共查询到19条相似文献,搜索用时 105 毫秒
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组织工程滑膜化肌健移植的实验研究 总被引:1,自引:0,他引:1
目的:观察用组织工程学方法形成的滑膜化肌鞘内移植后的形态变化。方法:在30只兔后肢的第2践腱鞘内移植入滑膜化肌腱段替代趾深屈肌腱。在不同时相点观察移植肌腱的愈合状况,粘连程度及屈趾功能。结果:滑膜化肌腱与受体肌腱之间形成了牢固的纤维性结合,粘连轻。结论:用组织工程学方法构建的滑膜化肌腱可以作为一种新的肌腱移植材料。 相似文献
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在解剖教学过程中,于一男性成人标本上,发现罕见的副长屈肌1例,现报道如下。副长屈肌紧贴于长屈肌下部的后外方,距内踝8cm处起始于胫后血管神经束外侧筋膜及小腿深筋膜,肌腹长5.5cm,宽1.5cm,厚0.3cm,肌腱长11cm。肌腹向下位于胫后血管神经束深面移行为细长的肌腱通过屈肌支持带深面的踝管至足底,沿长屈肌腱外侧共同向前,经趾长屈肌腱深面,并与其交叉,但无腱束合并。副长屈肌的肌腱继续沿足底向前,腱束与收肌斜头肌腱合并,共同止于趾第一节趾骨底。此外、趾长屈肌腱五条,经内踝后方和分… 相似文献
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对新鲜成人足61只(左38只右23只)用剥离法自内踝上5.0cm前内侧到足底直至足趾末端,逐层剥离,剖开踝管,显露胫骨后肌腱,趾长屈肌腱,胫后静脉,胫后动脉,胫神经及(足母)长屈肌腱。然后剥去跖腱膜,趾短屈肌,(足母)长展肌,小趾展肌及结缔组织等。结果如下:1.单支型:在足底内侧(足母)长屈肌腱与趾长屈肌腱交叉后,于第一楔骨近端中部,(足母)长屈肌腱发出一束与本身几乎等粗的肌纤维来,由此向前外方向斜行,在第一、二楔骨之间中部,与尚未分支的趾长屈肌膜会合,参与趾长屈肌腱的组成,分布到各趾去。本型计18例,占29.5%。2.双支型: 相似文献
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Noboru Tanaka M.D. D.D.S. Takeshi Asao 《Virchows Archiv : an international journal of pathology》1978,379(3):261-268
Summary A huge tumor mass arising from the soft tissue of the nape of the neck, which histologically resembled chordoma is reported. This case had a history of over 30 years after onset at around 37 years of age. With frequent recurrence and re-excision after en bloc radical resection, performed at 47 years of age, this female patient expired at the age of 66, 20 years after the first radical operation.At operation, the mass was found to be firmly attached to the dorsal soft tissue. There was no connection with any bony structure, such as the cervical vertebrae or skull. Chordoma-like histological features were unchanged throughout the next 20 years. This unusual malignant neoplasm appears to correspond to the chordoid tumor or chordoid sarcoma of soft tissue, a term coined by F.W. Stewart in 1948. Alternatively the name chondroid chordoma used by Heffelfinger, Dahlin and others may be employed. 相似文献
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外鼻软组织厚度的测量及其临床意义 总被引:9,自引:0,他引:9
目的为隆鼻术提供国人的外鼻软组织厚度的解剖学资料.方法20具经常规防腐处理的成年尸体标本,将外鼻分为眉间点、鼻根点、鼻背点、鼻尖上点、鼻尖点、鼻尖下点,鼻小柱前点和鼻翼顶点,进行各点外鼻软组织厚度测量.同时测量鼻翼软骨外脚距鼻翼缘的距离,鼻中隔软骨前端距鼻尖点和鼻中隔软骨下缘距鼻下点的距离.结果眉间点软组织厚度(4.42±0.86)mm,鼻根点(4.42±0.99)mm,鼻背点(2.67±0.87)mm,鼻尖上点(4.60±0.98)mm,鼻尖点(4.03±1.56)mm,鼻尖下点(2.67±0.62)mm,鼻小柱前点(2.41±0.57)mm,鼻翼软骨外脚距鼻翼缘的距离,高点(3.14±0.51)mm,中点(4.79±2.33)mm,下点(11.92±2.68)mm.鼻中隔软骨前端距离皮肤表面(4.94±2.50)mm,鼻中隔软骨距鼻下点距离(7.59±2.18)mm.鼻中线各点软组织厚度存在明显差异,其中以鼻背点和鼻尖下点为最薄,鼻尖点较厚,但个体变异大.结论了解外鼻被覆软组织的分布不均,有利于改善隆鼻手术的效果和避免手术并发症. 相似文献
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Yangyang Ma Jicui Zheng Shaobao Yang Haitao Zhu Kuiran Dong Xianmin Xiao Lian Chen 《International journal of clinical and experimental pathology》2015,8(10):13584-13589
Melanotic neuroectodermal tumor of infancy is rare. Only 3 cases have been reported in the soft tissue of the extremities up to date. It has a typically biphasic feature in morphology. Epithelial and melanotic markers are positive in the epitheliod cells and neuron-specific enolase or synaptophysin is positive in the small blue round cells in immunohistochemistry. Radical resection and close follow-up is the treatment strategy in general situation. Here we report one case of MNTI in the upper extremity with review of the literature. This is the first case of MNTI in the forearm. 相似文献
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目的 探讨软组织网状神经束膜瘤的临床病理特点和鉴别诊断。方法 对1例网状神经束膜瘤进行光镜、免疫组化和电镜观察。结果 肿瘤位于左尺骨远端软组织。长而纤细的肿瘤细胞突起网状、格子样、吻合状生长,排列于黏液水肿性、纤维性和胶原化的背景中,细胞纺锤状,胞质弱嗜酸性,核星形,无核分裂象。免疫表型:肿瘤细胞EMA和Vim阳性。电镜:肿瘤细胞可见长形的纤细的胞质突起,突起上有较多的吞饮小泡。结论网状神经束膜瘤是软组织神经束膜瘤的富有特征性的亚型,预后良好,诊断主要依靠常规病理、免疫组化和超微结构的综合观察。 相似文献
