颈动脉切除术的临床研究

目的 探讨颈部恶性肿瘤侵犯颈总动脉和I或颈内动脉以及颌面部难控制大出血时对颈总动脉和颈内动脉的外科处理方法及其并发症、后遗症的预防。方法 回顾性分析1990年－2000年行颈总或I和颈内动脉结扎、切除术的6例临床资料。结果 本组均为男性，年龄17－66岁。其中颈部复发性转移癌浸润颈总动脉、颈内动脉3例，鼻咽癌放疗后颈部溃疡侵犯颈总动脉1例，上颌骨中央性血管瘤大出血1例，鼻咽纤维轿管瘤术中、术后大出血1例。单纯结扎、切除颈总动脉4例，颈总及颈内动脉同时结扎、切除2例。经随访，术后短暂性肢体偏瘫2例，脑梗塞、永久性偏瘫1例，无任何并发症3例。无手术死亡病例。结论 颈动脉切除术对已累及颈动脉的颈部恶性肿瘤是一种有效的治疗手段，对于颌面颈难以控制的致命性大出血是一种有效的急救措施。单纯切除颈总动脉所产生的术后并发症的发生率比颈总动脉和颈内动脉同时切除低；而已先期或同时切除颈外动脉，出现并发症的机会更大。术后酌用抗凝或溶栓药物对于脑血栓、脑梗塞的防治作用有待进一步研究。     

Needle tract recurrences after closed biopsy for sarcoma: Three cases and review of the literature

Background: Percutaneous closed needle biopsy of musculoskeletal neoplasms has gained in popularity. However, it remains controversial whether or not to resect the needle tract for fear of a local recurrence. A single published case report exists, noting the lone tract recurrence of an extremity skeletal osteosarcoma. Methods: We report on three additional individuals who demonstrated that tract local recurrences may occur after a closed needle biopsy for nonosteosarcoma, nonextremity sarcomas. For perspective, the world literature is reviewed to identify tract recurrences for other malignancies and the results of needle biopsy in musculoskeletal neoplasms. Results: Eighty-nine percent of needle tract local recurrences occur when carcinomas are subjected to biopsy, as reported in the literature. Forty-seven cases since 1950 are described representing essentially all tumor types. The nature of musculoskeletal neoplasms makes closed biopsy more difficult than for softer, more homogeneous, and easier to access neoplasms. Conclusions: Local recurrences of sarcoma may occur in closed needle biopsy tracts. Strong consideration should be given to open biopsy and tract resection.     

Solid variant of odontogenic keratocyst

A case of an unusual lesion from the maxilla is presented. Macroscopically, the lesion was solid and histologically consisted of 'multiple separate keratocysts' of varying size that infiltrated into the surrounding bone and soft tissues. Panoramic image and CT scans showed a multilocular honeycomb ill-defined radiolucency with infiltration into the maxillary sinus and floor of orbit. This lesion should be differentiated from similar odontogenic lesions, such as keratoameloblastoma and papilliferous keratoameloblastoma. As there was no evidence of follicles, islands of ameloblastoma, or papilliferous structures in the entire specimen, the lesion could not be diagnosed as either a keratoameloblastoma or a papilliferous keratoameloblastoma. The invasive and destructive growth behavior, the histopathological features, and the histochemical pattern of the collagen stroma imply that this solid lesion is a neoplasia. It is suggested that the proper term for this lesion is solid variant of odontogenic keratocyst.     

高频灰阶超声鉴别良恶性胸肌淋巴结

目的:评价灰阶超声在鉴别良、恶性胸肌淋巴结中的应用价值.材料和方法:研究对象为43枚乳癌患者的胸肌淋巴结,其中16枚为转移性胸肌淋巴结、27枚为非转移性胸肌淋巴结;另有19枚乳腺良性病变患者的胸肌淋巴结和22枚正常者的胸肌淋巴结作为对照组.使用仪器为HDI-3000型彩色多普勒超声诊断仪,配备5～12MHz宽频控头.运用超声测量胸肌淋巴结的长径、轮廓形态、长径-厚度比、髓皮质厚度比,作为鉴别良、恶性胸肌淋巴结的参数,比较良、恶性胸肌淋巴结在形态学上差异.结果:良、恶性胸肌淋巴结的长径、轮廓形态、髓皮质厚度比无显著性差异;恶性淋巴结长径-厚度比(1.7±0.4)明显低于良性淋巴结(2.0±0.5),P＜0.05.结论:灰阶超声在鉴别良、恶性胸肌淋巴结中具有一定的应用价值.     

