Abdominal ultrasound in the diagnosis and management of recurrent pancreatic pseudocyst in children – case report

Author(s):  
V Hurduc ◽  
D Plesca ◽  
A Zamfirescu ◽  
D Dragomir ◽  
V Cretu ◽  
...  
2017 ◽  
Vol 4 (2) ◽  
pp. 42-45
Author(s):  
Saravana Karthikeyan Balasubramanian ◽  
◽  
Divya Vinayachandran ◽  
Sankara Aravind Warrier ◽  
Ananthi Sankar ◽  
...  

Author(s):  
B. Ouafidi ◽  
H. Kiram ◽  
H. Benaguida ◽  
A. Lamrissi ◽  
K. Fichtali ◽  
...  

Cephalalgia ◽  
2021 ◽  
pp. 033310242110068
Author(s):  
Marleen H van Coevorden ◽  
Mariëtte WCJ Schoofs ◽  
Jeroen Venhovens

Background Paroxysmal localized hyperhidrosis is a rare disorder of the central autonomic nervous system. No association between paroxysmal hyperhidrosis and severe headache has been previously described in literature. Case description: A 65-year-old woman with idiopathic paroxysmal localized hyperhidrosis combined with severe holocranial headache attacks is described in this case report. Extensive diagnostic testing by means of laboratory examinations, 24-hour urinalyses, chest X-ray, abdominal ultrasound and computed tomography scans, and brain and spinal cord magnetic resonance imaging could not identify an underlying disorder. A diagnosis of idiopathic paroxysmal localized hyperhidrosis was made, and the patient was successfully treated with clonidine 0.075 mg three times a day, without any side effects. Conclusion Paroxysmal localized hyperhidrosis is a rare central autonomic nervous system disorder that can occur in combination with severe headache. Both the headache and paroxysmal hyperhidrosis complaints were treated effectively with clonidine in the patient described in this case-report.


2011 ◽  
Vol 21 (03) ◽  
pp. 203-204 ◽  
Author(s):  
A. Papparella ◽  
F. Nino ◽  
S. Coppola ◽  
D. Donniacono ◽  
P. Parmeggiani

2021 ◽  
Vol 05 (03) ◽  
Author(s):  
Isadora Langoni Amorim Barbosa ◽  
Tayenne do Vale Cabral ◽  
Mariana Carraro ◽  
Mariana Castro Loureiro Borges e Curi

2021 ◽  
pp. 153857442110462
Author(s):  
Ahmed A. Sorour ◽  
Levester Kirksey ◽  
Sarah Keller ◽  
Michael S. O’Connor ◽  
Sean P. Lyden

Catastrophic antiphospholipid syndrome (CAPS) is a rare life threatening presentation of antiphospholipid syndrome. Surgery has been proposed as one of the triggering factors for this life threatening entity. There are no detailed published reports in the current literature describing CAPS as a complication after surgery. We report a case of a 21 year old that developed CAPS postoperatively and discuss the multidisciplinary approach for diagnosis and management.


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