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A case of dilated cardiomyopathy in a venezuelan patient with polymyositis

Un caso de cardiomiopatía dilatada en un paciente venezolano con polimiositis

Miguel Bayones MD1, Ana Ramírez MD1, Jose Ruiz MD2, Carlos Sierra MS3, Claudio Tombazzi4
1Internal Medicine Service, Bejuma District Hospital, Bejuma, Venezuela
2Research Service, Memphis VA Medical Center, Memphis, USA
3University of Kentucky School of Medicine, University of Kentucky, Lexington, USA
4University of Tennessee School of Medicine, University of Tennessee, Memphis, USA

DOI: 10.15568/am.2017.801.cc05

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Resumen / Abstract

Abstract

Polymyositis is an autoimmune disease, characterized by the inflammation of muscular tissues. It belongs to the family of inflammatory myopathies, along with dermatomyositis, inclusion-bodies myositis and necrotizing autoimmune myositis. In this case report we present a 39 year old male patient admitted to the Bejuma District Hospital in October of 1991, where the patient is evaluated for 21 days. Electromyography, skeletal muscle biopsies, and further lab tests were performed; posing a diagnostic impression of Polymyositis. After the analysis of these results, the patient is discharged with pharmacological treatment; however, he denies taking the medications. In March of 2007 patient is seen at the Bejuma District Hospital after complaining of respiratory distress during mild efforts, concomitantly non-productive cough and palpitations. It is concluded that the rate of cardiovascular deterioration without constant medical treatment is secondary to untreated Polymyositis.

Keywords: Polymyositis, dilated cardiomyopathy, inflammatory myopathy

Resumen

La polimiositis es una enfermedad autoinmune, caracterizada por la inflamación de los tejidos musculares. Pertenece a la familia de las miopatías inflamatorias, junto con dermatomiositis, miositis de cuerpos de inclusión y miositis autoinmune necrotizante. En este caso presentamos un paciente varón de 39 años admitido en el Hospital del Distrito de Bejuma en octubre de 1991, donde el paciente es evaluado durante 21 días. Se realizaron electromiografía, biopsias del músculo esquelético y más pruebas de laboratorio; lo que supone una impresión diagnóstica de Polimiositis. Después del análisis de estos resultados, el paciente es dado de alta con tratamiento farmacológico; sin embargo, niega tomar los medicamentos. En marzo de 2007 el paciente es visto en el Hospital del Distrito de Bejuma después de quejarse de dificultad respiratoria durante los esfuerzos suaves, concomitantemente tos no productiva y palpitaciones. Se concluye que la tasa de deterioro cardiovascular sin tratamiento médico constante es secundaria a la polimiositis no tratada.

Palabras clave: Polimiositis, miocardiopatía dilatada, miopatía inflamatoria


INTRODUCTION

Polymyositis is an autoimmune disease which belongs to the family of inflammatory myopathies, along with dermatomyositis, inclusion-bodies myositis and necrotizing autoimmune myositis (1,2). It affects the muscle tissue through an inflammatory and necrotizing process that results in progressive weakness. It may also affect the cardiac muscle. The average age of presentation ranges between 45 and 60 years, and it seldom occurs during childhood (3).

Due to its uncommon nature; we present the study of a clinical case in which a patient with a diagnosis of Polymyositis attends to the Bejuma District Hospital, State of Carabobo, Venezuela, with manifestations of dilated cardiomyopathy class III.

