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Childhood Mediastinal Actinomycosis - Case Report
By Dr. Hussain Al-Mukharraq, MBChB. DCH. ABMSP
 
Chief of Medical Staff & Consultant Pediatrician
Email to : HMukharriq@health.gov.bh
Salmaniya Medical Complex
State of Bahrain
  • Abstract:

Mediastinal actinomycosis in children is rare. A 11 year old Bahraini girl presented with fever, generalized weakness and body aches. A CT scan thorax confirmed the presence of a mass lesion in the mediastinum. The mass was surgically removed and the biopsy confirmed the diagnosis of actinomycosis.

  • Introduction:

Actinomycosis is a chronic granulomatous suppurative disease characterized by peripheral spread with extension to contigous tissue in the formation of multiple draining sinus tract. These infection usually involve the cervico facial, thoracic, abdominal or pelvic region. Actinomycosis israeli is the predominant organism causing disease in human. Other implicated species in order of importance include: Arachriapropionica, A. Odontolyticus, A. meyeri, A. naeslundii, A. viscous and Bifido bacterium eriksonii1,2. The three important sites of actinomycosis infection in order of frequency are cervicofacial, abdominal and thoracic. A British epidemiological surveys for the years 1971 and 1972 recorded 67 cases of actinomycosis, only six paediatric cases were described and none had intra thoracic involvement3. We report a child with a mediastinal actinomycosis, the clinical presentation and treatment.

  • The Case:

A 11 year old Bahraini girl presented with fever, generalised weakness and body aches. Physical examination revealed febrile, pale asthenic girl, not in respiratory distress, with diminished air entry by ausculation on the right side of the chest and bronchial breathing. There were no lymphadenopathy neither hepatosplenemegaly. Investigation showed the Hemoglobin of 8 g%, platelets 827 x 109/L, white blood cells 21.3 x 10 9/L (polymorph 66%, Lymphocytes 25%). ESR was 115 mm in 1 hr, chest radiograph (figure 1) showed a mass on the anterior mediastinum. CT scan of chest confirmed the presence of a large mass in the upper mediastinum extending anterio posteriorly to the paravertebral region (Figure 2). Tubercurbin, cold agglutination tests were negative. Fine needle aspiration revealed the presence of inflammatory lesion, not malignant or tuberculous. Thoractomy done which demonstrate a vascular mass extending from the posterior to anterior mediastinum, biopsy taken demonstrated the presence of colonies of fungi surrounded by neutrophills which is combined with the actinomycosis laying over vascular malformation. She was treated with intravenous penicilline G 200,000 unit / kg/day until the sedimentation rate returned to normal, and then she was maintained on oral pencillin G 500 mg 4 times daily for 6 months. She showed a dramatic improvement in her physical and general condition and the last chest radiograph (figure 3) showed complete resolution of upper mediastinal mass and her ESR was normal.

Figure 1. Chest x-ray showing mass in the anterior mediastinum
Figure 2. CT Scan of chest showing the presence of a large mass
Figure 3. Chest x-ray showing complete resolution of upper mediastinal mass

  • Discussion

Actinomycosis is usually not included in the differential diagnosis of mediastinal and pulmonary masses in children4,5. As demonstrated by our case, actinomycosis should be considered whenever there is a slowly progressive pulmonary or mediastinal mass accompanied by symptoms, sign and laboratory evidence of chronic infection. Of the four species of actinomyces capable of producing infections in man, A. Israelii is the primary pathogen. A. Israelii is a normal saprophyte of the oral cavity and nasopharynx and can be cultured from carious teeth, periodontal tissue, tonsillar crypts and para nasal sinuses6.

There was no clear evidence to support the pathogenisis of pulmonary actinomycosis but dental manipulation immunodeficiency and foreign body could be favoured actinomycosis infection7,8. mediastinal involvement probably is the result of direct extention from lungs or may result from spread via lymphatic channels connecting the mediastum and oral pharynx9.

The nature course of thoracic actinomycosis was described in details by Bates and Cruick Shank9 Of their 85 patients, 67% had primary disease and 7% had primary mediastinal involvement. Children between the ages of 3 and 20 years accounted for 27% of the cases. This was thought to be secondary to the prevalence of dental caries in this age group.

The most common symptoms were pleuritic pain, cough, fever, sputum production and weight loss. Retrosternal and back pain occurred with mediastinal involvement. Pulmonary actinomycosis should be considered in the differential diagnosis of pulmonary and mediastinal mass lesion in children10,11. The early roentgenographic manifestation of actinomycosis include patchy pulmonary infiltrates, and cavitory or mass lesion12.

The main stay of treatment for pulmonary actinomycosis is prolonged antibiotics and an appropriate surgical approach to sinus tract and abscesses. The drug of choice for treatment is penicillin, a recommended treatment schedule is 12 - 18 month of 2 - 5 million units of oral penicillin daily and should be tailored to each clinical situation13.

  • Conclusion

Mediastinal actinomycosis is a rare disease in children. It should be considered in the differential diagnosis of pulmonary and mediastinal lesion. Surgical resection of the mass lesion and prompt treatment with appropriate antibiotics could result in a high cure rate.

  • References
  1. Holm G. Studies on the etiology of human actinomycosis the other microbes of actinomycosis and their importance. Acta Pathol Microbial Scand 1950; 27: 736.
  2. Waksman SA, Henrici AT. The nomenclature and classification of the Actinomycis. J Bacteriol 1942; 40:337.
  3. Actinomycosis, Editorial. Br. Med. J 1973; 1: 365.
  4. Baum GD: Textbook of Pulmonary Disease. Boston, little Brown & Co:1974.
  5. Henshaw HC: Disease of the chest. Philadelphia, WB Saunders Co:1969.
  6. Hylton RP, Samuels HS, Oates GW Jr. Actinomycosis - is it really rare? Oral Surg 1970; 29: 138 - 147.
  7. Garini G; Bordi C; Mazzi A; Savazzi G; Tosu C. Thoracic actinomycosis with lung, mediastinal and pericardial involvement. A case report. Recenti Prog Med 1995 ; 86 (3): 107 - 11.
  8. Moesta RT; Totakas S; Schlag PM. Foreign body induced thoracic actinomycosis as differential mediastinal space - occupying lesion diagnosis. Chirurg 1999 ; 7065: 602 - 4.
  9. Bates M, Cruickshank G; Thoracic actinomycosis.Thorax 1957; 12: 99 - 124.
  10. Spinola SM; Bell RA; Henderson FW. Actinomycosis. A cause of pulmonary and mediastinal mass in children. Am J Dis Child 1981 ; 135(4): 336-9.
  11. Benammar S; Helardot PG; Sapin E; Adamsbaum C; Raymond J. Childhood actinomycosis; A report of two cases. Eur J Pediatrc Surgery, 1995; 5; 180 - 3.
  12. Balikian JP. Cheng TH, Costello P, et al: Pulmonary actinomycosis. Radiology 1978: 128: 613 - 6.
  13. Utz JP, Krovets HM, Einstein HE, et al; Chemotherapeutic agents For the pulmonary actinomycosis. Report of the committee on Fungus Disease and the sub committee on therapy. Chest 1971; 60; 260-2.

 

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