探讨原发性软组织淋巴瘤的临床病理特征。
To explore the clinicopathologic features of primary lymphoma in soft tissue.
目的探讨肝黏膜相关淋巴组织淋巴瘤的临床病理特征。
Purpose To investigate the clinicopathological characteristics of mucosa associated lymphoid tissue lymphoma in the liver.
方法对17例病理确诊胃粘膜相关淋巴组织淋巴瘤患者内镜下表现进行回顾性分析。
Methods endoscopic features of 17cases with gastric mucosa associated lymphoid tissue lymphoma diagnosed by pathology were reviewed and analyzed.
目的探讨胃粘膜相关淋巴组织淋巴瘤的临床、内镜及病理特征，以提高早期诊断水平。
Objective to investigate the features of clinical, endoscopic and pathologic of gastric mucosa associated lymphoid tissue lymphoma in order to improve diagnostic level in the early stage.
方法分析手术切除并经病理证实的78例胃粘膜相关淋巴组织淋巴瘤患者的临床、内镜和病理资料。
Methods Clinical, endoscopic and histological data of 78 patients with gastric mucosa associated lymphoid tissue lymphoma diagnosed surgically and pathologically were reviewed and analyzed.
结论：对于具备手术条件的胃黏膜相关淋巴组织淋巴瘤患者应尽早行手术治疗，可提高患者的生存率。
Conclusions: Early surgical treatment can improve the survival rate of patients with gastric mucosa-associated lymphoid tissue lymphoma.
目的：研究冬凌草甲素诱导人组织淋巴瘤u 937细胞凋亡的机制及ERK激酶在凋亡过程中的作用。
Objective: to study the mechanisms of oridonin-induced U937 cell apoptosis, and to examine the role of ERK MAPK.
那组织为白血病和淋巴瘤研究筹集资金。
The organization raises money for leukemia and lymphoma research.
目的：探讨胃粘膜相关淋巴组织(MALT)淋巴瘤的病理特征、临床诊断和治疗。
Objective: To study the pathologic features, clinical diagnosis and treatment of gastric mucosa associated lymphoid tissue (MALT) lymphoma.
目的：探讨胃黏膜相关淋巴组织(MALT)淋巴瘤的内镜特征。
Objective: To study the endoscopic features of gastric mucosa associated lymphoid tissue (MALT) lymphoma.
目的提高对胃粘膜相关淋巴组织(MALT)淋巴瘤的认识和诊疗水平。
Objective To improve the knowledge and diagnosis and treat level of gastric mucosa associated lymphoid tissue (MALT) lymphoma.
累及眼眶的恶性淋巴瘤的最常见的细胞学类型是组织细胞和淋巴细胞型。
The most common cytologic forms of malignant lymphoma involving the orbit are the histiocytic and lymphocytic types.
结论：本瘤是累及皮下脂肪组织的，具有独特临床病理特征的特殊类型的皮肤淋巴瘤。
Conclusions This tumor is a special type of skin lymphoma involving subcutaneous fat tissue and special clinicopathological features.
结果NK/T淋巴瘤组织结构特点为多形性淋巴细胞增生，大片的凝固性坏死和血管浸润，免疫组化表达CD3、CD45和CD56阳性。
Results Proliferation of pleomorphic lymphocyte, coagulation necrosis of massive tissue and vaso-infiltration were showed in the NK/T lymphoma; tumor cells were positive for CD3, CD45 and CD56.
目的：运用组织芯片及常规病理切片检测活化的细胞毒性细胞在各型淋巴瘤中的表达分布情况，为临床治疗和判断预后提供依据。
Objective: To detect the expression and distribution of activated cytotoxic cells in types of lymphoma with tissue microarray, and provide evidences for clinical treatment and prognosis.
目的：探讨原发性肝黏膜相关淋巴组织(MALT)淋巴瘤的临床病理特征及治疗方法。
Objective: To investigate clinical and pathological features of primary hepatic lymphoma of mucosa-associated lymphoid tissue (MALT) and explore the methods for its treatment.
