Zobrazeno 1 - 10
of 578
pro vyhledávání: '"pulmonary langerhans cell histiocytosis"'
Publikováno v:
Respirology Case Reports, Vol 12, Iss 9, Pp n/a-n/a (2024)
Abstract Pulmonary Langerhans cell histiocytosis (PLCH) is a subtype of Langerhans cell histiocytosis, a rare neoplastic disease characterized by lung involvement. Here, we present a case involving a patient with multiple cavitary nodules who was dia
Externí odkaz:
https://doaj.org/article/cdfaad4b08ca43978c1e964b9f0be51b
Autor:
Atif Saleem Siddiqui
Publikováno v:
Respirology Case Reports, Vol 12, Iss 9, Pp n/a-n/a (2024)
Key message Pulmonary Langerhans cell histiocytosis can be associated with subglottic adenoid cystic carcinoma.
Externí odkaz:
https://doaj.org/article/3fb5ddb207774d9f94fc0703431d74ae
Autor:
Joseph Inauen, Simone Barry
Publikováno v:
Respirology Case Reports, Vol 12, Iss 9, Pp n/a-n/a (2024)
Abstract This clinical case highlights the diagnostic challenges encountered in a young adult smoker presenting with undifferentiated pulmonary nodules. Initial investigations were inconclusive, necessitating surgical lung biopsy due to the nodules'
Externí odkaz:
https://doaj.org/article/b829b255deb24f388a15e4c92c70ba74
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message A comprehensive diagnostic approach, including immunohistochemistry, is crucial for confirming pulmonary Langerhans cell histiocytosis in adults. Individualized treatment with dynamically adjusted chemotherapy based on therapeuti
Externí odkaz:
https://doaj.org/article/89f594b58fd64ea2a2a21aae8944aff2
Autor:
Silvia Barril, Paloma Acebo, Paloma Millan-Billi, Alfonso Luque, Oriol Sibila, Carlos Tarín, Abdellatif Tazi, Diego Castillo, Sonsoles Hortelano
Publikováno v:
Respiratory Research, Vol 24, Iss 1, Pp 1-13 (2023)
Abstract Background Pulmonary Langerhans cell histiocytosis (PLCH) is a rare interstitial lung disease (ILD) associated with smoking, whose definitive diagnosis requires the exclusion of other forms of ILD and a compatible surgical lung biopsy. Bronc
Externí odkaz:
https://doaj.org/article/d060923586194a658656afb262de5679
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-4 (2023)
Abstract Background Pulmonary Langerhans cell histiocytosis (PLCH) only with airway involvement manifested as diffuse thickening of the tracheobronchial walls is rare. Case report A 26-year-old male was admitted to the hospital with progressive wheez
Externí odkaz:
https://doaj.org/article/9c1667180f284d5ab8d28a80f7f8e080
Autor:
Franciosi, Alessandro N. a, b, Gupta, Nishant c, Murphy, David J. b, d, Wikenheiser-Brokamp, Kathryn A. e, f, McCarthy, Cormac a, b, ∗
Publikováno v:
In Chest
Case of pulmonary Langerhans cell histiocytosis presenting as ground-glass opacity in the lower lung
Publikováno v:
Respiratory Medicine Case Reports, Vol 51, Iss , Pp 102095- (2024)
Nodules and cysts with upper lobe predominance on chest computed tomography (CT) are highly suggestive of pulmonary Langerhans cell histiocytosis (PLCH). Herein, we describe a case of PLCH that presented with the unusual CT findings of subpleural gro
Externí odkaz:
https://doaj.org/article/b3fe53473a5946c48c09fabda8fc5718
Publikováno v:
Journal of Infection and Public Health, Vol 16, Iss 4, Pp 526-530 (2023)
Diffuse cystic lung disease (DCLD) is a complex disease that can be caused by various reasons. Although the chest CT scan plays a vital role in suggesting the etiology of DCLD, it is apt to lead to misdiagnosis simply based on the CT image of the lun
Externí odkaz:
https://doaj.org/article/aff38f53c08d4fdeb95897d805a71f49
Publikováno v:
In Immunology and Allergy Clinics of North America May 2023 43(2):273-287