1997
DOI: 10.1016/s0305-4179(96)00026-5
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A shorter lag period of mesenchymal malignancy on Marjolin's ulcer

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Cited by 26 publications
(28 citation statements)
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“…3 Last, miscellaneous factors, such as irritation, poor lymphatic regeneration, antibodies, DNA mutations, and local toxins, have also been incriminated. 23 Most authors agree that prolonged healing of severe burn wounds (and therefore chronically abnormal keratinocyte cell biological activity) is the major potential risk factor for the development of scar carcinoma. 8,9 TYPES Two main types of Marjolin's ulcer have been described: acute and chronic.…”
Section: Pathogenesismentioning
confidence: 99%
See 1 more Smart Citation
“…3 Last, miscellaneous factors, such as irritation, poor lymphatic regeneration, antibodies, DNA mutations, and local toxins, have also been incriminated. 23 Most authors agree that prolonged healing of severe burn wounds (and therefore chronically abnormal keratinocyte cell biological activity) is the major potential risk factor for the development of scar carcinoma. 8,9 TYPES Two main types of Marjolin's ulcer have been described: acute and chronic.…”
Section: Pathogenesismentioning
confidence: 99%
“…1,4,6,9,14,23,26 The lag period before induction of malignancy is inversely proportional to patient's age at the time of burn injury. 4 Thus, younger patients tend to develop cancer after a much longer period of time.…”
Section: Latent Periodmentioning
confidence: 99%
“…In the previous literature, 24 cases of burn scar sarcomas have been reported. [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19] Of 24 cases, only 1 case of dermatofibrosarcoma protuberans (DFSP) has been reported. 19 We encountered a second case of DFSP arising in a chronic, severe burn scar, which we present herein.…”
mentioning
confidence: 99%
“…Factors believed to contribute to the development of malignancy include release of local toxins following injury, poor lymphatic regeneration in scars, chronic irritation, and existence of multiple dividing cells which are susceptible to mutations [14]. Somatic mutations of the Fas (Apo-1/ CD-95) gene and deletions of the p53 oncogene have been suggested to be predisposing factors in the development of Marjolin's ulcer, but most patients have no genetic predisposition [15,16].…”
Section: Discussionmentioning
confidence: 99%