01 January 2003
Pulmonary actinomycosis with chest wall infiltration, pleural effusion and lymph node enlargement
Elżbieta Radzikowska, Mariusz Chabowski, Renata Langfort, Lilia PawlickaCase Rep Clin Pract Rev 2003; 4(4):315-318 :: ID: 476416
Abstract
Background: Actinomycosis is a rare infection caused by anaerobic or facultatively anaerobic, asporogenous, non-motile, Gram-positive, non acid-fast bacteria. The disease develops as a result of aspiration or inhalation of organisms from oropharynx, hemtogenous dissemination or extension
from adjacent-infected tissue.
Case report: 37 year old man was admitted to hospital with two months history of a fever, dry cough, chest pain and the large induration in the left part of the chest wall. Chest CT scan revealed the infiltration in the lingula with pleural thickening and effusion. Also, chest wall invasion without
rib destruction and enlargement of a lymph node next to vena cava superior were observed. Pleural biopsy revealed sulphur granules and the diagnosis of actinomycosis was established. Patient was treated by intravenous penicillin G (24 million units /day) for 6 weeks, after that period by oral ampicyllin 4g/d up to 6 months. Therapy was effective.
Conclusions: Awareness of actinomycosis is required in differential diagnosis of chronic inflammatory changes involving lungs and thoracic cavity. The suspicion of this disease is a key to proper techniques of collecting, and submitting specimens, and finally for diagnosis, and treatment.
Keywords: Actinomycosis, infiltration of the chest wall, Pleural Effusion, pleural needle biopsy
279
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946411
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946041
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.947953
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946932
Most Viewed Current Articles
21 Jun 2024 : Case report
96,778
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
52,393
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133
20 Nov 2023 : Case report
31,818
DOI :10.12659/AJCR.941424
Am J Case Rep 2023; 24:e941424
18 Feb 2024 : Case report
23,483
DOI :10.12659/AJCR.943030
Am J Case Rep 2024; 25:e943030