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The potential for genetic aberrations such as ETV6\u2010NTRK3 fusion raises the potential for targeted treatments in certain patients. The optimum mode and frequency of surveillance is unclear. This study aims to assess this institution's experience with CMN and long\u2010term outcomes.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>A single centre retrospective review was performed of all confirmed cases of CMN between October 2001 and January 2021.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Nine cases of CMN in patients under 12\u2009months of age were identified. The histopathology, management and outcomes of these patients are discussed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>CMN overall has a very good prognosis, but a subgroup does exist that will have poor outcomes. 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