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versão impressa ISSN 0037-8682
Rev. Soc. Bras. Med. Trop. vol.45 no.4 Uberaba jul./ago. 2012
CASE REPORT RELATO DE CASO
Actinomicose comprometendo a medula espinhal: um relato de caso
Maria Isabela Alves RamosI; Jair Almeida CarneiroII; Fabiano de Oliveira PoswarII; Daniella Cristina NassauIII; Fernando Antônio ColaresIV
ICurso de Medicina, Universidade Estadual de Montes Claros, Montes Claros, MG
IIPrograma de Pós-Graduação Strictu Sensu em Ciências da Saúde, Universidade Estadual de Montes Claros, Montes Claros, MG
IIIHospital Universitário Clemente de Faria, Universidade Estadual de Montes Claros, Montes Claros, MG
IVDepartamento de Clínica Médica, Universidade Estadual de Montes Claros, Montes Claros, MG
Actinomycosis is a rare, chronic, suppurative, granulomatous infection caused by a group of gram-positive anaerobic bacteria belonging to the natural flora of the oral cavity and gastrointestinal and urogenital tracts. It may involve several organs. This case study refers to pulmonary actinomycosis with chest wall involvement and cord compression in a 29-year-old male who presented with fever, cough, hemoptysis, neck pain, and paresis and plegia of the lower limbs of 5-month duration.
Keywords: Actinomycosis. Lung. Chest wall.
A actinomicose é uma infecção rara, crônica, supurativa e granulomatosa, causada por um grupo de bactérias anaeróbias Gram-positivas que pertencem à flora natural da cavidade oral, do aparelho gastrointestinal e urogenital. Pode envolver diversos órgãos. O estudo refere-se à actinomicose pulmonar com envolvimento da parede torácica e compressão medular em um paciente masculino com 29 anos que apresentava febre, tosse, hemoptise e cervicalgia, além de paresia e plegia em membros inferiores com cinco meses de evolução.
Palavras-chaves: Actinomicose. Pulmão. Parede torácica.
Actinomycosis is a rare, suppurative, granulomatous disease that may involve several organs. It is more common in males (3:1) and in immunocompromised patients1. It is a chronic infection caused by gram-positive anaerobic commensal bacteria (Actinomyces) that normally colonize the oral cavity and gastrointestinal and urogenital tracts2. A total of 14 species have been identified, 6 of which are pathogenic to humans; the most common is Actinomyces israelii, followed by A. naeslundii, A. odontolyticus, A. viscosus, A. meyeri, and A. gerencseriae3. The risk factors include aspiration of oropharyngeal or gastrointestinal contents as well as poor hygiene and oral health. There is higher prevalence in chronic alcoholics and in patients with structural lung disease3. Five clinical forms have been described: cervicofacial (55%), abdominopelvic (20%), thoracic (15%), as well as in various organs (10%) due to hematogenous dissemination of occult lung injury, mimicking tumors in skin, brain, pericardium, and thighs4.
Chest wall involvement occurs in 12% of pulmonary cases4,5. Actinomycosis can also invade the spinal canal and cause cord compression. This event is extremely rare and occurs in <5% of infections6.
This study reports a case of pulmonary actinomycosis with chest wall involvement and cord compression.
O.R.S., a 29-year-old man, was admitted with complaints of fever, cough, hemoptysis, urinary incontinence, neck pain, and paresis and plegia of the lower limbs for ~5 months.
The patient also reported alterations in bowel habits, which oscillated between bouts of diarrhea and constipation. At the time of ectoscopy, the patient was dehydrated and malnourished, with diffuse atrophy, edema in the lower limbs, and pressure ulcers over the sacrum, trochanters, and heels. The vital signs evidenced blood pressure of 110 × 75 mmHg, heart rate of 132 bpm, respiratory rate of 20 rpm, and temperature of 38.2 ºC. Auscultation of the respiratory system revealed decreased breath sounds and diffuse rhonchi. Neurological examinations showed an absence of force, abolition of reflexes and sensation in the lower limbs, and no changes of the cranial nerves. The blood count showed anemia (hemoglobin, 6.5 g%) with an erythrocyte count of 2,420,000/mm3, hematocrit of 20.5%, total leukocyte count of 9,200/mm3, and platelet count of 312,000/mm3. He underwent blood cultures, urine culture, and serology for the human immunodeficiency virus, all of which yielded negative results; furthermore, purified protein derivative (PPD) tuberculin was not reactive.
A computed tomography (CT) scan (Figure 1) and magnetic resonance imaging (MRI) scan of the chest (Figure 2) revealed the presence of a nodular lesion in the right pulmonary apex and an infiltrative mass affecting the vertebral bodies, elements in the upper thoracic and lower cervical posterior arches, ribs, and paravertebral soft tissue, with involvement of the spinal canal. A third biopsy was performed in the right upper lung; pathology showed inflammation, suggestive of actinomycosis (Figure 3). Antibiotic therapy involving penicillin (5.0 × 106IU, every 4h for 2 months) and clindamycin (600mg, every 8h for 14 days) was initiated. The pressure ulcers were treated with papain and silver alginate. After 23 days of hospitalization in our hospital, the patient was transferred to another institution for surgical decompression of the spinal canal.
Actinomycosis is a non-transmissible infection caused by human commensal microbes, which may be complicated by the action of other pathogens. Because of the rarity of actinomycosis, diagnosis and appropriate treatment may be postponed, leading to significant morbidity7. A reduction in the incidence of this disease may be related to improved oral hygiene and the proper use of antibiotics in infections by other agents8. Actinomycosis can affect individuals of all ages.
