|Year : 2010 | Volume
| Issue : 4 | Page : 250-256
Clinical, electrophysiologic, and histopathologic profile, and outcome in idiopathic inflammatory myositis: An analysis of 68 cases
KN Ramesha1, Abraham Kuruvilla1, PS Sarma2, VV Radhakrishnan3
1 Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India
2 Department of Biostatistics, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India
3 Department of Neuropathology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India
|Date of Submission||06-Mar-2010|
|Date of Decision||13-Apr-2010|
|Date of Acceptance||20-Jul-2010|
|Date of Web Publication||24-Dec-2010|
Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India - 695 011
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Objectives: To study the electroclinical and histopathologic profile of idiopathic inflammatory myositis (IIM) with reference to prognosis and survival rate. Materials and Methods: Diagnosis of IIM was based on the Bohan and Peter criteria. Patients who improved and those whose condition worsened or who expired due to IIM per se at last follow-up were classified to have favorable and poor outcomes, respectively. Fisher's exact test was used for univariate analysis of prognostic factors. Results: The study cohort consisted of consecutive 68 patients with IIM. The mean age at diagnosis was 36.5 years and females constituted 71%. Of these patients, 62% had definite IIM, 49% had polymyositis, 20% had dermatomyositis, and 29% had overlap syndrome. The mean follow-up period was 5.4 years. Prednisolone alone was used in 55 (80%), and azathioprine (1-3 mg/kg/day) alone in 12 (17.6%) as the initial treatment. Relapse of IIM with drug withdrawal was seen in 15 patients (22%); 70% had favorable outcome and 16% had expired. The treatment delay of ≤6 months (P = 0.001), absence of cardiac or lung involvement (P < 0.001), and positive biopsy (P = 0.033) were predictive of a favorable prognosis in the univariate analysis. In multivariate analysis, only the duration of illness of ≤6 months (P = 0.008) and the absence of cardiac or lung involvement (P = 0.001) predicted the favorable outcome at last follow-up. Cumulative survival rate was 95% at 1 year, 86% at the 5th year, and 80% at the 10th year. Conclusions: Approximately, two-thirds of the patients showed good electroclinical and histopathologic correlations and an equal number improved with treatment. The treatment delay (≥6 months), presence of cardiac or pulmonary involvements, and negative muscle biopsy are bad prognostic factors.
Keywords: Final outcome, myositis, prognosis, survival rate
|How to cite this article:|
Ramesha K N, Kuruvilla A, Sarma P S, Radhakrishnan V V. Clinical, electrophysiologic, and histopathologic profile, and outcome in idiopathic inflammatory myositis: An analysis of 68 cases. Ann Indian Acad Neurol 2010;13:250-6
|How to cite this URL:|
Ramesha K N, Kuruvilla A, Sarma P S, Radhakrishnan V V. Clinical, electrophysiologic, and histopathologic profile, and outcome in idiopathic inflammatory myositis: An analysis of 68 cases. Ann Indian Acad Neurol [serial online] 2010 [cited 2021 Apr 18];13:250-6. Available from: https://www.annalsofian.org/text.asp?2010/13/4/250/74190
| Introduction|| |
The idiopathic inflammatory myositis (IIM) is a rare heterogenous group of disorders in which the primary pathologic process is inflammation within the muscle. , The disease has been divided into dermatomyositis (DM), polymyositis (PM), IIM associated with other connective tissue disorders (overlap syndromes), neoplasia-associated IIM, and inclusion body myositis (IBM). , The diagnosis and treatment are straightforward and rewarding in a majority of the cases. , The treatment is based both on expert opinion , and systematic analysis of a few randomized controlled trials.  Mortality is mainly because of other organ involvement or due to underlying malignancy. , The outcome and prognostic factors in IIM vary widely in the literature. ,,,,,,,, In this background, we aimed to evaluate the clinical, electrophysiologic, and histopathologic profile and their correlations in IIM and also to estimate the overall response rates to standard treatment and relapse rate with drug tapering, to assess the potential prognostic factors and to calculate the mortality rates and their causes in the study cohort.