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AIMS: Ossifying fibromyxoid tumour is a rare lesion that generally occurs in the soft tissues of proximal limbs/girdle, or head and neck. Histologically, it usually consists of bland, mitotically inactive, S100+ cells in a fibromyxoid matrix with a characteristic peripheral ossification. However, we present two cases that deviated from this pattern. MATERIAL AND METHODS: One tumour, which was removed from the axilla of a 55-year-old female, was unusual in its large size (120 mm in diameter) and in its restriction of bone formation to its central zones. The other tumour, which occurred in a 62-year-old female, was remarkable in its acral location on the hand and high mitotic activity (four mitoses per high-power field). These features caused concern and follow-up of the patients was recommended. So far there have been no recurrences (25 and 18 months after surgery, respectively). An additional previously undescribed feature was the presence of fibronexus-like structures by electron microscopy in the second case. However, a myofibroblastic phenotype was not supported by the immunohistochemical findings. CONCLUSION: Though a distinct entity, ossifying fibromyxoid tumour may exhibit a wider clinicopathological spectrum than generally recognized. 相似文献
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Application of markers in the diagnosis of soft tissue tumours 总被引:2,自引:0,他引:2
In this review we describe the application of markers which are useful for the diagnosis of soft tissue tumours in paraffin sections. Detection of intermediate filament proteins appears to be most useful for first screening of these neoplasms because all, except neuroblastomas, express vimentin; cytokeratin is expressed in synovial sarcomas, epithelioid sarcomas and mesotheliomas; desmin in myogenic tumours and glial fibrillary acidic protein in astrocytomas and gliomas. Tissue-specific markers are: factor VIII--related antigen-endothelial cells; myoglobulin and skeletal muscle myosin--skeletal muscle cells; neuron specific enolase--neurons and cells of the APUD systems; and leukocyte-associated antigen--leukocytes. Markers which are present in a variety of cell types and therefore do not serve as tissue-specific markers are; S-100 proteins, alpha-1-antichymotrypsin, creatine kinase M and actin. The S-100 antigens have been detected in melanomas, granular cell tumours, chondrosarcomas and in some schwannomas and liposarcomas. Alpha-1-antichymotrypsin has been found in fibrohistiocytic and 'true' histiocytic tumours and creatine kinase M and actin in myogenic tumours. No specific markers have, as yet, been described for fibrosarcomas, Ewing's sarcomas and hemangiopericytomas. 相似文献
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Alexander C. L. Chan Theo G. Lorentz Lily Ma Annie N. Y. Cheung Simon K. M. Tse 《Diagnostic cytopathology》1993,9(5):576-580
A 99-yr-old Chinese woman with cutaneous malakoplakia and concomitant urinary tract infection was reported. The patient presented with an ulcerated right lower quadrant mass and computerized tomography showed that it was limited to the skin and subcutaneous tissue with no extension to the pelvic or abdominal structures. The patient also suffered from urinary tract infection and was treated with oral norfloxacin. The ulcerated subcutaneous mass disappeared on follow-up visit 6 months after presentation. The cytologic (fine-needle aspiration), histologic (trucut biopsy) and ultrastructural features of cutaneous malakoplakia were described. The possible usefulness of fine-needle aspiration in the diagnosis of this condition was discussed. 相似文献