Actinomycosis

Etiology

Actinomyces normally colonize the human mouth, urogenital tract, and gastrointestinal (GI) tract. As it is a commensal organism, it is very difficult to determine normal flora colonization versus infection.[4][5][6]

Thoracic actinomycosis may occur in patients with alcohol use disorder and seizure disorders. Pulmonary infection usually occurs as a complication of aspiration. Rarely disease can result from a human bite. Infection in the cervical and facial areas typically occurs following oral cavity surgery in patients with poor oral hygiene. Pelvic actinomycosis has been associated with the use of intrauterine devices (IUDs). Abdominal actinomycosis has been reported after any abdominal surgery but is most commonly seen after an appendectomy.

Epidemiology

The incidence of the disease is greater in males age 20 to 60 years with a peak incidence in 40 to 50 years. The male to female ratio for incidence is 3:1. The use of IUD contraceptive devices in females has increased the incidence. The infection has a higher prevalence within areas with low socioeconomic status. There is no racial predilection.[7]

Pathophysiology

Actinomyces are part of the normal flora of the human oral cavity, GI tract, and female urogenital tract. The organism is not virulent and only invades the body to cause deeper infections when there is tissue injury and a subsequent break in the normal mucosal barrier. Infection is mostly polymicrobial, with as many as 5 to 10 other bacterial species present. The infection is established with the help of a companion bacteria by inhibiting host defenses, reducing oxygen tension, or by producing a toxin that facilitates the inoculation of actinomycoses. [8][9][10]

Once mucosal barriers are breached, and infection is established, the human host responds by initiating an intense inflammatory response which is suppurative and granulomatous. The infection does not respect tissue planes and spreads contiguously. This results in draining sinus tracts, tiny yellow clumps called sulfur granules, and the result may be intense fibrosis of tissue.

Around 60% of infections are cervicofacial and described as “lumpy jaw syndrome.” The predisposing risk factors for cervicofacial infection include infection in erupting teeth, dental caries, gingivitis, and dental extraction, diabetes, alcohol use disorder, malnutrition, and malignancy.

HIV, solid organ transplantation of lungs or kidneys, biologic agents like infliximab, and acute lymphoblastic leukemia treated with chemotherapy are other risk factors.

Pulmonary infections are primarily due to the aspiration of oral and GI secretions. Risk factors include the diseases mentioned above, as well as any chronic lung disease that lead to tissue destruction and break in normal mucosal defenses such as chronic obstructive pulmonary disease (COPD), bronchiectasis, tuberculosis (TB), silicosis, among others. It can be a direct or indirect extension from a cervicofacial infection. From the lungs, Actinomyces can easily spread to mediastinum and pleura. Bronchial and laryngeal infections are rare. Vocal cord infection may mimic cancer.

The second most frequent site for Actinomyces infection is the genitourinary tract. The primary risk factor is the use of the intrauterine device.

Abdominal actinomycosis is most common in the appendix, cecum, and colon. Abdominal surgery is the most significant risk factor.

Skin and soft tissue actinomycosis is rare but can occur secondary to skin injury.

Hematogenous dissemination is extremely rare.

Histopathology

Gram staining of infected tissue or purulent material is more useful and sensitive than culture, as, in 50% of cases, culture may be negative. The negative rate is high due to previous antibiotic therapy, polymicrobial infection where other organisms present inhibit growth, failure to maintain an anaerobic environment during transportation and culture, or short-term incubation. [11]

The characteristic of the disease is the yellow sulfur granules. They are formed primarily by mycelial fragments with some proteinaceous polysaccharide complexes, which act as a resistance mechanism to avoid and inhibit phagocytosis. The most common microscopic finding is necrosis of yellowish sulfur granules and the filamentous gram-positive bacteria. The most appropriate specimen is a tissue biopsy of the infected site or pus. For better results, the clinician should note their suspicion for the infection to the microbiologist or pathologist. This will ensure anaerobic cultures are performed for prolonged time frames to ensure an optimal growth environment. [12]

Immunofluorescence has poor sensitivity but high specificity and can be used to confirm the diagnosis. [13]

History and Physical

The clinical presentation depends upon the site of infection and can vary accordingly. Taking a detailed history, which includes risk factors, is essential. [14][15]

Cervicofacial

This is the most common, constituting approximately 60% of infections and usually involves the tissues surrounding the maxilla and lower mandible (almost 50% of all cases). The most common presentation is a progressive, painless mass that is indurated with or without reddish or bluish discoloration of overlying skin and eventually evolves into multiple abscesses with sinus tract formation, which drains yellow sulfur granules. The patient may give a history of an oral procedure or injury. Difficulty in chewing food and trismus can occur in chronic stages of infection. Lymphadenopathy is not associated with the disease process.

Genitourinary

History of IUD use is common. The symptoms mostly mimic gynecological tumors, both malignant and benign. The presentation could be with lower abdominal pain, constipation, and vaginal discharge. Fever is rare unless the disease spreads to the peritoneum.

GI

The patient might have a history of abdominal surgery, especially appendectomy, perforated viscus, or ingestion of a fish bone. It can involve the esophagus, appendix, cecum, and colon, and presentation depends upon the site of infection. In esophageal disease, dysphagia is the most common symptom. At other gastrointestinal sites, the infection presents with nonspecific symptoms of low-grade fever, weight loss, fatigue, nausea, vomiting, change in bowel habits, and abdominal pain with or without a palpable mass. Rarely, the liver and biliary tract are involved, in which case, there may be right upper quadrant pain and jaundice.

