2014
DOI: 10.1007/s11552-013-9590-x
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An Unusual Presentation of a Digital Schwannoma: Case Report

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Cited by 7 publications
(6 citation statements)
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“…Plexiform schwannomas are not visible on radiographs but have a hyperintense signal on T2 on magnetic resonance imaging, as seen in this case. 1 Many plexiform schwannomas observed in a patient at once may be classified as schwannomatosis; there is a higher association of schwannomatosis with neurofibromatosis type 2 than of solitary masses. 2 Although plexiform schwannomas have no mitoses and lack the potential for malignant transformation, pleomorphic nuclei are commonly seen on histologic investigation, although this was not seen here.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Plexiform schwannomas are not visible on radiographs but have a hyperintense signal on T2 on magnetic resonance imaging, as seen in this case. 1 Many plexiform schwannomas observed in a patient at once may be classified as schwannomatosis; there is a higher association of schwannomatosis with neurofibromatosis type 2 than of solitary masses. 2 Although plexiform schwannomas have no mitoses and lack the potential for malignant transformation, pleomorphic nuclei are commonly seen on histologic investigation, although this was not seen here.…”
Section: Discussionmentioning
confidence: 99%
“…These masses account for approximately 5% of all tumors involved with the upper extremities and 2.8% of biopsied benign, soft-tissue tumors of the hand and wrist. 1 These lesions typically occur along peripheral nerves and/or along the volar aspect of digits, hands, or arms. They may be associated with neurofibromatosis type 2, although they may also occur sporadically.…”
mentioning
confidence: 99%
“…A glomus tumour is very painful and may be associated with localised subungal discolouration. Intraosseous glomus tumours18 or schwannomas19 are very rare.…”
Section: Differential Diagnosismentioning
confidence: 99%
“…4 PS is not associated with neurofibromatosis type 1 (NF1), but it may occur in cases of NF2 and schwannomatosis. [5][6][7] PS is a superficial soft tissue tumor in young adults and occurs commonly as a solitary, slow-growing, asymptomatic nodule on the head, neck, trunk, or upper extremities. 1,3…”
Section: Introductionmentioning
confidence: 99%