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  <channel rdf:about="http://repositorio.ufc.br/handle/riufc/391">
    <title>DSpace Coleção:</title>
    <link>http://repositorio.ufc.br/handle/riufc/391</link>
    <description />
    <items>
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        <rdf:li rdf:resource="http://repositorio.ufc.br/handle/riufc/65513" />
        <rdf:li rdf:resource="http://repositorio.ufc.br/handle/riufc/65489" />
        <rdf:li rdf:resource="http://repositorio.ufc.br/handle/riufc/64760" />
        <rdf:li rdf:resource="http://repositorio.ufc.br/handle/riufc/64335" />
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    <dc:date>2026-04-08T22:39:19Z</dc:date>
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  <item rdf:about="http://repositorio.ufc.br/handle/riufc/65513">
    <title>Aneurisma de artéria pulmonar como apresentação clínica de uma doença de Behçet: a propósito de um caso</title>
    <link>http://repositorio.ufc.br/handle/riufc/65513</link>
    <description>Título: Aneurisma de artéria pulmonar como apresentação clínica de uma doença de Behçet: a propósito de um caso
Autor(es): Rodrigues, Lara Martins; Liberato, Benedita Tatiane Gomes; Carneiro, Ana Rita Sampaio; Paixão, Miguel Wesley Nogueira; Ponte, Maycon Fellipe da
Abstract: Objective: To present clinical aspects and radiological changes observed in a case of Behçet’s disease. Methodology: The&#xD;
research was conducted through the investigation of a patient diagnosed with Behçet’s disease presenting with pulmonary artery&#xD;
aneurysm. Case description: Patient with a history of recurrent painful oral and genital ulcers. He presented with edema and&#xD;
pain in the cervical region, being diagnosed with internal jugular vein thrombosis and right brachiocephalic vein. The patient&#xD;
developed dyspnea, chest pain, hemoptysis, hematemesis, and pulmonary artery aneurysm was diagnosed, as well as painful&#xD;
ulcers, and Behçet’s disease was diagnosed. Discussion: From the International Study Group for Behçet’s Disease classification,&#xD;
the presence of recurrent oral ulcers and two of the following alterations - genital ulcers, typical eye lesions (uveitis, retinal&#xD;
vasculitis), characteristic skin lesions, or a positive patergia test define the diagnosis of Behçet’s disease. Although rare, affecting&#xD;
less than 5% of patients, pulmonary artery involvement is the most feared form of vascular complication. Conclusion: We can&#xD;
conclude that it is important to consider the diagnosis of Behçet, as this pathology can affect several vessels of any caliber in the&#xD;
body and may result in thrombophlebitis, arterial stenosis, occlusions and aneurysms.
Tipo: Artigo de Periódico</description>
    <dc:date>2022-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repositorio.ufc.br/handle/riufc/65489">
    <title>Protocolo de cuidado ocular em pacientes internados nas unidades de tratamento intensivo</title>
    <link>http://repositorio.ufc.br/handle/riufc/65489</link>
    <description>Título: Protocolo de cuidado ocular em pacientes internados nas unidades de tratamento intensivo
Autor(es): Aragao, Ricardo Evangelista Marrocos de; Araruna, Loianne Pereira; Sousa, Mayara Pereira; Santos, Erika Andrade; Gomes, Lorena Maria Araújo
Abstract: Patients  in  intensive  care  unit  require  a  high  standard  of  medical  and  nursing  practice,  they  are  critically  ill  and  dependent  on  &#xD;
technology  and  medication,  however,  they  are  potentially  vulnerable  to  ocular  surface  disease,  mostly  those  sedated  and  at  &#xD;
mechanical  ventilation,which  are  at  risk  for  exposure  keratopathy.  This  condition  predisposes  to  microbial  keratitis  that  may  &#xD;
lead to corneal perforation and permanent visual loss. For these reasons eye care with regular cleaning of the eyes, installation &#xD;
of lubricating drops and ointments are recommended. Meta-analysis showed that moisture chambers are significantly better than &#xD;
lubrification at prevent exposure keratopathy. We reviewed some studies that showed the superiority of the moisture chamber in &#xD;
prevent ocular surface disease in patient in intensive care units.
