scholarly journals Hoffman's syndrome: pseudohypertrophic myopathy as initial manifestation of hypothyroidism. Case report

2003 ◽  
Vol 61 (3B) ◽  
pp. 851-854 ◽  
Author(s):  
Luiz Felipe Rocha Vasconcellos ◽  
Maria Claudia Peixoto ◽  
Tatiana Nunes de Oliveira ◽  
Glória Penque ◽  
Ana Claudia Celestino Leite

The frequency of myopathy in hypothyroidism ranges from 30 to 80%. The major symptoms related are weakness, muscular cramps and myalgia. The pseudohyperthrophic form is called Hoffman's syndrome. The electrophysiological study reveals myopathy, neuropathy or mixed pattern. Laboratorial investigation generally shows increased levels of muscle enzymes and low serum thyroid hormones, with thyrotrophic-stimulating hormone (TSH) elevated. The treatment consists in hormone replacement and the prognosis is good in most of the cases. We report an adult male who developed muscular cramps, myalgia, weakness, pseudohyperthrophy, associated with facial edema and alteration of his voice. The muscle enzymes were increased and T4 was undetectable with a raised level of TSH. The myopathy was the initial manifestation of hypothyroidism in this case.

1970 ◽  
Vol 8 (1) ◽  
pp. 32-36
Author(s):  
Md Abul Kalam Azad ◽  
Shaheen Lipika Quayum ◽  
Md Shamsul Haque ◽  
Md Azizul Islam ◽  
KAK Azad ◽  
...  

Although hypothyroidism may cause a wide range of muscle disturbances, an overt myopathy may rarely present as an isolated initial presentation of hypothyroidism. The frequency of myopathy in hypothyroidism ranges from 30 to 80%. The major muscular symptoms are weakness, muscular cramps and myalgia. Laboratorial investigation generally shows increased levels of muscle enzymes and low serum thyroid hormones, with high thyrotrophic-stimulating hormone (TSH) elevated. The electrophysiological study reveals myopathy, neuropathy or mixed pattern. The treatment consists in hormone replacement and the prognosis is good in most of the cases. We report two cases that developed cramps, myalgia, and weakness, one of them presented as a polymyositis-like syndrome. The muscle enzymes were increased with a raised level of TSH. The myopathy was the initial manifestation of hypothyroidism in these cases. Both the patient was treated by replacement of thyroxin with significant clinical and biochemical improvement. DOI = 10.3329/jom.v8i1.1379 J MEDICINE 2007; 8 : 32-36


2007 ◽  
Vol 10 (4) ◽  
pp. E329-E330 ◽  
Author(s):  
Jia-Lin Chen ◽  
Tsai-Wang Huang ◽  
Po-Shun Hsu ◽  
MD Chao-Yang, ◽  
Chien-Sung Tsai

Author(s):  
Sandesh Kini ◽  
Yellanthoor Ramesh Bhat ◽  
Lakshmikanth Halegubbi Karegowda

AbstractTorticollis refers to a condition in which the head is persistently tilted to one side, sometimes associated with pain. Torticollis in a child can be congenital or acquired. Torticollis as an initial manifestation of an underlying demyelinating syndrome is quite rare in children. Here, we report a 7-year-old girl who presented with persistent torticollis. Neuroimaging of the brain revealed features of a demyelinating disease. Further studies did not show any evidence of multiple sclerosis. Cerebrospinal fluid was negative for antiaquaporin-4 antibodies, antimyelin oligodendrocyte glycoprotein antibodies, and oligoclonal bands. A seronegative demyelinating disorder was considered. She was treated with pulsed methylprednisolone therapy. She responded well to steroids with no progression of illness during follow-up. Torticollis was partially improved.


PM&R ◽  
2009 ◽  
Vol 1 ◽  
pp. S246-S246
Author(s):  
Jasmine Martinez-Barrizonte ◽  
Kresimir Banovac ◽  
Alberto Martinez-Arizala

2016 ◽  
Vol 5 (2) ◽  
pp. 114
Author(s):  
Vitorino Modesto Santos ◽  
Renata Faria Silva ◽  
Viviane Vieira Passini ◽  
Mayza Lemes Duarte ◽  
Leandro Pretto Flores

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