scholarly journals Unusual case of gastro jejuno-colic fistula with perforation: a rare case report

2014 ◽  
Vol 18 ◽  
Author(s):  
Sundeep Ashokkumar Naik ◽  
Srinivas Pai
2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841


2010 ◽  
Vol 3 (4) ◽  
pp. 185-187 ◽  
Author(s):  
Manikandhan Ramanathan ◽  
Mathew Pynumootil Cherian

This is an unusual case of isolated bilateral zygomatic complex and arch fracture, which is extremely rare. The literature has no such report of a case.


2021 ◽  
pp. 40-43
Author(s):  
Seema Patil ◽  
M. Ekta ◽  
Asha. R. Iyengar ◽  
Revan Kumar Joshi ◽  
Ritika Agarwal ◽  
...  

Heck's disease is a familial benign lesion affecting the oral mucosa and skin caused by Human papilloma viruses 13 and 32. This condition is quite rare in the Indian subcontinent and till date less than 10 case reports have been published. Females are predominantly affected. It is important for an oral physician to be aware and possess sufcient knowledge about these lesions as these lesions are highly contagious. Further, the presence of these lesions may indicate an underlying immunodecient state of the patient. This paper reports an unusual case of Heck's disease in a 30 year old Indian male.


2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Elke R. Ahlmann ◽  
Yanling Ma ◽  
Vonny Tunru-Dinh

Gorham's disease is a rare disorder involving the proliferation of endothelial channels resulting in resorption and disappearance of bone. An unusual case of polyostotic Gorham's disease affecting the scapula, humerus, radius, and ulna in a 39-year-old woman is described. The patient had extensive disease spreading across both the glenohumeral and humeroulnar joints. This is the first report of Gorham's disease spreading across multiple joints in the upper extremity.


2014 ◽  
Vol 24 (2) ◽  
pp. 86-88
Author(s):  
Mohammad Shahidul Islam ◽  
Humayara Tabassum ◽  
Sharah Jahan ◽  
Mohammad Shahin Masud ◽  
Muhammad Al Amin ◽  
...  

Heart failure may present with diverse manifestation. It is far most common cause of bilateral transudative pleural effusion. In very unusual case, it may present with only massive transudative pleural effusion without cardiomegaly and other features of heart failure such as leg odema, tender hepatomegaly or congested liver. We presented a case that present with massive transudative pleural effusion with mediastinal lymphadenopathy evidenced by CT scan of chest and treated successfully with diuretics. DOI: http://dx.doi.org/10.3329/bjmed.v24i2.20223 Bangladesh J Medicine 2013; 24 : 86-88


2017 ◽  
Vol 4 (10) ◽  
pp. 3532
Author(s):  
Atish Kumar ◽  
Dharani Priya ◽  
Jayesh S. ◽  
Kamal Kataria

Lipoma, though one of the most common benign mesenchymal neoplasms, its presentation in hand is very rare. It can be located in various planes. Intramuscular lipomas are uncommon and usually occur in the proximal muscles of the extremities. Intramuscular lipoma of hand is extremely rare and only very few cases have been reported in the literature. Lipomas of hand may present with neurovascular deficit due to compression. We present here an unusual case of intramuscular lipoma of thenar region with no neurovascular deficit which was surgically excised under local anaesthesia with good cosmetic and functional outcome. 


Author(s):  
Ezhil Rajan B. ◽  
Reshma S.

<p>Foreign bodies in the knee joint are uncommon, particulary those not related to surgical procedures. We present a rare case of an intraosseous metallic foreign body penetrating the lateral femoral condyle at left knee causing pain, which was removed with complete resolution of the symptoms due to walking – running injury in a child.</p>


Author(s):  
Shubham Satyaprakash Gupta ◽  
Sangita Jogdand Shinde ◽  
Raju K. Shinde ◽  
Shweta Pandey

Splenic Hydatid Cyst is a very rare presentation with less than 5% of total incidences of Cystic Echinococcosis. It is usually due to spread of cysts from other regions leading to secondaries. Primary isolated splenic hydatid cyst without involvement of any other organs is even rarer. We report an unusual case of a female who presented as Abnormal Uterine Bleeding (AUB) with an incidental finding of Isolated Splenic Hydatid Cyst with absence of involvement of any other organ. Patient underwent laparotomy and total splenectomy was done. This case report targets to report a rare case of incidental finding of isolated unilocular hydatid cyst of spleen and describes its management.


2020 ◽  
pp. 263246362096054
Author(s):  
Sweta Singh ◽  
Uday Shanker Singh

Nocardia farcinia endocarditis is an extremely rare phenomenon. It is an opportunistic ubiquitously present pathogen in the environment. Here, we present an unusual case of septic embolism with infective endocarditis due to Nocardia spp. in a 55-year-old chronic alcoholic male. Radiological imaging techniques and microbiological investigations helped in the timely diagnosis. Timely institution of treatment based on sensitivity results resulted in favorable outcome in the patient.


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