mainly composed of neuroendocrine cells derived from the embryonic neural crest, with the ability to secrete catecholamines. Most paragangliomas of parasympathetic origin are located in the neck and skull base, along the branches of the glossopharyngeal and vagus nerves. They most commonly arise from the carotid body, less frequently from jugulotympanic and vagal paraganglia, and rarely from laryngeal paraganglia. Carotid body paragangliomas account for&#xD;
0.5-0.6% of head and neck tumors and approximately 60% of cervical paragangliomas. These tumors are typically asymptomatic and grow indolently but may progress to larger, symptomatic, and potentially secreting lesions. In this case report, we present a male patient with a painless cervical bulge on the right side. During the diagnostic workup, a neck AngioCT revealed a 5.5 x 4.3 x 1.0 cm mass at the carotid bulb, followed by a urinary catecholamine assessment. The typical location of this rare&#xD;
neoplasm, the carotid bulb, is a critical area that requires detailed preoperative planning with imaging studies, obviating the need for biopsy. However, in this case, a biopsy was performed before the patient was referred to the UFRJ service. The tumor is highly vascularized, and catecholamine assessment is essential to prevent complications from adrenergic release during surgery. In this case, the catecholamine test was negative. The patient underwent resection of the cervical mass, requiring permanent ligation of the external carotid artery. In surgical planning, it is crucial for the team and the patient to be fully informed about the complexity of the procedure, especially the possibility of sacrificing the carotid artery and its branches. The development of a detailed surgical plan should include strategies for cervical revascularization to ensure adequate perfusion and minimize risks. However, in some cases, revascularization may be unnecessary if appropriate tests confirm the competence of the circle of Willis, ensuring effective cerebral circulation.
Publisher: Universidade Federal do Rio de Janeiro
Type: Trabalho de conclusão de especialização</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/11422/26139</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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