自体软骨碎屑回植对肋软骨修复再生的影响

Objective To investigate the influence on costal cartilage reparative regeneration by replanting the small blocks of autogeneic cartilage into the perichondrial pocket at the donor-site. Methods 16 rabbits (8-10 weeks old, 1.8-2. 2 kg) were randomly divided into four groups as three experimental groups and one control group. The 1.5 cm in length of costal cartilage defect was made in experimental groups with the perichondrium and costochondral junction left completely intact. The cartilage defect was cloesd by 3 methods as suturation directly, or replanting the small blocks of autogeneic cartilage, or plugging bioprotein jelly after cartilage replanting. Each experimental group was handled with two methods in two sides of costal cartilage. No operation was performed in control group. All the rabbits were sacrificed 16 weeks after operation. The appearance of thoracic cage and new-formed tissue at the defect site were examined grossly. Haematoxylin-eosin staining was performed to evaluate the characteristics of new-formed tissues and biomechanical detection was used to measure intension of new-formed tissues. Results The appearance of thoracic cage was normal in every experimental group. Histological study showed that the defect was filled with abundant fibrous tissue in each group. The chipping of cartilage survived effectively with little proliferation. Biomechanical detection showed that the intension of new-formed tissue in the non replanted group [( 193. 92 ± 41. 41 ) N] was obviously less than that in the replanted group [( 318. 88 ±28. 28)N] ,or bioprotein jelly group[(301. 00 ±39. 52) N] , or control group[(300. 54 ±38. 35) N] (P <0. 01). Furthermore, there was no statistical difference between the latter three groups ( P > 0. 05 ) . Conclusions Although replanting the chipping of cartilage can' t promote reparative regeneration of hyaline cartilage, it can definitively strengthen the intensity of new-formed tissue, reinforce thoracic stability. It may also indirectly decrease the incidence rate of postoperative chest wall deformity.     

New β Ti alloy mini-prosthesis with low elastic modulus resurfacing articular surface defect in dogs

Objective To assess the effect of a new β Ti alloy mini-prosthesis with low elastic modulus on resurfacing the full-thickness Surface defect of the knee joint in dogs.Methods A full-thickness osteochondral defect of 7 mm in diameter was created at the medial femoral condyle of both hind limbs in 8 healthy adult dogs.The titanium alloy mini-prostheses with high-modulus of elasticity were implanted on the right side(control group)and those with low-modulus of elasticity on the left side(experiment group)to repair the cartilage defects.After 3 months,all the 8 dogs were sacrificed to harvest the specimens.Radiographic,histologic and micro-CT examinations were conducted to observe stability of the mini-prostheses and growth of the bone and cartilage surrounding the implants. Results Radiographic evaluation revealed no indications of device disassembly or subsidence.Bone trabeculae surrounding anchoring screws in the experiment group was visibly more and denser compared with the control group.Micro-CT data revealed that the bone volume fraction,trabecular thickness,trabecular number and tissue mineral density were 0.389%±0.025%,0.049±0.002 μm,8.9±0.4 mm-1 and 652.7 ±12.6 mg/mm3 respectively in the experiment group,compare with 0.253%±0.024%,0.038±0.002 μm,5.9±0.4 mm-1 and 595.2±7.6 mg/mm3 in the control group,with statistically significant differences between the 2 groups(P<0.05).Cartilage around the cap grew well and the surface remained smooth.Periphery of the resurfacing implant was covered by an extension of the superficial cartilage emanating from the defect margins. Conclusions The new β Ti alloy mini-prosthesis with low elastic modulus is favorable toward resurfacing the articular surface defect.The low-modulus of elasticity can improve new bone formation on the implant-bone interface.     

