双侧垂体腺瘤伴发1型多发性内分泌肿瘤。
Bilateral pituitary adenomas occurring with multiple endocrine neoplasia type one.
作者信息
Sahdev A, Jäger R
机构信息
Department of Imaging, Middlesex Hospital, London, UK.
出版信息
AJNR Am J Neuroradiol. 2000 Jun-Jul;21(6):1067-9.
Abstract
We report a case of synchronous bilateral pituitary adenomas in a patient with multiple endocrine neoplasia type one (MEN1). The patient was previously known to have a pancreatic gastrinoma and had first-degree relatives with MEN1. Both adenomas were concurrently revealed by high-resolution MR imaging of the pituitary gland as part of the investigation of the patient's severe, persistent headaches and elevated serum prolactin level.
摘要
我们报告一例患有1型多发性内分泌肿瘤（MEN1）的患者发生同步双侧垂体腺瘤的病例。该患者既往已知患有胰腺胃泌素瘤，且有患MEN1的一级亲属。作为对该患者严重、持续性头痛和血清催乳素水平升高进行调查的一部分，通过垂体高分辨率磁共振成像同时发现了这两个腺瘤。
相似文献
1
Bilateral pituitary adenomas occurring with multiple endocrine neoplasia type one.双侧垂体腺瘤伴发1型多发性内分泌肿瘤。
AJNR Am J Neuroradiol. 2000 Jun-Jul;21(6):1067-9.
2
Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma.1型多发性内分泌腺瘤病变异型，常伴泌乳素瘤，罕见胃泌素瘤。
J Clin Endocrinol Metab. 2004 Aug;89(8):3776-84. doi: 10.1210/jc.2003-031511.
3
[Multiple Endocrine Neoplasia I (Wermers Syndrome), Forms of Clinical Manifestation, 5 Case Studies].[多发性内分泌腺瘤病I型（韦默斯综合征），临床表现形式，5例病例研究]
Vnitr Lek. 2016 Fall;62(9 Suppl 3):140-149.
4
A novel germline mutation of multiple endocrine neoplasia type 1 (MEN1) gene in a Japanese MEN1 patient and her daughter.一名日本多发性内分泌腺瘤 1 型（MEN1）患者及其女儿中 MEN1 基因的一种新型种系突变。
Endocr J. 1999 Apr;46(2):325-9. doi: 10.1507/endocrj.46.325.
5
New therapies for patients with multiple endocrine neoplasia type 1.1 型多发性内分泌肿瘤患者的新疗法。
Ann Endocrinol (Paris). 2021 Apr;82(2):112-120. doi: 10.1016/j.ando.2021.03.005. Epub 2021 Apr 8.
6
Gigantism in sibling unrelated to multiple endocrine neoplasia: case report.与多发性内分泌腺瘤无关的同胞手足巨人症：病例报告
Neurosurgery. 1994 Nov;35(5):952-5; discussion 955-6. doi: 10.1227/00006123-199411000-00023.
7
Monosomy of chromosome 11 in pituitary adenoma in a patient with familial multiple endocrine neoplasia type 1.
Clin Endocrinol (Oxf). 2001 Jan;54(1):117-20. doi: 10.1046/j.1365-2265.2001.01031.x.
8
[Various neuroendocrine tumors in a family with multiple endocrine neoplasia type 1].[1型多发性内分泌腺瘤病家族中的各种神经内分泌肿瘤]
Orv Hetil. 2013 Dec 22;154(51):2037-42. doi: 10.1556/OH.2013.29772.
9
MEN1 935-1G>C splicing mutation in an Indian patient with multiple endocrine neoplasia type 1.一名患有1型多发性内分泌肿瘤的印度患者中存在MEN1 935-1G>C剪接突变。
Mol Diagn Ther. 2007;11(2):129-31. doi: 10.1007/BF03256233.
