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与1型神经纤维瘤病相关的自发性肠血肿。

Spontaneous intestinal haematoma associated with neurofibromatosis type-1.

作者信息

Hassan Syed, Yee Victoria, Amer Syed, Alkhatib Yaser

机构信息

Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan, USA.

出版信息

BMJ Case Rep. 2013 Aug 23;2013:bcr2013010512. doi: 10.1136/bcr-2013-010512.

DOI:10.1136/bcr-2013-010512
PMID:23975920
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3761687/
Abstract

Vasculopathy in patients with neurofibromatosis-1 are rare but serious and have potentially life-threatening complications. It mostly involves the thoracic, abdominal and intracranial vessels. In this case study we describe the first reported case of spontaneous intestinal haematoma in a young male patient. The first episode occurred at the age of 30, following which 2 years later the second episode was noted at the same anatomical site, which was spontaneous without any inciting event.

摘要

1型神经纤维瘤病患者的血管病变罕见但严重,并有潜在的危及生命的并发症。它主要累及胸、腹和颅内血管。在本病例研究中,我们描述了首例年轻男性患者自发性肠血肿的报告病例。首次发作发生在30岁时,两年后在同一解剖部位出现第二次发作,此次发作是自发的,没有任何诱发事件。

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Spontaneous intestinal haematoma associated with neurofibromatosis type-1.与1型神经纤维瘤病相关的自发性肠血肿。
BMJ Case Rep. 2013 Aug 23;2013:bcr2013010512. doi: 10.1136/bcr-2013-010512.
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Intramural haematoma of the duodenum.十二指肠壁内血肿
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本文引用的文献

1
Massive spontaneous hemorrhage in giant type 1 neurofibromatosis in soft tissue of chest wall.
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Spontaneous intramural duodenal hematoma--a rare cause of upper gastrointestinal obstruction.自发性十二指肠壁内血肿——上消化道梗阻的罕见原因。
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Intramural hematoma of the duodenum.十二指肠壁内血肿
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