Evidence map›Paper›PMID 40262506›Full record

ArticleInternational journal of surgery case reports2025

Retinal detachment in a neonate with congenital chylothorax and purpura fulminans associated with the PAK2 genetic variant: A case report.

Arijit Lodha, Majeeda Kamaluddeen, Stephanie Dotchin, Julie Lauzon, Patrick Mitchell

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Article in International journal of surgery case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Arijit LodhaFaculty of Medicine & Dentistry, University of Alberta, Edmonton, Canada.
Majeeda KamaluddeenDepartment of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, Canada. Electronic address: Majeeda.kamaluddeen@ahs.ca.
Stephanie DotchinDepartment of Ophthalmology & Visual Sciences, Cumming School of Medicine, University of Calgary, Calgary, Canada.
Julie LauzonDepartment of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, Canada; Department of Genetics, Cumming School of Medicine, University of Calgary, Calgary, Canada.
Patrick MitchellDepartment of Ophthalmology & Visual Sciences, Cumming School of Medicine, University of Calgary, Calgary, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introduction and importanceA potential relationship between bilateral retinal detachment, chylothorax, and purpura fulminans in a female neonate with a PAK2 gene variant is not commonly reported. This emphasizes the significance of early ophthalmologic assessment in neonates with congenital chylothorax. CASE PRESENTATION: A full-term female infant weighing 2.775 kg was delivered by cesarean section due to breech presentation. Prenatal imaging revealed fetal bilateral pleural effusion, suggestive of chylothorax. The neonate developed respiratory distress and purpura fulminans after birth. The absence of the red reflex in the right eye prompted a detailed ophthalmologic examination using a portable slit lamp and an indirect ophthalmoscope. The right eye revealed an ectatic pupil with posterior synechia extending from approximately 6 o'clock to 9 o'clock. Fundus examination of both eyes revealed funnel retinal detachment with multiple chronic features. A small amount of retina was draped between 4 and 7 o'clock, which may have been attached. Further ophthalmologic investigation under anesthesia, using B-scan ultrasonography and intravenous fluorescein angiography, confirmed bilateral retinal detachment. Genetic investigations revealed a PAK2 c.1115A>T, p.(Asp372Val) variant. CLINICAL DISCUSSION: In addition to presenting our case report, we reviewed other recent case reports similar to ours. Retinal detachment and bilateral pleural effusions in neonates with Knobloch syndrome have been recently reported, but without purpura fulminans. Retinal detachment in neonates can result from both congenital and acquired conditions, and requires a thoughtful approach to establish the diagnosis and provide future counseling.

conclusionBilateral retinal detachment, chylothorax, and purpura fulminans in a neonate with a PAK2 genetic variant is uncommon. This case underscores the importance of early ophthalmologic assessment and genetic testing for both neonates and their family members.

Indexed as

Case reportChylothoraxNewbornPleural effusionRetinal detachment

Identifiers

PMID40262506
PMCPMC12047482

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