Evaluation of reparative cartilage after autologous chondrocyte implantation for osteochondritis dissecans: histology,biochemistry, and MR imaging

Background The aim of this study was to investigate the biochemical properties, histological and immunohistochemical appearance, and magnetic resonance (MR) imaging findings of reparative cartilage after autologous chondrocyte implantation (ACI) for osteochondritis dissecans (OCD). Methods Six patients (mean age 20.2 ± 8.8 years; 13–35 years) who underwent ACI for full-thickness cartilage defects of the femoral condyle were studied. One year after the procedure, a second-look arthroscopic operation was performed with biopsy of reparative tissue. The International Cartilage Repair Society (ICRS) visual histological assessment scale was used for histological assessment. Biopsied tissue was immunohistochemically analyzed with the use of monoclonal antihuman collagen type I and monoclonal antihuman collagen type II primary antibodies. Glycosaminoglycan (GAG) concentrations in biopsied reparative cartilage samples were measured by high performance liquid chromatography (HPLC). MR imaging was performed with T₁- and T₂-weighted imaging and three-dimensional spoiled gradient-recalled (3D-SPGR) MR imaging. Results Four tissue samples were graded as having a mixed morphology of hyaline and fibrocartilage while the other two were graded as fibrocartilage. Average ICRS scores for each criterion were (I) 1.0 ± 1.5; (II) 1.7 ± 0.5; (III) 0.6 ± 1.0; (IV) 3.0 ± 0.0; (V) 1.8 ± 1.5; and (VI) 2.5 ± 1.2. Average total score was 10.7 ± 2.8. On immunohistochemical analysis, the matrix from deep and middle layers of reparative cartilage stained positive for type II collagen; however, the surface layer did not stain well. The average GAG concentration in reparative cartilage was 76.6 ± 4.2 μg/mg whereas that in normal cartilage was 108 ± 11.2 μg/mg. Common complications observed on 3D-SPGR MR imaging were hypertrophy of grafted periosteum, edema-like signal in bone marrow, and incomplete repair of subchondral bone at the surgical site. Clinically, patients had significant improvements in Lysholm scores. Conclusions In spite of a good clinical course, reparative cartilage after ACI had less GAG concentration and was inferior to healthy hyaline cartilage in histological and immunohistochemical appearance and on MRI findings.     

双扩张器重叠扩张无需植皮的全耳成形术

Objective To investigate a method of auricular reconstruction with overlapping tissue expansion techniques and without skin graft. Methods Two tissue expanders were implanted subcutaneously at the mastoid. 6 patients with microtia(overlapping group)were treated. After completion of skin expansion, the expanders were removed. The autolognus rib cartilage or Medpor scaffolds were implanted. The flap A made by the upper expanded flap was used to cover the upper part of the front and the back of the framework. The flap B made by lower expanded flap was transplanted to cover the lower part of the back of frameworks. The remaining expanded skin was designed to cover the postanricular wound. The other thirteen microtia patients who treated by the traditional auricular reconstruction were selected as control(traditional group). Results Skin graft was not necessary in the patients of overlapping groups. The appearance of the reconstructed ear was very satisfactory. Epidermal necrosis of 0.5 cm × 0.5 cm happened at the distal end of postauricular flap in one case. All the other cases had no complication of infection or framework exposure. The patients were followed up for 3～6 months. Compared with the traditional group, the scar in the costal donor site was inconspicuous in overlapping group(P <0.05). The complication rate was lower and satisfactory rate was higher in overlapping group (P < 0.01 and P < 0.05). But there was hair growth in the helix of reconstructed ear in overlapping group. Conclusions The overlapping expansion can provide enough skin for ear reconstruction. The skin graft is not necessary, resulting less donor site scar and low complications.     

