Anyiam Oluwaseun, Wallin Elizabeth, Kaplan Felicity, Lawrence Christopher
Imperial College London, London, UK.
East and North Hertfordshire NHS Trust, Stevenage, UK.
Case Rep Med. 2019 Dec 25;2019:2349470. doi: 10.1155/2019/2349470. eCollection 2019.
Renal Fanconi syndrome (RFS) is characterised by generalised dysfunction of the proximal renal tubules, resulting in excessive urinary loss of solutes, most notably bicarbonate, and type II (proximal) renal tubular acidosis. It is a rare condition, and literature around its management through pregnancy is limited. We present the management of a 37-year-old woman with RFS secondary to the HNF4A p.R63W mutation, through her third pregnancy. She presented at 28 + 5 weeks with dehydration, low serum bicarbonate, and profound metabolic acidosis. Daily infusions of sodium bicarbonate were necessary, and the requirements increased throughout the pregnancy. She also demonstrated both fasting hypoglycaemia and episodes of postprandial hyperglycaemia which required complex management. Due to concerns around fetal health, an elective caesarean section was performed at 34 weeks, delivering a healthy baby girl. This case highlights the potential complexity of pregnancy in patients with RFS and the need for a multidisciplinary approach to its management.
肾性范科尼综合征(RFS)的特征是近端肾小管广泛功能障碍,导致溶质过度经尿液丢失,最显著的是碳酸氢盐,以及II型(近端)肾小管酸中毒。这是一种罕见病症,关于其孕期管理的文献有限。我们介绍了一名37岁继发于HNF4A p.R63W突变的肾性范科尼综合征女性患者第三次怀孕期间的管理情况。她在孕28 + 5周时出现脱水、血清碳酸氢盐水平低和严重代谢性酸中毒。每日输注碳酸氢钠是必要的,且整个孕期需求不断增加。她还出现空腹低血糖和餐后高血糖发作,需要复杂的管理。由于担心胎儿健康,在34周时进行了择期剖宫产,产下一名健康女婴。该病例突出了肾性范科尼综合征患者孕期可能存在的复杂性以及对其管理采取多学科方法的必要性。