Results Multisystem were damaged,such as peripheral, hepatomegaly, splenomegaly,lymphadenectasis, endocrinopathy, skin changes, edema and plastcytosis in bone marrow are all more common damages, all of them peripheral neuropathy is the most characteristic manifestation.

結(jié)果本病是累及多系統(tǒng)的疾病wwwjizzjizzjizz，以周?chē)窠?jīng)病最具有特征性屌屄黄色视频，肝亚洲欧美一区日韩一区a国产传媒、脾和淋巴結(jié)腫大，內(nèi)分泌的病變看美曰欧国AV毛片，皮膚改變人人超碰喷潮人人，水腫及骨髓漿細(xì)胞增多比較常見(jiàn)。

Results In the medium and high dose F0 groups, it was observed that the atrophy and incrassation of seminiferous tubule, decrease of spermatogenesis, hyperplasia of interstitial tissue, especially in high dose groups spermatozoon abnormality and nucleolus concentration in the rats testis after DU ingestion for 14 months. The changes became more severe with the prolongation of DU ingestion. Such changes occurred in filial rats (F1) after DC ingestion for 5 months. In the medium and high dose F0 groups, it was observed that a little atrophy of kidney glomerulus, hyperplasia of interstitial tissue after DC ingestion for 14 months, and kidney glomerulus fibrosis happened after DC ingestion for 20 months, such changes occurred in filial rats (F1) after DC ingestion for 5 months In the medium and high dose F0 groups, splenic germinal center and periarterial lymphatic sheaths were hyperplasia , companies with lymphopoiesis after DC ingestion for 7 months, splenic white pulp became more small and sparse after DC ingestion for 20 months.

結(jié)果 F0代的中中文自拍日韩视频在线、高劑量組大鼠攝入貧鈾14個(gè)月后可見(jiàn)雄性的精曲小管萎縮免费欧美性交，管壁增厚呈空虛網(wǎng)狀，生精細(xì)胞層次減少黄色网站网址大全欧美，間質(zhì)細(xì)胞增生日本h片在线播放免费网站，但仍見(jiàn)有精子生成；高劑量組可見(jiàn)到精子呈異型性改變日本www.XⅩxx，細(xì)胞核濃縮深染久久天堂网av，且隨著攝入時(shí)間延長(zhǎng)改變愈趨明顯；F1代大鼠攝入貧鈾5個(gè)月后就有上述改變且更為嚴(yán)重日韩中文视频。F0代中一级a片黄片夫妻免费看、高劑量組大鼠攝入貧鈾14個(gè)月后腎小球輕度萎縮，間質(zhì)增生明顯亚洲偷自拍国综合第一页手机，20個(gè)月時(shí)腎小球萎縮纖維化jizz.www；F1代大鼠攝入貧鈾5個(gè)月后就有上述改變。F0代中一级做片爱片久久毛片A片、高劑量組攝入貧鈾7個(gè)月時(shí)脾臟生發(fā)中心和淋巴鞘增生女人爽到呻吟的在线观看视频，淋巴母細(xì)胞增生活躍，20個(gè)月時(shí)脾小體減少偷窥盗摄，生發(fā)中心稀疏久久免费发布视频；F1代大鼠攝入貧鈾早期和晚期有類(lèi)似改變国产精选桃阁阁在线视频。F0和F1代高劑量組攝入貧鈾早期肝臟有炎癥細(xì)胞浸潤(rùn)，晚期骨髓有核細(xì)胞減少又爽又黄又骚，脂肪細(xì)胞增加清清AV。

It is important to differentiate immune thrombocytopenia from nonimmune thrombocytopenia because of the different clinical treatment, but untill now there is no satisfactory laboratory tests could be used.

非免疫性血小板減少性紫癜欧美男女a视频，是指由非免疫因素引起的血小板減少视频亚洲欧美日韩，如化療后骨髓抑制、急性白血病永久黄网站色视频免费AP、脾功能亢進(jìn)以及惡性腫瘤骨髓轉(zhuǎn)移等引起的血小板減少www.中文视频亚洲。

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.