Experimental study on mechanism of vertebral osteophyte formation

Objective:The purpose of this experimental study was to explore the mechanism of the vertebral osteophyte formation.Methods:An experimental model of cervical spondylosis in rabbits was established by resection of the cervical supraspinous and interspinous ligaments and detachment of the posterior paravertebral muscles from cervical vertebrae.Because of individual difference,The natural development procedure of the vertebral osteophyte formation could be seen with a microscope by dynamic observation.Results:The cartilage end-plate was divided into a growth cartilage layer and an articular cartilage layer.Vertebrae and discs from the 3-month control group rabbits showed normal structure.The changes of cartilage plates from the 3-monthe experimental group and the 8-month control group animals showed proliferation in peripheral articular cartilage.The osteophytes from the 8-monthe experimental group animals could be seen.The osteophyte obviously arised from proliferation,calcification and ossification of the peripheral articular cartilage.Conclusions: The vertebral osteophyte arises from proliferation of peripheral articular cartilage which undergoes cartilaginous osteophyte,and then changes into bony osteophyte through an endochondrqal calcification and ossification.     

几丁糖对扩张后皮瓣纤维包膜影响的实验研究

Objective To investigate the effect of chitosan on the capsule inside the expanded flap. Methods The expanders were implanted in animals with the treatment of chitosan(experimental group, n=15) or without(control group, n=15). After taking out the expanders, the flap contraction rate was calculated. The samples were observed through HE, Masson dyeing and CD34 immunohistochemical study. The thickness of capsule inside the expanded flap was measured under microscope. The samples were also studied under electron microscope. Results The thickness of capsule was 516.000±128.491 μm in the experimental group, and 833.000±227.379 μm in the control group(P < 0.05). The number of microvessels was 8.200±2.150 per visual in experimental group, and 7.900±1.729 per visual in control group(P > 0.05). Under the electron microscope, the rough endoplasmic reticulum(RER) in the capsule in experimental group decreased and enlarged with degranulation. The mitochondria emerged or disappeared. The number of ribosome was reduced. In the control group, the PER enlarged without degranulation, the mitochondria was intact. The number of ribosome was not reduced. Conclusions The chitosan can effectively reduce the contraction of expanded flap through collagen secretion of fibroblast, delaying the differentiation from fibroblast to fiber cell, inhibiting thansform from fibroblast to myofibroblast. It has no effect on the microvascular generation and expansion, so the flap blood supply will not be affected with thicker capsule.     

Microsurgical repair at early stage for soft tissue defect of limbs wounded by modem firearm

Objective: To explore an early stage repair method for soft tissue defect of limbs of modern firearm wound,and to hnprove treating result. Methods: Defects of the hind limbs of dogs were relmired with skin, muscle and myocutaneous flaps. Results: Wounds healed within 2 weeks in the experimental group except one that healed in 3 weeks because of infection. Limb function was close to normal.The treatment result was better in the experimental group than the control. Conclusions: Skin, muscle and myocutaneous flaps can cover soft tissue defect at an early stage, prevent and reduce infection, promote the healing and recovery of combined injury, reduce the time of treatment and disability rate.     

