ArticleCureus2025
Managing Pneumothorax in Neurofibromatosis Type 1: A Report of a Rare Case.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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Who cites it
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Neurofibromatosis is a rare genetic disorder with variable manifestations, primarily involving neural and connective tissues. Although pulmonary complications such as pneumothorax are uncommon, they can significantly impact patient outcomes. We report the case of a 48-year-old male with a 10-year history of neurofibromatosis who presented with acute thoracic pain and dyspnea. Imaging revealed a pneumothorax requiring urgent thoracic drainage. Subsequent surgical exploration via thoracoscopy revealed apical bullae and vascularized adhesions, along with multiple intact cystic formations in the lung parenchyma. Surgical management included apical bullectomy using a mechanical stapler and talc pleurodesis. The patient's postoperative recovery was uneventful, with complete lung re-expansion confirmed on imaging. This case underscores the importance of tailored surgical intervention in managing rare complications of neurofibromatosis, emphasizing thoracoscopy as a minimally invasive and effective approach.
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