scholarly journals Ruptured anterior communicating artery aneurysm with spontaneous ventriculitis: An unusual case report with review of literature

2017 ◽  
Vol 31 (2) ◽  
pp. 211-214
Author(s):  
Mayank Sinha ◽  
Ashok Gupta ◽  
Amit Pratap Singh Deora ◽  
Mukesh Vij
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Unusual Case ◽  
Artery Aneurysm ◽  
Anterior Communicating Artery ◽  
Review Of Literature ◽  
Appropriate Treatment ◽  
Life Threatening ◽  
Unusual Case Report

Abstract Ventriculitis is a potentially life-threatening infection, and an early diagnosis is essential for the appropriate treatment of ventriculitis. Unsuspected ventriculitis might be a source of persistent infection and therapeutic failure in the management of meningitis. We present a rare case of spontaneous ventriculitis in a patient of acomm aneurysm who was neither immunocompromised nor any intervention was done on him.

Natural Course of Myxopapillary Ependymoma: Unusual Case Report and Review of Literature

2019 ◽  
Vol 121 ◽  
pp. 239-242 ◽  
Author(s):  
Serhat Pusat ◽  
Yahya Cem Erbaş ◽  
Selçuk Göçmen ◽  
Murat Kocaoğlu ◽  
Ersin Erdoğan
Keyword(s):  
Case Report ◽  
Unusual Case ◽  
Natural Course ◽  
Myxopapillary Ependymoma ◽  
Review Of Literature ◽  
Unusual Case Report

scholarly journals Unruptured anterior communicating artery aneurysm presenting as depression: A case report and review of literature

2016 ◽  
Vol 7 (19) ◽  
pp. 495 ◽  
Author(s):  
Adomas Bunevicius ◽  
Paulius Cikotas ◽  
Vesta Steibliene ◽  
VytenisP Deltuva ◽  
Arimantas Tamsauskas
Keyword(s):  
Case Report ◽  
Artery Aneurysm ◽  
Anterior Communicating Artery ◽  
Review Of Literature ◽  
Anterior Communicating Artery Aneurysm

scholarly journals Recurrent Ameloblastoma in the Free Fibula Flap: Review of Literature and an Unusual Case Report

2015 ◽  
Vol 14 (3) ◽  
pp. 821-825 ◽  
Author(s):  
Salih Onur Basat ◽  
Ali Rıza Öreroğlu ◽  
Cagdas Orman ◽  
Tolga Aksan ◽  
İlker Üsçetin ◽  
...  
Keyword(s):  
Case Report ◽  
Unusual Case ◽  
Review Of Literature ◽  
Free Fibula Flap ◽  
Fibula Flap ◽  
Free Fibula ◽  
Unusual Case Report

ENTRAPMENT OF THE MEDIAN NERVE BETWEEN SUBLIMIS TENDONS AFTER DISTAL FOREARM FRACTURE: AN UNUSUAL CASE REPORT

Hand Surgery ◽  
2008 ◽  
Vol 13 (02) ◽  
pp. 111-114
Author(s):  
Y. Taniguchi ◽  
T. Kitano ◽  
T. Shimoe ◽  
M. Yoshida
Keyword(s):  
Case Report ◽  
Median Nerve ◽  
Rare Case ◽  
Nerve Palsy ◽  
Unusual Case ◽  
Forearm Fracture ◽  
Distal Forearm ◽  
Distal Forearm Fracture ◽  
Median Nerve Palsy ◽  
Unusual Case Report

We present a rare case of entrapment of the median nerve between sublimis tendons after fractures of the distal radius and ulna in an 80-year-old woman. The entrapped median nerve was elongated redundantly with two regions of constriction. To our knowledge, no case of median nerve palsy caused by such a factor has been previously reported.

scholarly journals Large Complex Odontoma of Mandible in a Young Boy: A Rare and Unusual Case Report

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
G. Siva Prasad Reddy ◽  
G. V. Reddy ◽  
B. Sidhartha ◽  
K. Sriharsha ◽  
John Koshy ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
Facial Asymmetry ◽  
Surgical Excision ◽  
Radiographic Examination ◽  
Rare Tumor ◽  
Complex Odontoma ◽  
Compound Odontoma ◽  
Unusual Case Report

Odontomas are the most common odontogenic tumors. They are broadly classified in to Compound Odontoma and Complex Odontoma. Among them complex odontoma is a rare tumor. Occasionally this tumor becomes large, causing expansion of bone followed by facial asymmetry. Otherwise these tumors are asymptomatic and are generally diagnosed on radiographic examination. We report a rare case of complex odontoma of mandible in a young boy. The tumor was treated by surgical excision under general anesthesia.

Schwannoma of lower lip: an unusual case report and review of literature

2015 ◽  
Vol 4 (12) ◽  
pp. 1781
Author(s):  
Gayithri Kulkarni ◽  
Ehtesham Iqbal ◽  
Harish Kulkarni ◽  
Shahanavaj Khaji ◽  
Jyoti Biradar
Keyword(s):  
Case Report ◽  
Unusual Case ◽  
Review Of Literature ◽  
Lower Lip ◽  
Unusual Case Report

scholarly journals Gorlin-Goltz Syndrome - An Unusual Case Report

2016 ◽  
Vol 5 (1) ◽  
pp. 1071
Author(s):  
B. Thayumanavan ◽  
T. Jeyanthikumari ◽  
P. Meghalapriya
Keyword(s):  
Case Report ◽  
Unusual Case ◽  
Autosomal Dominant ◽  
Keratocystic Odontogenic Tumor ◽  
Review Of Literature ◽  
Autosomal Dominant Disorder ◽  
Goltz Syndrome ◽  
Multisystemic Disease ◽  
Consistent Feature ◽  
Unusual Case Report

Gorlin-Goltz syndrome is an uncommon autosomal dominant disorder manifesting as a multisystemic disease. Keratocystic odontogenic tumor (KCOT) is considered as the most consistent feature of this syndrome. Dentists play a key role in making early diagnosis of this syndrome. Here we present a case of Gorlin- Goltz syndrome identified by multiple multilocular radiolucencies in the mandible. A review of literature of different diagnostic criteria for Gorlin-Goltz syndrome is also discussed.

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