软骨细胞与骨髓基质细胞共培养体外构建软骨组织的实验研究

Objective To investigate the feasibility of chondrogenesis in vitro with bone marrow stromal cells (BMSCs) induced by the co-cultured chondrocytes. Methods The BMSCs and chondrocytes were separated from pig and cultured. The supernatant of chondrocytes was used as the inducing solution for BMSCs from the 2nd generation. 7 days later, samples were taken and underwent immunohistochemistry and RT-PCR for detection of the expression of specific type Ⅱ cartilage collagen,type Ⅱ collagen and aggrecan mRNA. The cultured BMSCs and chondrocytes were mixed at a ratio of 8:2(BMSC: cartilage cell) and were inoculated into a polyglycolic acid/polylactic acid (PGA/PLA) scaffold at the final concentration of 5.0 × 107/ml. The cartilage cells and BMSCs were also inoculated seperately at the same concentration as the positive and negative control. Pure cartilage cells at 20% of the abovementioned concentration (1.0 × 107/ml) were used as the low concentration cartilage cell control group. Samples were collected 8 weeks later. General observations, wet weight, glycosaminoglycans (GAGs) determination and histological and immunohistochemistry examinations were performed. Results The expression of type Ⅱ collagen, type Ⅱ collagen and aggrecan mRNA were positive in induced BMSCs.In the co-cultured group and the positive control group, pure mature cartilage was formed after 8 weeks of culture in vitro, and the size and shape of the scaffold were maintained. The newly formed cartilage in the two groups were almost the same in appearance and histological properties. The immunohistochemistry results indicated that the cartilage cells of the two groups all expressed ample cartilage-specific type Ⅱ collagen. The average wet weight and GAG content in the co-cultured group reached more than 70% of those in positive control group. Only an extremely small amount of immature cartilage tissues was formed in local regions in pure BMSC group, and the scaffold was obviously shrunk and deformed. Although the wet weight of newly generated cartilage tissue in the low concentration cartilage cell group reached 30% of that in positive control group, the scaffold was obviously shrunken and deformed. Only regional and discontinuous cartilage tissues were formed, and the amount of newly formed cartilage was obviously less than that in the co-culture group and the positive control group. Conclusions Chondrocytes can provide a micro-environment for the formation of cartilage, and also effectively induce BMSC to differentiate into chondrocytes and form tissue-engineered cartilage in vitro.     

Injury of ~(125)Ⅰ seeds implants to trachea and esophagus of rabbits

Objective To evaluate the impact of 1125 seeds para-tracheal braehytherapy on regional tissue injury in rab-bit models. Methods 42 rabbits were randomized into 7 groups. Group 1 to 6 belong to study groups (in which 1,4,5 and 6 belong to "dose gradient" subgroup, while 2,3 and 4 to "chronologic" subgroup) , while the last group acts as negative con-trol. The activity of seeds in study group were 0.3 mCi in group 1, 0.5 mCi in group 2 to 5, 0.7 mCi in group 5, and 0.9mCi in group 6. False seeds (0 mCi) were used for the negative control. 4 seeds with equal dosage were implanted between trachea and esophagus in each rabbit under general anesthesia. Seeds arrangement was made according to Paris principle. For the tissue injury evaluation, group 2 was sacrificed by the end of first month post-operatively, group 3 at the end of the second month, and group 4 end of the third month. The rest of rabbits were also sacrificed at the end of the third month. Pieces of adjacent e-sophagus and trachea were sampled from each rabbit. Tissue injury features such as inflammation, edema, congestion or fibrosis as evaluated histologically. Results All rabbits were healthy during study period except 5. Histological analysis revealed that trachea samples from all groups had lymphocytas and plasma cells infiltration as signs of chronic inflammation, hut fibrosis was nut clearly visible. There were no differences between study and control groups with respect to inflammation, edema and con-gestion scores. But in groups which received the highest doses of radiation or sacrificed at 60 d showed more eosinophil infiltra-tion and epithelum degeneration, and statistical significance was reached between these groups and control. Esophageal samples had less histological changes compared with trachea. Conclusion Para-tracheal implantation of ~(125)Ⅰ seeds with therapeutic or higher dosage only induce minor and reversible damage to the regional tissue. This implies that ~(125)Ⅰ implants adjacent to trachea or esophagus are clinically safe.     

Protective effect of ischemic postconditioning on lung ischemia-reperfusion injury in rats and the role of heme oxygenase-1

