CHEST 1158 Postgraduate Education Corner CHEST 2014; 145 ( 5 ): 1158 1161 A 50-year-old man presented with a 1-week history of a painful hard lump above his right nipple. He attended the Accident and Emergency Department when the lump suddenly grew bigger and more pain- ful. He had been unwell for 4 weeks, with a produc- tive cough, loss of appetite, and weight loss. He was normally well, and there was no relevant medical his- tory. He smoked 50 cigarettes a day and drank exces- sive quantities of alcohol each week. He worked in a warehouse and had not traveled outside the United Kingdom. On examination, he was comfortable at rest and did not look unwell. He was apyrexial, and oxygen saturations were 98% on room air. His BP was 110/70 mm Hg, and pulse rate was 90 beats/min. There was a large, hard, tender mass above his right nipple associated with some bruis ing of the skin. On auscultation of his chest, a few crackles were audible. His dentition was poor. The remainder of his physical examination was normal. Case Report Laboratory workup showed a hemoglobin concen- tration of 9.7 g/dL, WBC count of 21,000 cells/ m L, neutrophils count of 19,000 cells/ m L, platelet count of 438,000 cells/ m L, sodium concentration of 127 mmol/L, potassium concentration of 3.6 mmol/L, creatinine concentration of 56 m mol/L, and C-reactive protein level of . 150 mg/L. An HIV test result was negative. The patient underwent a chest radiograph ( Fig 1 ) and a contrast-enhanced CT chest scan ( Figs 2 - 4 ). The chest radiograph showed multifocal, bilateral consoli- dation and diffuse, poorly marginated, increased opacity A 50-Year-Old Man With a Cough and Painful Chest Wall Mass Quentin Jones , MBBS ; Rachel Benamore , MBBChir ; Eve Fryer , BMBCh ; and Anny Sykes , PhD Manuscript received September 3 , 2013 ; revision accepted December 28 , 2013 . Afliations: From the Oxford Centre for Respiratory Medi- cine (Drs Jones and Sykes) and the Department of Radiology (Dr Benamore), Churchill Hospital; and the Department of His- topathology (Dr Fryer), John Radcliffe Hospital, Oxford, England. Correspondence to: Quentin Jones, MBBS, Oxford Centre for Respiratory Medicine, Churchill Hospital, Oxford, OXE 7L3, England; e-mail: quentinjones7@hotmail.com 2014 American College of Chest Physicians. Reproduction of this article is prohibited without written permission from the American College of Chest Physicians. See online for more details. DOI: 10.1378/chest.13-2039
Figure 1. Chest radiograph showing multifocal bilateral consoli- dation. There is a diffuse, poorly marginated, increased opacity in the right midzone and enlargement and increased density of the soft tissues, suggestive of a chest wall mass.
Figure 2. The CT scan shows multifocal, bilateral, nodular, and mass-like consolidation. Downloaded From: http://journal.publications.chestnet.org/ by M Darwich on 10/15/2014 CHEST / 145 / 5 / MAY 2014 1159 journal.publications.chestnet.org in the right midzone and enlargement and increased density of the adjacent soft tissues, suggestive of a chest wall mass. The CT scan showed multifocal bilat- eral nodular and mass-like consolidation, which con- tained areas of low attenuation in keeping with necrosis ( Figs 2 , 3 ). The mass-like consolidation in the middle lobe was causing rib erosion and extended directly into the anterior chest wall, deep to the pectoralis major muscle, where there was a multiseptated low-density collection ( Figs 3 , 4 ). An ultrasound of the right anterior chest wall was performed, which conrmed that the swelling was caused by a localized uid collection. Image-guided aspiration yielded frank pus. Gram stain showed gram-positive lamentous rods.
Figure 3. CT scan showing the mass-like consolidation in the middle lobe contains areas of low attenuation in keeping with necrosis and is causing rib and costal cartilage erosion; it extends directly into the anterior chest wall, deep to the pectoralis major muscle, where there is a multiseptated low-density collection.
