The diagnosis of solitary fibrous tumor(SFT)is usually straightforward if the typical morphologicfeatures,including a wide variety of growth patterns,are identified. We report the clinical,radiologic,and pathologic findings of a rare case of intraoral SFT which exhibited a predominant leiomyomatous-like appearance,closely reminiscent of a leiomyoma,at both incisional and excisional biopsy.Histologically, the tumor was composed predominantly of intersecting fascicles of eosinophilic spindle-shaped cells, variably set in a fibrous stroma.A focal hemangiopericytoma-like growth pattern withalternating hypercellular and hypocellular areas, as well as the deposition of dense keloid-type collagen,raising the suspicion of SFT,could be identified only after a careful examination of the whole tumor.Immunohistochemistry was helpful in confirming the diagnosis of SFT,revealing a diffuse staining ofneoplastic cells for vimentin,CD34,bcl-2 protein,and,focally,CD99.Myogenic markers(alpha-smoothmuscle actin,desmin,h-caldesmon)were not expressed.The pathologist should be aware of this variant of intraoral leiomyomatous-like SFT to avoid amisdiagnosis of leiomyoma.The distinction of SFT from leiomyoma in the oral cavity is important toassure both correct treatment and prognostic information.

Solitary fibrous tumor of the oral cavity with a predominant leiomyomatous-like pattern: A potential diagnostic pitfall

MAGRO, Gaetano Giuseppe
2010-01-01

Abstract

The diagnosis of solitary fibrous tumor(SFT)is usually straightforward if the typical morphologicfeatures,including a wide variety of growth patterns,are identified. We report the clinical,radiologic,and pathologic findings of a rare case of intraoral SFT which exhibited a predominant leiomyomatous-like appearance,closely reminiscent of a leiomyoma,at both incisional and excisional biopsy.Histologically, the tumor was composed predominantly of intersecting fascicles of eosinophilic spindle-shaped cells, variably set in a fibrous stroma.A focal hemangiopericytoma-like growth pattern withalternating hypercellular and hypocellular areas, as well as the deposition of dense keloid-type collagen,raising the suspicion of SFT,could be identified only after a careful examination of the whole tumor.Immunohistochemistry was helpful in confirming the diagnosis of SFT,revealing a diffuse staining ofneoplastic cells for vimentin,CD34,bcl-2 protein,and,focally,CD99.Myogenic markers(alpha-smoothmuscle actin,desmin,h-caldesmon)were not expressed.The pathologist should be aware of this variant of intraoral leiomyomatous-like SFT to avoid amisdiagnosis of leiomyoma.The distinction of SFT from leiomyoma in the oral cavity is important toassure both correct treatment and prognostic information.
2010
Solitary fibrous tumor, Oral cavity, Pathological findings
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/54027
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