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febrile tropical splenomegaly相关的网络例句

查询词典 febrile tropical splenomegaly

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Results Of these 26 patients with IM, male was more than female with average age of 36.6 years old. Liver function of 85 percent patients were abnormal, while 65% splenomegaly, 81% skin rash, 100%EB virus-IgM positive and 50% hepatomegaly.

结果 本组患者中男性多于女性、成人多于儿童,平均年龄36.6岁。65%有脾大,50%有肝大,81%有皮疹,85%有肝功能异常,100%的EB病毒IgM抗体阳性。

Liver function of 85 percent patients were abnormal, while 65% splenomegaly, 81% skin rash, 100%eb virus-igm positive and 50% hepatomegaly.

结果 本组患者中男性多于女性、成人多于儿童,平均年龄36.6岁。65%有脾大,50%有肝大,81%有皮疹,85%有肝功能异常,100%的eb病毒igm抗体阳性。

Results plasmodium falciparum were detected from smears of 65 baby and infant falciparum malaria cases. clinical manifestations were fever (100%), vomiting in 32 cases (49.2%), diarrhea in 23 cases (36.9%), cough in 27 cases (41.5%), convulsions in 12 cases (18.5%), disturbance of consciousness in 19 cases (29. 1%), anemia in 52 cases (80.0%), splenomegaly in 46 cases (71.6%), hepatomegaly in 41 cases (63.1%), meningeal thorn forward levy in 19 cases (29. l%). sixty patients cured after treated wth artesunate and 5 cases died.

结果 65例恶性疟疾婴幼儿的血涂片均见到恶性疟原虫;临床表现以发热(100%),呕吐32例(49.2%),腹泻23例(36.9%),咳嗽27例(41.5%),抽搐12例(18.5%),意识障碍19例(29.1%),贫血52例(80.0 %),脾肿大46例(71.6%),肝肿大41例(63.1%),脑膜刺激征19例(29.1%)。65例均接受青蒿琥酯抗疟的综合治疗,治愈60例,死亡5例。

Methods Percutaneous liver biopsy guided by ultrasound was carried out in 37 clinical diagnosed infants with IHS. All the infants were presented with jaundice, hepatomegaly, splenomegaly or liver function damage.

方法按全国小儿病毒性肝炎防治座谈会制定的标准诊断为IHS的患儿37例,全部病例有黄疸、肝大或肝脾大及肝功能损害。

The main manifestations of typical IAHS are continuing hyperpyrexia, hepatomegaly and splenomegaly; laboratory findings are decrease of white blood count, hemoglobin or blood platelet, hypertriglyceridemia, liver disfunction, elevation of serum ferritin, and the hemophagocytes in bone marrow.

典型的儿童感染相关性噬血细胞综合征临床以持续高热、肝脾大为主要表现,实验室检查以白细胞计数、血红蛋白及血小板中两系或三系减少、低纤维蛋白血症、高三酰甘油血症、肝功能异常及血清铁蛋白升高,骨髓找到噬血细胞为主要特点。

Common clinical characteristics included marked neoplastic lymphocytosis, systemic lymphadenopathy, splenomegaly, and bone marrow involvement.

这5例共同的临床特征包括显著的肿瘤性淋巴细胞增生,系统性的淋巴结病、脾肿大及骨髓受累。

Either of them predisposes the spleen to torsion.1 Acquired wandering spleen can also arise in multiparous women during pregnancy when ligamentous laxity occurs owing to hormonal changes.2 Chronic torsion can cause splenomegaly.

腹痛由脾脏包膜的收缩或局部腹膜炎引起。此外,尚可见贫血、白细胞计数增多,乳酸脱氢酶升高等。影像检查主要包括超声、CT、核素成像、血管造影。

The diagnosis of ITP is made clinically by exclusion of other causes of thrombocytopenia, the absence of splenomegaly, and the finding of normal or increased megakaryopoiesis on bone marrow examination. The nonimmune thrombocytopenia is caused by some nonimmune factors, such as acute leukemia, hypersplenism and post-chemotherapic bone marrow suppression.

特发性血小板减少性紫癜的诊断仍只是一种排除性的临床诊断,其国内诊断标准为多次化验检查血小板计数减少,脾脏不增大或仅轻度增大,骨髓检查巨核细胞数增多或正常,有成熟障碍,并且具备以下五点中的任何一点:泼尼松治疗有效,切脾治疗有效,血小板相关抗体增多,血小板相关补体增多,血小板寿命测定缩短,同时应排除继发性血小板减少症。

Symptoms of splenomegaly and hypersplenism were obviously relieved. Relevant laboratory detections revealed distinct redintegration of platelets, common serous bilirubin, serous protein, PT and SGPT.

脾肿大及脾功能亢进症状得到明显缓解,相关实验室检查包括:血小板、血清总胆红素、血清蛋白、PT、SGPT等均有明显恢复。

One of the most common findings with portal hypertension is splenomegaly , as seen here.

门脉高压最常见的临床表现为脾肿大。

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