scholarly journals Neonatal intestinal obstruction associated with situs inversus totalis: two case reports and a review of the literature

2017 ◽  
Vol 11 (1) ◽  
Author(s):  
Rahul Gupta ◽  
Varsha Soni ◽  
Prakash Devidas Valse ◽  
Ram Babu Goyal ◽  
Arun Kumar Gupta ◽  
...  
1991 ◽  
Vol 65 (4) ◽  
pp. 286-288 ◽  
Author(s):  
J. B. Mpairwe

ABSTRACTTwo cases of intestinal obstruction due to Ascaris lumbricoides infection are reported from Ishaka Adventist Hospital, in south western Uganda. One was a male aged two and a half years and another was a female aged twenty. They were both treated surgically with good results. A review of the literature also revealed that intestinal obstruction due to A. lumbricoides is a common complication, though other surgical and nutritional complications also seem to be common, they are less reported.


2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Xu-Yong Sun ◽  
Ke Qin ◽  
Jian-Hui Dong ◽  
Hai-Bin Li ◽  
Liu-Gen Lan ◽  
...  

It is critical to effectively use every available organ to meet the increasing demands for liver transplantation. Situs inversus is a rare congenital anomaly caused by obstruction of viscus rotation during embryonic development. Situs inversus was once regarded as a contraindication to liver transplantation because of the technical difficulties associated with the unique vascular anatomy and concern about achieving accurate graft positioning. Here, we present a successful case of liver transplantation using a graft from a donor with situs inversus totalis. The related experience will contribute to opening up new realms for the use of such rare organ resources.


2020 ◽  
Vol 48 (9) ◽  
pp. 030006052094410
Author(s):  
Li-Juan Chen ◽  
Xuan Qiu ◽  
Hui Sun ◽  
Peng-Fei Xu ◽  
Fa-Ming Yin ◽  
...  

Situs inversus totalis (SIT) is a rare congenital anatomical variation. However, patients with SIT combined with cancer are rare and these patients with two types of lung cancer have not been reported. We report here a case of combined lung adenocarcinoma and solitary fibrous tumor of the pleura with SIT and discuss its clinicopathological features and outcomes. A 68-year-old asymptomatic woman was referred to the Affiliated Hospital of Qingdao University because of an abnormal shadow on chest radiography. Computed tomography showed SIT and an irregularly shaped nodule (measuring 38 × 27 mm in diameter) in the pleural area of the left lower lobe and a 5-mm nodule in the dorsal segment of the lower lobe of the left lung. Surgery was then performed. For such patients, we should eliminate anxiety in patients, perform regular reexaminations, focus on the individual features of these patients, and avoid misdiagnosis because of habitual thinking. At the same time, the lymph nodes should be completely removed and different parts of the tumor with different properties should be treated differently according to the situation.


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