milk allergy

牛奶过敏
  • 文章类型: Case Reports
    在新生儿的脐带血细胞中发现了对牛奶过敏原的细胞增殖。虽然这反映了胎儿生命中的敏感性,其临床意义和疾病,尤其是它的非常规演讲,基本上没有得到护理提供者的认可。这里,我们报告了三例母亲在怀孕期间食用乳制品的婴儿,患有严重便秘的产前和产后肠道。胎粪的通过显着延迟,随后的早发性婴儿便秘难以治疗,但当牛奶蛋白被抑制时,缓解,当重新引入牛奶蛋白质时复发,并在转换为广泛水解或基于氨基酸的婴儿配方食品时再次解决。基于这一点和其他观察,据认为,这些婴儿必须在出生前开始和/或发展牛乳蛋白过敏。我们建议对这些早发性便秘的新生儿进行为期2周的避免牛乳蛋白的试验,然后根据当前指南对先天性巨结肠和其他疾病进行不必要的侵入性检查。
    A cellular proliferation to milk allergens has been found in the cord blood cells of neonates. While this reflects a sensitivity during the fetal life, its clinical significance and disease, particularly its unconventional presentations, have remained largely unrecognized by care providers. Here, we report three cases of infants whose mothers consumed dairy products during pregnancy, who developed a severely constipated pre- and postnatal bowel. The passage of meconium was significantly delayed with subsequent early-onset infant constipation that was intractable to conventional therapies but remitted when milk proteins were withheld, recurred when milk proteins were reintroduced, and resolved again when switched to an extensively hydrolyzed or amino acid-based infant formula. Based on this and other observations, it is believed that these infants must have initiated and/or developed cow\'s milk protein allergy prenatally during fetal life. We suggest that a 2-week trial of cow\'s milk protein avoidance be applied to these neonate infants with early-onset constipation before an unnecessary invasive work-up for Hirschsprung disease and others is initiated per the current guidelines.
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  • 文章类型: Journal Article
    8806H配方是日本唯一可用于患有慢性肾脏疾病的儿科患者的肾脏配方。1个月大的女婴由于牛奶过敏而不能给药8806H。给予聚苯乙烯磺酸钠治疗的低钾抗过敏配方维持了足够的血清钾水平,腹膜透析的引入可能会延迟。患者患有严重的肾功能不全,继发于双侧增生性和多囊性肾脏。尽管她收到了8806H配方,该产品被转换为水解酪蛋白配方,因为她在28日龄时对8806H过敏,导致了高钾血症.我们在40日龄时开始用聚苯乙烯磺酸钠治疗,以降低牛奶中的钾浓度,预防高钾血症并维持患者的营养状况,以确保适当增加体重。我们监测了牛奶中的电解质水平,并在喂食前确认了钾水平的降低。尽管这种情况很少见,并且很少有抗过敏配方中钾减少的报道,对于因牛奶过敏而无法接受肾脏配方治疗的肾功能不全患儿,此策略可能有用.
    The 8806H formula is the only renal formula available for pediatric patients with chronic kidney disease in Japan. A 1-month-old female infant could not be administered 8806H because of milk allergy. Administration of low-potassium anti-allergic formula treated with sodium polystyrene sulfonate maintained adequate serum potassium levels, and introduction of peritoneal dialysis could be delayed. The patient had severe renal dysfunction secondary to bilateral hypoplastic and multi-cystic kidneys. Although she received the 8806H formula, this product was switched to hydrolyzed casein formula because she developed allergy to 8806H at 28 days of age, which led to hyperkalemia. We initiated treatment with sodium polystyrene sulfonate at 40 days of age to lower the potassium concentration in milk, which prevented hyperkalemia and maintained the patient\'s nutritional status to ensure appropriate increase in body weight. We monitored electrolyte levels in milk and confirmed reduction in potassium levels before feeding. Although such condition is rare and there are few reports of potassium reduction in anti-allergic formulas, this strategy may be useful for pediatric patients with renal insufficiency who cannot be treated with renal formulas because of milk allergy.
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  • 文章类型: Journal Article
    我们研究了牛奶过敏(CMA)与幼年特发性关节炎(JIA)之间的关系。本病例对照研究的材料是从2000年至2010年在芬兰出生并被诊断为JIA(n=1,298)和年龄-的所有儿童的国家登记册中收集的。sex-,和地点匹配的对照(n=5,179)。我们确定了235名CMA儿童;其中66名儿童也患有JIA。进行了条件逻辑回归分析,以评估CMA和JIA之间的关联,并测试抗生素暴露是否会成为这种关联的协变量。在男孩(但不是女孩),CMA的诊断和婴儿期使用低变应原性配方与JIA的后期发展相关(比值比=2.4,95%置信区间:1.6,3.6).这种关联在3岁之前被诊断为JIA或被诊断为主要胃肠道症状的CMA的男孩中最为明显。在JIA的后期发展中,CMA与抗生素暴露之间没有统计学上显着的累加相互作用。这些关联可能反映了有JIA风险的男孩肠道免疫和完整性的成熟受损。与JIA发病机制相关的诱发因素似乎显示出与性别相关的差异。
    We examined the association between cow\'s milk allergy (CMA) and juvenile idiopathic arthritis (JIA). The material for this case-control study was collected from national registers of all children born in Finland between 2000 and 2010 and diagnosed with JIA (n = 1,298) and age-, sex-, and place-matched controls (n = 5,179). We identified 235 children with CMA; 66 of these children also had JIA. A conditional logistic regression analysis was performed to evaluate the association between CMA and JIA and to test whether exposure to antibiotics would be a covariate for this association. In boys (but not in girls), a diagnosis of CMA and the use of hypoallergenic formula in infancy were associated with the later development of JIA (odds ratio = 2.4, 95% confidence interval: 1.6, 3.6). The association was most evident in boys who were diagnosed with JIA before age 3 years or diagnosed with CMA with predominantly gastrointestinal symptoms. There was no statistically significant additive interaction between CMA and antibiotic exposure in the later development of JIA. These associations may reflect impaired maturation of intestinal immunity and integrity in boys with a risk of JIA. Predisposing factors related to JIA pathogenesis seem to display a sex-linked disparity.
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