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
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