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marrow biopsy
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  骨髓活检
     Methods: Collect marrow biopsy samples of 45 childhood acute leukemia(including 25 first diagnosed children and 20 remission children) , and 20 contrasts.
     方法:收集儿童急性白血病骨髓活检标本45例(包括初诊组25例和缓解组20例),以及对照组非白血病患儿骨髓活检标本20例。
短句来源
     Results 1. Bone marrow biopsy has high successful rate of obtaining biopsy samples, the rate of failure was only 3.39%, and the rate of failure for puncture biopsy was 11.72%.
     结果①骨髓活检取材成功率高,失败率仅占3.39%,而穿刺失败率为11.72%。
短句来源
     A Preliminary Study on Expression of Adhesion Molecule LFA-1/ICAM-1 on Marrow Biopsy Section in Acute Myeloid Leukemia and Its Clinical Implication
     急性髓系白血病骨髓活检切片中粘附分子LFA-1/ICAM-1表达及其临床意义的初步研究
短句来源
     Methods:Bone marrow biopsy plastic embedded section stained by H Giemsa E,PAS and Alcin blue.
     方法 :骨髓活检塑料包埋切片 ,H- Gmiesa- E,Gomori,PAS,Alcin blue染色。
短句来源
     Pathological diagnosis of hematopathy by bone marrow biopsy: an analysis of 75 cases
     75例血液病骨髓活检病理诊断分析
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  “marrow biopsy”译为未确定词的双语例句
     Results After bone marrow biopsy and pathological analyses,the final diagnosis was 2 cases of CIMF,15 AA,9 MDS,3 PCM,2 ALL,1 CML,22 anemia with unknown causes,16 pancytopenia,4 leukopenia and 1 unknown fever.
     其中CIMF2例、AA15例、MDS9例、PCM3例、ALL2例、CML1例、贫血待查22例、全血细胞减少16例、白细胞减少4例、发热待查1例,确诊率61.33%。
短句来源
     The results of marrow biopsy in 59 cases showed that 30 had the dysmorphic cell ( 50.8 %), and 29 ALIP ( 49.2 %).
     59例行骨髓病理学检查3系不同程度病态造血30例(50.8%),粒系幼稚前体细胞异常定位(ALIP)29例(49.2%)。
短句来源
     The results of marrow biopsy in 118 cases showed that 60 had the dysmorphic cell(50.8%),and 58 ALIP(49.2%).
     118例行骨髓病理学检查:3系不同程度病态造血60例(50.8%),粒系幼稚前体细胞异常定位(ALIP)58例(49.2%)。
短句来源
     The results showed that the agreement of diagnosis between bone marrow biopsy and aspira- tion smear was 72. 1%, and disagreement 27. 9%;
     结果表明,活检切片和穿刺涂片诊断一致者达72.1%,不一致27.9%;
短句来源
     the confirmed diagnosis rate was 88. 5% in aspira- tion smear, and 81. 7% in bone marrow biopsy. It would reach 99% if both of the two techniques were used.
     骨髓穿刺涂片确诊率88.5%,活检切片确诊率81.7%,二项联合应用确诊率99%。
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  相似匹配句对
     Histopathological Diagnosis of Leukemias by Bone Marrow Biopsy
     白血病骨髓穿刺活检的病理诊断(附128例病理分析)
短句来源
     The diagnosis mainly depends on marrow aspirate and biopsy.
     多发性骨髓瘤临床表现多样,极易漏诊和误诊,骨髓细胞学检查是确诊MM的主要指标之一。
短句来源
     Bone marrow was normal.
     骨髓造血细胞无明显异常。
短句来源
     Repression of marrow was light.
     毒副反应主要为消化道反应 ,骨髓抑制较轻。
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  marrow biopsy
Specific chemotherapy was followed by both clinical improvement of the polyradiculopathy and complete remission on a second bone-marrow biopsy.
      
Aberrant mast cell surface marker expression can be detected in the bone marrow aspirate by .ow cytometry, even in patients with limited disease that lacks histopathologically detectable aggregates of mast cells in bone marrow biopsy sections.
      
Is it justified to perform a bone marrow biopsy examination in sustained erythrocytosis
      
No infiltration by atypical plasma cells could be documented in the bone marrow biopsy and aspirate.
      
He was also anemic and was diagnosed with acute myeloid leukemia (AML) after a bone marrow biopsy.
      
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After the investigation of 1,000 bone marrow biopsies, using the six staining procedures in every instance, i.e.,H.E., Giemsa,reticulin,collagen, PAS and Prussian blue reaction, the authors discuss the following ten aspects: the percentage of cellularity, the granulocytc to nucleated red blood cell ratio ( M : E ratio ) , the process of matura-tion of hematopoietic cells, the content of plasma cells, the content of megakaryocytes, edema and hemorrhage, the modification of reticulin fibres, the modification...

After the investigation of 1,000 bone marrow biopsies, using the six staining procedures in every instance, i.e.,H.E., Giemsa,reticulin,collagen, PAS and Prussian blue reaction, the authors discuss the following ten aspects: the percentage of cellularity, the granulocytc to nucleated red blood cell ratio ( M : E ratio ) , the process of matura-tion of hematopoietic cells, the content of plasma cells, the content of megakaryocytes, edema and hemorrhage, the modification of reticulin fibres, the modification of collagen fibres,the modification of bone trabeculae, and the evaluation of iron stores. In addition, some criteria for the basic lesions under microscopic observation are proposed.

