TY - JOUR
T1 - Manifestations cliniques et traitement de courte durée de l'actinomycose pulmonaire
AU - Abdulkarim, Aziz
AU - Pouxe, Marie
AU - De Vallière, Serge
AU - Beigelman, Catherine
AU - Favrat, Bernard
AU - Kokkinakis, Ioannis
N1 - Publisher Copyright:
© 2022 Editions Medecine et Hygiene. All rights reserved.
PY - 2022/11/16
Y1 - 2022/11/16
N2 - Actinomycosis is an uncommon disease caused by Actinomyces, a commensal of the oropharyngeal, digestive, and genital tract. Commonly, it manifests as cervicofacial infection and is often related to poor oral health, smoking, chronic alcoholism or immune deficiency. Pulmonary actinomycosis is a rare disease, characterized by unspecific clinical, biological, and radiological manifestations that may be confused with other diseases. It should always be considered in patients suspected of having tuberculosis, lung abscess or pulmonary neoplasia. We describe a case of pulmonary actinomycosis treated successfully with short-term antibiotic therapy of three months, with a short review of the literature.
AB - Actinomycosis is an uncommon disease caused by Actinomyces, a commensal of the oropharyngeal, digestive, and genital tract. Commonly, it manifests as cervicofacial infection and is often related to poor oral health, smoking, chronic alcoholism or immune deficiency. Pulmonary actinomycosis is a rare disease, characterized by unspecific clinical, biological, and radiological manifestations that may be confused with other diseases. It should always be considered in patients suspected of having tuberculosis, lung abscess or pulmonary neoplasia. We describe a case of pulmonary actinomycosis treated successfully with short-term antibiotic therapy of three months, with a short review of the literature.
UR - http://www.scopus.com/inward/record.url?scp=85142402553&partnerID=8YFLogxK
U2 - 10.53738/REVMED.2022.18.804.2177
DO - 10.53738/REVMED.2022.18.804.2177
M3 - Article
C2 - 36382979
AN - SCOPUS:85142402553
SN - 1660-9379
VL - 18
SP - 2177
EP - 2180
JO - Revue Medicale Suisse
JF - Revue Medicale Suisse
IS - 804
ER -