皮萎缩病

基本解释 (translations)

atrophoderma  ·  atrophodermatosis

与皮萎缩病相关的网络例句 [注：此内容来源于网络，仅供参考]

Of the many clinical symptoms, the frequently seen are seborrheic dermatitis, proliferation of blood vessels around cornea, cheilitis, corners of mouth look wet, white, thicker than usual, black and blue with swelling, nipple hypertrophy or atrophy, and often complicated by scrotal dermatitis.

维生素B2缺乏病临床症状较多，常见的有脂溢性皮炎、角膜周围血管增生、唇炎、口角湿白增厚、青红肿、乳头肥大或萎缩，常并发有阴囊皮炎。

Small intestinal biopsies showed subepithelial collagen deposition with varying degrees of villous atrophy and varying numbers of intraepithelial lymphocytes. Four patients had previous biopsies showing enteropathic changes without collagen deposition. Seven cases were associated with collagenous colitis and 1 also had features of lymphocytic colitis. Three patients also had collagen deposition in gastric biopsies. One case was associated with lymphocytic gastritis. Celiac disease (CD, gluten-sensitive enteropathy) was documented in 4 patients. Five patients made a clinical improvement with combinations of a gluten-free diet and immunosuppressive therapy. Two patients died of complications of malnutrition and 1 of another illness. Clonal T-cell populations were identified in 5 of 6 cases tested. Four of these patients improved clinically after treatment but 1 has died. Collagenous sprue evolved on a background of CD in 4 cases. There was no history of CD in others and these cases may be the result of a biologic insult other than gluten sensitivity.

小肠活检表现为上皮下胶原沉积，绒毛萎缩程度不一，上皮内淋巴细胞浸润数量不等。4例患者以往曾做过活检，表现为其他肠病改变，并没有胶原沉积。7例患者合并胶原性结肠炎，且1例还有淋巴细胞性结肠炎的特征。3例患者胃活检也发现有胶原沉积。1例患者合并淋巴细胞性胃炎。4例患者有乳糜泻（CD，谷蛋白敏感性肠病）病史。5例患者经无麸质饮食和免疫抑制治疗后，临床症状有所改善。2例患者因营养不良合并另一种疾病而死亡。6例患者做了T细胞受体基因重排，其中5例发现有克隆性T细胞群，这5例中有4例治疗后临床症状加重，且1例死亡。4例患者在CD的基础上病发胶原性口炎性腹泻；其余患者无CD病史，他们的发病也许是生物源性损害，而非谷蛋白敏感。

Such as inflammation of joints, the lower leg, such as chronic venous insufficiency lead to long-term sustainability of the skin caused by congestive hairy; hyperthyroidism in Pretibial myxedema patch Department often long acuminatum out; hypothyroidism and limbs of children in the back outside a large number of hair growth; children with viral encephalitis and inter-brain barrier after mumps-induced systemic hairy; head injury, especially after the children more prone to hair; children with primary malnutrition or enteropathy, or other malabsorption, or severe infections caused by malnutrition could rise to a large number of multi-body hair; anorexia nervosa patients in the face, trunk and upper limbs have more hair grow; infant limb pain patients in the limbs, face, trunk and more hair; dermatomyositis patients, mainly in children can be located hairy forearm, leg and temporal, but also a broader scope; Berordinelli syndrome, that is, growth and maturity accelerated from an early age, and accompanied by malnutrition and intestinal muscle atrophy, common hepatomegaly and high blood fat, the skin of patients with rough, often hairy; addition of certain drugs such as streptomycin, such as cortisone can cause iatrogenic hairy; some women as a result of adrenal, ovarian and other diseases caused by increased androgen can also result in more hair.

如炎症性关节，小腿慢性静脉机能不全等导致长期持续的皮肤充血造成多毛；甲状腺机能亢进者在胫前粘液性水肿的斑块处常有粗毛长出；甲状腺机能减退的儿童背部和四肢外侧有大量毛发生长；儿童在病毒性脑炎及流行性腮腺炎后间脑障碍所致的全身性多毛；头部外伤后特别是儿童易发生多毛；儿童原发性营养不良或肠病，或其他吸收不良，或严重感染引起的营养不良均可引起大量全身性多毛；神经性厌食症患者可在面部、躯干和上肢有较多的毛发长出；婴儿肢痛病患者可在四肢、面部、躯干部多毛；皮肌炎患者，主要发生于儿童中，多毛可位于前臂、小腿和颞部，但范围也更广泛；Berordinelli综合征，即生长和成熟从小就加速，并伴有肠营养不良和肌肉萎缩，常见肝肿大和高血脂，其患者皮肤粗糙，常多毛；此外某些药物如链霉素、可的松等可造成医源性多毛；某些妇女因肾上腺、卵巢等疾病致雄性激素增多也可造成多毛。

Preliminary animal experiment have shown that WYIH have significant curative effect on the CAG model rats,as well as reverse intestines epidermis vegetate to some extent.

