scholarly journals A case of late-onset paraphrenia in a very elderly patient receiving home medical care

2018 ◽  
Vol 55 (4) ◽  
pp. 675-678
Author(s):  
Yoshimasa Takase ◽  
Kaori Okuyama ◽  
Motohiro Nozawa ◽  
Katsuyoshi Mizukami
2020 ◽  
Vol 123 (8) ◽  
pp. 722-728
Author(s):  
Miki Enomoto ◽  
Ryo Kitajima ◽  
Kazuhiko Fukumoto

2013 ◽  
Vol 4 ◽  
pp. S27-S28
Author(s):  
J. Piqueras Flores ◽  
V. Hernández Jiménez ◽  
V. Mazoteras Muñoz ◽  
M.T. López Lluva ◽  
A. Moreno Arciniegas ◽  
...  

BMC Neurology ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Yiming Zheng ◽  
Yawen Zhao ◽  
Wei Zhang ◽  
Zhaoxia Wang ◽  
Yun Yuan

Abstract Background Late-onset multiple acyl-CoA dehydrogenase deficiency (MADD) is a rare and treatable inherited lipid storage myopathy. Here, we report an elderly patient with MADD mimicking myositis. Case presentation An 80-year-old woman had progressive weakness in her limbs, exercise intolerance, and no muscle pain for 3 months. The patient’s serum creatine kinase level was slightly elevated. The initial diagnosis was myositis. However, muscle biopsy showed many cytoplasmic vacuoles stained with oil red O, indicating the presence of lipid storage myopathy. The plasma acylcarnitine profile showed increased medium-chain and long-chain acylcarnitine species, consistent with the diagnosis of MADD. Riboflavin treatment dramatically improved muscle weakness. Conclusions MADD should be considered when evaluating elderly patients with subacute muscle weakness.


2015 ◽  
Vol 16 (4) ◽  
pp. 271-280
Author(s):  
Takuma Kimura ◽  
Teruhiko Imanaga ◽  
Makoto Matsuzaki ◽  
Tohru Akahoshi

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