Tipo: Artigo de Periódico</description>
    <dc:date>2022-04-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repositorio.ufc.br/handle/riufc/64760">
    <title>Resultados do transplante alogênico de células tronco hematopoiéticas em síndrome mielodisplásica do Hospital Universitário Walter Cantídio</title>
    <link>http://repositorio.ufc.br/handle/riufc/64760</link>
    <description>Título: Resultados do transplante alogênico de células tronco hematopoiéticas em síndrome mielodisplásica do Hospital Universitário Walter Cantídio
Autor(es): Cordeiro, Missielle Duarte; Gonçalves, Romélia Pinheiro; Duarte, Fernando Barroso
Abstract: Introduction: Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematopoietic disorders that are more&#xD;
likely to progress to acute myeloid leukemia (AML). Alogenic Haematopoietic Stem Cell Transplantation (HSCT) represents&#xD;
the most effective curative treatment for MDS to date. Objectives: To describe the profile of patients with MDS, who performed&#xD;
HSCT at the Walter Cantídio Universitary Hospital (HUWC) in Fortaleza, Ceará. Methodology: Retrospective observational&#xD;
and descriptive study with eleven patients with newly diagnosed MDS who performed HSCT in the period of February, 2015&#xD;
to June, 2018. Results: Total of eleven patients, age at diagnosis from nineteen to sixty-six years (mean age 46 years). Three&#xD;
deletion patients of the 5q (two with additional alterations), four hypocellular, one with multiple lineage dysplasia (p53 positive&#xD;
in immunohistochemistry), two with excess type 2 blasts, one with ring sideroblasts (low risk). Ten related donors with peripheral&#xD;
blood cell source and one non-related source of bone marrow. Deaths: a patient with excess blasts and a patient with multilinear&#xD;
dysplasia. Conclusion: It is possible to identify patients with low-risk MDS who have an indication for Alogenic Hematopoietic&#xD;
Stem Cell Transplantation. Additional cytogenetic abnormalities at the 5q deletion had no negative impact. We also reinforced the&#xD;
prognostic significance of p53.
Tipo: Artigo de Periódico</description>
    <dc:date>2022-03-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repositorio.ufc.br/handle/riufc/64335">
    <title>Síndrome mielodisplásica variante hipoplásica: análise estatística no serviço de transplante de medula óssea do Hospital Universitário Walter Cantídio</title>
    <link>http://repositorio.ufc.br/handle/riufc/64335</link>
    <description>Título: Síndrome mielodisplásica variante hipoplásica: análise estatística no serviço de transplante de medula óssea do Hospital Universitário Walter Cantídio
Autor(es): Martins, Henrique Girão; Barroso, Karine Sampaio Nunes; Leitão, João Paulo de Vasconcelos; Araujo, Beatriz Stela Gomes de Souza Pitombeira; Duarte, Fernando Barroso
Abstract: Objectives:&#xD;
 To analyze, in patients with myelodysplastic syndrome (MDS) hypoplastic variant of the Bone Marrow Transplant &#xD;
service, the response to the transplant and perform a comparison with data from the MDS Latin American database. &#xD;
Methodology:&#xD;
Analytical,  cross-sectional  and  retrospective  study  by  analyzing  medical  records,  including  all  patients  diagnosed  with  MDS  &#xD;
undergoing  bone  marrow  transplantation,  evaluation  of  post-transplantation  follow-up,  overall  survival  and  complications.  &#xD;
Comparison with data from the database of the MDS Latin American Society. Statistical analysis using the JAMOVI and MedCalc &#xD;
programs. &#xD;
Results:&#xD;
 A total of 13 MDS patients received an allogenic bone marrow transplant, of which 6 had hypoplastic variant, &#xD;
corresponding to 46.15%. Compared to data from the Latin American database, this percentage is only 12.75%. &#xD;
Conclusions:&#xD;
 Our &#xD;
service presented a higher frequency of hypoplastic variant MDS than that described in the medical literature, which corresponds &#xD;
to only 10-15%. Of the 6 patients with hypoplastic MDS, two died, reaching 33.3% against 13.5% in the Latin American database. &#xD;
The other transplanted patients are in remission so far with an overall 2-year survival rate of 83.3%, showing good results compared &#xD;
to the world literature.
Tipo: Artigo de Periódico</description>
    <dc:date>2022-03-01T00:00:00Z</dc:date>
  </item>
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