ArticleJournal of obstetrics and gynaecology of India2025
Management of Pregnancy in a Case of Endolymphatic Sac Tumour as a Part of Von Hippel-Lindau Syndrome Complex: A Case Report and Review of Literature.
Article in Journal of obstetrics and gynaecology of India, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Endolymphatic sac tumor (ELST) is a rare (1/30000) neoplasm with less than 200 cases reported. It is seen in 24-30% of patients with Von Hippel-Lindau (VHL) syndrome. We present a case of a woman diagnosed to have left cerebello pontine angle endolymphatic sac tumour with low grade adenocarcinoma, underwent left radical mastoidectomy and tumour decompression; developed left cerebellar vermian haemangioma and a left occipito temporal haemangioblastoma who successfully conceived and had an uneventful pregnancy and Caesarean delivery with good maternal and neonatal outcome, due to its rarity. High index of suspicion for an early diagnosis and a planned delivery in a tertiary care centre with a multidisciplinary approach are crucial for successful outcomes.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.