Laval Nancy, Kleiber Niina, Soucy Jean-François, Dubois Josée, Assaad Michael-Andrew
Neonatology, Centre Hospitalier Universitaire Sainte-Justine, Montréal, CAN.
Neonatology, Centre Hospitalier Chrétien MontLégia, Liège, BEL.
Cureus. 2024 Apr 28;16(4):e59243. doi: 10.7759/cureus.59243. eCollection 2024 Apr.
Activating mutation of PIK3CA is linked with cases of overgrowth syndromes and belongs to the PIK3CA-related overgrowth spectrum (PROS). Mutations in this gene are associated with vascular malformations, brain abnormalities, and an increased risk for certain tumors. We report the case of a newborn girl, preterm at 34 weeks of gestation, referred to our center for atypical necrotizing enterocolitis (NEC). At laparotomy, the appearance of the intestinal tract was described as puffy, cauliflower-like with a dark purplish coloration. Subsequently, the colostomy was described as having a consistent proliferative appearance. Medical treatment with sirolimus resulted in minimal improvement. There are no reported cases in the literature of association between NEC and PIK3CA mutation. It is possible that PIK3CA mutation, including the related vascular anomalies, plays a role in the pathogenesis of NEC with this condition.
PIK3CA的激活突变与过度生长综合征病例相关,属于PIK3CA相关过度生长谱系(PROS)。该基因的突变与血管畸形、脑部异常以及某些肿瘤的风险增加有关。我们报告了一名妊娠34周早产的新生女婴的病例,她因非典型坏死性小肠结肠炎(NEC)被转诊至我们中心。剖腹手术时,肠道外观被描述为肿胀、呈菜花状且颜色为深紫色。随后,结肠造口术被描述为具有持续的增殖外观。使用西罗莫司进行药物治疗仅取得了轻微改善。文献中没有关于NEC与PIK3CA突变之间关联的报道病例。PIK3CA突变,包括相关的血管异常,有可能在这种情况下的NEC发病机制中起作用。