Epithelioid hemangioma was firstly described by Enzinger and Weiss. It belongs to a group of unusual vascular proliferation accompanying prominent eosinophilic infiltration and synonymous with angiolymphoid hyperplasia with eosinophilia(ALHE). Histopathologically, the lesion is characterized by localized, marginated and relatively symmetrical proliferation of capillaries around a medium-sized vessel with an epithelioid hyperplasia of endothelial cell and marked infiltration of inflammatory cells, eosinophils and lymphocytes. The lesion occurs usually in the dermal and subcutaneous tissue of the head and neck area. We report a case of epithelioid hemangioma occuring on the nasal tip in a 72-years-old man. Microscopically, the lesion consisted of a proliferating vessels surrounded by inflammatory infilatration predominantly composed of eosinophils and lymphocytes. But vessels were lined by conventional-appearing endothelial cells.
Angiolymphoid Hyperplasia with Eosinophilia ; Capillaries ; Endothelial Cells ; Eosinophils ; Head ; Hemangioma* ; Hyperplasia ; Lymphocytes ; Neck ; Subcutaneous Tissue

This study was performed to investigate the in vitro proliferation and migration of rabbit auricular chondrocytes into the various sized pore of PLLA and PLGA scaffolds. The chondrocytes were harvested, expanded, and seeded onto PLGA(50 : 50, 75 : 25, 85 : 15) and PLLA scaffold having either small(50 - 100 micrometer) or large(300 - 350 micrometer) pores. On the 4th and 8th week after culture, histologic observation and quantitative DNA assay were done. We noted that the largest amount of DNA was found in the 85 : 15 PLGA sponges than others, and in the 4th and 8th week, some amount of DNA was detected in the lower portion of 85 : 15 PLGA sponge only, and DNA amounts were increased during the culture period in the 85 : 15 PLGA, significantly. We also found that the numbers of cells were low in middle portion of scaffolds, and in large pore-sized group of 85 : 15 PLGA, there were many cells in the lower portion of the scaffolds more than that of small pore group. In conclusion, the pore size of the scaffold for chondrocyte culture is important for cell migration and proliferation, and PLGA, especially 85 : 15 PLGA with 300- 350 micrometer sized pore is the more suitable biomatrix for proliferation and migration of the chondrocytes.
Cell Movement ; Chondrocytes* ; DNA ; Porifera

Polyurethane foam dressings are becoming widely used in partial and full thickness skin wounds since they are safe and convenient for both patients and physicians. However, the influence of polyurethane foam dressings on epithelialization has not been fully determined yet. This study was designed to compare 2 internationally available polyurethane foams and 3 locally made polyurethane foams as to their effects on the epithelialization in vivo. Twenty white rats were used. A 5 mm punch was employed to excise skin and subcutaneous tissue in a round fashion at six sites in the back area of 10 rats. After creating 6 open wounds, above mentioned 5 polyurethane foams and gauze dressings were applied. On the 5th day the lengths of the nonepithelialized area were measured under light microscope. In addition, partial thickness wounds were created using carbon dioxide laser at six sites on the back of the another 10 rats. Six dressings were applied on the wounds as same as above. On the 4th day the degree of the epithelialization was measured and compared. In full thickness wound study the best wound closing was also seen in chitin mixed Medifoam-N group. In partial thickness wound study the best epithelialization was seen in chitin mixed Medifoam-N and chitosan mixed Medifoam-N groups. These results demonstrated that polyurethane foam dressings influenced the epithelialization, and chitin mixed Medifoam-N showed the best result.
Animals ; Bandages* ; Chitin ; Chitosan ; Humans ; Lasers, Gas ; Polyurethanes* ; Rats* ; Skin ; Subcutaneous Tissue ; Wounds and Injuries

