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bilateral
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  双侧
    Nelson's syndrome following bilateral adrenalectomy,report of 5 cases
    双侧肾上腺切除术后Nelson氏综合征5例报告
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    Bilateral Breast Cancer (A Report of 14 Cases)
    双侧乳腺癌(附14例报告)
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    Bilateral Primary Breast Cancer
    双侧原发性乳腺癌16例报告
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    Primary bilateral breast cancer: a report of 25 cases
    原发性双侧乳腺癌25例报告
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    Bilateral Acoustic Neurinoma (NF Ⅱ)
    双侧听神经瘤(NFⅡ)
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  “bilateral”译为未确定词的双语例句
    Study of Rb Gene Deletions in Bilateral Retinoblastomas
    双眼视网膜母细胞瘤Rb基因缺失研究
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    Genetic Epidemiology and a Matched Case─control Study of Bilateral Breast Cancer inShanghai
    上海市女性乳腺癌的遗传流行病学及病例对照研究
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    Detection of Heterozygous Mutations of Rb1 Gene in Bilateral Retinoblastoma Patients
    Rb1基因在双眼视网膜母细胞瘤病人体细胞中杂合性突变的检测
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    Clinical analysis of bilateral neck dissection in patients with laryngeal cancer
    喉癌患者同时双颈廓清术临床分析
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    A noval 21 base pair heterozygous deletion of Rb1 gene in a bilateral retinoblastoma patient
    Rb1基因第16内含子内21个碱基缺失1例
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  bilateral
Our approach is rooted in a dominated ergodic theorem of Mart\'{\i}n--Reyes and de la Torre which assigns $T$ a canonical family of bilateral $A_{p}$ weight sequences.
      
After surgical operation, the operation group undertook bilateral common carotid artery permanent ligation, while the other group did not.
      
The mice were pretreated with heat stress followed by ischemia/reperfusion by clipping bilateral cervical common arteries for 7 min.
      
There were 54 patients with unilateral or bilateral hyperplasia and 25 patients with adenoma according to the CT scan.
      
Numerical investigation on the dryout point of annular flow in the upward narrow annuli with bilateral heating
      
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111 Cases of renal embryonal carcinosarcoma were treated from 1959-1978 inclusive, among which were 68 males and 43 females. 71 patients were less than 3 years old. The occurrence of tumor was nearly same on either side and 2 cases had bilateral tumors. The operated 86 cases fell into 5 different stages. 100 cases were followed for 2-19 years, having an over-all 2 years survival rate of 39.7%, 5 years survival 28.2% and 10 years survival 10.2%. All the non-operated cases died within 1 year, and 88% died...

111 Cases of renal embryonal carcinosarcoma were treated from 1959-1978 inclusive, among which were 68 males and 43 females. 71 patients were less than 3 years old. The occurrence of tumor was nearly same on either side and 2 cases had bilateral tumors. The operated 86 cases fell into 5 different stages. 100 cases were followed for 2-19 years, having an over-all 2 years survival rate of 39.7%, 5 years survival 28.2% and 10 years survival 10.2%. All the non-operated cases died within 1 year, and 88% died within 6 months. In contrast, 28.2% of the operated cases lived more than 5 years and 10.2% lived longer than 10 years. Of the 31 cases survived over 2 years postoperatively, 20 were below 2 years of age. This suggested that the younger the patient, the better the outcome after treatment. In the years 1969-1978, chemotherapy was applied in addition to surgery with or without radiotherapy. The 2 years sur- vival rate was thus increased from 21.6% of the first 10 year cases to 34.1% of the second 10 year cases.