| Materials and Methods|| |
All the consecutive cases of IIM treated in the Department of Neurology at Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India, from 1990 to April 2004 were reviewed from the medical records. The patients with a discharge diagnosis of IIM from April 2004 to December 2006 were prospectively followed-up for a minimum period of 2 years. A systematic chart review was done to collect the demographic data, clinical features, and investigations, including serum enzyme assay, electromyography (EMG) and muscle biopsy findings, treatment details, and complications related to treatment. The patients were followed-up initially at 3-month intervals till the end of the 1st year after the diagnosis, then yearly till last follow-up wherever possible. Patients who did not come for follow-up were contacted either by letter or by telephone regarding their treatment and health status at last follow-up. During each follow-up, clinical features, serum creatine phosphokinase (CPK) value and erythrocyte sedimentation rate (ESR) were noted along with the response to treatment.
The diagnosis of IIM was made according to diagnostic criteria proposed by Bohan and Peter.  They were subclassified into PM, DM, IBM, overlap syndrome with other connective tissue disorders and neoplasia-associated IIM. Patients with symptoms for less than 3 months duration at presentation were classified as having acute IIM. Grading of muscle weakness was done according to the standard MRC grading system. For prognostication, a muscle power of 4/5 and ≤3/5 at hip girdle and shoulder region were taken as mild and severe weakness, respectively.
The outcome at last follow-up was divided into excellent, favorable, and poor outcome. One who continued to be in complete remission after stopping the treatment was classified to have excellent outcome. Those who improved from the baseline neurologic status or became asymptomatic were classified to have favorable outcome. Those who expired due to IIM per se and those who worsened or did not improve with treatment were classified to have poor outcome. EMG was done by experts in the interpretation of EMG. Histopathology of the muscle was interpreted by expert neuropathologist, and hematoxylin and eosin stain, modified Gomori's trichrome stain, and periodic acid Schiff (PAS) were used in all patients. Dystrophinopathies were ruled out by appropriate immunohistochemistry in patients with atypical clinical features.
For statistical analysis, Fisher's exact test was used for the univariate analysis of various prognostic factors. The factors that were found either showing a positive trend or having a statistically significant bearing on the outcome were then subjected to multiple logistic regression analysis. Cumulative survival rate at each year up to last follow-up were calculated by Kaplan-Meier method. The P value ≤ 0.05 was considered as statistically significant.
| Results|| |
A total of 85 cases were collected in the retrospective group from 1990 to 2004, but six of them were excluded from the study as biopsy and EMG study unequivocally showed an alternate diagnosis. The prospective group included nine cases, which were recruited from April 2004 to December 2006. Patients with IBM (n=3), children below the age of 16 (n=12), and those with less than 2 years of follow-up (n=5) were excluded from the analysis. Hence, study cohort totally included 68 cases of IIM.
The mean age at presentation was 36.5 years (range, 16-68 years), 13% of the patients were older than 50 years, 72% were females, 25% had presentation less than 3 months after the onset of symptoms, and 50% patients had muscle pain. Half of them had tenderness on examination, 30% and 66% had severe and mild weakness in the shoulder girdle, respectively, whereas 35.2% and 62.4% had severe and mild weakness in the hip girdle, respectively. Two patients had upper girdle onset and 38% were not ambulant without support at the time of presentation. All had symmetrical weakness. Fasciculation was noted in only three patients. A significant muscle wasting was seen in 28.5% patients and all of them were symptomatic for more than 6 months prior to presentation. Seventy-six percent of the patients had neck muscle weakness at the time of initial evaluation. The neck flexion was more affected than neck extension. Thirty-four percent of the patients had bulbar muscle weakness in the form of dysphagia and nasal regurgitation. More than half of the patients with dysphagia had DM. A mild degree of bifacial weakness was seen in 20%. Deep tendon reflexes were brisk in 10%, sluggish 37%, and were absent in 15%.
Anemia and leukocytosis were seen in 9.5% and 33% cases, respectively. ESR was raised in 38%. Serum enzymes (SGOT and SGPT) were raised in 62% and serum CPK was high in 85%, normal in 14.8%, and more than 1000 IU in 51% of the cases. Mean CPK was 3200 IU/L in the cases with value more than 1000 IU/L. Highest CPK was 25,000 IU/L. Antinuclear antibody was positive in 23 out of the total 36 patients in whom it was tested (63.9%).
