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1.
Bol. Asoc. Méd. P. R ; 90(4/6): 82-84, Apr.-Jun. 1998.
Artigo em Inglês | LILACS | ID: lil-411395

RESUMO

We report the case of a uretero-arterial fistula (UAF) formation in a 68 years old male who had previously undergone an Aortobifemoral graft. He got complicated with occlusion and infection of the right lower extremity requiring a right hip disarticulation for its management. This was followed by groin infection and graft protusion, managed by transabdominal resection of the right graft limb, at which time the right ureter was lacerated and repaired. Several months later, he presented with gross hematuria found to be secondary to UAF. The diagnostic and management steps leading to this patient care will be reviewed, together with a review of the literature pertinent to this case report


Assuntos
Humanos , Masculino , Idoso , Aorta Abdominal/patologia , Doenças da Aorta/patologia , Complicações Pós-Operatórias/patologia , Doenças Ureterais/patologia , Fístula Urinária/patologia , Fístula Vascular/patologia , Aorta Abdominal , Aorta Abdominal/cirurgia , Doenças da Aorta/etiologia , Doenças da Aorta , Doenças da Aorta/cirurgia , Complicações Pós-Operatórias/etiologia , Complicações Pós-Operatórias , Complicações Pós-Operatórias/cirurgia , Doenças Ureterais/etiologia , Doenças Ureterais , Doenças Ureterais/cirurgia , Fístula Urinária/etiologia , Fístula Urinária , Fístula Urinária/cirurgia , Fístula Vascular , Fístula Vascular/cirurgia , Complicações Intraoperatórias , Ureter/lesões , Ureter/cirurgia
2.
Bol. Asoc. Méd. P. R ; 90(4/6): 79-81, Apr.-Jun. 1998.
Artigo em Inglês | LILACS | ID: lil-411396

RESUMO

Primitive neuroectodermal or neuroepithelial tumors are names used to describe neoplasias composed of undifferentiated cells resembling germinal cells of the embryonic neural tube. These tumors are small round cell malignancies of the neural crest origin arising outside the central and sympathetic nervous system. They are described as peripheral and central neuroectodermal tumors related to the original malignant cell. A great number of tumors are described under this classification in spite of the fact that there is no an universal acceptance that these small-cell neoplasms, regardless of their primary site, are derived from immature neuroectoderm tissue. Because one tumor resembles others in terms of its phenotypic expression, multiple specific studies such as clinical profile, ultrastructural, immunocytochemical, and cytogenetic features should be studied, since no single clinical or laboratory marker is by itself diagnostic. However, there is a chromosomal reciprocal translocation, t(11;22)(q24;q12), which is unique to Primitive Neuroectodermal Tumor (PNET)


Assuntos
Humanos , Masculino , Feminino , Recém-Nascido , Lactente , Pré-Escolar , Criança , Adolescente , Adulto , Tumores Neuroectodérmicos Primitivos/epidemiologia , Neoplasias Ósseas/epidemiologia , Neoplasias Ósseas/patologia , Neoplasias Ósseas/terapia , Neoplasias Retroperitoneais/epidemiologia , Neoplasias Retroperitoneais/patologia , Neoplasias Retroperitoneais/terapia , Neuroblastoma/epidemiologia , Neuroblastoma/patologia , Neuroblastoma/terapia , Prognóstico , Porto Rico/epidemiologia , Estudos Retrospectivos , Sarcoma de Ewing/epidemiologia , Sarcoma de Ewing/patologia , Sarcoma de Ewing/terapia , Tumores Neuroectodérmicos Primitivos/patologia , Tumores Neuroectodérmicos Primitivos/terapia
3.
Bol. Asoc. Méd. P. R ; 90(1/3): 37-39, Jan.-Mar. 1998.
Artigo em Inglês | LILACS | ID: lil-411406

RESUMO

This is a review of a child who developed symptomatic anemia secondary to a huge Meckel's Diverticulum (MD). The patient presented with multiple complications, such as: neoplasia, occult chronic bleeding, giant size MD, partial intestinal obstruction and severe symptomatic anemia. There was complete resolution of the condition after resection and ileo-ileal anastomosis. After revision of the literature, this case is the first report of MD occurring concomitantly with such a myriad of signs and symptoms


Assuntos
Humanos , Masculino , Adolescente , Divertículo Ileal/complicações , Hemorragia Gastrointestinal/etiologia , Divertículo Ileal/cirurgia , Leiomioma/complicações , Leiomioma/cirurgia , Neoplasias do Íleo/complicações , Neoplasias do Íleo/cirurgia , Reto
4.
Bol. Asoc. Méd. P. R ; 90(1/3): 34-36, Jan.-Mar. 1998.
Artigo em Inglês | LILACS | ID: lil-411407

RESUMO

This is a review of two children who developed acute glomerulonephritis (AGN) following acute gangrenous appendicitis (AGA) with periappendicular collections. The first patient presented with AGN during the course of appendicitis. The second patient developed AGN after appendectomy. Both patients did not have any other predisposing factors. AGN resolved in both patients after massive intravenous antibiotics. This is the first report of acute appendicitis as a predisposing factor for AGN


Assuntos
Humanos , Masculino , Criança , Adolescente , Apendicite/complicações , Glomerulonefrite por IGA/etiologia , Doença Aguda , Apendicectomia , Antibacterianos/uso terapêutico , Apendicite/tratamento farmacológico , Apendicite/cirurgia , Glomerulonefrite por IGA/cirurgia
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