Late puerperal hemorrhage of a patient with Klippel-Trenaunay syndrome: A case report.
Journal
Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
entrez:
20
12
2019
pubmed:
20
12
2019
medline:
1
2
2020
Statut:
ppublish
Résumé
The Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder. The obstetric course of women with KTS varies. Complications include bleeding, disseminated intravascular coagulation (DIC), thromboembolic events, etc. PATIENT CONCERNS:: Here, we report a case of late puerperal hemorrhage of a Chinese puerpera with KTS. The repeating severe hemorrhage, the DIC, and the Kasabach-Merrit syndrome made the treatment more difficult. KTS is a mixed malformation with a vascular component that is characterized by abnormal development of veins, capillaries, and lymphatics. Our patient was first diagnosed with KTS at the last trimester of pregnancy. Massive infusion of blood products, two laparotomies, as well as bilateral internal iliac artery embolization was carried out. Although the patient survived from the life-threatening hemorrhage, she lost her uterus forever. An interdisciplinary cooperation of obstetrician, anesthesiologist, vascular surgeon, and intensive care physician is highly recommended. Prophylactic anticoagulation is generally advised in the gestational and postpartum period.
Identifiants
pubmed: 31852150
doi: 10.1097/MD.0000000000018378
pii: 00005792-201912130-00090
pmc: PMC6922477
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e18378Références
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