Fusobacterium necrophorum Mediastinal Abscess Presenting as an Anterior Chest Wall Mass in a Child: A Case Report

2005 ◽  
Vol 44 (1) ◽  
pp. 73-75 ◽  
Author(s):  
Mary Mancao ◽  
Elizabeth Manci ◽  
Maria Figarola ◽  
Benjamin Estrada
2021 ◽  
Vol 5 (3) ◽  
pp. 316-319
Author(s):  
Haley Vertelney ◽  
Margaret Lin-Martore

Introduction: Chest wall masses are rare in children, but the differential diagnosis is broad and can include traumatic injury, neoplasm, and inflammatory or infectious causes. We report a novel case of an eight-year-old, previously healthy female who presented to the emergency department (ED) with one month of cough, fevers, weight loss, and an anterior chest wall mass. Case Report: The patient’s ultimate diagnosis was necrotizing pneumonia with pneumatocele extending into the chest wall. This case is notable for the severity of the patient’s pulmonary disease given its extension through the chest wall, and for the unique speciation of her infection. Conclusion: Although necrotizing pneumonia is a rare complication of community-acquired pneumonia, it is important for the emergency physician to recognize it promptly as it indicates severe progression of pulmonary disease even in children with normal and stable vital signs, as in this case. The emergency physician should consider complications of pneumonia including pneumatocele and empyema necessitans when presented with an anterior chest wall mass in a pediatric patient. Additionally, point-of-care ultrasound was used in the ED to facilitate the diagnosis of this illness and was particularly useful in determining the continuity of the patient’s lung infection with her extrathoracic chest wall mass.


2016 ◽  
pp. bcr2016214797
Author(s):  
Ku Hung Hsieh ◽  
Grace Tan Hwei Ching ◽  
Angela Chong Phek Yoon ◽  
Melissa Teo

CHEST Journal ◽  
2002 ◽  
Vol 121 (5) ◽  
pp. 1692-1694
Author(s):  
George S. Stoica ◽  
Harry N. Steinberg ◽  
Leonard J. Rossoff

2021 ◽  
Vol 108 (Supplement_6) ◽  
Author(s):  
R Reid ◽  
F Alakhras Aljanadi ◽  
R Beattie ◽  
A Graham

Abstract Aim We aim to present here a case of a painless anterior chest wall mass which was first noted during routine follow up post coronary artery bypass graft surgery Case presentation An 80-year-old male developed an asymptomatic slow growing pronounced swelling over the right anterior chest wall post CABG. His other past medical history includes chronic obstructive pulmonary disease, pulmonary fibrosis, ischaemic heart disease, an AICD for complete heart block, hypertension, hyperlipidaemia and osteoarthritis. A CT scan demonstrated a 10 x 12 x 6.5 cm subcutaneous lesion at the mid-line of the lower chest wall adjacent to the xiphisternum and the previous sternotomy site. On clinical examination there was a large non-tender cystic swelling with peripheral calcifications, but overlying skin was normal. Fluid was aspirated from the lesion and cytology showed a paucicellular specimen with features in keeping with seroma. Due to the progressive increase in size patient underwent surgical resection. A gelatinous bloody fluid was aspirated from the lesion and it was then resected enbloc. The tumour base appeared to arise from 6/7th costal cartilage and tumour was shaved away. The mass was confirmed histologically to be chondrosarcoma. Conclusions Given the uncommon prevalence of malignant primary chest wall tumours this case highlights the importance of high clinical suspicion even after developing post CABG.


2018 ◽  
Vol 35 (10) ◽  
pp. 586-586
Author(s):  
Claire Elaine Richards ◽  
Ahmed Mamdouh Taha Mostafa ◽  
Amr Elmoheen

Clinical introductionA 24-year-old Filipino man attended the ED with a 1-month history of a discrete swelling over his upper anterior chest wall that was rapidly increasing in size and tenderness. He denied any other symptoms. His medical history was unremarkable.Examination revealed a tender, 7 cm × 6 cm mass over the upper part of the sternum (figure 1). The surface was smooth, it was immobile, non-compressible and the overlying skin was normothermic but mildly erythematous. Cervical lymphadenopathy was present. His vital signs were normal.Figure 1Chest wall mass.QuestionWhat is the most likely diagnosis?LipomaChondrosarcomaLymphomaMycobacterium tuberculosis (TB)


2013 ◽  
Vol 6 (1) ◽  
pp. 48 ◽  
Author(s):  
Mohamed Leye ◽  
Modou Jobe ◽  
Souleymane Diatta ◽  
Mouhamadou Ndiaye ◽  
Fatou Aw ◽  
...  

2017 ◽  
Vol 50 (4) ◽  
pp. 308-311
Author(s):  
Junghyeon Lim ◽  
Sung Woo Cho ◽  
Hee Sung Lee ◽  
Hyoung Soo Kim ◽  
Yong Han Kim ◽  
...  

2009 ◽  
Vol 88 (5) ◽  
pp. e58-e59 ◽  
Author(s):  
Gary S. Schwartz ◽  
Liliana Rios ◽  
Tracy Zivin-Tutela ◽  
Faiz Y. Bhora ◽  
Cliff P. Connery

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