The patient under study was 29 years old and belonged to the age group most commonly affected by the disease, since the majority of cases involve adults aged between 20 and 50 years9. Actinomycetes are prevalent in the normal flora of the oral cavity but are less prominent in the lower gastrointestinal, respiratory, and urogenital tracts. These microorganisms are not virulent and require a break in mucosal integrity or the presence of devitalized tissue to invade other structures of the body and cause disease7,9. Typically, the infection spreads contiguously, ignores anatomical planes, and invades surrounding tissues or adjacent organs. Hematogenous dissemination to distant organs can occur at any stage of infection, while lymphatic spread is uncommon.
Aspiration of oropharyngeal secretions containing actinomycetes is the usual mechanism of infection that leads to pulmonary actinomycosis. However, the disease can result from the introduction of microorganisms through the perforation of the esophagus by direct propagation of an infectious process in the neck or abdomen, and by hematogenous spread from a distant lesion. It presents as a pulmonary infiltrate or mass, which, if untreated, may involve the pleura, pericardium, and chest wall7.
Symptoms related to pulmonary disease are as follows: hemoptysis (42%), persistent cough (37%), and chest pain. The nonspecific symptoms are as follows: fever (28%), loss of appetite, weight loss, and anemia1,4. Pulmonary actinomycosis is a difficult clinical diagnosis. Less than 10% of cases are diagnosed at initial presentation, finding themselves in situations such as differential diagnosis of lung abscess, tuberculosis, or lung neoplasm. This can lead to delays and even therapeutic and diagnostic errors, including conducting unnecessary surgery2.
It is noted that in addition to paresis and plegia of the lower limbs for ~5 months, this patient expressed virtually every major nonspecific symptom of the disease and some of the symptoms related to pulmonary involvement, indicating rapid progression and aggressive disease with central nervous system involvement. Probably, the disease first affected the apex of the right lung and spread contiguously, involving the chest wall and then the paravertebral soft tissues, vertebral bodies, and spinal canal. A computed tomography (CT) scan is the best diagnostic test because it shows the degree of damage and related complications4,5, while MRI is helpful in differentiating lesions infiltrating the chest wall4. These tests were helpful in the management of this case since they revealed the presence of a nodular lesion in the right pulmonary apex, an infiltrative mass affecting the vertebral bodies and elements of the upper thoracic and lower cervical posterior arches, ribs, and paravertebral soft tissue, with involvement of the spinal canal.
The definitive diagnosis of actinomycosis is obtained by biopsy (bronchoscopic, thoracoscopic, or open), pulmonary resection, or drainage of an abscessed material that is gelatinous, dark with sulfur granules, similar to sand or yellowish, odorless, and interspersed with a winy content4,5. The histological material obtained from a biopsy of the pulmonary right upper third of the patient showed an inflammatory process, suggestive of actinomycosis. This analysis enabled precise diagnosis of the case and choice of appropriate therapy. Treatment of pulmonary actinomycosis with chest wall involvement and cord compression consists of a combination of long-term antibiotic therapy and, if necessary, surgical resection of the lung and/or decompression of the spinal canal.
The antibiotic of choice is penicillin. In most cases, the antibiotic should be administered orally at the maximum tolerated dose. In severe or rapidly progressive cases, penicillin should be started intravenously at high doses (10-20 × 106 IU/d). Other antibiotics can be used orally, namely, ampicillin, tetracycline, and clindamycin, with good therapeutic results10. Several authors suggest the use of intravenous penicillin G for 1 month, and then replaced by oral penicillin for 6-12 months, or by amoxicillin5. In patients allergic to penicillin, sulfonamides, clindamycin, erythromycin, and chloramphenicol can be used4,5. The use of tetracycline and trimethoprim-sulfamethoxazole has also been described in the treatment of actinomycosis5. Actinomycosis has a high tendency to relapse, which is why the treatment should be extended for 6-12 months. The prognosis is excellent, with a cure rate of ~90% when the disease is diagnosed early and the antibiotics are effectively administered8.
The involvement of the spinal cord is extremely rare. We performed a search of the PubMed and Scopus databases with the keywords actinomycosis and spinal cord, and retrieved 25 published cases of actinomycosis with involvement of the spinal cord. Most patients share the same demographical characteristics of patients without cord compression, being mostly males (84.2%) and between 20 and 50 years of age (78.9%). In the majority of cases, the thoracic (47.6%) or cervical levels of the spine (28.6%) were affected. The entire spinal cord was affected in 1 case11. For clinical history, fever (84.6%), pain (78.6%), and weight loss (60%) were frequently described. Neurological findings were variable, reflecting the extension of the cord compression. Actinomycosis of the central nervous system can be responsible for significant neurological sequelae. Nevertheless, complete resolution was described in 50% of the cases. The best results are probably associated with early treatment12.
Actinomycosis provides a diagnostic challenge because it is a rare disease that presents with nonspecific symptoms, an insidious course, and a variety of clinical manifestations. Therefore, its diagnosis and appropriate treatment can be postponed, leading to significant morbidity. Pulmonary actinomycosis with chest wall involvement and cord compression, as evidenced in this study, shows rapid progression and can be considered an aggressive disease because the central nervous system is compromised.
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Dr. Fabiano de Oliveira Poswar
Av Cula Mangabeira 562, Bairro Santo Expedito
39401-001 Montes Claros, MG, Brasil
Phone: 55 38 3224-8327
Received in 25/07/2011
Accepted in 14/12/2011