Kamari Yehuda, Sharabi Yehonatan, Leiba Adi, Peleg Edna, Apter Sara, Grossman Ehud
Department of Internal Medicine D and Hypertension Unit, The Chaim Sheba Medical Center, Tel-Hashomer, Affiliated to the Sackler School of Medicine, Tel-Aviv University, Israel.
Am J Hypertens. 2005 Oct;18(10):1306-12. doi: 10.1016/j.amjhyper.2005.04.021.
Pheochromocytoma, a rare and usually curable cause of hypertension, is characterized by symptoms and signs related to increased catecholamine secretion. Pregnancy can elicit clinical manifestations of otherwise unrecognized pheochromocytoma.
Four women, ranging in age from 27 to 37 years, were referred to the hypertension clinic with the following presentations: 1) a 35-year-old woman, diagnosed with gestational hypertension and headaches during the third trimester of her pregnancy and 5 months after delivery, was hospitalized with pulmonary edema. Echocardiography revealed severe dilated left ventricular (LV) dysfunction. Cardiac function was normalized after surgical resection of a pheochromocytoma from her left adrenal; 2) a 37-year-old woman suffered from preeclampsia, persistent hypertension and orthostatic hypotension after a cesarean section. A diagnostic work-up revealed a catecholamine-secreting paraganglioma in the retroperitoneum. The patient underwent a laparosopic resection of the tumor; 3) a 27-year-old woman suffered from hypertension and episodes of palpitations, sweating, and dyspnea in the first trimester of her pregnancy. An ultrasound revealed a 5-cm mass in the left adrenal. She underwent a left adrenalectomy at the 17th week of pregnancy, which confirmed the diagnosis of pheochromocytoma; 4) a 34-year-old woman, at the 26th week of pregnancy, presented with an acute loss of vision and blood pressure of 230/140 mm Hg. Fundoscopy showed papilledema with soft exudates in both eyes. Chemical studies were positive and imaging revealed a left adrenal pheochromocytoma. Despite aggressive medical treatment, fetal distress mandated a laparotomy at the end of the 28th week of pregnancy. A healthy newborn was delivered and resection of the adrenal tumor confirmed the diagnosis of pheochromocytoma.
Although rare, pheochromocytoma can cause severe peripartum hypertension. Screening for pheochromocytoma, ideally with plasma-free metanephrines, should be considered in cases of peripartum hypertension.
嗜铬细胞瘤是一种罕见但通常可治愈的高血压病因,其特征为与儿茶酚胺分泌增加相关的症状和体征。妊娠可引发原本未被识别的嗜铬细胞瘤的临床表现。
4名年龄在27至37岁之间的女性因以下症状被转诊至高血压门诊:1)一名35岁女性,在妊娠晚期及产后5个月被诊断为妊娠高血压和头痛,因肺水肿住院。超声心动图显示严重的左心室扩张功能障碍。切除左侧肾上腺的嗜铬细胞瘤后心脏功能恢复正常;2)一名37岁女性在剖宫产术后患有先兆子痫、持续性高血压和体位性低血压。诊断性检查发现腹膜后有一个分泌儿茶酚胺的副神经节瘤。患者接受了腹腔镜肿瘤切除术;3)一名27岁女性在妊娠早期患有高血压、心悸、出汗和呼吸困难发作。超声检查发现左侧肾上腺有一个5厘米的肿块。她在妊娠第17周接受了左侧肾上腺切除术,确诊为嗜铬细胞瘤;4)一名34岁女性在妊娠第26周时出现急性视力丧失,血压为230/140毫米汞柱。眼底检查显示双眼视乳头水肿伴软性渗出物。化学检查呈阳性,影像学检查发现左侧肾上腺嗜铬细胞瘤。尽管进行了积极的药物治疗,但胎儿窘迫促使在妊娠第28周结束时进行剖腹手术。分娩出一名健康新生儿,肾上腺肿瘤切除确诊为嗜铬细胞瘤。
尽管罕见,但嗜铬细胞瘤可导致严重的围产期高血压。对于围产期高血压病例,应考虑筛查嗜铬细胞瘤,理想的筛查方法是检测血浆游离甲氧基肾上腺素。