2012
DOI: 10.9738/cc2.1
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Giant Neurofibroma in the Right Lower Limb of a 26-Year-Old Woman: Report of a Case

Abstract: Neurofibromatosis (NF) is a genetically inherited, autosomal-dominant disease with an incidence of 1 in 3000 live births. There are two types of NF, NF 1 and NF 2, and NF 1 is the most common. This study reports on the diagnosis, treatment, and related family medical history of a rare case with NF-1 in the right lower limb.

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Cited by 12 publications
(11 citation statements)
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“…To ensure optimal outcomes a multidisciplinary surgical team is advantageous. There are very few case reports that discuss plexiform neurofibroma resections in the lower limbs [9–13] and our case adds to the evidence for preoperative embolization to ensure safe resection. There are also reports in the literature of a resection of a plexiform neurofibroma infiltrating the middle and lower parts of the patient's face [14] and reports of spinal neurofibromas removal [15] .…”
Section: Discussionmentioning
confidence: 67%
“…To ensure optimal outcomes a multidisciplinary surgical team is advantageous. There are very few case reports that discuss plexiform neurofibroma resections in the lower limbs [9–13] and our case adds to the evidence for preoperative embolization to ensure safe resection. There are also reports in the literature of a resection of a plexiform neurofibroma infiltrating the middle and lower parts of the patient's face [14] and reports of spinal neurofibromas removal [15] .…”
Section: Discussionmentioning
confidence: 67%
“…[46] However, we agree that the most difficult challenge for this surgery is the variation of anatomy and unclear tumor margin. In addition, the tumor contains thickened cord of nerves along with abundant abnormal vessels; therefore, excessive hemorrhage during the operation is also a brainteaser.…”
Section: Discussionmentioning
confidence: 95%
“…9 There are very few case reports that discuss plexiform neurofibroma resections in the lower limbs. 10,11,12 Giant neurofibroma is a poorly defined term used to describe a neurofibroma that has grown to a significant but undefined size. However, the term "giant neurofibroma" be used for referring to those neurofibromas weighing 20% or more of the patient's total corporal weight.…”
Section: Case Reportmentioning
confidence: 99%