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International Journal of Pharmaceutical Science Invention
ISSN (Online): 2319 – 6718, ISSN (Print): 2319 – 670X
www.ijpsi.org Volume 2 Issue 10‖ October 2013 ‖ PP.01-03

Myoedema: A Presenting Symptom of Hypothyroid Myopathy.
Dr. Priti Panchal
Associate Professor (Internal Medicine) ESIPGIMSR, Andheri, Mumbai.

ABSTRACT:The incidence of Hypothyroidism is rising in our country. However, in this era of exhaustive
investigations, where clinical signs often get overlooked, Myoedema is one such clinical sign, that very
conclusively guides the clinician towards the diagnosis of Hypothyroidism. This case report highlights the
importance of eliciting Myoedema to corroborate the diagnosis of Hypothyroidism.

KEYWORDS : Hypothyroidism; Myoedema.
I.

INTRODUCTION

Hypothyroidism is a relatively common endocrine disorder with a characteristic clinical picture, which
may be associated with a variety of clinical features of Myopathy, Mononeuropathy and Sensorimotor axonal
polyneuropathy 14, 12,8,10. .The clinical evidence of Hypothyroid Myopathy has been reported in 20-88% of
patients14, 11, 12, 13, 15; the symptoms being proximal weakness, cramps, painful muscles, myoedema on
percussion, delay in deep tendon reflexes and development of muscle hypertrophy 12, 13, 10. Severity of Myopathy
generally correlates with the duration and the degree of thyroid hormone deficiency 11, 15. Serum Creatine Kinase
(CK) elevation is usually observed even in the absence of overt muscle weakness 11,10 .
CASE REPORT
31 year old male came with complaints of giddiness since 8 days. He noticed a gradual change in voice
over one year. He complained of easy fatigability and difficulty in getting up from squatting position. All the
above complaints progressed gradually over an year. There was no history of prolonged fever prior to these
symptoms or indulging in any vigorous muscular activity or any history of being on any prolonged
medication.Examination revealed normal vital parameters with no signs of malnutrition, oedema feet or
puffiness of face. The grade of power in proximal muscles was 4/5 and in the distal muscle was 5/5. All the deep
tendon reflexes were grossly delayed. On tapping biceps muscle gently there was slow and sustained contraction
of muscle lasting for few seconds which is a classical sign of Myoedema. All the other systems including the
Nervous system, especially higher functions were normal. Investigation revealed : Haemoglobin of 11.5gm/dl,
the total count was 5500/cmm, platelet 2.18lakh/cmm.The Liver and Renal Function Tests were normal. Serum
calcium and Vitamin D3 was normal. CPK was elevated 670 IU/L (Normal range 20-170IU/L). Serum
cholesterol was 303mg/dl, serum triglyceride 143 mg/dl.MRI brain showed ischemic changes in both
peritrigonal areas on T2 flair images which was not significant. Electrocardiogram was normal.
Echocardiography showed mild pericardial effusion. Thyroid function test was done in view of clinical
symptom and sign of Myoedema. It was suggestive of hypothyroidism with serum T3 80ng/100ml (70 200ng/100ml), T4 2.9µg/100ml (5-13µg/100ml), TSH 75µIU/ml (0.3-5µIU/ml).In view of above investigation
diagnosis of hypothyroidism was made and patient was started on L–Thyroxine 100µgm per day. Patient
showed remarkable symptomatic improvement with disappearance of Myoedema within a month and a marked
fall in the CPK level. The Thyroid function test were repeated at two monthly intervals, which showed gradual
fall in TSH levels. After 6 months Thyroid function tests became normal and there was complete resolution of
proximal muscle weakness and normalisation of voice. Raised serum CPK, low T4 and high TSH, and their
reversibility with L-thyroxine treatment supported the diagnosis of Hypothyroid Myopathy.
DISSCUSSION
Muscle weakness, aches and cramps, stiffness and delayed tendon jerk relaxation are usual features of
Hypothyroid Myopathy (30–80%),while muscle hypertrophy, myoedema and wasting are occasionally
seen.(1&2)Delayed relaxation of tendon jerks and proximal muscle weakness correlate with biochemical severity
of hypothyroidism (serum T4 <20 ng/ml).(3). Acute myoedema are, however, distinctly rare. (2
&4
)Musculoskeletal symptoms are very common in hypothyroidism, and they may improve or disappear with
correction of the hypothyroid state. [5] . The elevation of serum creatine phospho kinase (CK) was reported in
80% of the patients with hypothyroidism even with the absence of muscle involvement 4, 8,9,10. Elevation of CPK
levels was detected in our patient as well. With the thyroid hormone replacement therapy the serum levels of

