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Kluger N et al. – The true origin of these cells remains unclear. Some authors have speculated a histiocytic origin. However, immuno–chemical staining in this case failed to confirm this hypothesis and instead supported a fibroblastic/myofibroblastic origin. Given the clinical course and the histological and immunohistochemical results, the authors suggest that FR should be added to the group of fibromatoses.

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