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具有激素分泌功能的肾上腺节细胞神经瘤一例临床分析 被引量：3

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摘要 节细胞神经瘤（ganglioneuroma，GN）是一类少见的起源于神经脊的良性肿瘤，组织学上主要由成熟的神经节细胞、Schwann细胞、神经组织和神经纤维构成，通常起源于脊柱旁的交感神经链。肿瘤大多数位于后纵隔、腹膜后，原发于肾上腺髓质者偶见。通常GN很少分泌儿茶酚胺及类固醇激素，不具分泌功能。因此即使肿瘤较大，也常不会表现出明显临床症状。然而，本院收治1例肾上腺节细胞神经瘤（adrenal ganglioneuroma，AGN）患者内分泌功能活跃，呈低肾素性原发性醛固酮增多症表现。现对其临床表现、诊断及治疗措施进行讨论。
作者 于俊杰 温儒民 陈家存 李望 陈仁富 朱海涛 薛松
机构地区 徐州医学院附属医院泌尿外科
出处 《中华临床医师杂志（电子版）》 CAS 2015年第3期144-146,共3页 Chinese Journal of Clinicians(Electronic Edition)
关键词 肾上腺节细胞神经瘤 内分泌功能 类固醇激素 临床分析 SCHWANN细胞 原发性醛固酮增多症 良性肿瘤 神经节细胞
分类号 R736.6 [医药卫生—肿瘤]
  • 相关文献

参考文献20

  • 1Sasald S, Yasuda T, Kaneto H, et al. Large adrenal ganglioneuroma[J]. Intern Med, 2012, 51(17): 2365-2370.
  • 2Qing Y, Bin X, Jian W, et al. Adrenal ganglioneuromas: A 10-year experience in a Chinese population[J]. Surgery, 2010, 147(6): 854-860.
  • 3Rondeau C Nolet S, Latour M, et al. Clinical and biochemical features of seven adult adrenal ganglionenromas[J]. J Clin Endocrinol Metab, 2010, 95(7): 3118-3125.
  • 4Maweja S, Mateme R, Detremblenr N, et al. Adrenal ganglioneuroma. A neoplasia to exclude in patients with adrenal incidentaloma[J]. Acta Chit Belg, 2007, 107(6): 670-674.
  • 5梅骅,陈凌武,高新.泌尿外科手术学[M].3版.北京:人民卫生出版社,2007:855-856.
  • 6Linos D, Tsirlis T, Kapralou A, ct al. Adrenal ganglioneuromas: IncidentalomaS with misleading clinical and imaging features[J]. Surgery, 2011, 149(1): 99-105.
  • 7Erem C, Kocak M, Cinel A, et al. Dopamine-secreting adrenal ganglioncuroma prcscnting with paroxysnhal hypertension attacks[J]. Saudi Med J, 2008, 29(1): 122-125.
  • 8Geoerger B, Hero B, Harms D, et al. Metabolic activity and clinical features of primary gangLioneuromas[J]. Cancer, 2001, 91(10): 1905-1913.
  • 9Gvltekin M, Dursun P, Salman C, et al. Ganglioneuroma mimicking ovarian tumor: A report of a case and review of the ganglioneuromas[J]. Arch Gynecol Obstet, 2005, 271(1): 66-68.
  • 10Lora MS, Waguespack SC Moley JF, et al. Adrenal ganglioneuromas in children with multiple endocrine neoplasia type 2: A report of two cases[J]. J Clin Endocrinol Metab, 2005, 90(7): 4383-4387.

二级参考文献20

  • 1梅骅,陈凌武,高新.泌尿外科手术学[M].3版.北京:人民卫生出版社,2007:855-856.
  • 2Sasald S, Yasuda T, Kaneto H, et al. Large adrenal ganglioneuroma[J]. Intern Med, 2012, 51(17): 2365-2370.
  • 3Qing Y, Bin X, Jian W, et al. Adrenal ganglioneuromas: A 10-year experience in a Chinese population[J]. Surgery, 2010, 147(6): 854-860.
  • 4Rondeau C Nolet S, Latour M, et al. Clinical and biochemical features of seven adult adrenal ganglionenromas[J]. J Clin Endocrinol Metab, 2010, 95(7): 3118-3125.
  • 5Maweja S, Mateme R, Detremblenr N, et al. Adrenal ganglioneuroma. A neoplasia to exclude in patients with adrenal incidentaloma[J]. Acta Chit Belg, 2007, 107(6): 670-674.
  • 6Linos D, Tsirlis T, Kapralou A, ct al. Adrenal ganglioneuromas: IncidentalomaS with misleading clinical and imaging features[J]. Surgery, 2011, 149(1): 99-105.
  • 7Erem C, Kocak M, Cinel A, et al. Dopamine-secreting adrenal ganglioncuroma prcscnting with paroxysnhal hypertension attacks[J]. Saudi Med J, 2008, 29(1): 122-125.
  • 8Geoerger B, Hero B, Harms D, et al. Metabolic activity and clinical features of primary gangLioneuromas[J]. Cancer, 2001, 91(10): 1905-1913.
  • 9Gvltekin M, Dursun P, Salman C, et al. Ganglioneuroma mimicking ovarian tumor: A report of a case and review of the ganglioneuromas[J]. Arch Gynecol Obstet, 2005, 271(1): 66-68.
  • 10Lora MS, Waguespack SC Moley JF, et al. Adrenal ganglioneuromas in children with multiple endocrine neoplasia type 2: A report of two cases[J]. J Clin Endocrinol Metab, 2005, 90(7): 4383-4387.

共引文献5

同被引文献28

  • 1吉华明,陈自谦,丁洪彬,张波.节细胞神经瘤的CT和MR诊断[J].放射学实践,2006,21(4):333-335. 被引量：17
  • 2梅骅,陈凌武,高新.泌尿外科手术学[M].3版.北京:人民卫生出版社,2007:855-856.
  • 3Sasald S, Yasuda T, Kaneto H, et al. Large adrenal ganglioneuroma[J]. Intern Med, 2012, 51(17): 2365-2370.
  • 4Qing Y, Bin X, Jian W, et al. Adrenal ganglioneuromas: A 10-year experience in a Chinese population[J]. Surgery, 2010, 147(6): 854-860.
  • 5Rondeau C Nolet S, Latour M, et al. Clinical and biochemical features of seven adult adrenal ganglionenromas[J]. J Clin Endocrinol Metab, 2010, 95(7): 3118-3125.
  • 6Maweja S, Mateme R, Detremblenr N, et al. Adrenal ganglioneuroma. A neoplasia to exclude in patients with adrenal incidentaloma[J]. Acta Chit Belg, 2007, 107(6): 670-674.
  • 7Linos D, Tsirlis T, Kapralou A, ct al. Adrenal ganglioneuromas: IncidentalomaS with misleading clinical and imaging features[J]. Surgery, 2011, 149(1): 99-105.
  • 8Erem C, Kocak M, Cinel A, et al. Dopamine-secreting adrenal ganglioncuroma prcscnting with paroxysnhal hypertension attacks[J]. Saudi Med J, 2008, 29(1): 122-125.
  • 9Geoerger B, Hero B, Harms D, et al. Metabolic activity and clinical features of primary gangLioneuromas[J]. Cancer, 2001, 91(10): 1905-1913.
  • 10Gvltekin M, Dursun P, Salman C, et al. Ganglioneuroma mimicking ovarian tumor: A report of a case and review of the ganglioneuromas[J]. Arch Gynecol Obstet, 2005, 271(1): 66-68.

引证文献3

二级引证文献5

中华临床医师杂志（电子版）
2015年 第3期

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