病变

Pathological sites are involved in epidermis and hypodermis, the characteristics of it are cytometaplasia、 disappear of melanocyte、soakage of leukocyte and lymphocyte、vascular obstruction of hypodermis.

本病病变部位主要在表皮及真皮层，特点是细胞变性，黑色素细胞消失，不同程度的白细胞及淋巴细胞浸润，真皮层毛细血管闭塞。

Most children in the KBD endemic area showed lower T3 levels, which may act as a key factor for cartilage hypogenesis.

结论大骨节病病区乃当村大部份学龄前儿童存在低T3血症，可能是KBD软骨病变的始动病因。

Results (1) 6 cases of Tuberous Sclerosis. Diffused subependymal nodular calcification lesions were found in all cases on unenhenced CT. 4 patients are 2 pairs of mother/child relationship. Both of the two mothers are found to suffer from renal angiomyolipoma.(2)1 case of neurofibromatosis showed abnormal spinal canal: scoliosis of thoracic and lumbar spine, concave change of vertebral posterior border. Bilateral renal hypogenesis was found in this patient. Diffused hyper-density lesions were found in kidney and fatty accumulation was found in back skin.(3)6 cases of Sturge-Weber syndrome. On unenhenced CT, curving and strip-shaped calcifications were found along the parietal and occipital gyrus.

结果 ①结节性硬化6例，所有病例CT平扫见两侧脑室室管膜下多发小结节状高密度钙化灶，其中4例为两对母子关系，并见两位母亲合并有肾脏错构瘤，；②神经纤维瘤病1例，MRI表现为椎管异常，胸腰段脊柱侧弯，椎体后缘呈明显的切凹改变；伴有双肾发育不良，CT示肾内多个高密度影，背部皮肤多量脂肪堆积，③脑颜面血管瘤综合征6例， CT可见顶枕部沿脑回分布的弯曲的条状高密度钙化，部分延伸致侧脑室内，增强后见病灶内有扭曲的条状和结节状明显强化的血管影；④小脑血管瘤病4例，影像学表现为小脑内大囊、小结节样占位性病变。

Methods CTVE was performed with 3.0 mm at pitch 1.0 and 1.0 mm reconstruction interval in 10 normal subjects and 20 patients with larynx and hypopharynx diseases confirmed by pathology. The results were then compared with the findings of conventional laryngoscopy and operation.

采用层厚3.0 mm、螺距1.0、间隔1.0 mm对10例正常和20例经病理证实的喉及下咽部病变的患者进行CTVE成像，并与纤维喉镜、手术所见对照分析。

As is implied by the name, the most characteristic lesion is hypoplasia of the nasal turbinates

顾名思义，最特征的病变是鼻甲发育不全。

This patient was hypothyroid. This is the end result of Hashimoto's thyroiditis.

该病人甲状腺功能低下，此为桥本甲状腺炎的终末病变。

Joubert syndrome is an autosomal-recessive disorder, characterized by clinical presentation of hypotonia, ataxia, and global developmental delay.

jouber综合症是一种常染色体遗传性病变，临床表现为张力减低、共济失调、大脑半球发育延迟。

The cervical cone eletrocision through hysteroscope can identify the extent of affection in the diagnosis of CIN, determine the further treatments, and also is a suitable therapy for young patients in CIN Ⅲ level who have procreation requests.

宫腔镜宫颈锥形电切术在CIN的诊断中能明确病变程度，决定下一步处理方式，对年轻有生育要求的CIN Ⅲ患者是一个合适的方法。

Methods To compare the vaginal hysterotomy and the abdominal hysterotomy of 312 cases.Their positive physical sign,detection in operation,length of stay and were recorded.The postoperative recovery was observed.

回顾性分析比较阴式及腹式切除非脱垂病变子宫手术312例，记录患者的术前阳性体征、术中发现及术后恢复情况。

Its synthesis function has clinical significance in the iconographic diagnosis of endometria and tuble lesions.

阴道超声下行SHG检查是一种有效、简便、损伤小的方法，其包含有检查、诊断和治疗的综合功能，对子宫内膜和输卵管病变的影像学诊断有一定的临床意义。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。