Pirtskhalava N
O. Gudushauri National Medical Centre, Perinatal Department, Tbilisi, Georgia.
Georgian Med News. 2012 Jul(208-209):76-82.
Hypertension is the most common medical complication of pregnancy. Pheochromocytoma in pregnancy is rare, and if unrecognized, can cause serious perinatal morbidity and mortality. A patient with paroxysmal hypertension, postpartum intraabdominal bleeding, and a recognized pheochromocytoma is described. A 36-yr-old previously practical healthy woman (gravida 4, para 3) presented to our tertiary care centre at at 26 weeks four days gestation with a history of labile blood pressure and severe hypertension. A two week prior to admission she began having episodes of severe headache, sweating, nausea and dizziness. On an obstetric visit she was noted to be severely hypertensive with a blood pressure of 220/120 mmHg. Ultrasound imaging demonstrated a 11,6 cm x 9,2 cm right adrenal mass, biochemical investigations confirmed the diagnosis of pheochromocytoma. The patient was invasively monitored in the intensive care unit and treated with alpha-blockers and doxazosin. A multidisciplinary conference was organized involving endocrinology, anesthesiology, general surgery and obstetrics to determine the most appropriate management of the patient. Childbirth was performed by elective Cesarean Section with simultaneous laparatomic right-sided adrenalectomy. Postoperative period was complicated with intraabdominal bleeding consequently treated during relaparatomy. The primary goals in the management of pheochromocytoma in pregnancy are early diagnosis, usage of alpha-blockers, and avoidance of a hypertensive crises during delivery and definitive surgical treatment. Timing of surgical resection will depend on the gestational age at which diagnosis is made. Cesarean section is the preferred mode of delivery when the tumor is still present. Complications such is bleeding from adrenalectomy site should be considered. This case illustrates that with antenatal diagnosis, advanced methods of tumor localization, adequate preoperative adrenergic blockade and team planning, pheochromocytoma in pregnancy can be treated successfully even in complicated cases.
高血压是妊娠最常见的医学并发症。妊娠期嗜铬细胞瘤较为罕见,若未被识别,可导致严重的围产期发病和死亡。本文描述了一名患有阵发性高血压、产后腹腔内出血且已确诊嗜铬细胞瘤的患者。一名36岁、既往身体健康的女性(孕4产3),在妊娠26周零4天时因血压不稳定和严重高血压病史就诊于我们的三级护理中心。入院前两周,她开始出现严重头痛、出汗、恶心和头晕症状。在一次产科检查中,发现她血压严重升高,达220/120 mmHg。超声检查显示右侧肾上腺有一个11.6 cm×9.2 cm的肿块,生化检查确诊为嗜铬细胞瘤。患者在重症监护病房接受有创监测,并接受α受体阻滞剂和多沙唑嗪治疗。组织了一次多学科会议,涉及内分泌科、麻醉科、普通外科和产科,以确定对该患者最合适的治疗方案。通过择期剖宫产同时行腹腔镜右侧肾上腺切除术分娩。术后出现腹腔内出血并发症,随后在再次剖腹手术中进行了治疗。妊娠期嗜铬细胞瘤治疗的主要目标是早期诊断、使用α受体阻滞剂,避免分娩期间发生高血压危象以及进行确定性手术治疗。手术切除的时机将取决于诊断时的孕周。当肿瘤仍然存在时,剖宫产是首选的分娩方式。应考虑诸如肾上腺切除部位出血等并发症。该病例表明,通过产前诊断、先进的肿瘤定位方法、充分的术前肾上腺素能阻滞和团队规划,即使在复杂病例中,妊娠期嗜铬细胞瘤也可得到成功治疗。