Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
Autor: | Charlotte Casper, Agnès Sartor, Olivier Parant, Edith Brazet, Stéphane Decramer, Florence Cadoret, Isabelle Lacroix |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Adult
Male medicine.medical_specialty Urinary system medicine.medical_treatment 030232 urology & nephrology Prenatal diagnosis lcsh:Medicine Case Report 03 medical and health sciences Cystography 0302 clinical medicine Fetus Pregnancy Ascites Lymphangioma Medicine Humans Child Prenatal uroperitoneum Fetal ascites medicine.diagnostic_test Spontaneous Bladder Rupture Rupture Spontaneous business.industry lcsh:R Infant Newborn Urinary Bladder Diseases General Medicine Megacystis medicine.disease Morphine derivatives Surgery Fetal Diseases Fetal bladder rupture Nephrostomy Female medicine.symptom business 030217 neurology & neurosurgery |
Zdroj: | Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-5 (2020) Journal of Medical Case Reports |
ISSN: | 1752-1947 |
Popis: | Background Fetal bladder rupture causing urinary ascites is uncommon. It is generally related to invasive fetal medicine procedures or obstructive disorders such as in posterior urethral valves in male fetuses. An exceptional case of spontaneous bladder rupture in a female fetus occurred in a pregnant woman treated with high doses of opiates in an intensive care unit. This unusual obstetric situation leads to discussion of the possible causes of fetal bladder rupture, its management, and the pediatric prognosis. Case presentation We report the case of a 30-year-old nulliparous black woman with a history of mesenteric cystic lymphangioma and multiple bowel resections leading to chronic malabsorption. During her pregnancy, our patient presented with an occlusive syndrome and major bilateral renal dilation. Urinary derivation resulted in iatrogenic bilateral ureteral perforation. Our patient thus presented with major uroperitoneum, bilateral pleural effusion and acute renal failure, treated by thoracic drainage and bilateral nephrostomy. Postoperative pain required treatment with level III analgesics. In this context, 5 days after morphine treatment introduction an enlarged fetal bladder was observed, followed 3 days later by voluminous fetal ascites. The diagnosis of spontaneous bladder rupture was suspected. After multidisciplinary discussion, expectant management was decided. At 31 weeks and 4 days gestation, our patient went into spontaneous labor with a subsequent vaginal delivery. The infant required resuscitation and paracentesis of ascites at birth. Her neonatal course was favorable with a simple urethral bladder drainage. Cystography at day 9 was normal. At 2 years of follow-up, the mother and the child have a normal course. Conclusions An iatrogenic origin of megacystis in a female fetus must be evoked in the event of maternal administration of high doses of opiates in the second part of her pregnancy. In our case, the megacystis was followed by spontaneous bladder rupture at 30 weeks of gestation, with a favorable maternal fetal issue. |
Databáze: | OpenAIRE |
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