10
Multiple endocrine neoplasia type 1.1型多发性内分泌腺瘤病
Orphanet J Rare Dis. 2006 Oct 2;1:38. doi: 10.1186/1750-1172-1-38.
引用本文的文献
1
Importance of early detection in multiple endocrine neoplasia type 1: Clinical insights and future directions.1型多发性内分泌腺瘤病早期检测的重要性：临床见解与未来方向。
World J Gastrointest Oncol. 2025 Apr 15;17(4):100013. doi: 10.4251/wjgo.v17.i4.100013.
2
Expressions of Cushing's syndrome in multiple endocrine neoplasia type 1.库欣综合征在 1 型多发性内分泌肿瘤中的表现。
Front Endocrinol (Lausanne). 2023 Jun 20;14:1183297. doi: 10.3389/fendo.2023.1183297. eCollection 2023.
3
Is Routine Screening of Young Asymptomatic MEN1 Patients Necessary?对年轻无症状的MEN1患者进行常规筛查有必要吗？
World J Surg. 2017 Aug;41(8):2026-2032. doi: 10.1007/s00268-017-3992-9.
4
Multiple Pituitary Adenomas: A Systematic Review.多发性垂体腺瘤：一项系统评价
Front Endocrinol (Lausanne). 2016 Feb 1;7:1. doi: 10.3389/fendo.2016.00001. eCollection 2016.
5
Double pituitary adenomas.垂体腺瘤。
Endocrine. 2013 Apr;43(2):452-7. doi: 10.1007/s12020-013-9876-3. Epub 2013 Jan 17.
本文引用的文献
1
Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.1型多发性内分泌腺瘤病：遗传性内分泌肿瘤的临床和遗传特征
Recent Prog Horm Res. 1999;54:397-438; discussion 438-9.
2
MEN1 gene mutations in 12 MEN1 families and their associated tumors.
Eur J Endocrinol. 1998 Oct;139(4):416-20. doi: 10.1530/eje.0.1390416.
3
Multiple endocrine neoplasia type 1: clinical and genetic topics.1型多发性内分泌腺瘤病：临床与遗传学专题
Ann Intern Med. 1998 Sep 15;129(6):484-94. doi: 10.7326/0003-4819-129-6-199809150-00011.
4
Expression of the MEN-1 gene in a large kindred with multiple endocrine neoplasia type 1.
J Intern Med. 1998 Jun;243(6):465-70. doi: 10.1046/j.1365-2796.1998.00275.x.
5
Clinical studies of multiple endocrine neoplasia type 1 (MEN1).1型多发性内分泌腺瘤病（MEN1）的临床研究。
QJM. 1996 Sep;89(9):653-69. doi: 10.1093/qjmed/89.9.653.
6
Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1.
Arch Surg. 1996 Jul;131(7):699-702. doi: 10.1001/archsurg.1996.01430190021006.
7
Spectrum of pituitary disease in multiple endocrine neoplasia type 1 (MEN 1): clinical, biochemical, and radiological features of pituitary disease in a large MEN 1 kindred.
J Clin Endocrinol Metab. 1996 Jul;81(7):2642-6. doi: 10.1210/jcem.81.7.8675591.
8
Simultaneously occurring prolactinomas. Case report.同时发生的催乳素瘤。病例报告。
J Neurosurg. 1981 Jul;55(1):124-6. doi: 10.3171/jns.1981.55.1.0124.
9
Multiple secreting microadenomas as a possible cause of selective transsphenoidal adenomectomy failure. Case report.多发性分泌性微腺瘤可能是经蝶窦选择性腺瘤切除术失败的原因。病例报告。
J Neurosurg. 1983 Feb;58(2):267-9. doi: 10.3171/jns.1983.58.2.0267.
10
Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1.多发性内分泌腺瘤1型中肾上腺皮质病变的临床和遗传特征。
J Clin Endocrinol Metab. 1992 Jul;75(1):76-81. doi: 10.1210/jcem.75.1.1352309.
Zotero 插件