肺癌组织中血管内皮生长因子受体Flt1及KDR的表达及其与肿瘤转移和预后的关系

①目的　探讨肺癌中血管内皮生长因子受体Flt1、KDR的表达与其转移及预后的关系。②方法　应用免疫组织化学PowerVisionTM PV90 0 0法 ,测定 75例肺癌标本中Flt1、KDR的表达。③结果　肺癌组织中Flt1、KDR的表达较为广泛 ,主要位于肿瘤细胞胞浆及胞膜上 ,纤维母细胞和血管内皮细胞胞浆中亦有表达。Flt1、KDR在肿瘤细胞中的阳性率均显著高于在间质纤维母细胞中的表达 (χ2 =6 .0 7、5 .88,P <0 .0 5 )。肿瘤细胞及纤维母细胞中该两种受体的阳性率在不同年龄、不同性别及不同病理类型、不同病理分级之间差异均无显著性 (χ2 =0 .0 1～4 .84 ,P >0 .0 5 ;P =0 .2 9～ 0 .79)。肿瘤细胞中Flt1、KDR的阳性表达率在 3组不同大小的肿瘤间差异均有显著性(χ2 =1 0 .35、7.2 9,P <0 .0 5 ) ,而纤维母细胞中差异均无显著性 (χ2 =2 .86、2 .5 6 ,P >0 .0 5 ) ;肿瘤细胞及纤维母细胞中Flt1、KDR的阳性率在淋巴结有、无转移两组间的差异均有显著性 (χ2 =4 .72～ 9.32 ,P <0 .0 5 ) ,在 3组不同术后生存时间病人间亦均有显著性差异 (χ2 =8.81～ 1 9.1 9,P <0 .0 5 )。肿瘤细胞中Flt1、KDR的表达呈极显著性正相关 (r =0 .4 4 ,P <0 .0 1 )。④结论　肺癌的生长主要依赖自分泌机制 ,联合检测Flt1、KDR可能对肺癌转移     

腹腔镜诊断和治疗小肝癌临床研究的初步报告

目的　探讨腹腔镜对AFP阳性、而影像学检查阴性的小肝癌的诊断和治疗的价值。方法　对 5例AFP阳性、而B超、CT或 (和 )MRI阴性 ,高度怀疑早期肝癌者 ,进行了腹腔镜探查和手术治疗。结果　 5例均证实为小肝癌 ,肿瘤约 0 8～ 1 0cm ;4例实施了腹腔镜肝部分切除 ,1例中转开腹手术切除肿瘤。随访 4个月至 4年 ,5例均无瘤生存。结论　对AFP持续阳性 >1个月、而B超、CT或 (和 )MRI阴性 ,高度怀疑肝表面小肝癌者 ,进行腹腔镜探查和手术治疗可能是肝表面或肝边缘的小肝癌最佳的诊断和治疗手段。     

吲哚美辛对人结肠癌HCT116和SW480细胞的影响

目的：探讨吲哚美辛对人结肠癌HCT116和SW480细胞的影响。方法：体外培养细胞，采用MTT法分别检测吲哚美辛作用后两系细胞的生长情况，计算半抑浓度（IC50）；体内建立裸鼠皮下移植瘤模型，喂服吲哚美辛3 mg/(kg·d)共4周，隔日测瘤结节体积及鼠重，评价吲哚美辛的抑瘤效果。结果：吲哚美辛作用于结肠癌HCT116和SW480细胞48 h后，细胞的生长均受到明显抑制，呈剂量依赖效应，IC50分别为 (318.2±12.7) μmol/L和 (701.4±29.5) μmol/L；吲哚美辛显著减慢裸鼠皮下移植瘤的生长，用药4周后抑瘤率达44.6%，未见明显毒性反应。结论：吲哚美辛能抑制不表达环氧合酶的人结肠癌细胞（HCT116和SW480）生长，间接说明其抗癌作用不完全依赖环氧合酶途径，还存在其它的可能机制。     

胃上部癌经腹根治术的临床观察

目的探讨经腹根治胃上部癌的手术适应症及对本术式的评价。方法回顾总结1994-2004利用管型消化道吻合器经腹根治手术的125例胃上部癌的临床资料。结果经腹手术创伤小,出血少,并发症少,安全性较好,但亦有局限性。结论经腹手术路径的选择主要应根据肿瘤的具体情况而定,合理掌握指征,对于非贲门上部癌、食管侵犯≤2cm者以及BormannⅠ、Ⅱ型的胃上部癌应优先考虑经腹手术。     

Benign osteoblastoma of the occipital bone: Case report and literature review

We present a case of benign osteoblastoma of the occipital bone. Benign osteoblastoma is an uncommon primary bone tumor, which usually involves the vertebrae and the long bones. This tumor rarely develops in the calvaria, showing a preference for the temporal and frontal bones when it does. To the best of our knowledge, this case is only the eighth reported case of benign osteoblastoma confined to the occipital bone. A 20‐year‐old male presented with a mild tender mass lesion of the occipital area, just below the lambda. Plain X‐ray films and CT scans demonstrated an osteolytic mass surrounded by the sclerotic rim within the diploic space. MRI proved to be effective for the evaluation of the intracranial and intraosseous extensions of the tumor. However, it was very difficult to formulate a differential diagnosis against other osteoblastic tumors, or osteoid osteoma, in view of its radiological appearance. The final diagnosis was obtained by careful consideration of the histopathological characteristics of the tumor combined with its clinical and radiological features. Although generally regarded as benign, a complete resection is preferred over conventional curettage as this can guard against possible recurrence and malignant transformation.     

Malignant Rhabdoid Tumor of the Breast: A Case Report

A 66-year-old woman time of 10 days. One month after radicalmastectomy, there was local recurrence, followed by multiplepulmonary metastases, and the patient died of respiratory failure5 months after surgery. The gray-white-colored tumor measured13x12x;10 cm, and its border was well defined. The tumor wascomposed of diffusely growing round or polygonal cells withvesicular nuclei, prominent nucleoli, and ample cytoplasm containingeosinophilic inclusions. Lymph node involvement was widespread.Both vimentin and keratin were clearly demonstrated by immunohistochemicalstaining. Ultrastructural studies revealed that the MRT cellscontained cytoplasmic whorls of intermediate filaments.