The human acellular dermal graft provides safe and lasting volume gain for soft tissue augmentation in the face. However, variable amounts of the graft are gradually reabsorbed in the host tissue. The purpose of this experiment is to evaluate the absorption rates of the implanted acellular dermal grafts (SureDerm(R)) and to estimate the amount of overcorrection in the soft tissue augmentation. Twenty-eight New Zealand white rabbits were divided into 4 groups. A 2.0x 2.5 cm sized subcutaneous pocket was created on the dorsal surface of the ear. 10x10 mm sized SureDerm(R) sheets, each 1 mm, 2 mm, 3 mm and 4 mm in thickness were implanted into the pockets. Ear thickness was measured by Thickness Gauze at the time of pre-operative, immediate post-operative, 4, 8 and 12 weeks after implantation. Full thickness ear was harvested in 4, 8 and 12 weeks and examined histologically for graft thickness, host tissue ingrowth, neocollagen synthesis and inflammatory reaction. Ear thickness was mildly increased due to swelling and inflammatory reaction in the initial 4 weeks in all groups and then was decreased in 12 weeks by 84%. However, there was a significant decrease in the thickness of the graft itself (43%). There was no significant difference in the ear thickness among the groups (p<0.05) with time. Histological analysis of implanted SureDerm(R) sheets demonstrated progressive neovascularization, fibroblast infilteration, neocollagen bundle synthesis and organization. Our experimental study suggests that the absorption rate of SureDerm(R) is quite uniform regardless of the thickness of the graft. The amount of overcorrection is relatively predictable and 18% of overcorrection seems to be needed for satisfactory result.
Absorption* ; Ear ; Fibroblasts ; Humans* ; Rabbits ; Transplants

Chitosan is a polysaccharide obtained by deacetylating chitin which is the major constituent of the exoskeleton of crustaceous water animals. Chitosan has many useful biological properties such as biocompatibility, biodegradability, hemostatic effect, antimicrobial activity and the ease of chemical modification. In order to evaluate the efficacy of chitosan as a wound dressing material, authors prepared chitosan as a sponge form and compared it with ointment dressing material, amniotic membrane and hydrocellular dressing material through the animal experiment. Four round( 3 cm) full thickness skin defect were made bilaterally on the dorsolateral aspect of the New Zealand white rabbit's trunk and four groups of dressing material -chitosan sponge, ointment dressing material, amniotic membrane and hydrocellular dressing material-were applied on the wound and evaluated grossly and histopathologically. We compared gross finding by means of percentage of wound contraction, percentage of wound epithilization and percentage of wound healed by tracing the remained wound area every week and wound biopsy were performed every other day. Chitosan sponge group and amniotic membrane group show statistically higher percentage of wound contraction and higher percentage of wound healed than the other groups (p < 0.05). Hydrocellular dressing material group shows statistically lower percentage of wound epithelization than the others(p < 0.05). During the inflammatory phase (postwounding day 1-5) chitosan sponge group and amniotic membrane group absorbed exudate effectively and demonstrate less inflammatory cell infiltration, which induce faster angiogenesis and fibroblast proliferation than the other groups. This study suggest chitosan has a potential as a new dressing material because of high absorbency of exudate, promotion of wound contraction and reduction of inflammatory reaction during the inflammatory phase of wound healing.
Amnion ; Animal Experimentation ; Animals ; Bandages ; Biopsy ; Chitin ; Chitosan* ; Exudates and Transudates ; Fibroblasts ; New Zealand ; Porifera* ; Skin ; Wound Healing* ; Wounds and Injuries*