EMG findings were suggestive of myopathy in 59 cases (87%). Of the 59 cases, 40 cases had classical inflammatory myositis (59%) in the form of insertional irritability, fibrillations, positive sharp waves, and myopathic motor units. Yield of paraspinal EMG was very low (6%). EMG was inconclusive or normal in two, and showed changes of isolated neurogenic etiology in six cases (6.8%). Biopsy was suggestive of inflammatory muscle disease in 51 (75%) and normal or nonspecific in 14.8%. Classical perifascicular atrophy was seen in less than 50% of the cases with DM.
Final diagnosis at last follow-up
The mean and median follow-up period was 5.4 ± 4.0 years and 4.6 years, respectively (range 2-17 years). Forty patients had more than 5 years of follow-up. Definite IIM was seen in 62% of cases, probable IIM in 23% cases, and possible IIM in remaining 15% cases. The majority of patients were PM 33 (49%) followed by overlap syndrome 20 (29%), and DM 14 (20%).th
In the DM group, 80% had classical cutaneous manifestations, such as Gottron's scaly rashes and heliotrope eyelid rashes. In the remaining 20%, diagnosis was contributed by histopathology. In the category of overlap syndrome, out of 20 cases, seven had rheumatoid arthritis, six had systemic lupus erythematosis, and three each had systemic sclerosis and multiple connective tissue disorder. Three had calcinosis cutis. There was only one patient with IIM associated with malignancy .He succumbed to underlying carcinoma of lung with superior vena caval obstruction even though he made significant improvement in muscle power with treatment.
Prednisolone alone was used in 55 (80%) at 0.75-1 mg/kg/day in single daily dose), azathioprine (1-3 mg/kg/day) alone in 12 (18%), and combination of azathioprine and steroids was used as an initial treatment in one. Azathioprine was used in total 19 patients during the course of the treatment. Seven patients received azathioprine during the course of illness due to poor response to steroid or due to steroid-induced complications. In three patients, it was used in view of relapse as soon as steroids were tapered off. Steroids were tapered by the end of 3 and 6 months in 57% and 32% patients, respectively. A mean treatment duration was 2 years 6 months. Out of six patients who had respiratory compromise, intravenous immunoglobulin, and plasma exchange were used in two patients and intravenous methylprednisolone was used in four patients. Only two patients survived in this group. Methotrexate was used in three patients during follow-up. It was used as an adjunctive in one. In other two patients, it was introduced either due to steroid unresponsiveness or due to adverse effects of azathioprine and steroid. Two of them showed good improvement and one of them showed deterioration in muscle power [Table 1].
|Table 1: Comprehensive coverage of clinical features and investigations of study cohort of 68 cases|
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Complications related to drugs
Azathioprine-induced hepatitis was observed in three patients (15.8%) and leukopenia in two patients (10.5%). Both improved with discontinuation of the drug. Steroid-induced necrosis of bilateral head of femur was seen in two patients (3.6%). One patient improved with surgical replacement of head of femur. Steroid-induced transient systemic hypertension and diabetes mellitus were seen in 18 patients (27.0%). Two patients had steroid-induced psychosis.
Analysis of final outcome
Forty-eight (70%) had favorable outcome and 39 (57%) had excellent outcome at last follow-up. During follow-up, CPK started improving along with clinical improvement in most of the patients (38 out of 46 patients, 82.6%). Relapse rate was seen in 15 patients during the follow-up (22%) and 13 of them had short-term relapse (86%).
Cause of death
Eleven patients expired out of 68 cases (16%). Cause of death was directly related to illness in ten patients. The etiologies of death were multifactorial in four (aspiration pneumonia and septicemia related to bulbar weakness and cardiac arrhythmia), cardiac arrhythmia alone in two, and interstitial lung disease in four patients. Remaining one patient had cancer-associated delayed death. None died due to the complications of treatment. Mortality rate was same in PM and DM group. Total 13 had involvement of either myocardium or lung (15%), of which only three improved.
