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A Case of Pulmonary Sarcoidosis With Multiple Endobronchial Polypoid Structures and Partial Airway Obstruction.
J Investig Med High Impact Case Rep
January 2025
St. Joseph's University Medical Center, Paterson, NJ, USA.
We present a case of a 42-year-old male with sarcoidosis manifesting as endobronchial mass-like lesions, a rare and atypical presentation of the disease. Sarcoidosis typically involves the respiratory system, but its occurrence as endobronchial polyps mimicking malignancy is uncommon. The diagnosis was confirmed through bronchoscopy and biopsy, revealing non-caseating granulomas.
View Article and Find Full Text PDFA rare case report of endobronchial neurofibroma treated with transbronchial endoscopic resection and literature review.
Medicine (Baltimore)
September 2024
Department of Cardiology, Shaoxing People's Hospital (Shaoxing Hospital, Zhejiang University School of Medicine), Zhejiang Province, China.
Article Synopsis
- Endobronchial neurofibroma is a super rare type of tumor in the lungs that can cause symptoms like coughing and shortness of breath.
- A 57-year-old man was diagnosed with this condition and his tumor was successfully removed using special tools without needing traditional surgery.
- This case shows that new methods like electrical snaring and laser treatments can work well for certain lung tumors and could help other patients with similar issues.
Primary endobronchial multifocal Ewing's sarcoma: a rare case report.
Front Oncol
August 2024
Department of Radiology, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Extraskeletal Ewing's sarcoma (ES) has been reported to originate from various sites. Primary endobronchial ES is an extremely rare bronchial tumor, especially multifocal lesions. This report describes a rare presentation of primary bronchial ES in a 31-year-old female who was referred to the emergency department of our hospital due to suspicion of a foreign body in the bronchus.
View Article and Find Full Text PDFApplication of 18F-FDG PET/CT imaging in a primary angiomatoid fibrous histiocytoma of pulmonary bronchus: case report and literature review.
Front Med (Lausanne)
July 2024
Department of Nuclear Medicine, Jiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, Nanchang, Jiangxi, China.
Article Synopsis
- Angiomatoid fibrous histiocytoma (AFH) is a rare, low-grade malignant tumor, primarily affecting extremities and occasionally seen in the pulmonary bronchus.
- A 57-year-old female with a six-month cough was initially misdiagnosed with lung cancer based on imaging, but post-surgery pathology confirmed it as primary AFH of the bronchus.
- PAFH has low incidence, non-specific clinical and imaging features, making pathological diagnosis crucial while PET/CT can assist in identifying this tumor.
Endobronchial Obstruction: A Case of Well-Differentiated Liposarcoma.
Cureus
April 2024
Pulmonary and Critical Care Medicine, John H. Stroger, Jr. Hospital of Cook County, Chicago, USA.
Atypical lipomatous tumor/well-differentiated liposarcoma (ALT/WDL) is a rare subtype of endobronchial tumor that has been rarely reported in medical literature. Due to its low incidence, distinguishing it from endobronchial lipoma poses a significant diagnostic challenge, necessitating histopathologic and cytogenetic analysis. As of today, the treatment and surveillance protocols for these neoplasms remain poorly defined, often resulting in their misclassification and treatment as endobronchial lipomas.
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