共 50 条
Paraganglioma in Pregnancy: A Case Series and Review of the Literature
被引:33
|作者:
Wing, Laurie A.
[1
]
Conaglen, John V.
[1
,3
]
Meyer-Rochow, Goswin Y.
[2
,3
]
Elston, Marianne S.
[1
,3
]
机构:
[1] Waikato Hosp, Dept Endocrinol, Hamilton 3240, New Zealand
[2] Waikato Hosp, Dept Surg, Hamilton 3240, New Zealand
[3] Univ Auckland, Hamilton 3240, New Zealand
关键词:
CUSHINGS-SYNDROME;
UNDIAGNOSED PHEOCHROMOCYTOMA;
WOMAN;
RARE;
POSTPARTUM;
MANAGEMENT;
DIAGNOSIS;
PATIENT;
TERM;
D O I:
10.1210/jc.2015-2122
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Context: Pregnancies complicated by a pheochromocytoma or paraganglioma are very rare, being estimated to occur in 0.007% of all pregnancies. Both the well-being of the mother and fetus need to be considered, and management can be challenging. The optimal management of women with a pheochromocytoma or paraganglioma in pregnancy is not well established. Objective: The objective of the study was to assess whether there is a difference in fetal or maternal mortality between pheochromocytomas and paragangliomas in pregnancy. Design: We present an experience of eight pregnancies in four SDHB germline mutation-positive women with sympathetic paragangliomas, followed by a systematic review of the literature to compare the outcome of paragangliomas with that of pheochromocytomas occurring in pregnancy. Results: In our case series, favorable fetal and maternal outcomes were seen in all eight pregnancies. From the systematic review, maternal and fetal mortality were lower in women with paragangliomas, at 3.6% and 12% respectively, compared with 9.8% and 16% in women with pheochromocytomas. Conclusion: Pregnant women with paragangliomas may be at a lower risk of adverse outcome than those with pheochromocytomas, but both maternal and fetal mortality rates are still higher than that of the general obstetric population.
引用
收藏
页码:3202 / 3209
页数:8
相关论文