scholarly journals SPONTANEOUS INTESTINAL PERFORATION: AN ATYPICAL PRESENTATION OF THE PATIENT WITH DIARRHEAE—A CASE REPORT.

2018 ◽  
Vol 6 (2) ◽  
pp. 1345-1347
Author(s):  
Reem Aljubab ◽  
◽  
Abdulwahab AlJubab ◽  
Mohammed Mallick ◽  
Ilhama Jafarli ◽  
...  
2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Aylin Canbolat Ayhan ◽  
Cetin Timur ◽  
Ersin Bocu ◽  
Neslihan Gulcin

Background. Neutropenic enterocolitis is one of the most common gastrointestinal complications seen in patients who are receiving chemotherapy for leukemia. Severe neutropenia is the main underlying factor of this pathology. It is characterized by fever and abdominal pain.Case Presentation. Herein, we report a case of neutropenic enterocolitis which presented with intestinal perforation in an afebrile patient who was diagnosed with acute lymphoblastic leukemia and was receiving induction chemotherapy.Conclusion. We aimed to emphasize the importance of enterocolitis and increase awareness against such severe complications which could have unexpected presentations.


2019 ◽  
Vol 18 (2) ◽  
pp. 90-96
Author(s):  
O. V. Shcherbakova

A rare clinical observation of spontaneous intestinal perforation into the free abdominal cavity in teenager with complicated Crohn's disease during steroids therapy is presented. The experience of exclusive enteral nutrition and the results of the first stricturoplasty in children are demonstrated.


Author(s):  
Shweta Sharma ◽  
Bharat Sharma ◽  
Shantnu Chauhan ◽  
Mir Aziz ◽  
Nalin Chugh ◽  
...  

Author(s):  
Raul-Ciprian Covrig ◽  
Jasmina Petridou ◽  
Ulrich J. Knappe

AbstractBrucellosis is a frequent zoonosis in some regions of the world and may cause various symptoms. Neurobrucellosis is a rare but serious complication of the infection. Our case report describes the course of neurobrucellosis in a patient who had received a ventriculoperitoneal shunt in his native country 13 years prior to diagnosis of brucellosis. He initially presented to us with symptoms of peritonitis, which misled us to perform abdominal surgery first. After the diagnosis of neurobrucellosis was confirmed and appropriate antibiotics were initiated, the symptoms soon disappeared. Although the ventriculoperitoneal shunt was subsequently removed, the patient did not develop a symptomatic hydrocephalus further on. This case displays the challenges in diagnosing an infection that occurred sporadically in Europe and may be missed by currently applied routine microbiological workup. Considering the political context, with increasing relocation from endemic areas to European countries, it is to be expected that the cases of brucellosis and neurobrucellosis will rise. Brucellosis should be considered and adequate investigations should be performed.


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