本文报道111例小儿肾胚胎瘤的临床资料,其中86例手术切除,25例未行手术。得到随访者100例,其中手术组78例,非手术组22例。手术组2年存活率为39.7%、5年为28.2%、10年为10.2%;存活最长者为19年。非手术组无1例存活1年以上者。根据随访结果,提出各期肾胚胎瘤的治疗方案。

111 cases of Cushing's syndrome were analysed in which 101 cases were pathologically proved and 10 were clinically diagnosed. The choice of treatment according to the different pathological types was discussed. In cases of bilateral hyperplastic type without evidence of pituitary tumor (52 cases), bilateral subtotal adrenalectomy followed by pituitary irradiation was preferred. In cases of hyperplastic type with apparent evidence of pituitary tumor (11 cases including one case of Nelson's syndrome),...

111 cases of Cushing's syndrome were analysed in which 101 cases were pathologically proved and 10 were clinically diagnosed. The choice of treatment according to the different pathological types was discussed. In cases of bilateral hyperplastic type without evidence of pituitary tumor (52 cases), bilateral subtotal adrenalectomy followed by pituitary irradiation was preferred. In cases of hyperplastic type with apparent evidence of pituitary tumor (11 cases including one case of Nelson's syndrome), operation on pituitary gland should be performed first irrespective of absence of compression syndrome and 3-6 months later followed by subtotal adrenolectomy if necessary, o,p'-DDD and adrenal blockers were used in some of these patients or just pre-operatively. In cases of adrenal cortical adenoma (29 cases), simple unilateral adrenolectomy would produce satisfactory results. Adenocarcinomas of adrenal cortex (8 cases) should receive radical operation while in late inoperable cases, o,p'-DDD was the drug of choice. In one case of ectopic ACTH syndrome, hypercortisolism remitted after an effective treatment of the primary lesion.

本文结合111例皮质醇增多症的临床分析,根据其不同病理类型,对治疗方案的选择进行了讨论。增生型无明确垂体瘸者主张肾上腺次全切除加垂体放疗;有明显垂体瘤者,不论有无压迫症状均主张先行垂体手术,3~6月后皮质醇增多症症状未缓解者,再行肾上腺次全切除术。肾上腺腺瘤手术疗效满意。腺癌应手术根治,晚期不能手术者可用二氯苯二氯乙烷治疗。异位ACTH综合征根治原发病灶后皮质醇增多症可期缓解。

Arare case of mixed TSH-PRL pituitary adenoma secondary to hypo-thyroidism which had never reported before was treated surgically in 1980. Hypothyroidism, amenorrhea, galactorrhea, impairment of vision and bilateral hemianopsia were chief symptoms and signs. Laboratory examinations revealed low thyroxin (T4, T3U), high titer of microsomall thyroid antibodies and strong TRH reaction after TSH stimulation. Postoperative electromicroscopic examination revealed TSH and PRL secreting granules with microtubulars...

Arare case of mixed TSH-PRL pituitary adenoma secondary to hypo-thyroidism which had never reported before was treated surgically in 1980. Hypothyroidism, amenorrhea, galactorrhea, impairment of vision and bilateral hemianopsia were chief symptoms and signs. Laboratory examinations revealed low thyroxin (T4, T3U), high titer of microsomall thyroid antibodies and strong TRH reaction after TSH stimulation. Postoperative electromicroscopic examination revealed TSH and PRL secreting granules with microtubulars in tumor cells. Visual function soon recovered after operation, menstruation reappeared 11/2months later, galactorrhea disappeared and serum levels of TSH and PRL dropped near normal.

甲状腺低功所致垂体促甲状腺素、催乳素混合腺癌很罕见。本例的临床及实验室主要特征为:甲状腺低功,闭经,溢乳,视力左0.1,右0.3,双颞侧偏盲,血清T_4、T_3U值下降及PRL升高,甲状腺微粒抗体增加,TRH对TSH刺激试验呈过强反应。术后肿瘤超微结构检查发现瘤细胞内有TSH、PRL分泌颗粒及微小管。术后视功能迅速恢复,1个半月后月经来潮,溢乳停止,血TSH、PRL接近正常。

 
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