scholarly journals Intermittent claudication caused by compression of tibial vessels as a result of calf muscle hypertrophy: case report

1992 ◽  
Vol 16 (1) ◽  
pp. 116-120 ◽  
Author(s):  
Angela Mailis ◽  
Alan Lossing ◽  
Peter Ashby ◽  
Jacob Abarbanel
1992 ◽  
Vol 16 (1) ◽  
pp. 0116-0120 ◽  
Author(s):  
Daniel L. Diamond ◽  
Angela L. Mailis ◽  
Alan L. Lossing ◽  
Peter L. Ashby

2016 ◽  
Vol 8 (1) ◽  
pp. 89-92
Author(s):  
E. Ernst ◽  
S. Peter ◽  
A. Matrai ◽  
L. Kollar

2015 ◽  
Vol 16 (2) ◽  
pp. 112-114
Author(s):  
NS Neki ◽  
Ishu Singh ◽  
Jasbir Kumar ◽  
Ankur Jain ◽  
Tamil Mani

Hoffman syndrome is characterized by pseudohypertrophy of muscles, muscle’s weakness & stiffness complicating hypothyroidism. We describe the disorder in a 45 years old female admitted with complaints of myalgia, proximal muscle weakness & calf muscle hypertrophy since 11 months. Thyroid function tests, marked elevation of muscle enzyme, electromyogram & muscle biopsy established the diagnosis of thyroid myopathy with Hoffman’s syndrome. Therapy with levothyroxine resulted in marked clinical & biochemical improvements.J MEDICINE July 2015; 16 (2) : 112-114


2001 ◽  
Vol 59 (3A) ◽  
pp. 582-586 ◽  
Author(s):  
Rosana Herminia Scola ◽  
Lineu Cesar Werneck ◽  
Cássio Slompo Ramos ◽  
Ricardo Pasquini ◽  
Hans Graf ◽  
...  

The authors report one case of amyloidosis associated with muscular pseudohypertrophy in a 46-year-old woman, who developed weakness, macroglossia and muscle hypertrophy associated with primary systemic amyloidosis. Electromyography showed a myopathic pattern and bilateral carpal tunnel syndrome. The muscle biopsy presented with a type I and II fiber hypertrophy and infiltration of amyloid material in the interstitious space and artery walls. She underwent bone marrow transplantation with stabilization and subjective improvement of the clinical picture.


2019 ◽  
Vol 7 ◽  
pp. 2050313X1882335
Author(s):  
Dante Palumbo ◽  
Aden Miller ◽  
Elliott Smock ◽  
Scott Farner

Muscle herniation in the upper extremity is a rare but recognized phenomenon with a paucity of reports in the current literature. In the majority of cases, the herniation is secondary to trauma, with some of the cases due to muscle hypertrophy and increased intra-compartmental pressure from the forced exertion. Treatment for this condition ranges from nonsurgical, repair, or reconstruction to fasciotomy of the flexor carpi ulnaris fascia. Here, we present a case of flexor carpi ulnaris herniation after an open in situ cubital tunnel release in a 57-year-old male 6 years after initial surgery. The patient’s symptoms did not improve with conservative management, and the patient subsequently underwent endoscopic fasciotomy with resolution of his symptoms and maintenance of his wrist and grip strength. The rationale for the treatment chosen is discussed.


2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Takuhei Kozaki ◽  
Akihito Minamide ◽  
Hiroshi Iwasaki ◽  
Yasutsugu Yuakawa ◽  
Muneharu Ando ◽  
...  

Author(s):  
Masayuki Tsuneki ◽  
Satoshi Maruyama ◽  
Manabu Yamazaki ◽  
Kanae Niimi ◽  
Tadaharu Kobayashi ◽  
...  

2018 ◽  
Vol 18 (1) ◽  
Author(s):  
Jagath C. Ranasinghe ◽  
Chandani Wickramasinghe ◽  
Ganganath Rodrigo

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