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Morphological changes observed via fetal ultrasound in prenatally diagnosed and isolated congenital lymphangiomas: three case reports

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Abstract

We illustrate three cases of isolated congenital lymphangioma (CL). Fetal ultrasound (US) demonstrated uniloculated cystic masses that changed to multiloculated, subcutaneous, hypoechoic, avascular cystic masses with thin septations without solid components. Case 1: CL of the right forearm; Case 2: CL of the right hypochondrium; and Case 3: CL of the left upper posterior back. Postnatal US detected multiloculated, subcutaneous, hypoechoic, avascular cystic masses with thin septations without solid components or invasive developments. We prenatally and postnatally diagnosed them as isolated CL cases due to focal, soft, bulging masses with unclear margins. Due to our correct diagnosis and precise evaluation of sizes and locations, no perinatal complications occurred. In this case series, uniloculated features changed to multiloculated features and the largest macrocyst size decreased, whereas the sizes of the smaller microcysts increased. These morphological changes observed via fetal US represent intermittent CL growing processes.

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References

  1. Oh KY. Lymphangioma. In: Woodward PJ, Kennedy A, Sohaey R, et al., editors. Diagnostic imaging obstetrics, section 5. 2nd ed. Canada: Amirsys Inc; 2011. p. 36–9.

  2. Wiegand S, Eivazi B, Barth JP, et al. Pathogenesis of lymphangiomas. Virchows Arch. 2008;453:1–8.

    Article  PubMed  Google Scholar 

  3. Gonçalves LF, Rojas MV, Vitorello D, et al. Klippel–Trenaunay–Weber syndrome presenting as massive lymphangiohemangioma of the thigh: prenatal diagnosis. Ultrasound Obstet Gynecol. 2000;15:537–41.

    Article  PubMed  Google Scholar 

  4. Whimster IW. The pathology of lymphangioma circumscriptum. Br J Dermatol. 1976;94:473–86.

    Article  PubMed  CAS  Google Scholar 

  5. Giguère CM, Bauman NM, Smith RJ. New treatment options for lymphangioma in infants and children. Ann Otol Rhinol Laryngol. 2002;111:1066–75.

    PubMed  Google Scholar 

  6. Rasidaki M, Sifakis S, Vardaki E, et al. Prenatal diagnosis of a fetal chest wall cystic lymphangioma using ultrasonography and MRI: a case report with literature review. Fetal Diagn Ther. 2005;20:504–7.

    Article  PubMed  Google Scholar 

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Correspondence to Yusuke Inde.

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Inde, Y., Yamagishi, E., Kawabata, I. et al. Morphological changes observed via fetal ultrasound in prenatally diagnosed and isolated congenital lymphangiomas: three case reports. J Med Ultrasonics 40, 265–269 (2013). https://doi.org/10.1007/s10396-012-0421-4

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  • DOI: https://doi.org/10.1007/s10396-012-0421-4

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