Figure 4. CT scan sagittal view showing rib erosion. What is the diagnosis? Downloaded From: http://journal.publications.chestnet.org/ by M Darwich on 10/15/2014 1160 Postgraduate Education Corner Diagnosis: Actinomycosis with empyema necessitans Discussion Clinical Discussion Actinomycoses are commensals in the human oro- pharynx, GI tract, and female genitalia. Rarely, they cause chronic suppurative granulomatous inamma- tion with abscess and sinus tract formation. The most common sites of infection are the face, jaw, abdomen, pelvis, and lungs. 1 Pulmonary actinomycosis accounts for 15% to 20% of cases 1 , 2 and is associated with chronic respiratory disorders, alcoholism, and poor oral hygiene. 3 , 4 Aspiration of secretions containing actinomycosis is thought to be the mechanism of infection. 5 The disease is more common in men 2 ; it has been suggested that this may be because of poorer oral hygiene in men and higher rates of trauma from st ghts. 5 A clue to the diagnosis in this patient was the history of poor dentition and increased alcohol intake. On taking a more detailed history, it transpired that he had recently removed a rotten tooth himself with a pair of pliers. Like pneumonia, pulmonary actinomycosis fre- quently presents with a low-grade fever, cough, and shortness of breath. However, unlike in pneumonia, the history is often longer, and weight loss and chest pain may be prominent features (as in this patient). 6
There are usually pulmonary inltrates, which may invade surrounding structures including the ribs, mediastinum, and soft tissue of the chest wall, causing pain. This patient developed empyema necessitans caused by invasion of the pleural space followed by invasion of the chest wall. It is likely that the history of sudden chest pain and the increasing size of the chest wall mass were caused by rupture of the abscess though the chest wall. The mainstay of treatment of actinomycosis is pro- longed antibiotics. In vitro studies indicate that the organism is sensitive to a wide range of antibiotics, including penicillin. 7 Historically, treatment consisted of high-dose IV penicillin for a long duration (generally 6 weeks) followed by oral antibiotics for up to 6 to 12 months. 8 The risk of developing penicillin resis- tance is thought to be low. More recently, successful outcomes with a shorter duration of antibiotics have been reported. 9 In a series of 16 patients, cure was achieved after a median duration of 2 weeks of IV anti- biotics and 3 months of oral penicillin. 10 Erythromycin, clindamycin, and doxycycline are alternative antibiotics for patients allergic to penicillin. 11 , 12
Surgery may be needed in the treatment of large abscesses and empyema, especially if sinus tracts, s- tulas, or extensive necrotic tissue are present. 13 Surgery should also be considered in patients who respond poorly to antibiotics. A retrospective review identied ve patients who had responded poorly to initial anti- biotics and went on to have successful surgical treat- ment. 14 Prolonged antibiotic treatment is also necessary after surgery, because surgery alone is not curative. Prognosis in actinomycosis is generally excellent. 9
Radiologic Discussion Pulmonary actinomycosis may mimic other chronic suppurative lung diseases such as TB, nocardiosis, fun- gal disease, lung abscess, and thoracic malignancies. Radiographic ndings in actinomycosis are often non- specic, particularly in the early stages of infection. Various CT scan ndings have been described, includ- ing multifocal or mass-like consolidation, which may involve the chest wall and pleura and may cavitate and form abscesses and sinus tracts. There is often a peripheral and lower-lobe predominance of disease. 15
Unlike in most infections, regional lymphadenopathy is rare. The differential diagnoses of the radiologic ndings in actinomycosis include infection (TB, fungal dis- ease, invasive pulmonary aspergillosis, botryomyco- sis, nocardiosis, and other subacute bacterial necrotizing pneumonias), malignancy (multifocal adenocarcinoma, necrotic bronchogenic carcinoma, and lymphoma), and vasculitis (granulomatosis with polyangiitis [Wegener] and atypical granulomatosis with polyangiitis). In this patient, infection was most likely caused by the pre- sumed abscess formation in the chest wall. The diagnosis of pulmonary actinomycosis can be difcult. Up to one-quarter of cases may be misdiag- nosed initially as malignancy, leading to delay in treat- ment and unnecessary surgical procedures. 16 An added diagnostic difculty is that actinomycosis may colo- nize necrotic tissues and coexist with malignancy. 