scholarly journals Cavernoma presenting with an atypical clinico-radiological finding: a case report

2021 ◽  
pp. 101451
Author(s):  
Rajbhandari Suyasha ◽  
Rajbhandari Saujanya ◽  
Shrestha Pranaya ◽  
Rajbhandari Pravesh ◽  
Pant Basant
2011 ◽  
Vol 1 ◽  
pp. 43 ◽  
Author(s):  
Suresh Thirunavukarasu

Bilateral temporal and frontal lobe involvement is a common characteristic of herpes simplex encephalitis (HSE). Clinical sequelae of herpes simplex encephalitis may manifest sometimes as Kluver Bucy syndrome (KBS). In herpes simplex encephalitis, apart from frontal lobe, extra temporal involvement is rare and uncommon. We report a case of HSE manifesting clinically as KBS with a rare radiological finding of temporal and extratemporal involvement of pons.


2016 ◽  
Vol 73 (3) ◽  
pp. 277-279 ◽  
Author(s):  
Biljana Zvezdin ◽  
Nevena Savic ◽  
Sanja Hromis ◽  
Violeta Kolarov ◽  
Djordje Tausan ◽  
...  

Introduction. Chilaiditi's syndrome is a rare condition manifested by gastrointestinal symptoms, and radiologically verified by transposition of the large intestine loop. This radiological finding with no manifested symptoms is termed the Chilaiditi's sign. The aim of this case report was to remind the clinicians of the possibility of this rare syndrome, whose symptoms and signs may be misinterpreted and inadequately treated, with consequent diverse complications. Case report. We presented the theoretical facts and a patient in whom the diagnosis of Chilaiditi's syndrome was established incidentally, when hospitalized for an exacerbation of his chronic obstructive pulmonary disease. The Chilaiditi's sign was verified as an incidental finding on chest X-ray performed to evaluate the primary disease. Conclusion. Chilaiditi's syndrome is a benign condition which rarely requires surgery. Its clinical importance lies in adequate differential diagnostic approach and timely management of potentially serious complications.


2020 ◽  
Vol 58 (222) ◽  
Author(s):  
Suzit Bhusal ◽  
Uttara Gautam ◽  
Rajan Phuyal ◽  
Robin Choudhary ◽  
Sunil Raja Manandhar ◽  
...  

Autosomal dominant mutations in fibroblast growth factor receptor 3 cause achondroplasia, the most common form of dwarfism in humans. Achondroplasia is a genetic disorder causing rhizomelic shortening of limbs. Head is often large with prominent forehead causing vaginal delivery difficult. A twenty-one years old multipara mother gave birth to a baby with achondroplasia via spontaneous vaginal delivery with episiotomy without any complication. Achondroplasia, in this case, was diagnosed on the basis of antenatal ultrasonography finding, clinical features and radiological finding of the baby. He was admitted in the special baby care unit for observation and discharged on the next day as no complications were noted.


Author(s):  
Deepa Dubey ◽  
Sudhir Rishi ◽  
Pallavi Chawla ◽  
Vinay Badyal

The calcifying epithelial odontogenic tumor (CEOT) is a benign epithelial odontogenic lesion that accounts for less than 1% of all odontogenic tumors. CEOT is usually asymptomatic and an incidental radiological finding, often presenting as a mandibular radiolucency with flecks of calcified material. We report a case of CEOT in the right posterior maxilla of a 24-year-old female that was associated with an ectopic unerupted tooth. The tumour in this case caused mild pain and appeared radiographically similar to an odontoma or Ameloblastic fibro-odontome, due to its dense calcified contents. Diagnosis was confirmed through histopathology. This case report highlights the unusual clinical and radiographic appearence of Pindborg tumor.


2020 ◽  
Vol 102 (8) ◽  
pp. e213-e215
Author(s):  
O Barraclough ◽  
G Wilson ◽  
A Power

Synovial chondromatosis is a rare benign condition. It most commonly affects the large joints. Presentation in the temporomandibular joint is rare. Our case was an incidental radiological finding and not diagnosed immediately, highlighting the ease with which conditions such as this can be missed, particularly in asymptomatic patients. Only 45% of patients with synovial chondromatosis show radiographic changes. Findings as significant as ours are unusual. An increased professional awareness of the radiological signs of synovial chondromatosis would be beneficial to improve diagnosis and prognosis for patients.


2010 ◽  
Vol 4 ◽  
pp. CMC.S5677 ◽  
Author(s):  
James Ker

Simple hepatic cysts are a relatively common radiological finding. These cysts may be classified as parasitic and non-parasitic. They are usually asymptomatic, but may cause symptoms due to local compression. These compressive complications include: portal hypertension, edema due to caval compression, extrinsic gastric compression and duodenal compression with obstruction. However, no reports in the literature exist describing atrial compression by hepatic cysts. In this case report a simple hepatic cyst causing slight right atrial compression is described. This slight compression is the cause of atrial premature beats. It is proposed that simple hepatic cysts may be the cause of atrial premature beats.


Author(s):  
Deepa Dubey ◽  
Sudhir Rishi ◽  
Pallavi Chawla ◽  
Vinay Badyal

The calcifying epithelial odontogenic tumor (CEOT) is a benign epithelial odontogenic lesion that accounts for less than 1% of all odontogenic tumors. CEOT is usually asymptomatic and an incidental radiological finding, often presenting as a mandibular radiolucency with flecks of calcified material. We report a case of CEOT in the right posterior maxilla of a 24-year-old female that was associated with an ectopic unerupted tooth. The tumour in this case caused mild pain and appeared radiographically similar to an odontoma or Ameloblastic fibro-odontome, due to its dense calcified contents. Diagnosis was confirmed through histopathology. This case report highlights the unusual clinical and radiographic appearence of Pindborg tumor.


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