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Ginecología y Obstetricia de México

Federación Mexicana de Ginecología y Obstetricia, A.C.
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2018, Number 10

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Ginecol Obstet Mex 2018; 86 (10)

Giant placental chorioangioma. A case report

Ramírez-Cárdenas A, Licona-Venegas EE, Licona-Meníndez RD, Navarro- Muñoz FS
Full text How to cite this article

Language: Spanish
References: 10
Page: 692-698
PDF size: 456.68 Kb.


Key words:

Placental chorioangioma, Giant chorioangioma, Prenatal diagnosis.

ABSTRACT

Background: Chorioangioma is the most common benign placental tumour (1%). If these are greater than 5 cm, it can cause various maternal-fetal complications, so it is important to perform your prenatal diagnosis.
Clinic case: Female patient of 25 years-old, attended at the Hospital Español de Beneficencia de Pachuca with suggestive diagnosis with fetus of 19.2 weeks, according to the ultrasound of the first trimester; in the imaging study cranial oedema was observed; cardiac-thoracic area 0.55 (abnormal), compatible with severe cardiomegaly. The maternal Doppler ultrasound showed the placenta in the anterior location and tumour of 7.53 x 6.74 x 6.33 cm, with hyperechoic and hypoechoic zones, which protruded the fetal surface of the placenta, above the insertion of the umbilical cord; the feeding vessels with a maximum diameter of 3 mm, located superficially and close to the insertion of the cord. In the evaluation of fetal Doppler ultrasound: ACM-PVS: 33.5 cm/s, 1.37 MoM, mild anaemia and DV IP 1.02 (› p95 abnormal); In the cord umbilical vein pulsatile flow was observed, maximum pool of 5.81 cc and cervical length of 4 cm. While a multidisciplinary team was formed, expectant treatment was agreed upon until birth; however, soon after, the fetus died due to hemodynamic repercussions. The histopathological study confirmed the diagnosis of chorioangioma (placental hemangioma), 7 cm in greatest diameter.
Conclusions: It is important to report the cases of placental chorioangioma, with the purpose of contributing with the knowledge and estimating maternal-fetal morbidity and mortality rates.


REFERENCES

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  2. Haiyan Lui, Weirong Gu,Xiaotian Li. Natural history and pregnancy outcome in patients whit placental chorioangioma. JCU 2014;42(2):74-80. https://doi.org/10.1002/ jcu.22101

  3. Vega G, et al. Corioangioma gigante de la placenta: reporte de dos casos. Rev Chil Obstet Ginecol 2007;72(6): 407-11. http://dx.doi.org/10.4067/S0717-75262007000600009

  4. Pérez-García GE, et al. Corangioma placentario: enfoque clínico-patológico de un caso descrito en Colombia. Ginecol Obstet Mex 2013;81(2):109-114.

  5. Zoppi MA, et al. Color Doppler score: a new approach for monitoring a large placental chorioangioma. Case Reports in Obstetrics and Gynecology 2014, Article ID 723429. http://dx.doi.org/10.1155/2014/723429

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  7. Smeke BJ, et al. Corioangioma placentario gigante asociado a secuencia de Pierre Robin. An Med (Mex) 2011;56(1):38-43.

  8. Zanardini C, et al. Giant placental chorioangioma: natural history and pregnancy outcome. https://doi.org/10.1002/ uog.7451

  9. Lim F, et al. Giant chorioangiomas: perinatal outcomes and techniques in fetoscopic devascularization. Ultrasound Obstet Gynecol 2010;35:332-36. https://doi. org/10.1159/000363600

  10. Al Wattar, et al. Placenta chorioangioma: a rare case and systematic review of literature. J Matern Fetal Neonatal Med 2014;27(10): 1055-63. https://doi.org/10.3109/147 67058.2013.847424 DOI: https://doi.org/10.24245/gom.v86i10.2365 CITACIÓN ACTUAL




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Ginecol Obstet Mex. 2018;86