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首页> 外文期刊>Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association >Sudden death due to subarachnoid haemorrhage in an infant with autosomal dominant polycystic kidney disease
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Sudden death due to subarachnoid haemorrhage in an infant with autosomal dominant polycystic kidney disease

机译:患有常染色体显性遗传多囊肾的婴儿因蛛网膜下腔出血突然死亡

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摘要

Intracranial aneurysm rupture is the most serious and potentially lethal extra-renal manifestation of autosomal dominant polycystic kidney disease (ADPKD). Almost all cases of ruptured intracranial aneurysm occur in adult patients with a median age of rupture of 40 years. We report the occurrence of sudden death in a newborn infant born to a mother with typical ADPKD in the first week of life. Post-mortem examination revealed the cause of death to be subarachnoid haemorrhage with focal glomerular and tubular cysts detected in the kidney. This is the earliest reported case of intracranial aneurysm rupture in ADPKD and should raise awareness of this rare but lethal complication in younger patients.
机译:颅内动脉瘤破裂是常染色体显性多囊肾病(ADPKD)的最严重且可能致命的肾外表现。几乎所有颅内动脉瘤破裂病例都发生在中位破裂年龄为40岁的成年患者中。我们报告了在出生后第一周,一名患有典型ADPKD的母亲所生的新生儿突然死亡。验尸后发现死因是蛛网膜下腔出血,肾脏中发现了局灶性肾小球和肾小管囊肿。这是最早报道的ADPKD颅内动脉瘤破裂病例,应该提高对年轻患者这种罕见但致命的并发症的认识。

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