ArticleJournal of medical cases2026
Systemic Sarcoidosis With Neurosarcoidosis and Obstructive Hydrocephalus: A Radiologic-Pathologic Case Report.
Article in Journal of medical cases, 2026. 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
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sarcoidosis is a systemic granulomatous disease characterized by non-caseating granulomas, most commonly affecting the lungs and intrathoracic lymph nodes. Central nervous system involvement (neurosarcoidosis) is rare but associated with significant morbidity and mortality, particularly in advanced systemic disease. We report a fatal case of a 43-year-old man with long-standing pulmonary sarcoidosis who developed progressive neurosarcoidosis complicated by obstructive hydrocephalus and subsequent ventriculoperitoneal shunt infection. High-resolution computed tomography demonstrated advanced perilymphatic and peribronchovascular fibrosis with symmetric mediastinal lymphadenopathy, consistent with fibrotic pulmonary sarcoidosis (Scadding stage IV). Contrast-enhanced brain magnetic resonance imaging revealed a large, intensely enhancing mass-like lesion centered in the atrium of the right lateral ventricle, with extension into the posterior and temporal horns, causing near-complete obliteration of the ventricular lumen and secondary obstructive hydrocephalus. Autopsy showed extensive fibrotic and granulomatous remodeling of the lungs with non-caseating granulomas. Histological examination of tissue obtained from the central nervous system lesion demonstrated non-necrotizing granulomatous inflammation, supporting central nervous system involvement; however, the precise anatomical origin of the intraventricular lesion was not established microscopically. This case highlights a rare and fatal presentation of sarcoidosis with combined fibrotic pulmonary involvement and neurosarcoidosis. Mechanical obstruction by the mass-like intraventricular lesion played the principal role in the development of hydrocephalus. Radiologic-pathologic correlation provided important insights into the underlying disease mechanisms.
Indexed as
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.