Document Detail

Hematoma of the umbilical cord with acute antepartum fetal distress. A case report.
MedLine Citation:
PMID:  3950887     Owner:  NLM     Status:  MEDLINE    
In a case of spontaneous hematoma of the umbilical cord, no pathologic lesion was found in the umbilical blood vessels. However, an extremely short cord (14 cm) may have contributed to the vessel rupture. A prolonged deceleration discovered during a routine nonstress test led to emergency cesarean section, with delivery of a healthy neonate.
D Feldberg; M Ben-David; D Dicker; N Samuel; J Goldman
Related Documents :
1772557 - Characteristics of motor vehicle accidents resulting in spinal cord injury.
3785607 - Primary leptomeningeal glioma mimicking an acoustic neuroma: case report with review of...
3785497 - Acute spinal cord compression by spontaneous subarachnoid haematoma.
15123997 - Lumbar spinal angiolipomas: report of two cases and review of the literature.
20656457 - When is a retrobulbar haemorrhage not a retrobulbar haemorrhage?
9607497 - Cryptococcal rib osteomyelitis in a pediatric patient.
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Journal of reproductive medicine     Volume:  31     ISSN:  0024-7758     ISO Abbreviation:  J Reprod Med     Publication Date:  1986 Jan 
Date Detail:
Created Date:  1986-04-02     Completed Date:  1986-04-02     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0173343     Medline TA:  J Reprod Med     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  65-6     Citation Subset:  IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Cesarean Section
Fetal Distress / complications*
Hematoma / complications*,  pathology
Infant, Newborn
Umbilical Cord / pathology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Laser ablation of hymenal fissures.
Next Document:  Antepartum reversal of hematologic abnormalities associated with the HELLP syndrome. A report of thr...