1.Colchicine-Induced Neuromyopathy with Myotonic Discharges in a Patient Using Concomitant Diuretics
Dar-Eun JUNG ; Seung-Hee NA ; Yun-Jeong HONG ; Seong-Hoon KIM ; Tae-Won KIM ; Young-Do KIM
Journal of Electrodiagnosis and Neuromuscular Diseases 2024;26(1):9-13
		                        		
		                        			
		                        			 Colchicine is a widely used anti-inflammatory medication, but its neuromuscular adverse effects are under-recognized. One month ago, a 70-year-old woman presented to our clinic for an evaluation of general weakness. She had been taking colchicine and diuretics daily. The weakness, which began in both thighs and lower legs approximately 4 weeks before her visit, had progressively worsened. The patient also experienced mild paresthesia and hypoesthesia in both arms and legs. Her serum creatine kinase and aldolase levels were elevated, and nerve conduction studies indicated a motor-dominant sensorimotor polyneuropathy of the axonal type. Needle electromyography showed prominent fibrillation potentials, positive sharp waves, and myotonic discharges. Suspecting colchicine-induced neuromyopathy, we discontinued the colchicine and diuretics, after which her symptoms resolved. 
		                        		
		                        		
		                        		
		                        	
2.Coexistence of Posterior Cortical Atrophy and Parkinson’s Disease
Eun-Byul KO ; Il-Joong HWANG ; Jung-Woo KIM ; Dar-Eun JUNG ; Ju-Suk LEE ; Sang-Won YOO ; Joong-Seok KIM
Journal of the Korean Neurological Association 2023;41(3):216-219
		                        		
		                        			
		                        			 We report a rare and unique presentation of a patient with early and levodopa-responsive Parkinson’s disease (PD) who exhibited clinical features similar to posterior cortical atrophy (PCA). The imaging evidence suggested the coexistence of PD and PCA, without the presence of amyloid pathology. Although the present case lacks pathologic evidence, this case represents a distinct manifestation of PD characterized by a combination of parkinsonism and early prominent posterior cognitive deficits, reminiscent of the visual variant of Alzheimer’s disease. 
		                        		
		                        		
		                        		
		                        	
            
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