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1.
Pediatr Neurosurg ; 33(5): 265-269, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11155065

RESUMO

Ultrasonography revealed a suprasellar tumor in a fetus at 28 weeks of gestation. The male newborn, delivered 10 weeks later, was operated at the age of 17 days, and a craniopharyngioma was completely removed. Intraoperatively, inappropriate secretion of antidiuretic hormone occurred and was followed by diabetes insipidus causing imbalance of fluid and electrolytes. The tumor recurred and was totally removed 1 year later. Further development was uneventful and, at the age of 8 years, the boy is in generally good mental and physical condition except for a left-sided hemiparesis. In contrast to the poor outcome of neonatal craniopharyngioma reviewed in the literature, this case may encourage radical surgery even in the very young.


Assuntos
Neoplasias Encefálicas/diagnóstico , Neoplasias Encefálicas/cirurgia , Craniofaringioma/diagnóstico , Craniofaringioma/cirurgia , Doenças Fetais/diagnóstico , Procedimentos Neurocirúrgicos/métodos , Diagnóstico Pré-Natal , Sela Túrcica , Feminino , Humanos , Recém-Nascido , Imageamento por Ressonância Magnética , Masculino , Recidiva Local de Neoplasia , Gravidez , Sela Túrcica/diagnóstico por imagem , Sela Túrcica/patologia , Sela Túrcica/cirurgia , Tomografia Computadorizada por Raios X , Ultrassonografia Pré-Natal
2.
Z Geburtshilfe Perinatol ; 192(5): 192-6, 1988.
Artigo em Alemão | MEDLINE | ID: mdl-3062952

RESUMO

At the Gynecological Clinic of the Klinikum Ludwigshafen prenatal transabdominal diagnostic aspiration of villi was performed in 120 cases in the first and second trimesters between October 1986 and April 1988. The puncture was performed using a cannula system comprising a guide and an aspiration needle. The ultrasonographically controlled removal technique is described with special consideration of the procedure in cases with placental insertion in the posterior wall. Successful tissue removal (at least 5 mg of tissue) was achieved in 97.5% of the cases. Cytogenetic, biochemical, and molecular biologic studies were performed. The most frequent indication was to detect chromosome disorders in older mothers (74.2%). Such disorders were diagnosed in 4.2% of all cases and pregnancy was terminated in seven of them; the indications were aneuploidies, metabolic disease, or severe developmental anomalies detected by ultrasonography in normal karyotypes. In the remaining 113 pregnancies one miscarriage was seen nine weeks after aspiration of villi. On the basis of these results the abortion risk following transabdominal chorionic biopsy is 0.88% and is thus similar to that following amniocentesis.


Assuntos
Amostra da Vilosidade Coriônica/instrumentação , Aberrações Cromossômicas/diagnóstico , Aborto Eugênico , Aberrações Cromossômicas/genética , Transtornos Cromossômicos , Feminino , Humanos , Cariotipagem , Gravidez , Primeiro Trimestre da Gravidez , Segundo Trimestre da Gravidez , Fatores de Risco , Ultrassonografia/instrumentação
3.
Geburtshilfe Frauenheilkd ; 47(11): 792-5, 1987 Nov.
Artigo em Alemão | MEDLINE | ID: mdl-3319761

RESUMO

The article reports on the introduction of transabdominal chorionic biopsy in the Gynaecological Hospital of Ludwigshafen in cooperation with the Department of Human Genetics at the University of Heidelberg. After completion of a pilot study 15 diagnostic transabdominal chorionic biopsies were performed between the 15th and 23rd pregnancy week. Sampling was successful in all cases; the median estimated weight of the biopsied samples was 35 mg. Cytogenic, biochemical and molecular-genetic examinations were conducted. No complications were seen except for one subserous haematoma. Indications and time of performance are discussed. The transabdominal chorionic biopsy is easier to conduct in the 2nd trimenon than during the first, and can therefore be considered to be a favorable "entry" into the technique. Shifting the biopsy to an earlier date, namely, into the first trimenon, can be aimed at as the familiarity with the technique increases. The obvious advantages of transabdominal removal of villi compared with the transcervical method lead us to expect that in course of the time the transcervical method will be replaced by the transabdominal one. No indication for invasive prenatal diagnosis should be implied without previous detailed genetic counselling.


Assuntos
Vilosidades Coriônicas/patologia , Aberrações Cromossômicas/patologia , Diagnóstico Pré-Natal , Adulto , Biópsia por Agulha , Aberrações Cromossômicas/genética , Transtornos Cromossômicos , Feminino , Triagem de Portadores Genéticos , Humanos , Gravidez , Fatores de Risco , Ultrassonografia
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