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| http://dx.doi.org/10.1513/AnnalsATS.202103-317LE | DOI Listing |
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An immunocompetent lady with invasive aspergillosis presenting as disseminated lesions: a case report.
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Internal Medicine, Aga Khan University Hospital, Stadium Road, Gulshan-e-Iqbal, Karachi, Pakistan.
Background: Invasive Aspergillosis is a fungal infection caused by Aspergillus species, typically posing life-threatening risks to immunocompromised individuals. While occurrences in immunocompetent hosts are rare, a recent case report documented fulminant pulmonary aspergillosis in an immunocompetent patient during autopsy. Here, we present a case of invasive aspergillosis in an immunocompetent woman, manifesting with disseminated lesions.
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Internal Medicine, Pediatrics, Hurley Medical Center, Michigan State University (MSU), Flint, USA.
Systemic lupus erythematosus (SLE) is an autoimmune condition more commonly observed in women of childbearing age. The most commonly reported initial presentations were fatigue, arthritis, and skin manifestations. However, due to the involvement of a variety of organs, diagnosis remains a challenge for physicians.
View Article and Find Full Text PDFA ciliated adenocarcinoma of the lung mimicking lung abscess and pneumonia.
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Division of Respiratory Medicine, Center for Respiratory Diseases National Hospital Organization Kyoto Medical Center Kyoto Japan.
This case report describes a 78-year-old man initially treated for pneumonia and lung abscess who was resistant to antimicrobial treatment and was eventually diagnosed with ciliated adenocarcinoma. Ciliated adenocarcinoma, a rare non-terminal respiratory unit (TRU)-type lung adenocarcinoma, presents a unique diagnostic challenge because of its similarity to pneumonia and lung abscesses. Morphologically, the ciliated adenocarcinoma in this case appeared to be a non-TRU type adenocarcinoma, with partial mucous epithelium, no visible extracellular mucus, thyroid transcription factor (TTF)-1 negativity, and mucin (MUC) 5AC positivity on immunostaining.
View Article and Find Full Text PDFA Rare Presentation of Late-Onset Idiopathic Pulmonary Hemosiderosis: A Case Report.
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Respiratory Medicine, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune, IND.
Idiopathic pulmonary hemosiderosis (IPH) is a rare cause of diffuse alveolar hemorrhage (DAH). It is associated with a high mortality rate and recurrent episodes of widespread alveolar hemorrhage and most commonly affects children. Here, we present a rare occurrence of late-onset idiopathic pulmonary hemosiderosis in a 74-year-old male.
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Department of Vitreoretinal Services, Sankara Nethralaya, Chennai, India.
Article Synopsis
- * Despite initial treatment with adalimumab and corticosteroids, his condition did not improve after four months, prompting surgical intervention due to retino-retinal adhesions.
- * Post-surgery, the patient's vision improved significantly, and he has remained stable without recurrence of retinal detachment during a year of follow-up, highlighting the complexities of treating long-standing bullous retinal detachments.
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