Biochemical analysis of ascites fluid as an aid to etiological diagnosis: a series of 100 cases of nonimmune fetal ascites. (26th November 2014)
- Record Type:
- Journal Article
- Title:
- Biochemical analysis of ascites fluid as an aid to etiological diagnosis: a series of 100 cases of nonimmune fetal ascites. (26th November 2014)
- Main Title:
- Biochemical analysis of ascites fluid as an aid to etiological diagnosis: a series of 100 cases of nonimmune fetal ascites
- Authors:
- Dreux, Sophie
Salomon, Laurent J.
Rosenblatt, Jonathan
Favre, Romain
Houfflin‐Debarge, Véronique
Broussin, Bernard
Guimiot, Fabien
Fenaux, Honorine
Delezoide, Anne‐Lise
Muller, Françoise - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="pd4522-sec-0001" sec-type="section"> <title>Objective</title> <p>The aim of this study is to analyze the contribution of biochemistry and cytology of fetal ascites fluid to the etiological diagnosis of ascites after ultrasonographic scan, maternal blood sampling, and fetal karyotyping.</p> </sec> <sec id="pd4522-sec-0002" sec-type="section"> <title>Method</title> <p>This is a retrospective study of 100 consecutive cases of nonimmune fetal ascites in which ascites fluid was sampled. All women underwent referral ultrasound scan and fetal karyotyping. All cases of fetal ascites were studied by biochemistry (total protein, <italic>β</italic><sub>2</sub>‐microglobulin, IgM, gamma‐glutamyl transpeptidase, aspartate aminotransferase, aminopeptidase M, and intestinal isoform of alkaline phosphatase) and cytology (lymphocyte count and vacuolated cells).</p> </sec> <sec id="pd4522-sec-0003" sec-type="section"> <title>Results</title> <p>The etiology of ascites was diagnosed at ultrasound scan in only 50% of cases. We observed significantly (<italic>P</italic> &lt; 0.001) low levels of total protein in ascites of urinary origin, high levels of digestive enzymes in ascites of digestive origin, and high <italic>β</italic><sub>2</sub>‐microglobulin in infectious ascites. Vacuolated cells were observed in all ten storage metabolic diseases.</p> </sec> <sec id="pd4522-sec-0004" sec-type="section"> <title>Conclusion</title><abstract abstract-type="main"> <title>Abstract</title> <sec id="pd4522-sec-0001" sec-type="section"> <title>Objective</title> <p>The aim of this study is to analyze the contribution of biochemistry and cytology of fetal ascites fluid to the etiological diagnosis of ascites after ultrasonographic scan, maternal blood sampling, and fetal karyotyping.</p> </sec> <sec id="pd4522-sec-0002" sec-type="section"> <title>Method</title> <p>This is a retrospective study of 100 consecutive cases of nonimmune fetal ascites in which ascites fluid was sampled. All women underwent referral ultrasound scan and fetal karyotyping. All cases of fetal ascites were studied by biochemistry (total protein, <italic>β</italic><sub>2</sub>‐microglobulin, IgM, gamma‐glutamyl transpeptidase, aspartate aminotransferase, aminopeptidase M, and intestinal isoform of alkaline phosphatase) and cytology (lymphocyte count and vacuolated cells).</p> </sec> <sec id="pd4522-sec-0003" sec-type="section"> <title>Results</title> <p>The etiology of ascites was diagnosed at ultrasound scan in only 50% of cases. We observed significantly (<italic>P</italic> &lt; 0.001) low levels of total protein in ascites of urinary origin, high levels of digestive enzymes in ascites of digestive origin, and high <italic>β</italic><sub>2</sub>‐microglobulin in infectious ascites. Vacuolated cells were observed in all ten storage metabolic diseases.</p> </sec> <sec id="pd4522-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Sampling of fetal ascites fluid for biochemical and cytological examination provides important additional information. We propose a two‐step management: (1) detailed ultrasound scan examination, maternal blood analysis, and fetal karyotyping and (2) biochemical and cytological analyses. On the basis of such an approach, 63% and 96% of etiologies would have been identified in our series after the first and second steps, respectively. © 2014 John Wiley &amp; Sons, Ltd.</p> </sec> </abstract> … (more)
- Is Part Of:
- Prenatal diagnosis. Volume 35:Number 3(2015:Mar.)
- Journal:
- Prenatal diagnosis
- Issue:
- Volume 35:Number 3(2015:Mar.)
- Issue Display:
- Volume 35, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 35
- Issue:
- 3
- Issue Sort Value:
- 2015-0035-0003-0000
- Page Start:
- 214
- Page End:
- 220
- Publication Date:
- 2014-11-26
- Subjects:
- Prenatal diagnosis -- Periodicals
Fetus -- Diseases -- Diagnosis -- Periodicals
Electronic journals
618.32075 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/pd.4522 ↗
- Languages:
- English
- ISSNs:
- 0197-3851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6607.646000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3870.xml