There was statistically significant correlation between duration of illness before presentation, cardiac or lung involvement, and positive biopsy with the outcome at last follow-up in the univariate analysis [Table 2]. Duration of illness less than 6 months (86% vs 14%, P = 0.001), absence of cardiac or lung involvement (23.1% vs 76%, P ≤ 0.001), and positive biopsy (78% vs 21%, P = 0.033) had favorable outcome. There was positive trend for favorable outcome with early age of onset (less than 50 years) compared with those after the age of 50 years (76% vs 24%, P = 0.065). Other factors including various clinical variables, such as sex, presence or absence of neck or bulbar muscle involvement, extent of muscle weakness, EMG findings, serum CPK level, type of treatment received, and subclassification in the diagnosis did not have statistically significant correlation with the outcome at last follow-up. A multivariate logistic regression analysis was carried out on the factors that were found significant in the univariate analysis. In the multivariate analysis, only duration of illness less than 6 months (P = 0.008) and the absence of cardiac and lung involvement (P = 0.001) were found to be significant in predicting the favorable outcome [Table 3].
|Table 2: Prognostic factors analyzed and their statistical significance at last follow-up|
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There was statistically significant positive relationship between excellent outcome when the illness was less than 3 months duration (76.2% vs 50.8%, P = 0.047), absence of cardiac or lung involvement (63.4% vs 23.1%, P = 0.013), and positive biopsy (65.1% vs 33.3%, P = 0.021). There was also statistically significant positive relationship between the excellent outcome at last follow-up and the muscle weakness at 3 months (69.2% vs 38.5%, P = 0.056) after starting the treatment.
Cumulative survival rate was 95% at 1 year, 88% at 3 years, 86% at the end of 5 years, and 80% at 10th year by Kaplan-Meier method [Figure 1]. Survival rate was significantly better in patients without the involvement of myocardium or lung pathology (98.6%) than those with cardiac or pulmonary involvements (23.1%), P = 0.0000.
|Figure 1: Kaplan-Meier survival analysis of 68 cases with idiopathic inflammatory myositis to depict the mortality and survival rate during the follow-up period|
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| Discussion|| |
IIM is not a common neurologic illness. This study totally included 68 cases, which formed the 0.1% of 69,313 neurology outpatients and 0.6% of 14,706 neurology inpatients of this large neurology tertiary referral center in South India over 17 consecutive years. This is in agreement with the other published studies where annual incidence rate was calculated to vary between 1.9 and 7.7 per million , and prevalence rate to be 21.5, 50, and 63 per million in Canada, USA, and Japan, respectively. ,
The mean age and maximum number of patients at presentation in the current study were one to two decades less than that of the majority of the published studies. ,,,, However, sex ratio was similar to other studies. ,,, In this study, severe muscle weakness at the hip girdle and at the shoulder girdle were seen in 35% and 29%, respectively, which is in agreement with the study published by Hoffman et al.  The percentage of neck muscle involvement (76%) in the present study is much higher than in the study by Uthman et al.,  where it was seen in 23% only. One-fourth of our patients had bulbar muscle weakness at the time of initial evaluation, whereas it was only 10% in a study published by Rios et al. 
There has been a lot of variation in the prevalence of elevated CPK in IIM in various studies (64%-94%). ,,,,, CPK was elevated in 85% of cases in the current study, which was higher than that described by DeVere et al.  who found CPK elevation in 64% of cases. We found CPK value more than 1000 IU in 50% cases, which is in agreement with that found by Uthman et al.  who found CPK > 1000 IU in 43%. The variation in CPK level among various studies may be related to the variation in the method used for analysis or due to initiation of treatment before the CPK analysis.
EMG suggestive of myopathy in IIM varies between 66% and 86%. ,,, Myopathic features noted in our study (87%) are comparable to the aforementioned data. DeVere et al.,  Koh et al.,  and Tymms et al.  found positive biopsy in 65%, 76%, and 78% of cases, respectively. This is comparable to our data, which showed positive biopsy in 75%. The biopsy can be false negative because of patchy distribution of the pathology. Also precise diagnosis in IIM may not be easy as shown in a recent study from Mayo Clinic,  wherein they reviewed the clinical features, course of the disease during follow-up, and biopsy in 107 previously diagnosed cases of PM or sporadic IBM and found that 16 patients (37%) had biopsy features of PM, but clinical features of IBM. Hence they concluded that combined evaluation of biopsy and clinical features are crucial to subclassify different IIMs.