根据1,000例骨髓穿刺活检及近二年来采用H.E.、姬姆萨、网状纤维、胶原纤维、PAS及铁反应6种染色后的工作体会,对一些基本病变的观察作了分析和探讨.共讨论了10个问题:如造血组织与脂肪组织的比例、粒细胞与红细胞的比例、造血细胞成熟过程、浆细胞含量、巨核细胞含量、骨髓水肿与出血、网状纤维的变化、胶原纤维的变化、骨小梁变化及骨髓中贮存铁的观察等,并对其中某些内容提出了自己镜检的常规标准.

From 1955 to 1980,50 cases of primary myelofibrosis were treated in 13 hospitalsof Shanghai,with 48 cases confirmed by bone marrow biopsy and 2 by splenic evidenceof extramedullary hemopoiesis.Among the 50 cases,39 were male and 11 female,themedian age being 48.5.The common symptoms were fatigue(70%)and dizziness(58%).Splenomegaly was the most prominent sign(47.7%).Peripheral blood smears revealedtear-drop shaped erythrocytes in 11 cases,nucleated erythrocytes in 36 and younggranulocytes in 37.Myeloid...

From 1955 to 1980,50 cases of primary myelofibrosis were treated in 13 hospitalsof Shanghai,with 48 cases confirmed by bone marrow biopsy and 2 by splenic evidenceof extramedullary hemopoiesis.Among the 50 cases,39 were male and 11 female,themedian age being 48.5.The common symptoms were fatigue(70%)and dizziness(58%).Splenomegaly was the most prominent sign(47.7%).Peripheral blood smears revealedtear-drop shaped erythrocytes in 11 cases,nucleated erythrocytes in 36 and younggranulocytes in 37.Myeloid atrophy and fibrosis were the common histological patternsseen in bone marrow sections.The diagnosis,treatment by traditional and westernmedicine and the interrelationship between primary myclofibrosis and myeloproliferativedisorder were discussed.

本文总结1955~1980年的原发性骨髓纤维化共50例,其中48例经骨髓活检证实,另2例经脾脏病理检查证实有髓外造血而确诊.本组病例男性39例,女性11例。常见症状为乏力、头昏。脾脏肿大为最突出的体征,有5例在诊断本病前,已做了脾脏切除术。周围血有11例出现泪滴状红细胞,36例出现幼红细胞,有37例出现幼稚粒细胞。骨髓病理检查以骨髓萎缩与纤维化型最为常见。怍者对诊断、鉴别诊断、中西医结合治疗,以及本病与骨髓增殖性疾病间的关系作了讨论。

This article presents a olinicopathologic analysis of 28 pathologically confirmed cases of malignant histiocytosis. The main pathologic findings were infiltration of malignant histiocytes in the spleen (28 cases), liver (25), lymph nodes (24), and bone marrow (20). And involvement of the lung was found in 19 cases, kidney 14, and heart 13. The destruction of normal architectures of the spleen and lymph node had been severe. The malignant histiocytes invaded chiefly into the splenic red pulps, hepatic sinusoids,...

This article presents a olinicopathologic analysis of 28 pathologically confirmed cases of malignant histiocytosis. The main pathologic findings were infiltration of malignant histiocytes in the spleen (28 cases), liver (25), lymph nodes (24), and bone marrow (20). And involvement of the lung was found in 19 cases, kidney 14, and heart 13. The destruction of normal architectures of the spleen and lymph node had been severe. The malignant histiocytes invaded chiefly into the splenic red pulps, hepatic sinusoids, sinuses and pulps of lymph nodes, the wall of pulmonary alveoli and myocardial interstitial tissues. Autopsy disclosed ascites in 22, pleural effusion in 17, and pericardial effusion in 13 cases. Only 14 out of the 22 oases were found to hava ascites, and no pleural or pericardial effusion was detected in any of them beforo death. Clinically, fever was present in all the 28 cases. Besides splenomegaly, hepatomegaly and enlargement of lymph nodes, jaundice and pulmonary rales were also common signs. The liver function was impaired when the malignant infiltration in the liver and degenerative changes of hepatic cells were distinctive. In those cases with bone marrow involvement, the marrow puncture smears were positive in 8 out of 15 cases, and marrow biopsy positive in 3 out of 4. Eight of 9 cases of pulmonary infiltration as shown by chest films were confirmed by autopsy. It is concluded that the cardinal manifestations of malignant histiooytosis may serve as a clue to its diagnosis, and yet repeated bone marrow puncture and biopsy from different suspected parts are indispensable to the establishment of diagnosis. Peripheral lymph node biopsy should be made liberally. Liver puncture biopsy is dangerous and non-rewarding. Oytological study of pleural or peritoneal effusion, X-ray film of the chest, and radioisotope scanning of the liver are all of valuable diagnostic aids.

本文报告28例恶性组织细胞病,全部病例均经尸解证实。病变以浸润为主,常侵犯脾、肝、淋巴结、骨髓和胸腹等浆膜,累及肺、肾及心脏者也不少。临床上每例均有发热,除肝、脾、淋巴结肿大外,黄疸及肺部啰音也属常见。本病以累及多脏器为特点。病灶分布缺乏规律性。同一器官内恶组细胞浸润的程度也缺少均匀性,可散在浸润,也可聚集成粟粒样或肉芽肿样病灶。本病的诊断应该是综合性的:临床表现结合多部位骨髓穿刺和活检仍为主要诊断手段。应尽可能争取淋巴结活检。肝穿刺具有危险性而阳性率不高。浆膜腔积液的细胞学检查对确立本病的诊断有所帮助。

 
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