Pulmonary

The infection can be acute to subacute, but because the diagnosis is difficult most cases are diagnosed in the chronic phase. Initially, the patients may present with very nonspecific symptoms of mild fever and weight loss. The symptoms mimic other chronic lung infections and cancer. The most common symptoms are a chronic productive cough with or without hemoptysis, shortness of breath, and chest pain. Lung parenchymal infections can cavitate, forming sinus tracts, which are a pathognomonic finding. If the disease process is extensive, and the host is immunocompromised, the disease process can present with severe hypoxemia and florid respiratory failure with acute respiratory distress syndrome (ARDS).

Evaluation

A complete blood count (CBC) will show leukocytosis with elevated neutrophils. Nonspecific inflammatory markers such as C-reactive protein and erythrocyte sedimentation rate are elevated.[16][17][18]

The gold standard test for diagnosis is tissue biopsy culture with anaerobic pus cultures. Swabs from the infected sites should be avoided. Cultures can be falsely negative; gram-stain may demonstrate the presence of branched, beaded, gram-positive filamentous rods with sulfur granules, which helps in making a preliminary diagnosis. For examination, under the microscope, the granules should be crushed in between the two slides and then stained with methylene blue to identify the organism.

Serological tests do not help in making the diagnosis.

Imaging results will depend upon the site of infection and can mimic other chronic infections like nocardiosis, TB, and malignancy.

Cervicofacial

Imaging findings are nonspecific and are noncontributory in diagnosing the disease but will help in assessing the degree of soft tissue and bone involvement. Dental radiographs are helpful in evaluating the apical abscesses. CT and MRI studies may show osteolysis in the chronic form of infection.

Pulmonary

The imaging for actinomycosis is nonspecific. In the acute presentation, it can look like any other pneumonia. In chronic forms, it can present as a pulmonary mass or can cavitate. In the case of a mass malignancy, actinomycosis is an important diagnosis to consider. Especially when it cavitates, tuberculosis is an important differential diagnosis to consider. The computed tomography scan findings can vary depending upon the duration of illness and can include consolidation, cavitation, pleural effusion, lymph node enlargement, atelectasis, and ground glass opacification.

The gold standard test is a histological examination and bacterial culture of a biopsy, which can be obtained with bronchoscopy (pulmonologist), a CT-guided biopsy (interventional radiologist), or video-assisted thoracoscopic surgery (VATS) performed by a thoracic surgeon. Anaerobic cultures of pleural fluid rarely grow the organism. Sputum culture will not be useful unless the patient has a cavitary disease.

GI

Imaging of actinomycosis can be nonspecific; findings will depend upon the site of infection and chronicity. In chronic cases, a CT scan might show an enterocutaneous fistula with multiple abdominal abscesses. The best test is a culture of the infected site.

Genitourinary

A CT scan can show pelvic mass (6 to 7 cm) with the cystic lesion. Lymphadenopathy can be seen in 40% to 60% of cases. A tubo-ovarian abscess is highly suggestive of infection with actinomycosis. Bladder actinomycosis can present like bladder carcinoma, with bladder thickening and hematuria.

Pus samples can be taken after removing the IUD. Colonization must be differentiated from infection. Tissue biopsy should be taken in patients presenting with pelvic masses to rule out malignancy.

Treatment / Management

Most of the cases can be managed with antibiotics; surgery can be adjunctive.[19][20](A1)

Medical management in the form of antibiotics includes:

• Penicillin G
• Beta-lactams with a long course of oral amoxicillin
• Cephalosporin

If the patient is allergic to penicillin, alternatives include:

• Clindamycin
• Macrolides (erythromycin, clarithromycin or azithromycin)
• Doxycycline

A combination of metronidazole and a beta-lactamase inhibitor may be tried in polymicrobial infections.

Antimicrobial susceptibility testing is not indicated due to predictable antibiogram.

The duration of therapy is usually 6 to 12 months but can be shortened if surgical resection of the infected site has been performed. Type of surgery will depend upon the site and extent of the disease, but it usually involves incision and drainage of abscesses, decompression of closed space, and excision of sinus tracts.

The response to treatment can be monitored with imaging.

Differential Diagnosis

The differential will depend upon the site of infection. It is a slow-spreading infection that can mimic benign or malignant tumors, nocardiosis, and TB.

The other important differential diagnosis to consider are the following:

• Aspiration pneumonia
• Appendicitis
• Diverticulosis
• Crohn disease
• Lung abscess
• Fungal pneumonia
• Pelvic inflammatory disease
• Brain abscess
• Dental abscess

Prognosis

Prolonged antibiotic therapy is usually required, and the prognosis is excellent. With better oral hygiene, availability of antibiotics, and advanced surgical techniques, the outcome, and mortality have improved. For extensive and complicated disease, antibiotics and surgical treatment are required. In these cases, morbidity is high, and death may occur.

Complications

Complications of actinomycosis include the development of abscesses and the spread of the infection. Osteomyelitis is a possible complication with the involvement of the ribs, vertebrae, and the mandible. Nervous system involvement will include meningitis, brain abscess, actinomycetoma, cranial, epidural and subdural infection, and spinal epidural infection.

In addition, other complications are hepatic actinomycosis, endocarditis, and disseminated actinomycosis.