結締織病 的英文怎麼說
中文拼音 [jiēdìzhībìng]
結締織病
英文
desmosis-
Typical pathological changes is leprosy granulation swollen namely leprosy is nodal, by composition of place of afterbirth of large and small of connective tissue of embedded leprosy bacili, there is epithelial appearance cell, oar cell to reach fiber cell all round
典型病變是麻風肉芽腫即麻風結節，由內含麻風桿菌結締組織巨細胞所組成，四周有上皮樣細胞、漿細胞及成纖維細胞。People with injury to the penis, family history, or certain connective tissue diseases ( such as development of fibrosis in other elastic tissues of the body ) will have higher risk of developing peyronie s disease
不過陰莖曾經受傷、家族中有其它成員患上陰莖硬結癥、或患上過某些結締組織病（如在身體的其它彈性組織出現纖維化）的人士，都會有較高的風險患上陰莖硬結癥。The causes may be due to childbirth, connective tissue disease, increased intra - abdominal pressure or iatrogenic causes
陰道或子宮的支持組織發生缺陷的原因可能是分娩、結締組織疾病、腹腔壓力提高或其他醫療疾病引起。There are cystically dilated ducts, areas of lobules that are laced with abundant fibrous connective tissue ( sclerosing adenosis ), and stromal fibrosis
可見到囊性擴張導管、小葉區伴大量纖維結締組織（硬化性腺病）增生、間質纖維化。This article reviews the clinical manifestations, mutation feature, gene location and phenotype of different ischemic cerebrovascular disease caused by monogenic disorders, including coagulation disorders, erythrocytic disorders, inherited small vessel disease, metabolic disorders, connective tissue diseases, vasculopathies and disorders of unknown etiology
本文主要闡述了單基因遺傳障礙引起的缺血性腦血管病，包括凝血障礙、血細胞病、遺傳性小血管病、代謝障礙、結締組織病、大動脈病及不明原因引起缺血性腦血管病的臨床特徵、突變特點、基因定位及表型等遺傳學研究進展。The early clinical features of mctd are nonspecific, and may consist of general malaise, arthralgias, myalgias, and low - grade fever
混合性結締組織疾病早期的表現並不具特異性，常只是全身倦怠，關節肌肉酸痛及低熱，較特異的發現是抗核抗體的生成。Through farther diagnose, what just discover sun mou suffers from is actually " papula of phallic pearl shape ", it is not venereal, it is normal connective tissue hyperplasia only, need treatment far from
經過進一步確診，才發現孫某患的其實是「陰莖珍珠狀丘疹」 ，它不是性病，只是正常的結締組織增生，根本不需要治療。It is this marked increase in the dense fibrous tissue stroma that produces the characteristic hard " scirrhous " appearance of the typical infiltrating ductal carcinoma
緻密的纖維結締組織間質的顯著增生造成了典型浸潤性導管癌的特徵性病變硬癌特徵。Mental disorders due to disease of connective tissue
結締組織疾病所致精神障礙If pericarditis is suspected, the history should address exposure to infectious agents, connective tissue and immune diseases, and previous diagnosis of neoplasia
當懷疑有心包炎時，病史應注重感染原接觸史，結締組織和免疫性疾病史和以往的腫瘤診斷史。Data fail to confirm a relationship between lymphoid proliferation with immunoblastic morphology and connective tissue diseases
這些資料不能證實具有免疫母細胞形態的淋巴樣增生與結締組織病之間的關系。The morphological characteristics of desmoplastic fibroblastoma
促結締組織增生性纖維母細胞瘤的病理形態學特徵Mixed connective tissue disease ( mctd ) was defined as a connective tissue disorder characterized by the presence of high titers of a distinct autoantibody in combination with clinical features commonly seen in systemic lupus erythematosus ( sle ), scleroderma, and polymyositis ( referred to as overlap syndrome )
摘要混合性結締組織疾病是一種結締組織異常的疾病，合併有高價且明確的自體抗體，臨床上常有類似全身性紅斑性狼瘡，硬皮癥及多發性肌炎的表現。Overlapping connective tissue disease
重疊結締組織病Mixed connective tissue disease, mctd
混合結締組織病Analysis of connective tissue complicated with pneumocystis pneumonia in 7 cases
結締組織病並發肺孢子菌肺炎7例分析Mixed connected tissue
混合結締組織病Pulmonary connective tissue diseases
肺結締組織疾病Herein, we report a case of mctd presenting with chylothorax, which should be considered in the differential diagnosis of chylothorax
乳糜胸的?別診斷中必須將混合性結締組織疾病納入考慮。Rheumatoid arthritis and systemic lupus erythematosus have been reported to have chylothorax, but in only a limited number of cases
本篇報告一個呈現乳糜胸的混合性結締組織疾病病案，在以前的文獻中，鮮見類似個案的報導。分享友人