To investigate the effect of ischemic postconditioning (IPO) on acute lung ischemia-reperfusion (I/R) injury and the protein expression of haeme oxygenase-1 (H0-1), a cytoprotective defense against oxidative injury. Methods: After being anesthetized with chloralhy-drate, forty-eight healthy SD rats were randomly divided into 6 groups (8 in each): sham operation group (S group); I/R group: left lung hilum was clamped for 40 minutes followed by 105 minutes of reperfusion; IPO group: left lung hilum was clamped for40 minutes and postconditioned by 3 cycles of 30 seconds of reperfusion and 30 seconds of reocclusion; Hemin (HM)+ I/R group: hemin, an inducer of HO- 1 was injected intraperitoneally at 40 μmol.kg-1·day-1 for two con-secutive days prior to 40 minutes clamping of left lung hilum; ZnPPIX+IPO group: zinc protoporphyrin Ⅸ, an inhibitor of HO-1 was injected intraperitoneally at 20 mg·kg-1 24 hours prior to 40 minutes clamping of left lung hilum; and HM+S group: HM was administered as in the HM+I/R group without inducing lung I/R. Arterial partial pressure of oxygen (PaO2) and malondialdehyde (MDA) content in serum were assessed. The left lung was removed for determination of wet/dry lung weight ratio and expression of HO-1 protein by immuno-his-tochemical technique and for light microscopic examination. Results: The PaO2 was significantly lower in all the experimental groups compared with sham group (90 mm Hg ±11 mm Hg). However, the values ofPaO2 in IPO (81 mm Hg ±7 mm Hg) and HM+I/R (80 mm Hg±9 mm Hg) were higher than that in I/R (63 mm Hg±9 mm Hg) and ZnPPIX+IPO (65 mm Hg±8 mm Hg) groups (P<0.01). The protein expression of HO-1 in lung tissue was significantly increased in I/R group compared with S group (P<0.01). While the HO-1 protein expression was higher in IPO and HM+I/R groups as compared with I/R group (P<0.05, P<0.01). The lung wet/ dry (W/D) weight ratio and MDA content in serum were significantly increased in I/R group as compared with S or HM+S groups (P<0.01), accompanied by severe lung tissue histological damage, which was attenuated either by IPO or by HM pretreatment (P<0.01, IPO or HM+I/R vs. I/R). The protective effect of IPO was abolished by ZnPPIX. Condusion: Ischemic postconditioning can attenuate the lung ischemia-reperfusion injury through upregulating the protein expression of HO-1 that leads to reduced post-ischemic oxidative damage.     

Repairing articular cartilage defects with tissueengineering cartilage in rabbits

Objective: To investigate the effect of cancellous bone matrix gelatin ( BMG ) engineered with allogeneic chondrocytes in repairing articular cartilage defects in rabbits. Methods: Chondrocytes were seeded onto three-dimensional cancellous BMG and cultured in vitro for 12 days to prepare BMG-chondrocyte complexes. Under anesthesia with 2.5% pentobarbital sodium (1ml/kg body weight), articular cartilage defects were made on the right knee joints of 38 healthy New Zealand white rabbits (regardless of sex, aged 4-5 months and weighing 2. 5-3 kg) and the defects were then treated with 2. 5% trypsin. Then BMG-chondrocyte complex ( Group A, n = 18 ), BMG (Group B, n = 10), and nothing (Group C, n = 10) were implanted into the cartilage defects, respectively. The repairing effects were assessed by macroscopic, histologic, transmission electron microscopic ( TEM ) observation, immunohistochemical examination and in situ hybridization detection, respectively, at 2, 4, 8, 12 and 24 weeks after operation. Results: Cancellous BMG was degraded within 8 weeks after operation. In Group A, lymphocyte infiltration was observed around the graft. At 24 weeks after operation, the cartilage defects were repaired by cartilage tissues and the articular cartilage and subchondral bone were soundly healed. Proteoglycan and type II collagen were detected in the matrix of the repaired tissues by Safranin-O staining and immunohistochemical staining, respectively. In situ hybridization proved gene expression of type II collagen in the cytoplasm of chondrocytes in the repaired tissues. TEM observation showed that chondrocytes and cartilage matrix in repaired tissues were almost same as those in the normal articular cartilage. In Group B, the defects were repaired by cartilage-fibrous tissues. In Group C, the defects were repaired only by fibrous tissues. Conclusions: Cancellous BMG can be regarded as the natural cell scaffolds for cartilage tissue engineering. Articular cartilage defects can be repaired by cancellous BMG engineered with allogeneic chondrocytes. The nature of repaired tissues is closest to the normal cartilage. Local administration of trypsin can promote the adherence of repaired tissues to host tissues. Transplantation of allogeneic chondrocytes has immunogenicity, but the immune reaction is weak.     