Van der Meulen  et al. concluded that pure PM entity is rare. However, in our series, 50% had PM, 30% had overlap syndrome, and 20% had DM. In our study, 75% of PM group had favorable outcome at last follow-up. This indicates that pure PM is not a very rare condition as recently thought to be. However, very high proportion of IIM being PM in this study may be because of the following reasons: some of the patients with PM with poor outcome might have had IBM as we used electron microscopy in the histopathologic diagnosis in only three patients and a repeat muscle biopsy was done in only two. None of the poor responders had a history of early falls, distal > proximal weakness, quadriceps > hip weakness, finger and wrist flexor > shoulder weakness, and selective atrophy of forearm muscles. Also, none of the patients during follow-up with PM developed other connective tissue disorders or cutaneous rashes suggestive of DM. A study from Mumbai showed that a clinical scoring system can reliably differentiate chronic IIM from the muscular dystrophies. 
Hoffman et al.  in a study of 27 cases with IIM found that 64% had little to no weakness within 3 months of treatment with steroids. This is comparable to our study where steroids were tapered by the end of 3 and 6 months, respectively, in 57% and 32% of our patients with clinical improvement; 57% were in remission, two-thirds had favorable outcome, and 16% expired at terminal follow-up. Similar result was noted in a study by Rios et al.  and Marie et al.  wherein remission was reported in 51% and 43%, respectively. Only 17% had full remission in another study,  whereas Maugars et al.  reported a favorable outcome in 84%. In a study consisting 77 cases, short-term recurrences of PM/DM (during tapering of therapy) occurred in 47% patients and long-term recurrences (after discontinuation of therapy) in 12% patients.  The 22% recurrence rate noted in our study is comparable to the above series.
The early treatment initiated within 6 months of onset of illness, and absence of cardiac or lung involvement had statistically significant bearing on outcome in both univariate and multivariate analyses. There was a positive trend for good prognosis with early age of onset. This is in agreement with other studies. ,,, This is the first study that has shown positive correlation between positive biopsy and favorable prognosis. This may be because of the fact that 83% of patients who had treatment delay by less than 6 months had positive biopsy and 62% of patients who had treatment delay by more than 6 months had negative biopsy (P = 0.045). However, this was not found significant in multivariate analysis. Also, prognosis was excellent when improvement in muscle power was seen in the first 3 months of follow-up.
Sixteen percent mortality noted in our study was less than that reported in the majority of other studies, which ranged from 10% to 43%. ,,,,,,, The low mortality in the current study was probably due to the fact that there were very few cases of neoplasia-associated IIM and only 13% were older than 50 years. The low rate of malignancy-associated IIM was also noted in other Indian studies. , Mortalities were mainly due to myocarditis, interstitial lung disease, and aspiration pneumonias, which are in agreement with other studies except for the proportion of cancer-related deaths. ,,,,, There was a single mortality related to underlying malignancy in this study unlike in other studies where substantial numbers of mortalities were due to malignancy. ,,,,,,, We did not find any difference in the death rate or statistically significant difference in the outcome between PM and DM. Some studies have shown that DM has better prognosis than PM,  whereas other studies have shown vice versa. ,
The cumulative survival rate at 1st, 5th, and 10th year was 95%, 86%, and 80%, respectively, in the current study by Kaplan-Meier method. The survival rate in the current study was high as only one patient had malignancy and only three patients were older than 60 years. This may reflect the referral pattern. The comparison of the survival rate during follow-up between the various published studies on IIM and the current study is shown in [Table 4].
|Table 4: Comparison of the survival rate during follow-up in the various published studies on idiopathic inflammatory myositis and in the current study|
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Limitations of the study are retrospective collection of a relatively small number of cases and a minimum follow-up period of 2 years. Electron microscopy and major histocompatibility complex detection were not used in the histopathologic diagnosis, so some DM and IBM might have been misdiagnosed to have PM. Exhaustive workup for malignancy in DM were not carried out. Hence, there is a possibility of missing some malignancy-associated IIM.
