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  • Perinatal/Neonatal Case Presentation
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Perinatal/Neonatal Case Presentation

A catecholamine-secreting neuroblastoma leading to hydrops fetalis

Abstract

A case of fetal neuroblastoma of the right adrenal gland, with rapid development of hydrops fetalis due to catecholamine-induced cardiomyopathy, is reported. A fetus with a right suprarenal mass detected during ultrasonography at 32 weeks gestation progressively developed into hydrops fetalis by 35.2 weeks gestation. An emergent cesarean section was performed. At birth, the female neonate was hypertensive, with markedly elevated catecholamine levels; echocardiography showed poor contractility. Morphine, human atrial natriuretic peptide, milrinone, nitroprusside and dobutamine were initiated and her blood pressure was maintained within the normal range and her cardiac contractility improved 2 weeks after birth. Neuroblastoma cells were detected in the placenta, resulting in the right adrenal mass being diagnosed as a neuroblastoma. She was well, and the mass diminished in size within 4 months, without surgery. A fetus with suspected neuroblastoma, indicated by a suprarenal mass, should be managed with appropriate consideration of hydrops.

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References

  1. Wells HG . Occurrence and significance of congenital malignant neoplasms. Arch Pathol 1940; 30: 535–601.

    Google Scholar 

  2. Carlson P, Jefferies JL, Kearney D, Russell H . Refractory dilated cardiomyopathy associated with metastatic neuroblastoma. Pediatr Blood Cancer 2010; 55: 736–738.

    Article  Google Scholar 

  3. Ohyama M, Kobayashi S, Aida N, Toyoda Y, Ijiri R, Tanaka Y . Congenital neuroblastoma diagnosed by placental examination. Med Pediatr Oncol 1999; 33: 430–431.

    Article  CAS  Google Scholar 

  4. Moss TJ, Kaplan L . Association of hydrops fetalis with congenital neuroblastoma. Am J Obstet Gynecol 1978; 132: 905–906.

    Article  CAS  Google Scholar 

  5. Jennings RW, LaQuaglia MP, Leong K, Hendren WH, Adzick NS . Fetal neuroblastoma: prenatal diagnosis and natural history. J Pediatr Surg 1993; 28: 1168–1174.

    Article  CAS  Google Scholar 

  6. Lindner W, Behnisch W, Kunz U, Debatin KM, Pohlandt F . Congenital neuroblastoma mimicking early onset sepsis. Eur J Pediatr 2001; 160: 436–438.

    Article  CAS  Google Scholar 

  7. Kato M, Hirata S, Kikuchi A, Ogawa K, Kishimoto H, Hanada R . Neuroblastoma presenting with dilated cardiomyopathy. Pediatr Blood Cancer 2008; 50: 391–392.

    Article  CAS  Google Scholar 

  8. Cun L, Zhe M, Xinfeng Z, Guowei T, Shaoping L, Chuanxi L . Fetal neuroblastoma with fetal hypertension [letter]. Ultrasound Obstet Gynecol 2008; 31: 106–107.

    Article  CAS  Google Scholar 

  9. Steinmetz JC . Neonatal hypertension and cardiomegaly associated with a congenital neuroblastoma. Pediatr Pathol 1989; 9: 577–582.

    Article  CAS  Google Scholar 

  10. Halpérin DS, Oberhänsli I, Siegrist CA, Velebit L, Klauser P, Pilloud P et al. Intrathoracic neuroblastoma presenting with neonatal cardiorespiratory distress. Chest 1984; 85: 822–823.

    Article  Google Scholar 

  11. Selldén H, Kogner P, Sollevi A . Adenosine for per-operative blood pressure control in an infant with neuroblastoma. Acta Anaesthesiol Scand 1995; 39: 705–708.

    Article  Google Scholar 

  12. Wright KC, Agre JC, Wilson BC, Theologides A . Autonomic dysreflexia in a paraplegic man with catecholamine-secreting neuroblastoma. Arch Phys Med Rehabil 1986; 67: 566–567.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Shouichiro Amari, MD, Ikuko Hama, MD, Yukiko Tasaki, MD, Masao Kaneshige, MD, Sae Hanai, MD, Yuka Wada, MD, PhD, Shigehiro Takahashi, MD, Hideshi Fujinaga, MD, Keiko Tsukamoto, MD (Center for Maternal–Fetal and Neonatal Medicine, National Center for Child Health and Development) and Yasushi Misaki, MD (Division of Cardiology, National Center for Child Health and Development) for their helpful clinical suggestions.

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Correspondence to Y Ito.

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Inoue, T., Ito, Y., Nakamura, T. et al. A catecholamine-secreting neuroblastoma leading to hydrops fetalis. J Perinatol 34, 405–407 (2014). https://doi.org/10.1038/jp.2014.19

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