Plexiform neurofibromatosis is almost invariably associated with neurofibromatosis type I. A case of an isolated back plexiform neurofibroma, initially thought to be a lipoma, is presented, with emphasis on the importance of eliciting family history in reaching a diagnosis of neurofibromatosis. Currently, surgical resection is still the treatment of choice though a management plan is not well defined. Patients need appropriate regular follow-up to detect malignancy or early recurrence.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3028994 | PMC |
http://dx.doi.org/10.1136/bcr.01.2010.2696 | DOI Listing |
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