Fetal intraventricular haemorrhage in severe congenital protein C deficiency

Fetal intraventricular haemorrhage is a rare condition with heterogeneous causes. We report severe congenital protein C deficiency (SCPCD) in a neonate with a previous sibling who had a similar clinical presentation suggestive of the same disorder. The first neonate developed purpuric skin lesions, seizures and clinical features of coagulopathy shortly after birth and died in the early neonatal period; however, confirmatory laboratory or genetic testing was not available. In a subsequent pregnancy, antenatal ultrasonography at 32 weeks’ gestation demonstrated bilateral severe ventriculomegaly with echogenic intraventricular material suggestive of fetal intraventricular haemorrhage. The neonate developed purpuric lesions within hours of birth and died despite supportive management. Laboratory evaluation revealed undetectable protein C activity and genetic testing confirmed a homozygous pathogenic PROC variant. SCPCD should be considered in the differential diagnosis of unexplained fetal intraventricular or intracranial haemorrhage, particularly when associated with neonatal purpura fulminans or recurrence in siblings.

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Publication Details

Journal
BMJ Case Reports
Published
2026-11-01
DOI
https://doi.org/10.1136/bcr-2026-273866
Primary Topic
Blood Coagulation and Thrombosis Mechanisms
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article
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article

Fetal intraventricular haemorrhage in severe congenital protein C deficiency

Mandakini Pradhan, Monali Khergade, Kritika Agnihotri, Yogeshree Pradhan
BMJ Case Reports
Blood Coagulation and Thrombosis Mechanisms
article

Fetal intraventricular haemorrhage in severe congenital protein C deficiency

Mandakini Pradhan, Monali Khergade, Kritika Agnihotri, Yogeshree Pradhan
article en

Abstract

Fetal intraventricular haemorrhage is a rare condition with heterogeneous causes. We report severe congenital protein C deficiency (SCPCD) in a neonate with a previous sibling who had a similar clinical presentation suggestive of the same disorder. The first neonate developed purpuric skin lesions, seizures and clinical features of coagulopathy shortly after birth and died in the early neonatal period; however, confirmatory laboratory or genetic testing was not available. In a subsequent pregnancy, antenatal ultrasonography at 32 weeks’ gestation demonstrated bilateral severe ventriculomegaly with echogenic intraventricular material suggestive of fetal intraventricular haemorrhage. The neonate developed purpuric lesions within hours of birth and died despite supportive management. Laboratory evaluation revealed undetectable protein C activity and genetic testing confirmed a homozygous pathogenic PROC variant. SCPCD should be considered in the differential diagnosis of unexplained fetal intraventricular or intracranial haemorrhage, particularly when associated with neonatal purpura fulminans or recurrence in siblings.

BMJ Case ReportsVol. 19(11)
Sanjay Gandhi Post Graduate Institute of Medical Sciences (IN)
Openalex Percentile: Top 11%
Blood Coagulation and Thrombosis Mechanisms
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