脱细胞软骨支架材料修复兔关节软骨缺损

目的 观察异种异体脱细胞软骨支架材料(ACM)复合同种异体兔骨髓间充质干细胞(rBMSCs)修复兔股骨内髁关节软骨缺损的效果.方法 (1)密度梯度离心和差速贴壁法获得原代兔BMSCs,选择第3代BMSCs作为种子细胞;(2)利用冷冻干燥、胰酶消化和化学去垢剂等方法制备脱细胞软骨支架材料;(3)3个月龄新西兰兔股骨内髁制备直径4 mm,深3 mm砌关节软骨缺损模型,24只新西兰兔以2个时间段随机分为3组,Ⅰ ACM-BMSCs组:第3代BMSCs 1×106个/ml与ACM于37℃5%CO2饱和湿度复合48 h;Ⅱ ACM组;Ⅲ空白对照组.(4)移植6、12周后大体及组织学观察,免疫组织化学染色观察修复组织Ⅱ型胶原,Wakitani评分评估修复效果.结果 (1)大体观察及组织学观察:6和12周Ⅰ组再生组织与正常关节软骨面平齐,修复部位表面较平整,界限模糊,接近正常软骨.Ⅱ组修复组织表面不平整并有明显下陷,修复组织全层可见成纤维样细胞,深层可见极少数透明软骨样细胞.Ⅲ组未见明显修复,肉芽组织形成伴成纤维样细胞增生;(2)Wakitani组织学评分可见在不同的时间段I组和Ⅱ组均低于Ⅲ组,差异有统计学意义(P<0.05),Ⅰ组和Ⅱ组间组织学评分差异无统计学意义(P>0.05).(3)免疫组织化学:ACM-BMSCs组修复组织的细胞为软骨样细胞,可见柱状排列,周围软骨基质Ⅱ型胶原染色阳性.结论 以ACM为支架材料,同种异体BMSCs为种子细胞制备的组织工程化软骨对兔股骨内髁关节软骨缺损有修复作用,形成的新生软骨为透明软骨样组织.     

组织工程软骨对兔膝关节胫骨平台浅层全关节软骨缺损的修复作用

目的探讨组织工程软骨对兔膝关节胫骨平台外侧髁浅层全关节软骨缺损的修复作用，并检测其修复组织的软骨类型。方法取2周龄乳兔软骨细胞体外培养传代至第3代后，与人胎盘Ⅰ型胶原蛋白海绵复合后植入成年兔的胫骨平台外侧髁完全软骨缺损区，并设立空白对照组，分别于术后4、12、24周取材。观察修复效果。运用天狼星红染色检测Ⅰ型胶原，Ⅱ型胶原单克隆抗体检测Ⅱ型胶原的表达。结果实验组术后4周缺损表面未见明显的新生软骨形成，组织学切片上少数几个呈上皮样生长的软骨细胞，苏木素-伊红（HE）染色胞浆呈深蓝色，周围软骨基质染色成浅蓝色；12周，缺损表面有少量的新生软骨形成，组织学切片上可见软骨细胞呈边缘不规则的，小蜂窝状结构，软骨细胞周围有软骨陷窝形成；24周，缺损表面的新生软骨较4、12周的新生软骨明显，表面光滑，且与周围组织结合紧密，但仍存在部分缺损尚未修复，组织学切片上可见软骨细胞呈边缘不规则的，多层细胞的蜂窝状结构，软骨细胞周围有软骨陷窝形成，并分泌甲苯胺蓝异染的软骨基质。而对照组则均未见明显的修复；随着术后时间的延长，Ⅰ型胶原的表达呈逐渐减弱的趋势，而Ⅱ型胶原的表达呈逐渐增强的趋势。结论该方法制成的组织工程软骨对兔胫骨平台外侧髁全层软骨缺损有修复作用，运用该方法不能完全修复兔胫骨平台外侧髁软骨完全缺损；形成的新生软骨为透明软骨样组织。     

