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Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.

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ICD D36.1ORPHA:252183

Neurofibroma

A neurofibroma is a non-cancerous tumour that grows from the cells and tissue surrounding peripheral nerves. It can appear as a single lump on or under the skin, or as larger growths along deeper nerves. Many people with neurofibromas have neurofibromatosis type 1, though single tumours can occur without it. Management depends on symptoms and may include monitoring, surgery or targeted medicines.

This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.

391
Articles
119
Trials (4 AU)
Data refreshed
20 October 2026
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Common Questions

What is Neurofibroma?

A neurofibroma is a non-cancerous tumour that grows from the cells and tissue surrounding peripheral nerves. It can appear as a single lump on or under the skin, or as larger growths along deeper nerves. Many people with neurofibromas have neurofibromatosis type 1, though single tumours can occur without it. Management depends on symptoms and may include monitoring, surgery or targeted medicines.

How many clinical trials are available for Neurofibroma?

RareWays currently indexes 119 clinical trials for Neurofibroma, of which 16 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.

Where does the research data for Neurofibroma come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.

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