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一名患有多发性内分泌肿瘤综合征(2A型或西普尔综合征)的孕妇发生脑出血。

Cerebral haemorrhage in a pregnant woman with a multiple endocrine neoplasia syndrome (type 2A or Sipple's syndrome).

作者信息

Moraca-Kvapilová L, Op de Coul A A, Merkus J M

出版信息

Eur J Obstet Gynecol Reprod Biol. 1985 Oct;20(4):257-63. doi: 10.1016/0028-2243(85)90074-7.

DOI:10.1016/0028-2243(85)90074-7
PMID:2865176
Abstract

We present the case history of a 30-yr-old woman who suffered a cerebral haemorrhage toward the end of pregnancy (at 35 wk). The pregnancy was terminated by Caesarean section because aggravation of cerebral bleeding was feared. Extensive studies revealed that the patient was suffering from a multiple endocrine neoplasia syndrome (type 2A or Sipple's syndrome) with bilateral pheochromocytomas and a medullary thyroid carcinoma. She made an uneventful recovery. The relevant literature is discussed.

摘要

我们报告一名30岁女性的病史,她在妊娠晚期(35周时)发生脑出血。由于担心脑出血加重,通过剖宫产终止妊娠。广泛检查显示,该患者患有多发性内分泌肿瘤综合征(2A型或西普尔综合征),伴有双侧嗜铬细胞瘤和甲状腺髓样癌。她恢复顺利。并对相关文献进行了讨论。

相似文献

1
Cerebral haemorrhage in a pregnant woman with a multiple endocrine neoplasia syndrome (type 2A or Sipple's syndrome).一名患有多发性内分泌肿瘤综合征(2A型或西普尔综合征)的孕妇发生脑出血。
Eur J Obstet Gynecol Reprod Biol. 1985 Oct;20(4):257-63. doi: 10.1016/0028-2243(85)90074-7.
2
[Anesthesia for cesarean section and excision of pheochromocytoma caused by Sipple's syndrome].[嗜铬细胞瘤综合征所致剖宫产及嗜铬细胞瘤切除术的麻醉]
Ann Fr Anesth Reanim. 1991;10(1):84-7. doi: 10.1016/s0750-7658(05)80276-x.
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Medullary thyroid cancer in a Wisconsin kindred with Sipple's syndrome: the use of provoked calcitonin testing.威斯康星州一个患有西普尔综合征家族中的甲状腺髓样癌:激发降钙素检测的应用
Wis Med J. 1982 Nov;81(11):22-5.
4
Multiple endocrine neoplasia presenting as phaeochromocytoma during pregnancy.
Br J Obstet Gynaecol. 1993 Dec;100(12):1144-5. doi: 10.1111/j.1471-0528.1993.tb15185.x.
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Recurrence of phaeochromocytoma in pregnancy in a patient with multiple endocrine neoplasia 2A: a case report and review of literature.多发性内分泌腺瘤病2A患者妊娠期嗜铬细胞瘤复发:一例报告及文献复习
Gynecol Endocrinol. 2016 Nov;32(11):875-880. doi: 10.1080/09513590.2016.1236242. Epub 2016 Nov 3.
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[Paresthetic notalgia and multiple endocrine neoplasia type 2a (Sipple's syndrome): 3 cases].[感觉异常性疼痛和2a型多发性内分泌腺瘤病(西普尔综合征):3例]
Ann Dermatol Venereol. 1999 Jun-Jul;126(6-7):522-4.
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Multiple endocrine neoplasia type IIA (Sipple's syndrome) presenting in pregnancy.妊娠期出现的IIA型多发性内分泌腺瘤病(西普尔综合征)。
Aust N Z J Obstet Gynaecol. 2000 Nov;40(4):473-4. doi: 10.1111/j.1479-828x.2000.tb01188.x.
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Pheochromocytoma in multiple endocrine neoplasia type 2A: positive 123I MIBG with negative CT and equivocal 131I MIBG imaging.2A 型多发性内分泌肿瘤中的嗜铬细胞瘤:123I-MIBG 阳性,CT 阴性,131I-MIBG 显像结果不确定。
Clin Nucl Med. 2012 Jun;37(6):596-8. doi: 10.1097/RLU.0b013e31824c5f43.
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[Sipple's syndrome: a case report].[西普尔综合征:一例报告]
Hinyokika Kiyo. 1990 Nov;36(11):1309-12.
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[Relationship between types of hypertension and patterns of urinary catecholamine excretion in Sipple's syndrome].
Nihon Naibunpi Gakkai Zasshi. 1992 Jan 20;68(1):39-50. doi: 10.1507/endocrine1927.68.1_39.

引用本文的文献

1
Vaginal delivery in a patient with pheochromocytoma, medullary thyroid cancer, and primary hyperparathyroidism (multiple endocrine neoplasia type 2A, Sipple's syndrome).患有嗜铬细胞瘤、甲状腺髓样癌和原发性甲状旁腺功能亢进症(2A型多发性内分泌腺瘤病,西普尔综合征)患者的阴道分娩
Saudi J Anaesth. 2014 Jul;8(3):437-9. doi: 10.4103/1658-354X.136652.
2
Sonographic Findings of Medullary Thyroid Carcinoma Leading to Diagnosis of Multiple Endocrine Neoplasia Type 2a during Pregnancy.孕期甲状腺髓样癌的超声表现导致2a型多发性内分泌腺瘤病的诊断
AJP Rep. 2011 Sep;1(1):59-64. doi: 10.1055/s-0031-1280572. Epub 2011 Jun 9.
3
Intracerebral hemorrhage as the presenting feature of concurrent pheochromocytoma and paragangliomas.
脑出血作为并发嗜铬细胞瘤和副神经节瘤的首发表现。
J Clin Hypertens (Greenwich). 2008 Dec;10(12):941-4. doi: 10.1111/j.1751-7176.2008.00051.x.
4
Genetic prenatal RET testing and pregnancy management of multiple endocrine neoplasia Type II A (MEN2A): a case report.遗传性产前RET基因检测与IIA型多发性内分泌腺瘤病(MEN2A)的妊娠管理:一例报告
J Endocrinol Invest. 2004 Apr;27(4):357-60. doi: 10.1007/BF03351062.