Department of Nuclear Medicine, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, 310003, People's Republic of China.
Department of Radiology, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, 310003, People's Republic of China.
BMC Endocr Disord. 2019 Jul 29;19(1):82. doi: 10.1186/s12902-019-0409-9.
Primary hyperparathyroidism (PHPT), which is mostly caused by a parathyroid adenoma, is fairly common in postmenopausal women but is relatively rare in pregnant women. PHPT-induced pancreatitis during pregnancy is associated with significant maternal and foetal morbidity and mortality. Diagnosis is challenging because of non-specific symptoms and changes in maternal calcium homeostasis. Information about the optimal treatment strategy for the prevention of catastrophic consequences to the mother and foetus is limited. Here, we describe a rare lethal case of severe acute necrotizing pancreatitis due to a parathyroid adenoma in a woman in her third trimester of pregnancy.
A previously healthy 24-year-old Chinese woman at 37 weeks of gestation presented with persisting epigastric pain, nausea and bilious vomiting for 1 day. PHPT-induced acute necrotizing pancreatitis was diagnosed on the basis of her serum calcium, parathyroid levels and imaging results. A caesarean section and parathyroidectomy were performed at 1 day and 11 days after admission, respectively. Histological examination confirmed a right inferior parathyroid adenoma with a size of 2.0 × 1.5 cm. Following the parathyroidectomy, the patient had eucalcaemia and presented normal parathyroid hormone (PTH) levels. Although the foetus was normal, the patient died of multiple organ failure due to severe pancreatitis.
PHPT-induced acute necrotizing pancreatitis is a rare clinical entity and life-threatening condition to both the mother and the foetus during pregnancy. Early diagnosis can be challenging and is crucial. Appropriate treatment according to the patient's condition may effectively reduce maternal and foetal mortality.
原发性甲状旁腺功能亢进症(PHPT)主要由甲状旁腺瘤引起,在绝经后妇女中较为常见,但在孕妇中相对罕见。PHPT 引起的妊娠胰腺炎与母婴发病率和死亡率显著相关。由于母体钙稳态的变化和非特异性症状,诊断具有挑战性。关于预防对母婴灾难性后果的最佳治疗策略的信息有限。在这里,我们描述了一例罕见的致命病例,即妊娠晚期妇女因甲状旁腺瘤引起的严重急性坏死性胰腺炎。
一名 24 岁的中国健康初产妇,妊娠 37 周,持续上腹痛、恶心和胆汁性呕吐 1 天。根据血清钙、甲状旁腺水平和影像学结果诊断为 PHPT 诱导的急性坏死性胰腺炎。入院后 1 天和 11 天分别进行了剖宫产和甲状旁腺切除术。组织学检查证实为大小为 2.0×1.5cm 的右侧下甲状旁腺腺瘤。甲状旁腺切除术后,患者血钙正常,甲状旁腺激素(PTH)水平正常。尽管胎儿正常,但由于严重胰腺炎,患者死于多器官衰竭。
PHPT 诱导的急性坏死性胰腺炎是一种罕见的临床实体,对妊娠期间的母婴都是危及生命的情况。早期诊断具有挑战性,至关重要。根据患者的情况进行适当的治疗可能会有效降低母婴死亡率。