CLINICAL CASE

Case of a 39-year-old patient from Carabobo, Venezuela, that started exhibiting symptoms of the disease in August of 1991. The patient begins to exhibit proximal muscle weakness in the lower extremities in a progressive and symmetric manner. This progressive muscle weakness limits the patient’s 

ability to perform daily activities like walking and stair climbing. Concomitantly, the patient presents with moderate myalgia that was unresponsive to NSAIDS. Due to persistent symptomatology, the patient is admitted to the Bejuma District Hospital in October of 1991, where the patient is evaluated for 21 days. Electromyography, skeletal muscle biopsies, and further lab tests were performed; posing a diagnostic impression of Polymyositis. The results showed a CPK ( 1435 IU/L) and CK-MB (40 IU/L) elevation, electromyography of the anterior tibial, left vastus medialis, right deltoid, right quadriceps, right long supinator and left gastronecmius reported myopathic affection with proximal musculature predominance. After the analysis of these results, specialists concluded the diagnosis of Polymyositis. Oral Prednisone is indicated for 15 days. A Rheumatology service consultation is also requested. The patient did not follow treatment nor attended to the Rheumatologist evaluation.

In March of 2007, he returned to the center after complaining of respiratory distress during mild efforts, concomitantly non-productive cough and palpitations, which is why he was evaluated and admitted for 7 days. Physical examination showed: Patient in regular general conditions. Temperature: 36.5 ° C. Pulse: 100 b.p.m. Breathing: 20 b.p.m. Blood Pressure: 100 / 70mmHg. Hydrated skin without apparent lesions. Symmetric thorax, apex visible and palpable in 7th left intercostal space at 3cm outside of left midclavicular line, tachyarrhythmic cardiac sounds with holosystolic murmur grade II; Respiratory sounds present in both hemithorax with crackles in both pulmonary bases. Limbs showed decreased muscle strength in both upper limbs and mainly in lower limbs in its proximal portion, manifested by limitation to gait and incorporation in squatting position, muscular atrophy is evidenced at the predominance of bilateral femoral region, preserved osteotendinous reflexes, superficial and deep sensitivity conserved, no varices or edema are evident. Rest of the physical evaluation, without alterations. Machado Guerreiro test was negative, EKG showed Left Bundle Branch Blockade with Ventricular Extrasystoles, in the chest X-ray bibasal infiltrate, dilated cardiomyopathy is observed, and echocardiogram indicated dilated cardiomyopathy in four wells, left ventricular systolic function severely depressed with Ejection Fraction (EF) of 17% moderate mitral insufficiency, mild tricuspid insufficiency, without intracavitary thrombi. The patient is diagnosed with functional class III dilated cardiomyopathy.

After 7 days of hospitalizations the patient was discharged with Prednisolone P.O (1g/day) and medical treatment for cardiac insufficiency (lisinopril 2.5mg/day, spironolactone 5mg/day, metoprolol 25mg/day).

DISCUSSION

Polymyositis is an idiopathic inflammatory disease whose prevalence is estimated in one case per 100,000 inhabitants per year in the general population and an incidence of 5 to 10 cases per million in adults. The highest incidence occurs around the fifth decade of life and the woman / man ratio is 2: 1 (3,7). Being a disease of unusual appearance it is often considered by many specialists as a diagnosis of exclusion (1).

The factors that trigger polymyositis are still unknown. The theory of a viral cause such as Coxsackie virus, influenza virus and HIV infection has been proposed, the latter being the most accepted because of the development of inflammatory myopathies in patients infected with a retrovirus. However, several studies have yielded conflicting results. Likewise, the effect of genetic factors and environmental agents has been hypothesized (1, 4). Our patient wasn’t aware of the presence of polymyositis in his family and also denied the history of a viral infection. The ELISA test for HIV reported a negative result.

The etiopathogenesis of this disease is believed to have an autoimmune basis. The presence of a direct cytotoxicity phenomenon restricted to the expression of class 1 antigens of the major histocompatibility complex has been evidenced. Polymyositis as an isolated entity is rare; more commonly it appears along with some other inflammatory disorder, being denominated “overlap syndrome”. These include: mixed connective tissue disease (MCTD), scleroderma myositis overlap syndrome, and the antisynthetase syndrome. It is common to see physical findings such as sclerodactyly and Raynaud’s phenomenon (1,2,4). Due to institutional and economical limitations, it was not possible to perform the necessary laboratories for the detection of antibodies related to these entities.