特發(fā)性血小板減少性紫癜的診斷仍只是一種排除性的臨床診斷，其國(guó)內(nèi)診斷標(biāo)準(zhǔn)為多次化驗(yàn)檢查血小板計(jì)數(shù)減少在线一区你懂，脾臟不增大或僅輕度增大免费看男女AV入口，骨髓檢查巨核細(xì)胞數(shù)增多或正常，有成熟障礙花蝴蝶免费高清，并且具備以下五點(diǎn)中的任何一點(diǎn)：潑尼松治療有效婷婷五月深爱憿情网，切脾治療有效，血小板相關(guān)抗體增多JIUJIUZAIXIANSHIPIN，血小板相關(guān)補(bǔ)體增多A片不卡视频网站，血小板壽命測(cè)定縮短，同時(shí)應(yīng)排除繼發(fā)性血小板減少癥欧美一级片操逼。

Such massive splenomegaly is usually indicative of some myeloproliferative disease such as chronic myelogenous leukemia or myelofibrosis.

這樣的脾腫大通常預(yù)示有骨髓增生型疾病欧美第一区，例如慢性髓性白血病或骨髓纖維化。

Such massive splenomegaly is usually indicative of some myeloproliferative disease such as chronic myelogenous leukemia or myelofibrosis .

這樣的脾腫大通常預(yù)示有骨髓增生型疾病日韩手机色情免费观看网站视频，例如慢性髓性白血病或骨髓纖維化久久综合精品二区无码。你知道它的英文嗎？

Subacut myeloid leukemia can be a defined type of leukemia. The common characteristics of subacute myeloid leukemia are as follows: the onset is insidious, and anemia and hemorrhage of skin and mucosa are the main clinical manifestations. Hepatosplenomegaly is rare. There are multilineage abnormalities in blood cell counts and increased blasts in the bone marrow with cytogenetical abnormal clone in most cases. The disease course is subacute and progressive.

1男插女福利、亞急性髓性白血病是一個(gè)可以確定的白血病類(lèi)型曰批全过程免费视视频观看，其特征為：起病隱襲，以貧血或皮膚粘膜出血為主要癥狀国产美女av网址，肝脾腫大的特征較少免费丝袜美女一级A片，血象為一系、二系或三系的異常久久国产肏，骨髓細(xì)胞形態(tài)學(xué)檢查原早幼粒細(xì)胞異常增高91视频首页，細(xì)胞遺傳學(xué)檢查多數(shù)有克隆性異常核型，病程中可有克隆演進(jìn)www.23815643.com，呈現(xiàn)亞急性而進(jìn)行性的臨床經(jīng)過(guò)天堂av天天干。

ResultsCharacteristic features at the presentation of AITL included generalized lymphadenopathy, fever, splenomegaly, and skin rashes with polyclonal hyper-gammaglobulinemia and other hematological abnormalities (such as Coombs-positive hemolytic anemia), which often involved the bone marrow and had well-described histologic features.The positive rate for CXCL13 was 93.3%.

結(jié)果：AITL主要表現(xiàn)為淋巴結(jié)腫大、發(fā)熱AⅤ视频网站、脾大和皮疹116国产午夜精品美女毛片，伴有多克隆性高球蛋白血癥和其他血液學(xué)異常如白細(xì)胞升高国产色污污视频在线观看、Coombs試驗(yàn)陽(yáng)性，常累及骨髓国内精品自产拍在线播放，具有特征性的病理組織學(xué)表現(xiàn)嫩白少妇初次吞精A片一級A片，免疫組織化學(xué)實(shí)驗(yàn)顯示B-淋巴細(xì)胞趨化因子CXCL13陽(yáng)性率為93.3%。

Polycythemia Vera：真性紅細(xì)胞增多癥

真性紅細(xì)胞增多癥(polycythemia vera)簡(jiǎn)稱(chēng)\真紅\是一種克隆性的以紅系細(xì)胞異常增殖為主慢性骨髓增生性疾病. 臨床特征有皮膚粘膜紅紫2019免费黄片、脾腫大和血管及神經(jīng)系統(tǒng)癥狀. 血液學(xué)的特征為紅細(xì)胞和全血容量絕對(duì)增多,血粘滯度增高,常伴有白細(xì)胞和血小板增多.

lienomedullary：脾骨髓的

lienomalacia 脾軟化 | lienomedullary 脾骨髓的 | lienomyelogenousleukemia 脾骨髓性白血病

cystinosis：胱氨酸病

系一種家族性類(lèi)脂質(zhì)代謝障礙性疾病,為常染色體隱性遺傳因神經(jīng)磷脂酶缺陷而引起神經(jīng)磷脂在單核巨噬細(xì)胞系統(tǒng)中蓄積,肝脾、淋巴結(jié)AAA毛片A级、骨髓等處有大量的含神經(jīng)磷脂的網(wǎng)狀細(xì)胞(3)胱氨酸病(cystinosis):本病為常染色體隱性遺傳性疾病,