scholarly journals Two cases with dropped head syndrome caused by hypokalemic myopathy

2011 ◽  
Vol 51 (2) ◽  
pp. 110-113 ◽  
Author(s):  
Koichiro Taniguchi ◽  
Iwao Okino ◽  
Nobuaki Yamamoto ◽  
Shinichi Matsumoto ◽  
Naoko Tachibana ◽  
...  
Author(s):  
T. Shimizu ◽  
Y. Muranaka ◽  
I. Ohta ◽  
N. Honda

There have been many reports on ultrastructural alterations in muscles of hypokalemic periodic paralysis (hpp) and hypokalemic myopathy(hm). It is stressed in those reports that tubular structures such as tubular aggregates are usually to be found in hpp as a characteristic feature, but not in hm. We analyzed the histological differences between hpp and hm, comparing their clinical manifestations and morphologic changes in muscles. Materials analyzed were biopsied muscles from 18 patients which showed muscular symptoms due to hypokalemia. The muscle specimens were obtained by means of biopsy from quadriceps muscle and fixed with 2% glutaraldehyde (pH 7.4) and analyzed by ordinary method and modified Golgimethod. The ultrathin section were examined in JEOL 200CX transmission electron microscopy.Electron microscopic examinations disclosed dilated t-system and terminal cistern of sarcoplasmic reticulum (SR)(Fig 1), and an unique structure like “sixad” was occasionally observed in some specimens (Fig 2). Tubular aggregates (Fig 3) and honeycomb structure (Fig 4) were also common characteristic structures in all cases. These ultrastructural changes were common in both the hypokalemic periodic paralysis and the hypokalemic myopathy, regardless of the time of biopsy or the duration of hypokalemia suffered.


2021 ◽  
Vol 132 (8) ◽  
pp. e120
Author(s):  
Nurul Maisarah Sainuddin ◽  
Christopher Chua ◽  
Sibi Sunny ◽  
Joy Vijayan ◽  
Kay Ng

Neurology ◽  
1998 ◽  
Vol 51 (6) ◽  
pp. 1748-1751 ◽  
Author(s):  
J.-i. Satoh ◽  
Y. Kuroda ◽  
H. Nawata ◽  
T. Yanase

1971 ◽  
Vol 25 (2) ◽  
pp. 137-139
Author(s):  
Yoshiyuki MURAI ◽  
Nobuo MASUDA

2021 ◽  
Vol 26 (1) ◽  
Author(s):  
Kenji Endo ◽  
Jun Matsubayashi ◽  
Yasunobu Sawaji ◽  
Kazuma Murata ◽  
Takamitsu Konishi ◽  
...  

Abstract Background To date, the histopathologic characteristics of dropped head syndrome (DHS) have not been reported sufficiently. The present study investigates the histopathology of biopsy specimens from the cervical paravertebral region in patients with DHS. Methods Histopathological parameters were evaluated in biopsy specimens of the cervical paravertebral soft tissue from 15 patients with DHS. Results Among the 15 cases of DHS examined, skeletal muscle was identified in 7 cases, all of which showed necrosis, microvessel proliferation and atrophy. The ligament was identified in 12 cases, 8 of which showed degeneration. The lag time between the onset of symptoms and the performance of a biopsy in all 8 cases, which showed degeneration was over 3 months. Microvessel proliferation in the ligament was observed in 1 of the 4 cases, in which the lag time between the onset of symptoms and the performance of a biopsy was less than 3 months (acute or subacute phase), and in 7 of the 8 cases, in which the lag time between the symptoms and the performance of a biopsy was over 3 months (chronic phase). Chronic inflammation in the ligament was identified in 1 of the 12 cases. Conclusions The identification of necrosis, microvessel proliferation, and atrophy in the skeletal muscle of patients with DHS and the presence of ligament degeneration and microvessel proliferation in the chronic but not acute or subacute phases may suggest that persistent skeletal muscle damage of the cervical paravertebral region causes subsequent ligament damage in patients with DHS.


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