This study was designed to investigate the optimal poloxamer concentration in the mixed solution of recombinant human epidermal growth factor and poloxamer which can be effective in the wound healing process. Two full-thickness excisions were made on the back of the experimental animals. Recombinant human epidermal growth factors(RhEGF) containing different poloxamer concentrations were applied twice a day and the rates of wound closure were measured every day for 14 days. On the 7th and 14th postoperative day, the histological analysis for epithelization and granulation were performed using computerized imaging analysis system after Masson's trichrome stains. The healing times 50% were significantly reduced in the RhEGF containing 0, 3 and 6% poloxamer treated groups as compared with both the non treated control and vehicle control group(p < 0.05). However, there were no statistical differences in the healing times 50% in the RhEGF containing 10, 15 and 20% poloxamer treated groups as compared with both the non treated control and vehicle control group. Histological examinations revealed that epithelization and granulation were increased significantly in the RhEGF containing 0, 3 and 6% poloxamer treated groups as compared with control group and vehicle control group at the 7th day after operation(p < 0.05). In conclusion, these findings suggest that RhEGF may enhance the epithelial wound healing process through stimulating cell proliferation. The concentration of 0, 3 and 6% of poloxamers can be applied to stabilize and enhance the wound healing effect of RhEGF for clinical application.
Animals ; Cell Proliferation ; Coloring Agents ; Epidermal Growth Factor* ; Humans* ; Poloxamer* ; Rats* ; Wound Healing* ; Wounds and Injuries*

The wound healing effect of topical application of the recombinant human epidermal growth factor(rhEGF) on full-thickness dermal injury was investigated. Two full-thickness excisions were made on the back of the experimental animals. The rhEGF was applied twice a day and the rate of wound closure was measured every day for 14 days. On the seventh postoperative day, the histological findings of epithelization and granulation were examined by Massons tichrome stain, and immunohistochemical staining for proliferating cell nuclear antigen (PCNA) and alpha-smooth muscle actin(alpha-SMA). The wound size was a significant reduction in the rhEGF treated groups as compared with the control group (p<0.05). However, there was no statistical difference in the wound size among the concentrations of the rhEGF treated group. Histological examination revealed that epithelization and granulation was increased significantly in the rhEGF group compared to control group (p < 0.01, 0.05). PCNA and alpha-SMA immunoreactive cells were observed at the margin of wound and the rhEGF treatments significantly increased the number of PCNA and alpha-SMA immunoreactive cells as compared to those of control group (p < 0.01, 0.05). Taken together, these findings suggest that rhEGF enhance the epithelial wound healing by the stimulate of cell proliferation. The wound contraction might be also affected by rhEGF application.
Animals ; Cell Proliferation ; Epidermal Growth Factor* ; Humans* ; Proliferating Cell Nuclear Antigen ; Rats* ; Skin* ; Wound Healing ; Wounds and Injuries*

PURPOSE: Oncostatin M(OSM) is a multifunctional cytokine that belongs to the interleukin(IL)-6 family. Although there have been a number of studies that focused on the role and mechanism of OSM in various organs and tissues, there are few reports on its effect on wound healing. The final purpose of this project is to evaluate the effect of OSM on wound healing. This pilot study was designed to investigate the effect of OSM on proliferation and matrix synthesis of human dermal fibroblasts, which are the major components of the wound healing. METHODS: Excess skin that was obtained from patients who underwent skin grafts, was used for this study. From this material, fibroblasts were isolated and cultured. The cultured fibroblasts were treated with one of four concentrations of OSM. The OSM concentrations used were 0, 50, 100, and 200ng/ml, respectively. After the OSM treatment, cell proliferation was determined by the MTT assay, collagen synthesis by the C1CP method, GAG levels by the Blyscan Dye method. The parameter levels of each group were compared. RESULTS: OSM treatment increased all the components tested in the study. In particular, cell proliferation, GAG synthesis demonstrated statistically significant increases(p<0.05 in the Mann-Whitney U-test). The highest increase in all the components was obtained at a 100ng/ml concentration of OSM. CONCLUSION: The results of the present study indicate that OSM stimulates proliferation and matrix synthesis of human dermal fibroblast and the optimal concentration for wound healing is 100ng/mL.
Cell Proliferation ; Collagen ; Fibroblasts ; Humans ; Oncostatin M ; Pilot Projects ; Skin ; Transplants ; Wound Healing

No abstract available.
Anemia, Aplastic* ; Breast* ; Humans ; Skin* ; Ulcer*

No abstract available.
Breast Implants* ; Breast* ; Contracture* ; Pregnancy*