The diagnosis of inflammatory myositis is based on the presence of at least 3 clinical and laboratory findings, including: the presence of progressive weakness in the upper and lower extremities, elevation of muscle enzymes such as creatine kinase and transaminases, Electromyography and abnormal muscle biopsy. The presence of suggestive results in the aforementioned studies and the absence of dermatological findings such as Gottron’s papules and heliotrope rash excluded the possibility of a diagnosis of dermatomyositis (4,5). In our case, it would be necessary to do a differential diagnosis with Chagas disease, which can present peripheral muscle alterations, in addition to the characteristic heart affection. Due to its similar presentation, Chagas can be confused with Polymyositis (6). A test of Machado Guerreiro was indicated, which yielded negative results.

Among the various complications related to the diagnosis of polymyositis, the most common is the development of interstitial lung disease; which has been evidenced in almost 75% of the cases (7,8,9). Cardiovascular complications have an approximated prevalence of 9 to 72% of cases (10) It has been hypothesized suggested that the development of cardiac complications are the sum of traditional cardiovascular risk factors plus the characteristic systemic inflammation in Polymyositis , which may explain the long period of time before the onset of cardiac symptoms in our patient. Cardiac symptomatology is often related to a bad prognosis in patients with Polymyositis The progress to systolic heart failure, has been documented in case reports, however, there are no controlled studies exposing this complication (11).). The development of cardiac insufficiency by cardiomyopathy tends to be observed in patients with important peripheral musculature affection (12,13). Electrocardiographic manifestations include branch block, A-V block, prolonged PR interval, left ventricular abnormalities, ventricular extrasystoles, high-grade cardiac block, Q-wave abnormalities, and non-specific changes in the ST segment (10).

Due to economical causes, in Venezuela we do not have the steroids sparing immunotherapy medications for the treatment of inflammatory myopathies.

With the presentation of this case report, we would like to highlight the relevance of a proper patient education and medical follow up, which are the keys in the prevention of long term complications. Even thought, in the Venezuelan public health system, we don’t always count with the necessary diagnostic and therapeutic tools, we as physicians try to prioritize the use of a good clinical eye and a complete medical history to obtain the correct diagnosis give the best treatment option.

Acknowledgement: Bejuma District Hospital Epidemiology Service.

REFERENCES

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  10. Zhang L, Wang GC, Ma L, Zu N. Cardiac involvement in adult polymyositis or dermatomyositis: a systematic review. Clin Cardiol. 2012 Nov;35(11):686-91.
  11. Schwartz T, Diederichsen LP, Lundberg IE, Sjaastad I, Sanner H. Cardiac involvement in adult and juvenile idiopathic inflammatory myopathies. RMD Open. 2016 Sep 27;2(2):e000291.eCollection 2016.
  12. Afzal A, Higgins RS, Philbin EF. Heart transplant for dilated cardiomyopathy associated with polymyositis. Heart. 1999 Oct;82(4):e4.
  13. Coblyn JS, Weinblatt ME. Rheumatic diseases and the heart. In: Braunwald E, ed. Heart disease. A textbook of cardiovascular medicine. Philadelphia: WB Saunders & Co.1997:1779–80.

Jose Ruiz, MD
Av. 90. Urb. Las Chimeneas
Edif. San Andres VII, Apt. 10-C. Valencia, Edo Carabobo, Venezuela.
Telephone: +582418420996
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Actual. Med.
2017; 102: (801): 109-111
Enviado: 15-04-2017
Revisado: 20-05-2017
Aceptado: 10-06-2017

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Fundación Benéfica Anticancer San Francisco Javier y Santa Cándida

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Revista Actualidad Médica
ISSN: 0365-7965
(Edición impresa)
Edita la Real Academia de Medicina y Cirugía de Andalucía Oriental.
Avda. Madrid 11. 18012 Granada · España.