www.ijpsi.org

1|Page
Myoedema: A Presenting Symptom...
CPK decreased in parallel to the clinical improvement in 3 months. Myoedema is one of classical signs of
Hypothyroid Myopathy, which is uncommon and hence overlooked by clinicians in most instances. It is a
phenomenon of mounding of muscle tissue occurring after a light pressure stimuli. It is produced by flicking
across along the contours of bulk of arm involving biceps belly with the thumb and index fingers.(fig.1) This
causes a visible and palpable non-tender, firm, localized ridge in the muscle immediately under the point of
tactile stimulus.(fig. 2) The swelling reaches its maximal size after 1-2 seconds and gradually subsides over
some 5-10 seconds,(fig.3) following which the muscle resumes its normal smooth contour with no palpable
localized hardening.(fig.4) The swelling does not spread elsewhere along the muscle. The magnitude as well as
the duration of this phenomenon is quite variable, depending upon the thickness of the muscle and the overlying
soft tissues [6] and the intensity of the blow delivered. Myoedema is entirely reversible by thyroid hormone
replacement and it does not have any harmful effects. Myoedema is due to prolonged muscle contraction caused
by delayed calcium reuptake by sarcoplasmic reticulum, following local calcium ion release brought out by
percussion or pressure. The muscle involvement in hypothyroidism is caused by alterations in muscle fibres
from fast twitching type II to slow twitching type I fibres, deposition of glycosaminoglycans, poor contractility
of actin–myosin units, low myosin ATPase activity, and low ATP turnover in skeletal muscle. [7] In the past,
Myoedema was considered an insensitive and non-specific finding, occurring also in states of malnutrition,
hypovitaminosis, and hypoalbuminemia, in addition to hypothyroidism. However, in conditions suspicious of
overt hypothyroidism, elicitation of Myoedema significantly increases the probability of Hypothyroid
Myopathy. Hence, it's special clinical significance and the need for its validation in appropriate settings.

II.

CONCLUSION

Myoedema is uncommon feature of Hypothyroid Myopathy and Serum CPK levels - can be used as a
marker of Hypothyroid Myopathy; which effectively responds to L-Thyroxine Therapy.

ACKNOWLEDGEMENT
The author would like to thank the institution head: respected Dean for encouraging and permitting the
publication of this case report. The author would also like to thank the institution Neurologist and the
Department of Internal Medicine for providing the Clinical material for this Report. Lastly the author expresses
her gratitude to the Hospital and the patient for their cooperation.

REFERENCES:
[1]
[2]
[3]
[4]
[5]
[6]
[7]
[8]
[9]
[10]
[11]
[12]
[13]
[14]
[15]

