Behbehani A W, Lehnert W, Langenbeck U, Luthe H, Baumgartner R
Klin Padiatr. 1984 Mar-Apr;196(2):106-10. doi: 10.1055/s-2007-1025588.
Clinical course and special diagnostic procedures in a 7 1/2 weeks old dystrophic infant with propionic acidemia are described. The disorder manifested with vomiting and diarrhea within the first week of life when the child was on a cow milk formula. Parenteral nutrition with glucose and electrolytes led to improvement. When oral nutrition with a cow milk formula was implemented again, an acute deterioration with diarrhoea and vomiting occurred. Thus, a diagnosis of cow milk allergy was suggested. There was also a severe muscular hypotony. Oral nutrition with a soybean formula did not prevent further clinical deterioration. At 7 1/2 weeks of age the patient died with symptoms of cardiogenic shock. The correct diagnosis was considered too late and confirmed post mortem. Clinical symptoms in the neonatal period like vomiting, muscular hypotony and failure to thrive should alert the physician to a possible diagnosis of a hereditary organic aciduria. Gas chromatography-mass spectrometry of urinary organics acids, in the present case, established the diagnosis. On autopsy, spongy degenerations were found in CNS.
描述了一名7.5周大患有丙酸血症的营养不良婴儿的临床病程及特殊诊断程序。该疾病在患儿出生第一周食用牛奶配方奶时表现为呕吐和腹泻。给予葡萄糖和电解质的肠外营养后病情有所改善。当再次采用牛奶配方奶进行口服营养时,出现了伴有腹泻和呕吐的急性恶化。因此,有人提出牛奶过敏的诊断。患儿还存在严重的肌张力减退。采用大豆配方奶进行口服营养并未能阻止病情进一步恶化。患儿在7.5周龄时死于心源性休克症状。正确诊断做出得太晚,尸检后得以确诊。新生儿期出现的呕吐、肌张力减退和发育不良等临床症状应提醒医生考虑遗传性有机酸尿症的可能诊断。在本病例中,通过尿有机酸的气相色谱-质谱分析确诊了疾病。尸检时,在中枢神经系统发现了海绵状变性。