目的研究LMP1基因和蛋白在结外鼻型NK/T细胞淋巴瘤移植瘤模型传代组织中的稳定性和变异性。
Objective To assess the stability and variability of the LMP1 gene and protein in nude-mice transplanted tumor models of extranodal nasal type NK/T-cell lymphoma.
软组织肉瘤的组织起源和淋巴瘤的分类是重点中的难点。
Tissue origin of parenchyma tissue sarcoma and sorts of malignancy lymphoma are nodus.
并将各亚型与皮肤B细胞性假性淋巴瘤及组织细胞性淋巴瘤进行鉴别。
Differential diagnosis of CBCL between cutaneous B-cell pseudolymphoma and cutaneous genuine histiocytic lymphoma is discussed.
目的探讨淋巴组织细胞型间变性大细胞淋巴瘤（ALCL-LH）的病理形态学特点、诊断及鉴别诊断。
Objective To study the clinicopathological characteristics, diagnosis, differential diagnosis of anaplastic large cell lymphoma, lymphohistiocytic variant (ALCL-LH).
皮损组织病理及免疫组化标记确诊为原发性皮肤CD 30 +间变性大细胞淋巴瘤。
The diagnosis of primary cutaneous CD30 + anaplastic large cell lymphoma was established by means of histopathology and immunohistochemistry.
该病人七年前患何杰金淋巴瘤，所以医生在治疗前把她的一部分卵巢组织取出，并且把它们冷藏起来。
The patient developed Hodgkin's lymphoma seven years ago, so doctors removed and froze samples of her ovarian tissue before beginning cancer treatment.
目的 ：探讨胃粘膜相关淋巴组织 （MALT）淋巴瘤的病理特征、临床诊断和治疗。
Objective To study the clinicopathologic features of mucosa-associated lymphoid tissue lymphoma(MALToma) of intestines.
据NCI称，系统性alcl是一种罕见的恶性肿瘤(非霍奇金淋巴瘤)，可见于身体多个部位，包括淋巴结、皮肤、骨骼、软组织、肺或肝。
Systemic ALCL is a rare malignant tumor (non-Hodgkin lymphoma) that may appear in several parts of the body including the lymph nodes, skin, bones, soft tissue, lungs or liver, according to the NCI.
目的探讨诊断和鉴别诊断眼附属器黏膜相关淋巴组织(malt)型淋巴瘤和淋巴组织反应性增生的方法。
Objective To study the methods of differential diagnosis between mucosa-associated lymphoid tissue (MALT) type lymphoma and reactive lymphoid hyperplasia in ocular adnexa.
方法回顾性分析我院1986 ~ 1996年收治的10例真性组织细胞型淋巴瘤的临床和病理资料，并复习文献。
Methods The clinical and pathological data of 10 true histiocytic lymphoma patients admitted between 1986 and 1996 to our hospital was retrospectively reviewed.
与以前的报道相比，我们的结果表明胃malt淋巴瘤在诊断时组织学转化为大细胞淋巴瘤的比例更高。
Our results for gastric MALT lymphoma show a much higher rate of histological transformation to large-cell lymphoma at diagnosis than previously reported.
通常分为两型︰霍奇金氏病和非霍奇金氏淋巴瘤，每一型又可进一步细分。这两种类型都需要靠活组织检查来诊断，常取自淋巴结。
The two major types, Hodgkin disease and non-Hodgkin lymphoma, each have several subtypes. Diagnosis of either type requires Biopsy, usually from the lymph nodes.
方法获取10例淋巴瘤患者的活检淋巴结组织，以CGH技术检测淋巴瘤基因组d NA拷贝数的变化。
Methods Biopsy specimens of lymph nodes were obtained from 10 cases of lymphoma patients. The changes of DNA copies number (e. g. deletion and amplification) were detected using the CGH technique.
目的：对肾脏原发性淋巴瘤的临床病理特点、组织学起源、诊断及鉴别诊断等进行初步探讨。
Purpose to investigate the clinical pathologic characteristics and to probe into the histogenesis, diagnoses, and differential diagnoses of the primary lymphoma of the kidney.
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