Complete spontaneous resolution of severe nonimmunological hydrops fetalis with unknown etiology in the second trimester--a case report
- PMID: 12530111
- DOI: 10.1515/JPM.2002.082
Complete spontaneous resolution of severe nonimmunological hydrops fetalis with unknown etiology in the second trimester--a case report
Abstract
The incidence of nonimmunological fetal hydrops is between 1 in 1500 and 1 in 4000. Overall mortality for this condition is about 80%. This report describes a case of prenatally diagnosed hydrops fetalis with severe generalized edema, ascites and pleural effusion of unknown origin at 19 weeks of gestation. No symptoms were found of infections or anemia, no variabilities were observed in fetal blood analysis or in karyotyping. All signs of hydrops resolved completely after 6 weeks without treatment. The pregnancy continued with normal fetal development; labor was induced at 41 weeks of gestation. After vaginal delivery with vacuum extraction the child was completely healthy and demonstrated no signs of remaining hydrops fetalis or any other pathological parameters except an uncritical atrial septal defect type II which healed without any complications within 3 months post delivery.
Similar articles
-
Outcome of nonimmune hydrops fetalis diagnosed during the first half of pregnancy.Obstet Gynecol. 1997 Sep;90(3):321-5. doi: 10.1016/s0029-7844(97)00290-1. Obstet Gynecol. 1997. PMID: 9277637
-
Fetal critical aortic stenosis with natural improvement of hydrops fetalis due to spontaneous relief of severe restrictive atrial communication.J Obstet Gynaecol Res. 2015 Jul;41(7):1137-40. doi: 10.1111/jog.12681. Epub 2015 Mar 15. J Obstet Gynaecol Res. 2015. PMID: 25772579
-
Resolution of cystic hygroma, hydrops fetalis, and fetal anemia.Am J Perinatol. 1993 Nov;10(6):455-9. doi: 10.1055/s-2007-994631. Am J Perinatol. 1993. PMID: 8267813
-
Diagnosis and management of early non-immune hydrops fetalis.Prenat Diagn. 1997 Dec;17(13):1261-8. doi: 10.1002/(sici)1097-0223(199712)17:13<1261::aid-pd292>3.0.co;2-c. Prenat Diagn. 1997. PMID: 9509544 Review.
-
Resolution of hydrops fetalis in congenital cystic adenomatoid malformation after prenatal steroid therapy.J Pediatr Surg. 2003 Mar;38(3):508-10. doi: 10.1053/jpsu.2003.50089. J Pediatr Surg. 2003. PMID: 12632377 Review.
Cited by
-
Clinical characteristics and perinatal outcome of fetal hydrops.Obstet Gynecol Sci. 2015 Mar;58(2):90-7. doi: 10.5468/ogs.2015.58.2.90. Epub 2015 Mar 16. Obstet Gynecol Sci. 2015. PMID: 25798421 Free PMC article.
-
Isolated non-immune hydrops fetalis: an observational study on complete spontaneous resolution, perinatal outcome, and long-term follow-up.Arch Gynecol Obstet. 2023 Aug;308(2):487-497. doi: 10.1007/s00404-022-06731-w. Epub 2022 Aug 22. Arch Gynecol Obstet. 2023. PMID: 35994111 Free PMC article.
-
Comparative Proteomic Assessment of Normal vs. Polyhydramnios Amniotic Fluid Based on Computational Analysis.Biomedicines. 2022 Jul 28;10(8):1821. doi: 10.3390/biomedicines10081821. Biomedicines. 2022. PMID: 36009368 Free PMC article.
-
Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants.Clin Case Rep. 2021 Aug 10;9(8):e04624. doi: 10.1002/ccr3.4624. eCollection 2021 Aug. Clin Case Rep. 2021. PMID: 34401172 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources