1991
DOI: 10.1016/s0753-9053(05)80203-0
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Tumeur d'Abrikossoff de la main

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Cited by 4 publications
(13 citation statements)
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“…[3–6] The lesions are usually less than 3.0 cm in size and may undergo partial regression. [45] Multiple GCTs have only been reported in less than 10% of cases, especially in children and teenagers. [16] Multiple GCTs are reported in association with neurofibromatosis, Watson's syndrome, Lentiginosis profusa, Noonan syndrome, facial and ocular alterations, cardiovascular abnormalities, muscle and bones malformations, and neurologic deficits.…”
Section: Discussionmentioning
confidence: 99%
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“…[3–6] The lesions are usually less than 3.0 cm in size and may undergo partial regression. [45] Multiple GCTs have only been reported in less than 10% of cases, especially in children and teenagers. [16] Multiple GCTs are reported in association with neurofibromatosis, Watson's syndrome, Lentiginosis profusa, Noonan syndrome, facial and ocular alterations, cardiovascular abnormalities, muscle and bones malformations, and neurologic deficits.…”
Section: Discussionmentioning
confidence: 99%
“…[4–8] Though the most common site of involvement is the tongue, it can occur anywhere in the body. [359] A GCT usually presents as a small solitary painless firm nodule affecting the middle-aged people. [35681011] The GCT of hand is exceedingly rare with only 17 cases bieng reported in the literature till date.…”
Section: Introductionmentioning
confidence: 99%
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