Although pneumonia presents a relatively common diagnosis, it does not always present with classic clinical symptoms, nor does it follow a regular course without complications. The presented case describes a rare case of aspiration necrotizing pneumonia, which despite intensive therapy, progressed to lung gangrene and required a lung lobectomy. Another peculiarity is that the correct diagnosis was established only after the onset of abdominal pain, surprisingly by a trauma surgeon. This case emphasizes the necessity of a thorough general examination and draws attention to a rare, but conservatively intractable necrotizing pneumonia complicated by lung gangrene.
Download full-text PDF |
Source |
---|
Pathogens
November 2024
Division of Pulmonary, Critical Care, and Sleep Disorders, Department of Medicine, University of Louisville, Louisville, KY 40202, USA.
While rare, necrotizing pneumonia is a severe and potentially life-threatening manifestation of lung parenchyma infection. Initially documented in the 1940s, it was a significant contributor to mortality rates in both adults and children, with figures reaching up to 45%. Despite being a disease described in the literature for decades, data on the management of necrotizing pneumonia remain limited.
View Article and Find Full Text PDFTransplant Proc
November 2024
William S. Middleton Veterans Hospital, Lung Transplant Program Madison, Madison, Wisconsin; University of Wisconsin School of Medicine, Lung Transplant Program Madison, Madison, Wisconsin.
Pulmonary gangrene (PG) is a potentially devastating complication of necrotizing pneumonia. We describe successful nonsurgical management of PG in a lung transplant recipient. The patient presented with symptoms and imaging consistent with pneumonia.
View Article and Find Full Text PDFImmunotherapy
October 2024
Department of hematology, the first affiliated hospital of Anhui medical university, Hefei, 230022, China.
J Am Coll Cardiol
July 2024
Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA. Electronic address:
Systemic sclerosis (SSc), also called scleroderma, is an auto-immune rheumatic disease that is characterized by fibrosis of the skin and internal organs and vasculopathy. Three of the severe manifestations of the disease include a scleroderma renal crisis (SRC), pulmonary arterial hypertension, and digital ulceration. Vascular manifestations like Raynaud's phenomenon are an almost universal symptom in patients with SSc and are often the earliest manifestation of the disease.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!