Literature DB >> 21997954

Prenatal management of diaphragmatic rhabdomyosarcoma presenting with fetal hydrops.

A Reitter1, J Peters, B Wittekindt, H Buxmann, F Geka, U Rolle, R Schlösser, F Louwen.   

Abstract

Fetal malignant tumors are rare. We present a case of intrauterine diagnosis of a diaphragmatic tumor presenting with fetal hydrops at 32 weeks' gestation. The sonographic findings were bilateral pleural effusion, ascites and skin edema. A large right-sided diaphragmatic tumor was identified. Owing to the findings on ultrasound and magnetic resonance imaging a solid malignant tumor was suspected. The pleural effusions were drained and malignant cells identified. Because of rapid tumor progression Cesarean section was performed and a hydropic female newborn was delivered at 34 + 0 weeks' gestation. There was no sign of metastatic disease. Postnatally tumor biopsy revealed an alveolar rhabdomyosarcoma. Therapy included chemotherapy and secondary surgical intervention. After a good primary response with complete remission after 6 months, the rhabdomyosarcoma relapsed at 12 months with cerebral metastasis. The prognosis was poor.
Copyright © 2012 ISUOG. Published by John Wiley & Sons, Ltd.

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Mesh:

Year:  2012        PMID: 21997954     DOI: 10.1002/uog.10113

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  1 in total

Review 1.  Imaging findings in fetal diaphragmatic abnormalities.

Authors:  Leonor Alamo; François Gudinchet; Reto Meuli
Journal:  Pediatr Radiol       Date:  2015-08-09
  1 in total

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