Department of Medicine, Kasturba Medical College, Manipal, Manipal University, Karnataka, India.
Asian Pac J Trop Med. 2012 Aug;5(8):667-8. doi: 10.1016/S1995-7645(12)60137-0.
We present this rare occurrence of a 17 yr old boy, a known case of congenital hypoparathyroidism, who presented with fever and jaundice for 8 days and 2 episodes of generalised tonic-clonic seizures. Premorbidly patient was on regular oral calcium supplementations with normal serum calcium levels. Investigations revealed severe hypocalcaemia (3.2 mg/dL), low 25 hydroxyvitamin D levels and hypomagnesaemia. The marked elevation of serum bilirubin was accompanied by derangement of liver enzymes. Microbiological investigations were confirmatory for both hepatitis A and typhoid fever. In spite of the aggressive management with intravenous calcium gluconate infusion, refractory hypocalcaemia persisted with recovery only after gradual decline in the bilirubin levels. We inferred that the cholestatic process produced by both acute viral hepatitis A and typhoid fever precipitated this state of refractory hypocalcaemia in the previously well preserved patient.
我们呈现了这一罕见病例,一名 17 岁男孩患有先天性甲状旁腺功能减退症,他因发热和黄疸持续 8 天,并伴有 2 次全身性强直阵挛性癫痫发作而就诊。在发病前,患者一直在服用常规的口服钙剂,血钙水平正常。检查发现严重低钙血症(3.2mg/dL)、25-羟维生素 D 水平低和低镁血症。血清胆红素明显升高,同时伴有肝酶异常。微生物学检查证实了甲型肝炎和伤寒均为阳性。尽管给予了静脉注射葡萄糖酸钙输注的积极治疗,但难治性低钙血症持续存在,只有在胆红素水平逐渐下降后才得以恢复。我们推断,急性甲型肝炎和伤寒引起的胆汁淤积过程导致了这位之前情况良好的患者出现难治性低钙血症。