Ramsey I. Muscular abnormalities of hypothyroidism. In: Thyroid disease and muscle dysfunction. London: William
Heinemann, 1974; pp 126–171.
McArdle B. Metabolic and endocrine myopathies. In: Walton JN, Ed, Disorders of voluntary muscle. Edinburgh: Churchill
Livingstone, 1974; p 750.
Khaleeli AA, Griffith DG, Edwards RHT. The clinical presentation of hypothyroid myopathy and its relationship to
Abnormalities in structure and function of skeletal muscle.Clin Endocrinology 1983; 19:365–76.
Lochmuller H, Reimers CD, Fischer P, Heuss D, Muller-Hocker J, Pongratz DE. Exercise induced myalgia in Hypothyroidism.
Clin Invest 1993; 71:999–1001.
Cakir M, Samanci N, Balci N, Balci MK. Musculoskeletal manifestations in patients with thyroid disease. Clin Endocrinol. 2003;
59:162–7.
Jones MP, Parkes WE. Myoedema. Clin Sci. 1955; 14:97–100.
Wiles CM, Young A, Jones DA, Edwards RH. Muscle relaxation rate, fibre-type composition and energy turnover in hyper- and
hypo-thyroid patients. Clin Sci. 1979; 57:375–84.
Krupsky M, Flatau E, Yarom R Musculoskeletal symptoms as a presenting sign of long standing hypothroidism. Isr J Med Sci
(1987) 23:1110-1113
Kung AWC, Ma JTC, Yu YL Myopathy in acute hypothyroidism. Postgraduate Medical Journal (1987) 63; 661-663
Scott KR, Simmons Z, Boyer P. Hypothyroid myopathy with a strikingly elevated serum creatine kinase levels. Muscle and
Nerve (2002) 26:141-14 4
11.Evans R, Itaru W Central changes in hypothyroid myopathy: a case report. Muscle and Nerve (1990) 13:952-956
Klein I, Levey G Unusual manifestations of hypothyroidism. Arch Intern Med (1984)144:123-128
Ono S, Inouye K, and Mannen T Myopathology of hypothyroid myopathy. J Neurological Sciences (1987) 77:237-248
Ruurd FD, Bosch J, Laman DM Neuromuscular findings in thyroid dysfunction: a prospective clinical and electrodiagnostic
study. J Neurol Neurosurg Psychiatry (2000) 68:750-755
15.Torres CF, Moxley RT Hypothyroid neuropathy and myopathy: clinical and electrodiagnostic

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2|Page
Myoedema: A Presenting Symptom...

Figure 1 Resting phase

Figure 2 After flicking on biceps muscle belly

Figure 3 Mounding phase

Figure 4 Back to resting phase

www.ijpsi.org

3|Page

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International Journal of Pharmaceutical Science Invention (IJPSI)