前期研究已初步证实了胃炎Ⅰ号对脾胃虚弱型慢性萎缩性胃炎病人和CAG模型大鼠胃粘膜修复有很好的疗效，并有一定的抗肠上皮化生的作用。

Histologically, the seminiferous tubules contained numerous Sertoli cells and more Sertoli-spermatozoa complexes, accompanied by the depletion of Leydig cells with deeply stained nuclei. Mature spermatozoa were stored up in the epididymis, but only a few in the efferent ducts. In the second place was testicular atrophy（32/120; 26.7%）. The seminiferous tubules showed moderate to severe inactivity of spermiogenesis with evidence of only spermatogonia, spermatocytes and Sertoli cells. The Leydig cells were obviously decreased in numbers associated with decrease of lipid droplets in their cytoplasms. Testicular hypoplasia was the third disorders（22/120; 18.3%）. Only a few spermatogonia and Sertoli cells appeared without any spermiogenesis. The associated changes was decreased in Leydig cells and fibrous hyperplasia in the interstitium.Epididymal stones were sometimes found（12/120; 10%）. Grossly, yellowish-white nodules with various sizes and firm in consistency were observed in the epididymis and the front efferent ducts. Microscopically, the epididymal ducts were dilated with voluminous spermatozoa storage, even showed calcification in severe cases. The deposited calcium salts were stained positively by Von Kossa and Alizarin red methods.Amyloidosis was also detected in 10 roosters（8.3%）. Eosinophilic, homogeneous, amyloid-like substances were deposited mainly in the testicular interstitium and the periphery of blood vessels. These substances showed positive reaction by Congo red staining. Five roosters（4.2%）had Marek's lesions in the testis, epididymis and peripheral nerves with infiltration of pleomorphic lymphocytes. Only one case showed epithelial necrosis of seminiferous tubules accompanied by fibrous proliferation in the interstitium.

结果发现，在总共搜集的120个病例中，其中因年老所导致的产精力不佳为最多，占38例（31.7%），於镜下可见大量精虫黏附於Sertoli cell的表面，并可见Sertoli cell数量明显增多而Leydig cell明显减少，且其细胞核呈现浓染的现象，而在其副睪中仍可见到成熟精虫蓄留於管腔中，但在其输精管内却只有少量精虫存在；其次为睪丸萎缩，占32例（26.7%），镜下可见中度至重度无造精作用，其生精小管中只见到精母细胞、精原细胞及Sertoli cell存在，但Leydig cell数量明显减少且其细胞质内的脂质也明显减少；睪丸发育不全，占22例（18.3%），於生精小管内只见到精母细胞及少量Sertoli cell存在，不见造精细胞分化，於生精小管间质可见Leydig cell减少并伴随结缔组织增生；副睪结石，占12例（10%），肉眼下可在副睪及输精管前段见到黄白色大小不一的结节，触感坚硬，於镜下可见副睪管扩张并有大量成熟精虫蓄积，严重时可见钙化现象，以Von Kossa及茜素红染色均呈阳性反应；类淀粉沉著症，占10例（8.3%），镜下在睪丸间质及血管周围可见粉红均质样的物质沉积，以刚果红染色成阳性反应；马立克病，占5例（4.2%），镜下可在睪丸、副睪实质及周边神经内均可见到嗜碱性大小不一的淋巴样细胞浸润；睪丸坏死，占1例（0.8%），镜下可见生精小管上皮细胞坏死脱落及间质结缔组织增生。

与皮萎缩病相关的网络解释 [注：此内容来源于网络，仅供参考]

Alzheimer's disease unspecified：局限性脑萎缩

颧部钙化上皮瘤 Alveolitis of jaws | 局限性脑萎缩 Alzheimer's disease unspecified | 阿尔茨海默病,伴有晚期发病(老年性) Alzheimer's disease with early onset

beefy tongue：牛肉舌

(6)牛肉舌(beefy tongue):舌面绛红如生牛肉状,见于糙皮病(菸酸缺乏). (7)镜面舌:亦称光滑舌(sm()oth tongue),舌头萎缩,舌体较小,舌面光滑呈粉红 色或红色,见于缺铁性贫血、恶性贫血及慢性萎缩性胃炎. (8)毛舌:也称黑舌,

dermatitis：皮炎

酸性比较稳定缺乏症脚气病(beriberi)主要损害神经血管系统多发性神经炎、肌肉萎缩及水肿尼克酸(nicotinic acid)又名烟酸、维生素PP癞皮病(pellagra)早期:疲劳、记忆力减退、失眠. 典型:3D症状-皮炎(dermatitis)腹泻(diarrhea)抑郁(depression)

pellagra：癞皮病

抗脚气病因子,易因受热和氧化而遭到破坏,尤其在碱性环境中更是如此,酸性比较稳定缺乏症脚气病(beriberi)主要损害神经血管系统多发性神经炎、肌肉萎缩及水肿尼克酸(nicotinic acid)又名烟酸、维生素PP癞皮病(pellagra)早期:疲劳、记忆力

pigmentary purpuric dermatosis：色素*紫癜*皮病

白色萎缩 white atrophy, atrophite blanche | 痛*挫伤*综合征 painful bruising syndrome | 色素*紫癜*皮病 pigmentary purpuric dermatosis

atrophoderma：皮肤萎缩 皮萎缩 皮萎缩病

atrophique萎缩的 | atrophoderma皮肤萎缩 皮萎缩 皮萎缩病 | atrophodermamaculatum斑状皮萎缩

pial funnel：软脑膜漏斗

pia mater 软膜 | pial funnel 软脑膜漏斗 | Pick disease 皮克病,脑叶萎缩