# Unravelling fetal enigmas: a case of suprasellar lesion

**Authors:** Shravani Shinde, Dr Priscilla Joshi, Shriyash Pinglikar

PMC · DOI: 10.1093/bjrcr/uaaf029 · BJR | Case Reports · 2025-05-14

## Full-text entities

- **Genes:** NF1 (neurofibromin 1) [NCBI Gene 4763] {aka NFNS, VRNF, WSS}
- **Diseases:** Arachnoid cysts (MESH:D016080), CNS neoplasms (MESH:D016543), Holoprosencephaly (MESH:D016142), Pituitary hypoplasia (MESH:D010900), anomaly (MESH:D000013), CSP (MESH:C535562), Astrocytomas (MESH:D001254), suprasellar masses (MESH:D020863), Developmental anomalies (MESH:C566440), agenesis (MESH:C536482), Dandy-Walker malformation (MESH:D003616), endocrine dysfunction (MESH:D004700), calcification (MESH:D002114), Congenital malformations (OMIM:163000), intracranial tumours (MESH:D001932), obstruction of CSF flow (MESH:D002559), toxoplasmosis (MESH:D014123), Neoplastic lesions (MESH:D009062), fetal hydrops (MESH:D015160), congenital infections (MESH:D007239), Tumors (MESH:D009369), Hydrocephalus (MESH:D006849), intracranial lesion (MESH:D020765), Infectious (MESH:D003141), intracranial masses (MESH:C536030), midline anomalies (MESH:C538667), colloid cysts (MESH:D056364), intracranial abnormalities (MESH:D001927), Craniopharyngiomas (MESH:D003397), spinal abnormalities (MESH:D016472), Cystic (MESH:D018297), gliomas (MESH:D005910), NT (MESH:D053589), Central nervous system teratomas (MESH:D013724)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12267136