Thoracic Giant Venous Malformation in a Stillbirth with <i>Pik3ca</i> Somatic Mutation

<b>Introduction:</b> Congenital venous malformations (VMs) are typically located in the skin of the head and neck, but extension to deep tissues and visceral organs may occur. In 20% of cases, sporadic VMs are caused by somatic mutations in the <i>PIK3CA</i> gene, which determines aberrant angiogenesis. <b>Case report:</b> Intrauterine death of a fetus with a known extensive vascular lesion of the right hemithorax occurred at 28 weeks + 6 days. Autopsy revealed abundant bilateral pleural effusions, and histology showed a VM. High-depth next-generation sequencing for <i>PIK3CA</i> and <i>TEK</i> on amniocytes was negative. Postmortem real-time polymerase chain reaction for <i>PIK3CA</i> on paraffin-embedded samples of the lesion revealed somatic p.H1047X hotspot mutation in the exon 20. <b>Conclusion:</b> To the best of our knowledge, this is the first case of a VM in a stillbirth. Extensive lesions carry a high risk of fetal demise due to high-output cardiac failure.

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Publication Details

Journal
Fetal and Pediatric Pathology
Published
2025-04-24
DOI
https://doi.org/10.1080/15513815.2025.2493721
Citations
2
Primary Topic
Vascular Malformations and Hemangiomas
Type
article
Field-Weighted Citation Impact
4.01
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article

Thoracic Giant Venous Malformation in a Stillbirth with Pik3ca Somatic Mutation

Elisa Tidu, Nunzio Salfi, Mariano Lanna, Patrizio Antonazzo et al.
2 citations
Fetal and Pediatric Pathology
Vascular Malformations and Hemangiomas
4.01
article

Thoracic Giant Venous Malformation in a Stillbirth with Pik3ca Somatic Mutation

Elisa Tidu, Nunzio Salfi, Mariano Lanna, Patrizio Antonazzo, Enrico Farnetti, Maria Paola Bonasoni, Davide Nicoli, S. Faiola, A. Martinelli, Elisa Cattaneo, Sabrina Gismondi
article en
2 citations

Abstract

<b>Introduction:</b> Congenital venous malformations (VMs) are typically located in the skin of the head and neck, but extension to deep tissues and visceral organs may occur. In 20% of cases, sporadic VMs are caused by somatic mutations in the <i>PIK3CA</i> gene, which determines aberrant angiogenesis. <b>Case report:</b> Intrauterine death of a fetus with a known extensive vascular lesion of the right hemithorax occurred at 28 weeks + 6 days. Autopsy revealed abundant bilateral pleural effusions, and histology showed a VM. High-depth next-generation sequencing for <i>PIK3CA</i> and <i>TEK</i> on amniocytes was negative. Postmortem real-time polymerase chain reaction for <i>PIK3CA</i> on paraffin-embedded samples of the lesion revealed somatic p.H1047X hotspot mutation in the exon 20. <b>Conclusion:</b> To the best of our knowledge, this is the first case of a VM in a stillbirth. Extensive lesions carry a high risk of fetal demise due to high-output cardiac failure.

Fetal and Pediatric PathologyVol. 44(3)
Azienda Sanitaria Unità Locale di Reggio Emilia (IT), Ospedale Infermi di Rimini (IT), Ospedale dei Bambini Vittore Buzzi (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT)
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Openalex Percentile: Top 8%
Vascular Malformations and Hemangiomas
4.01
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Thoracic Giant Venous Malformation in a Stillbirth with <i>Pik3ca</i> Somatic Mutation — Elisa Tidu, Nunzio Salfi, et al. · Fetal and Pediatric Pathology (2025) | TGRS Research Map | TGRS