| Conclusion|| |
Clinical, electrophysiologic, and histopathologic correlations were seen in two-thirds of the patients with IIM. More than 50% had excellent outcome and two-thirds had a favorable outcome ultimately. Majority of the relapse was due to premature withdrawal of the medications. The early commencement of the treatment, absence of cardiac or pulmonary involvement, and positive muscle biopsy findings are good prognostic factors. Patients who are likely to show excellent improvement will likely show improvement in the initial 3 months of the treatment period.
| References|| |
|1.||Bohan A, Peter JB. Polymyositis and dermatomyositis (first of two parts). N Engl J Med 1975;292:344-7. |
|2.||Bohan A, Peter JB. Polymyositis and dermatomyositis (second of two parts). N Engl J Med 1975;292:403-7. |
|3.||Dalakas MC. Clinical, immunopathologic and therapeutic considerations of inflammatory myopathies. Clin Neuropharmacol 1992;15:327-51. |
|4.||Mastaglia FL, Phillips BA, Zilko P. Treatment of inflammatory myopathies. Muscle Nerve 1997;20:651-64. |
|5.||Choy EH, Hoogendijk JE, Lecky B, Winer JB. Immunosuppressant and immunomodulatory treatment for dematomyositis and polymyositis. Cochrane Database Syst Rev 2005;3:CD003643. |
|6.||Dalakas MC. Polymyositis, dermatomyositis and inclusion body myositis. N Engl J Med 1991;325:1487-98. |
|7.||Airio A, Kautiainen H, Hakala M. Prognosis and mortality of polymyositis and dermatomyositis patients. Clin Rheumatol 2006;25:234-9. |
|8.||Bronner IM, van der Meulen MF, de Visser M, Kalmijn S, van Venrooij WJ, Voskuyl AE, et al. Long-term outcome in polymyositis and dermatomyositis. Ann Rheum Dis 2006;65:1456-61. |
|9.||Marie I, Hachulla E, Hatron PY, Hellot MF, Levesque H, Devulder B, et al. Polymyositis and dermatomyositis: Short term and longterm outcome, and predictive factors of prognosis. J Rheumatol 2001;28:2230-7. |
|10.||Choy EH, Isenberg DA. Treatment of dermatomyositis and polymyositis. Rheumatology 2002;41:7-13. |
|11.||Oddis CV, Conte CG, Steen VD, Medsger TA Jr. Incidence of polymyositis-dermatomyositis: 20-year study of hospital diagnosed cases in Allegheny Country, PA 1963-1982. J Rheumatol 1990;17:1329-34. |
|12.||Araki S, Uchino M, Kumamoto T. Prevalence studies of multiple sclerosis, myasthenia gravis, and myopathies in Kumamoto district, Japan. Neuroepidemiology 1987;6:120-9. |
|13.||De Vere R, Bradley WG. Polymyositis: Its presentation, morbidity and mortality. Brain 1975;98:637-66. |
|14.||Koh ET, Seow A, Ong B, Ratnagopal P, Tjia H, Chng HH. Adult onset polymyositis/dermatomyositis: Clinical and laboratory features and treatment response in 75 patients. Ann Rheum Dis 1993;52:857-61. |
|15.||Holden DJ, Brownell AK, Fritzler MJ. Clinical and serologic features of patients with polymyositis or dermatomyositis. Can Med Assoc J 1985;132:649-53. |
|16.||Drouet B, Le Loët X, Vittecoq O, Nouvet G, Genevois A, Lauret P, et al. A study of long term survival, functional outcome and quality of life in patients with polymyositis or dermatomyositis. Rev Rheum Engl Ed 1996;63:321-30. |
|17.||Ehrenstein MR, Snaith ML, Isenberg DA. Idiopathic myositis: A rheumatological view. Ann Rheum Dis 1992;51:41-4. |
|18.||Porkodi R, Shanmuganandan K, Parthiban M, Madhavan R, Rajendran P. Clinical spectrum of inflammatory myositis in South India: A ten year study. J Assoc Physicians India 2002;50:1255-8. |
