Tissue-engineered mucosa graft for reconstruction of the intraoral lining after freeing of the tongue: a clinical and immunohistologic study

被引:20
作者
Feinberg, SE [1 ]
机构
[1] Univ Michigan, Ctr Med, Dept Oral & Maxillofacial Surg, Ann Arbor, MI 48109 USA
关键词
D O I
10.1053/joms.2001.20490
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
Purpose: This article describes the use of tissue-engineered mucosal grafts instead of split-thickness skin grafts after freeing of the tongue in patients who had previous resection of an oral squamous cell carcinoma and initial primary wound closure. Patients and Methods: Tissue-engineered mucosal grafts, up to 75 cm2 in size, were cultured from biopsy specimens of the hard palate in 6 patients, starting 3 to 4 weeks before the operation. After freeing of the tongue, the engineered mucosa was implanted on the wound surface by using vaseline gauze as carrier and fixed with an intraoral gauze wound dressing. Results: A good glossoalveolar sulcus was formed in 5 patients, resulting in good mobility of the tongue and a satisfactory denture-bearing surface. In 1 patient, there was a disturbance of wound healing, leading to severe shrinkage of the glossoalveolar sulcus and very limited improvement in tongue mobility. Preoperative bromodeoxyuridine (BrdU) labeling of the graft and postoperative immunohistochemical staining of biopsy specimens from the grafted areas with anti-BrdU showed that the cultured cells are integrated into the newly formed mucosal epithelium. Postoperative histologic investigations showed a differentiation process in the grafted mucosal epithelium, with a change in the expression of cytokeratins. At 6 months postoperatively, the typical pattern of normal nongrafted mucosa was regained. Conclusions: This investigation provides evidence that tissue-engineered mucosal cells can serve as a graft for large intraoral wounds. Complete intraoral lining is quickly reestablished, and normal epithelial differentiation is seen in the graft area within a 6-month postoperative period. © 2001 American Association of Oral and Maxillofacial Surgeons.
引用
收藏
页码:175 / 177
页数:3
相关论文
共 17 条
[1]
AUGER FA, 1995, IN VITRO CELL DEV-AN, V31, P432
[2]
CLUGSTON P A, 1991, Journal of Burn Care and Rehabilitation, V12, P533, DOI 10.1097/00004630-199111000-00008
[3]
Compton Carolyn C., 1993, Journal of Burn Care and Rehabilitation, V14, P653, DOI 10.1097/00004630-199311000-00010
[4]
DELLON AL, 1976, J ORAL SURG, V34, P789
[5]
DONOFF RB, 1976, J ORAL SURG, V34, P890
[6]
Gallico G G, 1995, Tissue Eng, V1, P231, DOI 10.1089/ten.1995.1.231
[7]
EFFECTS OF FIBROBLASTS OF DIFFERENT ORIGIN ON LONG-TERM MAINTENANCE OF XENOTRANSPLANTED HUMAN EPIDERMAL-KERATINOCYTES IN IMMUNODEFICIENT MICE [J].
INOKUCHI, S ;
SHIMAMURA, K ;
TOHYA, H ;
KIDOKORO, M ;
TANAKA, M ;
UEYAMA, Y ;
SAWADA, Y .
CELL AND TISSUE RESEARCH, 1995, 281 (02) :223-229
[8]
Ex vivo development of a composite human oral mucosal equivalent [J].
Izumi, K ;
Takacs, G ;
Terashi, H ;
Feinberg, SE .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1999, 57 (05) :571-577
[9]
Development and characterization of a tissue-engineered human oral mucosa equivalent produced in a serum-free culture system [J].
Izumi, K ;
Terashi, H ;
Marcelo, CL ;
Feinberg, SE .
JOURNAL OF DENTAL RESEARCH, 2000, 79 (03) :798-805
[10]
KERATO-DERMAL GRAFTS - THE IMPORTANCE OF DERMIS FOR THE IN-VIVO GROWTH OF CULTURED KERATINOCYTES [J].
KANGESU, T ;
NAVSARIA, HA ;
MANEK, S ;
FRYER, PR ;
LEIGH, IM ;
GREEN, CJ .
BRITISH JOURNAL OF PLASTIC SURGERY, 1993, 46 (05) :401-409