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：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.
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.
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.
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.
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.
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).
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.
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.
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.
淋巴结被小的淋巴瘤细胞浸润，浸润已经延伸到淋巴结的囊，浸润到周围的脂肪组织。
The lymph node is replaced by an infiltrate of small (mature-appearing) neoplastic lymphocytes, and the infiltrate extends through the capsule of the lymph node and into the surrounding fat.
组织学，病变特征性地表现为淋巴样细胞夹杂着大细胞弥漫浸润，高度可疑淋巴瘤。
Histologically, they are characterized by a dense lymphoid infiltrate with admixed large cells that is often suspicious for lymphoma.
方法对8例淋巴结及皮肤的间变性大细胞淋巴瘤组织学观察及免疫组化染色，并复习相关临床资料。
Methods: Histological and immunohistochemical methods were used to analyse 8 cases of ALCL located in the skin and in the lymphoid node, and the correlated clinical data were reviewed.
组织学上多形T细胞淋巴瘤5例，B细胞淋巴瘤4例，其中淋巴浆细胞样型和小细胞性各2例。
Histologically, 5 of 9 cases were polymorphoral(peripheral) T cell lymphoma, in the rest 4 of B cell lymphoma, 2 were lymphoplasmacytoid and the other 2 were small cell type.
组织学上多形T细胞淋巴瘤5例，B细胞淋巴瘤4例，其中淋巴浆细胞样型和小细胞性各2例。
Histologically, 5 of 9 cases were polymorphoral(peripheral) T cell lymphoma, in the rest 4 of B cell lymphoma, 2 were lymphoplasmacytoid and the other 2 were small cell type.
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