Evidence map›Paper›PMID 42340433›Full record

ArticleActa neurochirurgica2026

Case study of monozygotic triplets with identical pineal cysts. Is pineal cyst hereditary condition?

Neevya Balasubramaniam, Zdeněk Musil, Kateřina Chroboková, Michael Tonhajzer, Tomáš Moravec, David Netuka, Vladimír Beneš, Martin Májovský

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In one paragraph

Article in Acta neurochirurgica, 2026. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Neevya BalasubramaniamDepartment of Neurology and Neurosurgery, McGill University, Montreal, Canada.
Zdeněk MusilInstitute of Biology and Medical Genetics, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
Kateřina ChrobokováThird Faculty of Medicine, Charles University, Prague, Czech Republic.
Michael TonhajzerFaculty of Mechanical Engineering, Czech Technical University, 160 00, Prague, Czech Republic.
Tomáš MoravecDepartment of Neurosurgery and Neurooncology, First Faculty of Medicine, Charles University and Military University Hospital, Prague, Czech Republic.
David NetukaDepartment of Neurosurgery and Neurooncology, First Faculty of Medicine, Charles University and Military University Hospital, Prague, Czech Republic.
Vladimír BenešDepartment of Neurosurgery and Neurooncology, First Faculty of Medicine, Charles University and Military University Hospital, Prague, Czech Republic.
Martin MájovskýDepartment of Neurosurgery and Neurooncology, First Faculty of Medicine, Charles University and Military University Hospital, Prague, Czech Republic. martin.majovsky@uvn.cz.ORCID 0000-0001-7725-5181

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPineal cysts are common incidental findings of uncertain etiology, and the potential contribution of genetic factors to their development remains poorly understood. This study aimed to investigate the possibility of a hereditary predisposition to pineal cysts by examining a unique case of identical pineal cysts in a set of monozygotic triplets and by surveying familial occurrence of pineal cysts within an institutional patient database.

methodsA retrospective case study was conducted on 21-year-old monozygotic male triplets, each identified with a pineal gland cyst. All three underwent brain MRI with dedicated evaluation of the pineal region, independently reviewed by two board-certified neuroradiologists. One symptomatic triplet (T1) underwent surgical resection; peripheral blood and resected cyst tissue were subjected to whole-exome sequencing using an Agilent/Illumina NextSeq platform with variant analysis against the GRCh38 reference genome. Additionally, an institutional database of 243 patients with pineal cysts was reviewed for familial clustering.

resultsAll three triplets presented with morphologically identical 14 mm pineal cysts, despite variable clinical presentations. WES identified a germline HERC2 nonsense variant (c.7114G > T, p.Glu2372Ter) in peripheral blood and a somatic INO80E frameshift mutation (c.42del) in cyst tissue, suggesting a possible two-hit model. Database review revealed eight additional individuals across four unrelated families with pineal cysts, all first-degree relatives, with identical cyst sizes noted in three of the four families.

conclusionThese findings provide novel evidence supporting a potential hereditary component in pineal cyst formation. While causality cannot be established from this case series alone, the observed familial clustering and identified genetic variants suggest that genetic factors may contribute to pineal cyst formation in selected cases and merit further investigation as additional familial or genetically characterized cases become available.

Indexed as

Central Nervous System CystsCystsPineal GlandTripletsAdultGenetic Predisposition to DiseaseHumansMaleRetrospective StudiesYoung AdultFamilial clusteringHERC2Hereditary predispositionMonozygotic tripletsPineal cystWhole-exome sequencing

Identifiers

PMID42340433
PMCPMC13427959

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