  • 1. International Journal of Pharmaceutical Science Invention ISSN (Online): 2319 – 6718, ISSN (Print): 2319 – 670X www.ijpsi.org Volume 2 Issue 10‖ October 2013 ‖ PP.01-03 Myoedema: A Presenting Symptom of Hypothyroid Myopathy. Dr. Priti Panchal Associate Professor (Internal Medicine) ESIPGIMSR, Andheri, Mumbai. ABSTRACT:The incidence of Hypothyroidism is rising in our country. However, in this era of exhaustive investigations, where clinical signs often get overlooked, Myoedema is one such clinical sign, that very conclusively guides the clinician towards the diagnosis of Hypothyroidism. This case report highlights the importance of eliciting Myoedema to corroborate the diagnosis of Hypothyroidism. KEYWORDS : Hypothyroidism; Myoedema. I. INTRODUCTION Hypothyroidism is a relatively common endocrine disorder with a characteristic clinical picture, which may be associated with a variety of clinical features of Myopathy, Mononeuropathy and Sensorimotor axonal polyneuropathy 14, 12,8,10. .The clinical evidence of Hypothyroid Myopathy has been reported in 20-88% of patients14, 11, 12, 13, 15; the symptoms being proximal weakness, cramps, painful muscles, myoedema on percussion, delay in deep tendon reflexes and development of muscle hypertrophy 12, 13, 10. Severity of Myopathy generally correlates with the duration and the degree of thyroid hormone deficiency 11, 15. Serum Creatine Kinase (CK) elevation is usually observed even in the absence of overt muscle weakness 11,10 . CASE REPORT 31 year old male came with complaints of giddiness since 8 days. He noticed a gradual change in voice over one year. He complained of easy fatigability and difficulty in getting up from squatting position. All the above complaints progressed gradually over an year. There was no history of prolonged fever prior to these symptoms or indulging in any vigorous muscular activity or any history of being on any prolonged medication.Examination revealed normal vital parameters with no signs of malnutrition, oedema feet or puffiness of face. The grade of power in proximal muscles was 4/5 and in the distal muscle was 5/5. All the deep tendon reflexes were grossly delayed. On tapping biceps muscle gently there was slow and sustained contraction of muscle lasting for few seconds which is a classical sign of Myoedema. All the other systems including the Nervous system, especially higher functions were normal. Investigation revealed : Haemoglobin of 11.5gm/dl, the total count was 5500/cmm, platelet 2.18lakh/cmm.The Liver and Renal Function Tests were normal. Serum calcium and Vitamin D3 was normal. CPK was elevated 670 IU/L (Normal range 20-170IU/L). Serum cholesterol was 303mg/dl, serum triglyceride 143 mg/dl.MRI brain showed ischemic changes in both peritrigonal areas on T2 flair images which was not significant. Electrocardiogram was normal. Echocardiography showed mild pericardial effusion. Thyroid function test was done in view of clinical symptom and sign of Myoedema. It was suggestive of hypothyroidism with serum T3 80ng/100ml (70 200ng/100ml), T4 2.9µg/100ml (5-13µg/100ml), TSH 75µIU/ml (0.3-5µIU/ml).In view of above investigation diagnosis of hypothyroidism was made and patient was started on L–Thyroxine 100µgm per day. Patient showed remarkable symptomatic improvement with disappearance of Myoedema within a month and a marked fall in the CPK level. The Thyroid function test were repeated at two monthly intervals, which showed gradual fall in TSH levels. After 6 months Thyroid function tests became normal and there was complete resolution of proximal muscle weakness and normalisation of voice. Raised serum CPK, low T4 and high TSH, and their reversibility with L-thyroxine treatment supported the diagnosis of Hypothyroid Myopathy. DISSCUSSION Muscle weakness, aches and cramps, stiffness and delayed tendon jerk relaxation are usual features of Hypothyroid Myopathy (30–80%),while muscle hypertrophy, myoedema and wasting are occasionally seen.(1&2)Delayed relaxation of tendon jerks and proximal muscle weakness correlate with biochemical severity of hypothyroidism (serum T4 <20 ng/ml).(3). Acute myoedema are, however, distinctly rare. (2 &4 )Musculoskeletal symptoms are very common in hypothyroidism, and they may improve or disappear with correction of the hypothyroid state. [5] . The elevation of serum creatine phospho kinase (CK) was reported in 80% of the patients with hypothyroidism even with the absence of muscle involvement 4, 8,9,10. Elevation of CPK levels was detected in our patient as well. With the thyroid hormone replacement therapy the serum levels of www.ijpsi.org 1|Page
