Large chorioangioma: Antenatal color‐flow Doppler ultrasonic imaging and its correlation with postpartum pathology

Kung, Fu‐Tsai; Chen, Wei-Jen; Hsu, Pei-Hua; Wu, Jiashin; Tsai, Yao‐Chou; Chang, Shiuh‐Young

doi:10.1111/j.1600-0412.1997.tb07859.x

Cited by 8 publications

(9 citation statements)

References 5 publications

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“…13 Similar was the finding in our cases where we found calcification in the tumor with reduced flow of blood within the lesion. One of the case had a favourable outcome and pathological examination also confirmed the presence of calcifications.…”

Section: 12supporting

confidence: 78%

Large placental chorioangioma, cause for gross polyhydramnios; experience of two cases and review of literature

et al. 2016

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Section: 12supporting

confidence: 78%

Large placental chorioangioma, cause for gross polyhydramnios; experience of two cases and review of literature

et al. 2016

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“…11 Some studies have found only arterial blood flow in chorioangiomas, 12,13 some have found only venous waveforms, 14 and a few studies have demonstrated both arterial and venous waveforms. 9 Doppler flow characteristics include either abundant blood flow or a single large feeding vessel within the tumor with a branching pattern.…”

Section: Discussionmentioning

confidence: 99%

Chorioangioma of placenta: Sonographic features

Taori

Patil

Attarde

et al. 2007

J of Clinical Ultrasound

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“…Chorangiomas are solid or complex and Doppler analysis reveals abundant blood flow, which sometimes is pulsatile [Zalel et al, 2002]. Some tumors exhibit calcifications, reduced blood flow or foci of absent blood flow near term [Eldar‐Geva et al, 1988; Kung et al, 1997; Zalel et al, 2002]. These same rheologic features and other ultrasonographic findings are seen in solitary cutaneous RICH [Berenguer et al, 2003] and in solitary hepatic lesions [Dreyfus et al, 1996].…”

Section: Discussionmentioning

confidence: 99%

Multifocal rapidly involuting congenital hemangioma: A link to chorangioma

Mulliken

Bischoff

Kozakewich

2007

American J of Med Genetics Pt A

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Common infantile hemangioma is intriguing because of its variable presentation, rapid postnatal growth and slow regression in childhood. Interest in this tumor has increased with the recognition that it can be associated with structural anomalies in the craniofacial and ventral-caudal regions. The phenotype has expanded by characterization of rare vascular tumors that arise in the fetus and manifest at birth as rapidly involuting congenital hemangioma (RICH) or non-involuting congenital hemangioma (NICH). We describe a boy born with three RICH on the abdominal wall; one extended into the base of the umbilical cord. Two weeks later a small, infantile hemangioma arose on his neck. This patient stimulated a review of what is known about placental vascular tumors and their possible relationship to fetal and infantile hemangiomas. We suggest that chorangioma and umbilical cord hemangioma are clinically and histopathologically similar to cutaneous and hepatic RICH. These placental vascular tumors can also occur in conjunction with solitary and multiple infantile hemangiomas.

show abstract

Large chorioangioma: Antenatal color‐flow Doppler ultrasonic imaging and its correlation with postpartum pathology

Cited by 8 publications

References 5 publications

Large placental chorioangioma, cause for gross polyhydramnios; experience of two cases and review of literature

Large placental chorioangioma, cause for gross polyhydramnios; experience of two cases and review of literature

Chorioangioma of placenta: Sonographic features

Multifocal rapidly involuting congenital hemangioma: A link to chorangioma

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