scholarly journals Recurrent gastrointestinal bleeding in a patient with type 1 neurofibromatosis

2019 ◽  
Vol 12 (6) ◽  
pp. e226303
Author(s):  
Vidhyachandra Gandhi ◽  
Pratik Gautam ◽  
Taher Chharchhodawala ◽  
Nitin Pai

Type 1 neurofibromatosis (NF1) is a hereditary disorder with an incidence of approximately 1:3000 at birth. Gastrointestinal (GI) lesions occur in approximately one-third of the patients, with most being asymptomatic and diagnosed incidentally. Symptomatic lesions leading to GI bleeding are uncommon. We share our experience of an elderly man with NF1, who presented with massive recurrent GI bleeding secondary to jejunal neurofibromas. The lesions were identified on CT scan of abdomen, and the patient was managed with resection of the involved bowel segment.

2011 ◽  
Vol 141 (2) ◽  
pp. 437-782 ◽  
Author(s):  
Ming-Chang Ku ◽  
Chung-Ming Tsai ◽  
Yeu-Sheng Tyan

Heart Asia ◽  
2012 ◽  
Vol 4 (1) ◽  
pp. 27-30 ◽  
Author(s):  
Amit Malviya ◽  
Sundeep Mishra ◽  
Shyam S Kothari

2007 ◽  
Vol 54 (3,4) ◽  
pp. 354-358 ◽  
Author(s):  
Sara Simeoni ◽  
Antonio Puccetti ◽  
Marco Chilosi ◽  
Elisa Tinazzi ◽  
Daniele Prati ◽  
...  

Breast Cancer ◽  
2009 ◽  
Vol 17 (4) ◽  
pp. 306-309 ◽  
Author(s):  
Nikolaos S. Salemis ◽  
Georgios Nakos ◽  
Dimitrios Sambaziotis ◽  
Stavros Gourgiotis

2011 ◽  
pp. P1-722-P1-722
Author(s):  
Chiara Diazzi ◽  
Alessandro Guidi ◽  
Alessandra Luberto ◽  
Erica Taliani ◽  
Bruno Madeo ◽  
...  

2019 ◽  
Vol 16 (1) ◽  
pp. 62-71
Author(s):  
Natasha Harris ◽  
Alaa Rostom ◽  
Husein Moloo

Background:  Obscure gastrointestinal bleeding from idiopathic small bowel varices is both a diagnostic and management challenge for physicians. There are very few cases reported in the literature and there is no consensus on management recommendations. Aims:  To present the case of a 34-year-old male patient with bleeding from idiopathic jejunal varices and to review similar cases in the literature.  Methods:  A case of idiopathic jejunal varices is reported. A literature review was conducted and a total of 24 articles describing idiopathic small bowel varices were identified. Results:  Case Report: A 34-year-old gentleman was referred for worsening obscure gastrointestinal bleeding and anemia. Anterograde single balloon enteroscopy revealed several petechial like lesions that were not classic for angiodysplasia. These lesions were initially treated with argon plasma coagulation and clipped, which did not resolve the patient’s persistent anemia. No venous abnormalities were identified on computed tomography of the abdomen and pelvis with contrast. The patient underwent an endoscopically assisted exploratory laparoscopy that was converted to a laparotomy upon finding of grossly abnormal distal jejunum. Dilated and tortuous varicosities were identified involving approximately 150 cm of small bowel. It was decided to resect the 40 cm segment of jejunum in which varices were visible endoscopically. There was no evidence of thrombosis in the resected specimen. The patient suffered a pulmonary embolism post-operatively, believed to be provoked by the surgery.  The patient has had no re-bleeding 12 months post-resection. Literature Review: Both familial and non-familial accounts of small bowel varices in the absence of a primary cause have been reported in the literature. When supportive therapy is insufficient, the most common treatment modality chosen is surgical resection. Select cases have also demonstrated that sclerotherapy and varix dissection can be used for to treat these lesions. Conclusions:  Idiopathic small bowel varices pose both diagnostic and therapeutic challenges for physicians. In the literature, several treatment modalities have been shown to be successful; these include surgical resection, varix dissection and sclerotherapy. There is no consensus on the preferred treatment strategy. This report demonstrates endoscopically assisted surgical resection as a viable management strategy for bleeding of idiopathic small bowel varices, an uncommon cause of occult GI bleeding.


Urology ◽  
2011 ◽  
Vol 77 (6) ◽  
pp. 1339-1340 ◽  
Author(s):  
Dominik Abt ◽  
Diego De Lorenzi ◽  
Wolfgang Nagel ◽  
Hans-Peter Schmid ◽  
Stefan Preusser

2020 ◽  
Vol 3 (1) ◽  
pp. 64-66
Author(s):  
Prakash Poudel ◽  
Ramesh Dhakwa

Dieulafoy lesion is a rare cause of massive GI bleeding. It’s an abnormal sub-mucosal artery protruding from a minute mucosal defect (≤3 mm). A 31 yearold male presented with complaints of hematochezia. Preliminary investigations failed to locate the exact source of bleed. Enteroscopy suggested distal ileal bleed. At laparotomy, an ulcerated nodular lesion, approximately 0.5 cm was identified in distal ileum. 30 cm of ileum along with mesentery was resected. Histology revealed it to be Dieulafoy lesion. Dieulafoy lesion is uncommon but one of the causes of obscure gastrointestinal bleeding that could result in treacherous and life-threatening gastrointestinal haemorrhage. This lesion is difficult to identify and high index of suspicion is required to make diagnosis. Hence, it should be considered in the differential diagnosis of active GI bleeding. The definitive diagnosis is based only on histopathology.


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