Cystic lymphangiomatosis with severe intra‐abdominal bleeding in a newborn: Case report |
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Authors: | Didem Baskın Adnan Narcı Nazan Okur Meltem Uğraş Gülengül Nadirgil Köken Ahmet Ali Tuncer Çiğdem Tokyol Salih Çetinkurşun |
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Affiliation: | 1. Department of Pediatric Surgery, Afyon Kocatepe University Medical Faculty, Afyonkarahisar, Turkey;2. Department of Radiology, Afyon Kocatepe University Medical Faculty, Afyonkarahisar, Turkey;3. Department of Pediatrics, Afyon Kocatepe University Medical Faculty, Afyonkarahisar, Turkey;4. Department of Gynecology and Obstetrics, Afyon Kocatepe University Medical Faculty, Afyonkarahisar, Turkey;5. Department of Pathology, Afyon Kocatepe University Medical Faculty, Afyonkarahisar, Turkey |
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Abstract: | ![]() We report the case of a newborn girl with intestinal cystic lymphangiomatosis who presented with abdominal distension and intra‐abdominal bleeding following a prenatal ultrasound diagnosis of intestinal anomaly. Postnatal abdominal ultrasound revealed disseminated submucosal and intramural cystic dilatations of various sizes in the bowel and intestinal lymphangiomatosis was diagnosed. The presence of severe bleeding diathesis and widespread disease led to conservative treatment. The patient died on postnatal day 7 and postmortem examination confirmed cystic lymphangiomatosis. Detection of intestinal hyperechogenicity and/or dilatation in prenatal ultrasonography and the persistence of these findings during pregnancy are suggestive for pathologies such as meconium ileus, meconium peritonitis, and intestinal atresia. Although rare, intestinal lymphangiomatosis should be kept in mind in patients whose prenatal sonographic findings persist until birth. © 2012 Wiley Periodicals, Inc. J Clin Ultrasound, 2013 |
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Keywords: | lymphangiomatosis small intestine ultrasonography obstetrics abdomen |
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