Literature DB >> 12415484

Infrarenal aortic rupture secondary to neurofibromatosis.

George L Hines1, Laura Lefkowitz, Manucher Mohtashemi.   

Abstract

Neurofibromatosis is characterized by its cutaneous manifestations. It also is manifested by arterial lesions commonly found in arterioles and small arteries but rarely in large arteries. We present a patient with type I neurofibromatosis with spontaneous rupture of his abdominal aorta. He was found at the time of emergency laparotomy to have direct compression of his aorta by retroperitoneal neurofibromas and abnormal aortic structural wall integrity.

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Year:  2002        PMID: 12415484     DOI: 10.1007/s10016-001-0221-6

Source DB:  PubMed          Journal:  Ann Vasc Surg        ISSN: 0890-5096            Impact factor:   1.466


  3 in total

1.  Spontaneous aortic rupture in a patient with neurofibromatosis type 1.

Authors:  Yang Jin Park; Keun Myoung Park; Jiyoung Oh; Hong Suk Park; Jung-Sun Kim; Young-Wook Kim
Journal:  J Korean Surg Soc       Date:  2012-03-27

2.  Fatal acute retropharyngeal hemorrhage in neurofibromatosis type 1.

Authors:  Pierre-Antoine Peyron; Michael S Pollanen
Journal:  Forensic Sci Med Pathol       Date:  2017-10-28       Impact factor: 2.007

3.  Successful treatment of aortic rupture with endovascular stent grafting in a patient with mantle cell lymphoma.

Authors:  A T Sumbul; F Kose; L Oğuzkurt; C Karadeniz; N E Kocer; O Ozyilkan
Journal:  Case Rep Oncol       Date:  2012-05-30
  3 in total

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