Hejazi Arya, Hosseini Marzieh, Bahrani Mohammadreza
Department of Pathology Laboratory, Fars Legal Medicine Research Center, PO Box 71345-1864, Shiraz, Iran.
Am J Forensic Med Pathol. 2013 Jun;34(2):127-9. doi: 10.1097/PAF.0b013e31828d69da.
Acute arteritis of the aorta and the main pulmonary arteries is unusual in a newborn. This type of vasculitis should be described as a separate entity. There are many differences between this entity and polyarteritis nodosa or Takayasu disease. Moreover, neither Takayasu disease nor polyarteritis nodosa and other forms of classic primary large vessels vasculitis have been reported in a neonate until now. The presence of chronic inflammation, fibrosis, and calcification would suggest that this process had been present before birth.We report a 27-day-old newborn with acute necrotizing aortitis. The feature of this entity is not those of any of the classic entities described in infants or children.
新生儿主动脉及主要肺动脉的急性动脉炎并不常见。这种血管炎应被描述为一种独立的疾病实体。该实体与结节性多动脉炎或高安病有许多不同之处。此外,迄今为止,尚未有新生儿患高安病、结节性多动脉炎及其他经典原发性大血管血管炎的报道。慢性炎症、纤维化和钙化的存在提示该过程在出生前就已存在。我们报告一例患有急性坏死性主动脉炎的27日龄新生儿。该疾病实体的特征与婴儿或儿童中描述的任何经典实体均不相同。