2 The presence of air bronchograms within mass-like, pleural- based densities may help distinguish actinomycosis from malignancy; however, imaging alone is insuf- cient to make the diagnosis. Pathologic conrmation by culturing actinomycosis is vital. Pathologic Discussion Actinomycosis is a slow-growing, gram-positive rod that frequently branches. The organism was rst iso- lated in the nineteenth century from jaw abscesses in cattle. The name actinomycosis derives from the Greek term akino, which refers to the radiating appearance of sulfur granules and mykos, meaning fungus (a misnomer because the organism is actually a bacterium). Sulfur granules are colonies of organisms arranged in round basophilic masses with eosinophilic terminal clubs on staining with hematoxylin-eosin. Downloaded From: http://journal.publications.chestnet.org/ by M Darwich on 10/15/2014 CHEST / 145 / 5 / MAY 2014 1161 journal.publications.chestnet.org However, they are often best seen when stained with periodic acid shift diastase, which highlights their structure ( Fig 5 ). Sulfur granules can be distinguished from the Bollinger granules found in Botryomycosis (a rare granulomatous bacterial infection, usually caused by Staphylococcus aureus , which mimics acti- nomycosis). Bollinger granules are rings of bacteria surrounded by eosinophilic matrix but, unlike sulfur granules, they lack lamentous structures. Actinomycosis is a fastidious organism that may be difcult to isolate. Failure to culture the organism can be caused by antibiotic therapy, overgrowth by a contaminant, or inadequate culture technique. Less than 30 min of exposure to air may result in inhibition of actinomycosis. Protected specimen brushing with expedient transport of specimens and taking a sample prior to administering antibiotics may improve the yield. Bronchoscopy is usually not useful in making the diagnosis. Demonstration of a gram-positive lamentous branch- ing organism and sulfur granules on histologic examina- tion supports the diagnosis of actinomycosis. However, sulfur granules are not always present and can occur in other conditions, such as nocardiosis. If actino- mycosis is suspected, the microbiology laboratory should be asked specically for actinomycosis cul- tures. In general, the organism is identied by colony morphology and biochemical profiling. Molecular genetic techniques using polymerase chain reaction, 16s ribosomal RNA sequencing, and comparison with a database, or uorescence in situ hybridization can rapidly confirm the diagnosis. Direct staining with uorescent-conjugated monoclonal antibody may also allow rapid identication. Conclusions In this patient, cultures of pus aspirated from the chest wall grew Actinomyces meyeri. The chest wall abscess was incised and drained. A 32F chest drain was inserted into the pleural cavity, with a corregated drain into the subpectoral abscess cavity. The patient received 6 weeks of IV benzyl penicillin followed by 6 months of oral penicillin and made a good recovery. Acknowledgments Financial/nonnancial disclosures: The authors have reported to CHEST that no potential conicts of interest exist with any companies/organizations whose products or services may be dis- cussed in this article . Other contributions: CHEST worked with the authors to ensure that the Journal policies on patient consent to report information were met. References 1. Mabeza GF , Macfarlane J . Pulmonary actinomycosis . Eur Respir J . 2003 ; 21 ( 3 ): 545 - 551 . 2. Weese WC , Smith IM . A study of 57 cases of actinomycosis over a 36-year period. A diagnostic failure with good prognosis after treatment . Arch Intern Med . 1975 ; 135 ( 12 ): 1562 - 1568 . 3. Russo TA . Agents of actinomycosis . In: Mandell GL , ed. Prin- ciples and Practice of Infection Disease . 5th ed. New York, NY : Churchill Livingstone ; 1995 : 2645 - 2654 . 4. Brown JR . Human actinomycosis. A study of 181 subjects . Hum Pathol . 1973 ; 4 ( 3 ): 319 - 330 . 5. Bennhoff DF . Actinomycosis: diagnostic and therapeutic con- siderations and a review of 32 cases . Laryngoscope . 1984 ; 94 ( 9 ): 1198 - 1217 . 6. Kinnear WJ , MacFarlane JT . A survey of thoracic actinomy- cosis . Respir Med . 1990 ; 84 ( 1 ): 57 - 59 . 7. Smith AJ , Hall V , Thakker B , Gemmell CG . Antimicrobial susceptibility testing of Actinomyces species with 12 antimi- crobial agents . J Antimicrob Chemother . 2005 ; 56 ( 2 ): 407 - 409 . 8. Brook I . Actinomycosis: diagnosis and management . South Med J . 2008 ; 101 ( 10 ): 1019 - 1023 . 9. Wong VK , Turmezei TD , Weston VC . Actinomycosis . BMJ . 2011 ; 343 : d6099 . 10. Sudhakar SS , Ross JJ . Short-term treatment of actinomycosis: two cases and a review . Clin Infect Dis . 2004 ; 38 ( 3 ): 444 - 447 . 11. Fass RJ , Scholand JF , Hodges GR , Saslaw S . Clindamycin in the treatment of serious anaerobic infections . Ann Intern Med . 1973 ; 78 ( 6 ): 853 - 859 . 12. Kolditz M , Bickhardt J , Matthiessen W , Holotiuk O , Hffken G , Koschel D . Medical management of pulmonary actinomy- cosis: data from 49 consecutive cases . J Antimicrob Chemother . 2009 ; 63 ( 4 ): 839 - 841 . 13. Conant EF , Wechsler RJ . Actinomycosis and nocardiosis of the lung . J Thorac Imaging . 1992 ; 7 ( 4 ): 75 - 84 . 14. Song JU , Park HY , Jeon K , Um SW , Kwon OJ , Koh WJ . Treat- ment of thoracic actinomycosis: a retrospective analysis of 40 patients . Ann Thorac Med . 2010 ; 5 ( 2 ): 80 - 85 . 15. Kwong JS , Mller NL , Godwin JD , Aberle D , Grymaloski MR . Thoracic actinomycosis: CT ndings in eight patients . Radi- ology . 1992 ; 183 ( 1 ): 189 - 192 . 16. Slade PR , Slesser BV , Southgate J . Thoracic actinomycosis . Thorax . 1973 ; 28 ( 1 ): 73 - 85 .
Figure 5. Actinomycosis forming sulfur granules (periodic acid shift diastase, original magnication 3 100). Downloaded From: http://journal.publications.chestnet.org/ by M Darwich on 10/15/2014