目的:探讨高血压伴肾上腺增生患者的临床特点。
Objective To investigate the diagnosis and treatment of primary adrenal medullar hyperplasia(PAMH).
肾上腺病变11例,其中良性肿瘤7例,恶性肿瘤2例,2例肾上腺增生症在随访观察中。
Of 11 cases adrenal diseases, there were 7 cases adrenal malignant tumor and 2 cases benign tumor, 2 cases adrenal hyperplasia.
治疗一些类型的先天性肾上腺增生性肥大能够运用诸如羊水诊断或绒毛膜取样的产前检查被发现。
Treatment Some forms of CAH can be detected in prenatal tests like amniocentesis or villus sampling.
治疗一些类型的先天性肾上腺增生性肥大能够运用诸如羊水诊断或绒毛膜取样的产前检查被发现。
Treatment Some forms of CAH can be detected in prenatal tests like amniocentesis or chorionic villus sampling.
结果111例中有23例为库兴氏综合征,3例为原发性醛固酮增多症,其余85例为无激素分泌功能的肾上腺增生性疾病。
Results out of 111 patients, 23 had Cushing's syndrome, 3 had primary aldosteronism and 85 had adrenal gland hyperplastic diseases without secreted hormones.
结果4 5例中醛固酮瘤15例,误诊的双侧肾上腺增生3例,嗜铬细胞瘤8例,腺瘤、腺癌型皮质醇增多症4例和意外瘤15例。
Results Of 45 cases, 15 were with aldosterone producing adenoma (APA), 3 with of BAH, 8 pheochromocytoma, 4 adrenal tumor with hypercortisolism and 15 adrenal incidentaloma.
下边是皮质增生的肾上腺,可能是垂体腺瘤分泌acth (Cushing病),或异位分泌acth引起的库欣综合征,或特发性肾上腺增生。
This could be due to a pituitary adenoma secreting ACTH (Cushing's disease), or Cushing's syndrome from ectopic ACTH production, or idiopathic adrenal hyperplasia.
羊水细胞DNA分析是先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断的可靠方法。
DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
方法总结15例肾上腺性征综合征患者的临床资料,其中先天性肾上腺皮质增生13例,肾上腺皮质癌2例。
Methods The clinical data of 15 patients were summarized including 13 cases of congenital adrenal hyperplasia, and 2 cases of adrenocortical carcinoma.
熟悉肾上腺皮质增生和肿瘤的临床病理特点。
To be familiar with pathologic and clinical features of adrenal cortical hyperplasia and tumors.
目的探讨增生型肾上腺疾病的临床特点、诊断及治疗方向。
Objective: To investigate the clinical characters, diagnosis and treatment of hyperplastic adrenal disease.
目的探讨磁共振成像(MRI)对肾上腺腺瘤及增生的诊断价值。
Purpose To evaluate the adrenal neoplasms and cortical hyperplasia with MRI.
如何首乌近来研究证明有促进干细胞增生、增强或调节免疫功能、兴奋肾上腺皮质及皮质样作用。
Polygonum multiflorum has recently proved that if there is to promote stem cell proliferation, enhance or regulate the immune function, excitement and adrenal cortex-like role.
目的提高对肾上腺髓质增生症(amh)的诊断与治疗水平。
Objective To study the diagnosis and treatment of adrenal medullary hyperplasia (AMH).
方法回顾性分析3例肾上腺皮髓质增生患者的临床资料。
Methods The clinical data of 3 cases of adrenal cortex and medulla hyperplasia were analysed.
结论:TWEE能促进大鼠肾上腺皮质增生及促进皮质束状带细胞分泌皮质酮。
CONCLUSION: TWEE can promote the production of corticosterone and the proliferation of the cell of fascicular zone in adrenal cortex in SD rat.
结果:肾上腺皮质腺瘤45例,肾上腺皮质增生1例。
Results: Of which, 45 cases were adrenal adenomas and 1 adrenocortical hyperplasia.
目的:检测促肾上腺皮质激素(ACTH)在增生的肾上腺皮质组织中的表达,探讨肾上腺皮质球状带增生的发生机制。
Purpose:To detect the expression of adrenocorticotropin(ACTH) in adrenal cortex hyperplasia, and to explore the mechanism of adrenal cortex glomorulosa zona hyperplasia development.
目的开展新生儿先天性肾上腺皮质增生症筛查,降低残疾儿童的发生率,提高人口素质。
Objective to develop the neonatal screening for congenital adrenal hyperplasia in order to prevent children from congenital disability and improve the aristogenesis in our country.
用放免法检测肾上腺皮质增生症患者血浆ACTH的浓度,并与肾上腺皮质组织中局部表达ACTH的水平进行相关性分析。
The correlation between plasma ACTH concentration and expression level of ACTH in adrenal cortical tissue of patients with adrenal cortical hyperplasia was studied.
肾上腺皮质增生4例,行肾上腺全切术。
Unilateral total adrenalectomy was performed in 4 patients with adrenal hyperplasia.
结果102例患者中,术后病理证实94例为肾上腺肿瘤,3例为肾上腺囊肿,2例为肾上腺皮质增生,2例为肾上极肿瘤,1例为副脾。
ResultsAmong the 102 cases, 94 cases were with adrenal tumors, 3 with adrenal cyst, 2 with adrenal hyperplasia, 2 with renal tumor and with accessory spleen.
目的探讨肾上腺皮、髓质增生症的诊断和治疗。
Objective To study the diagnosis and treatment of adrenal cortical and medullary hyperplasia.
结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。
Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。
Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
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