GERYCHOVÁ, Romana, Jana PANNOVA, Filip SOKOL and Jan ŠENKYŘÍK. Prenatally detected rare case of the fetal facial rhabdomyosarcoma. In 24th World Congress on Ultrasound in Obstetrics and Gynecology, 14–17 September 2014, Barcelona, Spain. 2014. ISSN 0960-7692. doi:10.1002/uog.14197.
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Basic information
Original name Prenatally detected rare case of the fetal facial rhabdomyosarcoma
Name in Czech Prenatální diagnostika vzácného případu fetálního rhabdomyosarkomu
Authors GERYCHOVÁ, Romana (203 Czech Republic, guarantor, belonging to the institution), Jana PANNOVA (203 Czech Republic), Filip SOKOL (203 Czech Republic) and Jan ŠENKYŘÍK (203 Czech Republic).
Edition 24th World Congress on Ultrasound in Obstetrics and Gynecology, 14–17 September 2014, Barcelona, Spain, 2014.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 30214 Obstetrics and gynaecology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW http://onlinelibrary.wiley.com/doi/10.1002/uog.14197/pdf
Impact factor Impact factor: 3.853
RIV identification code RIV/00216224:14110/14:00077026
Organization unit Faculty of Medicine
ISSN 0960-7692
Doi http://dx.doi.org/10.1002/uog.14197
Keywords (in Czech) rhabdomyosarkom plodu; prenatální diagnostika
Keywords in English prenatal fetal rhabdomyosarcoma
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 25. 3. 2015 14:36.
Abstract
Rhabdomyosarcoma is a mesenchymal highly malignant neoplasm. RMS is the most common soft tissues tumor of childhood,but its prenatal occurence is very rare, but also can have a genetic underlay associated with some rare familial “cancer syndromes”.We present a case of 27-year old primigravida with the singleton pregnancy. She was referred to our department at 30 weeks of gestation with the suspected facial tumor. Anomaly scan at the first and second trimester were both normal. Ultrasound showed mostly solid mass 77x52 mm with the small cystic portion arising from the right orbit and dislocating the bulb. The third part of the tumor expanding intracranially. Doppler flow in the mass was present. MRI confirm our finding, amniocentesis showed normal karyotype 46 XX. Differential diagnosis we consider teratoma or rhabdomyosarcoma. Due to the rapid growth of the tumor, its inauspicious location and 31+5 gestational age parents decided to the late termination of the pregnancy. The fetocide was done and at the same day we vaginally delivered baby girl 2370g and 46cm without no maternal injury. Postnatal autopsy confirmed rhabdomyosarcoma. We would like to point out that the fetal occurrence of head-and-neck RMS is very rare but possible. The prognosis of RMS tumor finally depends on staging and histological subtype. We consider the prognosis of our fetus in such circumstances highly adverse.
Abstract (in Czech)
prenatální diagnostika a řešení vzácného případu rhabdomyosarkomu očnice plodu. RMS - častá malignita dětského věku, ale prenatální výskyt velmi vzácný. Nejčastěji sporadicky, případně jako součást některých "genetických syndromů".
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