  • 2. Myoedema: A Presenting Symptom... CPK decreased in parallel to the clinical improvement in 3 months. Myoedema is one of classical signs of Hypothyroid Myopathy, which is uncommon and hence overlooked by clinicians in most instances. It is a phenomenon of mounding of muscle tissue occurring after a light pressure stimuli. It is produced by flicking across along the contours of bulk of arm involving biceps belly with the thumb and index fingers.(fig.1) This causes a visible and palpable non-tender, firm, localized ridge in the muscle immediately under the point of tactile stimulus.(fig. 2) The swelling reaches its maximal size after 1-2 seconds and gradually subsides over some 5-10 seconds,(fig.3) following which the muscle resumes its normal smooth contour with no palpable localized hardening.(fig.4) The swelling does not spread elsewhere along the muscle. The magnitude as well as the duration of this phenomenon is quite variable, depending upon the thickness of the muscle and the overlying soft tissues [6] and the intensity of the blow delivered. Myoedema is entirely reversible by thyroid hormone replacement and it does not have any harmful effects. Myoedema is due to prolonged muscle contraction caused by delayed calcium reuptake by sarcoplasmic reticulum, following local calcium ion release brought out by percussion or pressure. The muscle involvement in hypothyroidism is caused by alterations in muscle fibres from fast twitching type II to slow twitching type I fibres, deposition of glycosaminoglycans, poor contractility of actin–myosin units, low myosin ATPase activity, and low ATP turnover in skeletal muscle. [7] In the past, Myoedema was considered an insensitive and non-specific finding, occurring also in states of malnutrition, hypovitaminosis, and hypoalbuminemia, in addition to hypothyroidism. However, in conditions suspicious of overt hypothyroidism, elicitation of Myoedema significantly increases the probability of Hypothyroid Myopathy. Hence, it's special clinical significance and the need for its validation in appropriate settings. II. CONCLUSION Myoedema is uncommon feature of Hypothyroid Myopathy and Serum CPK levels - can be used as a marker of Hypothyroid Myopathy; which effectively responds to L-Thyroxine Therapy. ACKNOWLEDGEMENT The author would like to thank the institution head: respected Dean for encouraging and permitting the publication of this case report. The author would also like to thank the institution Neurologist and the Department of Internal Medicine for providing the Clinical material for this Report. Lastly the author expresses her gratitude to the Hospital and the patient for their cooperation. REFERENCES: [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] [14] [15] Ramsey I. Muscular abnormalities of hypothyroidism. In: Thyroid disease and muscle dysfunction. London: William Heinemann, 1974; pp 126–171. McArdle B. Metabolic and endocrine myopathies. In: Walton JN, Ed, Disorders of voluntary muscle. Edinburgh: Churchill Livingstone, 1974; p 750. Khaleeli AA, Griffith DG, Edwards RHT. The clinical presentation of hypothyroid myopathy and its relationship to Abnormalities in structure and function of skeletal muscle.Clin Endocrinology 1983; 19:365–76. Lochmuller H, Reimers CD, Fischer P, Heuss D, Muller-Hocker J, Pongratz DE. Exercise induced myalgia in Hypothyroidism. Clin Invest 1993; 71:999–1001. Cakir M, Samanci N, Balci N, Balci MK. Musculoskeletal manifestations in patients with thyroid disease. Clin Endocrinol. 2003; 59:162–7. Jones MP, Parkes WE. Myoedema. Clin Sci. 1955; 14:97–100. Wiles CM, Young A, Jones DA, Edwards RH. Muscle relaxation rate, fibre-type composition and energy turnover in hyper- and hypo-thyroid patients. Clin Sci. 1979; 57:375–84. Krupsky M, Flatau E, Yarom R Musculoskeletal symptoms as a presenting sign of long standing hypothroidism. Isr J Med Sci (1987) 23:1110-1113 Kung AWC, Ma JTC, Yu YL Myopathy in acute hypothyroidism. Postgraduate Medical Journal (1987) 63; 661-663 Scott KR, Simmons Z, Boyer P. Hypothyroid myopathy with a strikingly elevated serum creatine kinase levels. Muscle and Nerve (2002) 26:141-14 4 11.Evans R, Itaru W Central changes in hypothyroid myopathy: a case report. Muscle and Nerve (1990) 13:952-956 Klein I, Levey G Unusual manifestations of hypothyroidism. Arch Intern Med (1984)144:123-128 Ono S, Inouye K, and Mannen T Myopathology of hypothyroid myopathy. J Neurological Sciences (1987) 77:237-248 Ruurd FD, Bosch J, Laman DM Neuromuscular findings in thyroid dysfunction: a prospective clinical and electrodiagnostic study. J Neurol Neurosurg Psychiatry (2000) 68:750-755 15.Torres CF, Moxley RT Hypothyroid neuropathy and myopathy: clinical and electrodiagnostic www.ijpsi.org 2|Page
  • 3. Myoedema: A Presenting Symptom... Figure 1 Resting phase Figure 2 After flicking on biceps muscle belly Figure 3 Mounding phase Figure 4 Back to resting phase www.ijpsi.org 3|Page