|19.||Hoffman GS, Franck WA, Raddatz DA, Stallones L. Presentation, treatment, and prognosis of idiopathic inflammatory muscle disease in a rural hospital. Am J Med 1983;75:433-8. |
|20.||Uthman I, Vázquez-Abad D, Senécal JL. Distinctive features of idiopathic inflammatory myopathies in French Canadians. Semin Arthritis Rheum 1996;26:447-58. |
|21.||Rios G. Retrospective review of the clinical manifestations and outcomes in Puerto Ricans with idiopathic inflammatory myopathies. J Clin Rheumatol 2005;11:153-6. |
|22.||Tymss KE, Webb J. Dermatopolymyositis and other connective tissue diseases: A review of 105 cases. J Rheumatol 1985;12:1140-8. |
|23.||Scola RH, Werneck LC, Prevedello DM, Toderke EL, Iwamoto FM. Diagnosis of dermatomyositis and polymyositis: A study of 102 cases. Arq Neuropsiquiatr 2000;58:789-99. |
|24.||Chahin N, Engel AG. Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBM. Neurology 2008;70:418-24. |
|25.||van der Meulen MF, Bronner IM, Hoogendijk JE, Burger H, van Venrooij WJ, Voskuyl AE, et al. Polymyositis: An over diagnosed entity. Neurology 2003;61:316-21. |
|26.||Khadilkar SV, Patil SG, Amin SN. Study of idiopathic inflammatory myopathies with special reference to borderland between idiopathic inflammatory myopathies and muscular dystrophies. Neurol India 2008;56:356-62. |
|27.||Sultan SM, Ioannou Y, Moss K, Isenberg DA. Outcome in patients with idiopathic inflammatory myositis: Morbidity and mortality. Rheumatology 2002;41:22-6. |
|28.||Maugars YM, Berthelot JM, Abbas AA, Mussini JM, Nguyen JM, Prost AM. Long term prognosis of 69 patients with dermatomyositis or polymyositis. Clin Exp Rheumatol 1996;14:263-74. |
|29.||Sharma A, Kumar S, Wanchu A, Sharma K, Sharma N, Singh R, et al. Clinical characteristics and predictors of mortality in 67 patients with primary polymyositis: A study from North India. Clin Rheumatol 2010;29:45-51. |
|30.||Shah PA, Hassan I, Choudhary ND, Nafae A. Clinical profile of polymyositis in Kashmir valley. J Assoc Physicians India 1999;47:480-2. |
|31.||Dankó K, Ponyi A, Constantin T, Borgulya G, Szegedi G. Long term survival of patients with idiopathic inflammatory myopathies according to clinical features: A longitudinal study of 162 cases. Medicine (Baltimore) 2004;83:35-42. |
|32.||Ponyi A, Constantin T, Garami M, András C, Tállai B, Váncsa A, et al. Cancer associated myositis: Clinical features and prognostic signs. Ann N Y Acad Sci 2005;1051:64-71. |
|33.||Torres C, Belmonte R, Carmona L, Gómez-Reino FJ, Galindo M, Ramos B, et al. Survival, mortality and causes of death in inflammatory myopathies. Autoimmunity 2006;39:205-15. |
|34.||Miró O, Laguno M, Alonso JR, Casademont J, Herrero C, Selva A, et al. Clinical course of idiopathic inflammatory myopathies: Complications, survival and prognosis factors. Med Clin (Barc)1999;112:521-6. |
|35.||Hilton-Jones D. Diagnosis and treatment of inflammatory muscle diseases. J Neurol Neurosurg Psychiatry 2003;74:ii25-31. |
|36.||Pautas E, Chérin P, Piette JC, Pelletier S, Wechsler B, Cabane J, et al. Features of polymyositis and dermatomyositis in the elderly: A case-control study. Clin Exp Rheumatol 2000;18:241-4. |
|37.||Tani K, Tomioka R, Sato K, Furukawa C, Nakajima T, Toyota Y, et al. Comparison of clinical course of polymyositis and dermatomyositis: A follow-up study in Tokushima University Hospital. J Med Invest 2007;54:295-301. |
[Table 1], [Table 2], [Table 3], [Table 4]
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