同种异体骨软骨移植修复关节软骨缺损的研究进展

同种异体骨软骨移植修复膝关节软骨和骨软骨缺损适用于大面积骨软骨缺损的修复,且不受缺损形状和面积的限制,在临床上已取得令人鼓舞的结果。现对国内外同种异体骨软骨移植修复关节软骨缺损的研究进展作一综述。     

Articular cartilage restoration with costal cartilage previously fused with bone

A novel procedure was developed for restoration of an articular cartilage defect using an autologous costal cartilage prepared with iliac bone, and the durability in vivo of this biologic construct was examined. First, an osteochondral complex was prepared (successful preparation, 67 of 80). Cancellous bone blocks isolated from the ilium of male Japanese White rabbits aged 5 months were implanted onto the surface of the costal cartilage before being tied by a pair of 3-0 silk thread sutures that were looped around the costal cartilage from behind. Second, 3 months later, the bone-attached costal cartilage was harvested and implanted into a full-thickness cartilage defect induced in a trochlear groove of the femur. All of the grafts were fixed to the recipient, maintaining its cartilage structure until 6 months (n = 28) and 12 months (n = 12) after implantation. However, when the costal cartilage without any bony portion was implanted into a similarly induced defect, 42% (10 of 24) were detached from the recipient before 12 months after implantation. The nontreated defect did not heal spontaneously to a satisfactory level (n = 12). These findings suggest that an osteochondral fragment, prepared by grafting cancellous bone onto costal cartilage, can be used for articular cartilage restoration.     

耳软骨整体再造鼻侧软骨的可行性分析

目的：以耳软骨为供区,探索整体再造鼻侧软骨的方法。方法：20具（40侧）尸体标本,取下耳软骨40枚,鼻侧软骨40枚。CT扫描后重建三维图像,测量鼻侧软骨各解剖分区的相关数据。设计耳软骨3个供区可整体移植再造同侧鼻侧软骨,测量相关的形态数据。结果：耳软骨3个供区的相关形态数据大于同侧鼻侧软骨的相应数据。结论：耳甲腔、耳屏及两者之间连接的峡部（CVIT区域）,三角窝、耳轮及两者的连接部（TFH区域）,耳甲艇、耳轮及两者之间的连接部分（CBH区域）可整体取下,修整后整体再造同侧鼻侧软骨。     

软骨代谢标志物对骨关节炎软骨改变的反映

目的研究血清中蛋白聚糖和Ⅱ型胶原水平与骨关节炎严重程度间的关系,及对手术后软骨代谢改变的反映。方法研究对象包括65例膝骨关节炎患者及22名正常人。45例患者分别行不同方式手术治疗,术后半年复查。正常人及患者术前和复查时抽取静脉血,摄下肢负重位X线片。应用酶联免疫吸附方法检测血清样本中蛋白聚糖及Ⅱ型胶原的水平。结果骨关节炎患者血清中蛋白聚糖及Ⅱ型胶原水平均显著高于正常对照组,差异有显著性意义(P<0.05)。血清中蛋白聚糖和Ⅱ型胶原水平在轻型骨关节炎组升高,在关节明显狭窄组水平最高,而在严重狭窄组明显降低。术后半年,全膝关节置换术组血清中蛋白聚糖水平较术前明显下降(P<0.05);截骨术组血清中Ⅱ型胶原水平较术前明显下降(P<0.05)。结论血清中蛋白聚糖和Ⅱ型胶原的水平与骨关节炎软骨的破坏程度、软骨细胞的合成反应及软骨的总量有关。蛋白聚糖和Ⅱ型胶原水平是反映软骨代谢改变的较敏感的指标。