Zobrazeno 1 - 10
of 1 714
pro vyhledávání: '"Pleuritis"'
Autor:
A. A. Klimenko, N. A. Demidova, V. V. Veselkin, T. A. Kirdyashkina, A. A. Chinova, Yu. A. Shandanovina
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 20, Iss 5, Pp 581-587 (2024)
Postmyocardial syndrome (Dressler syndrome) is a form of secondary pericarditis with or without pericardial effusion resulting from myocardial damage. Dressler syndrome is not a common disease, but it should be suspected in patients with pathognomoni
Externí odkaz:
https://doaj.org/article/3c346ee080c64441904e82de15920856
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract In a prospective cohort study, we evaluated plasma PCT levels in 48 TB lymphadenitis (TBLN) and 41 TB pleuritis (TBPE) patients. Measurements of PCT were done in unstimulated plasma of microbiologically and clinically confirmed TBLN and TBPE
Externí odkaz:
https://doaj.org/article/7c6b152c24b149d19cefa4ca39e92c84
Publikováno v:
Public Health Action, Vol 14, Iss 3, Pp 112-118 (2024)
BACKGROUND: Quantifying quality of life (QoL) in extrapulmonary TB patients is crucial yet often overlooked. This study examines the impact of tuberculous lymphadenitis and pleuritis on patients' QoL, associated factors, and recurrence. METHODS: Data
Externí odkaz:
https://doaj.org/article/47de502300a1404bbf87b62b97c97cd8
Publikováno v:
World Journal of Surgical Oncology, Vol 22, Iss 1, Pp 1-6 (2024)
Abstract Background Thymic mucosa-associated lymphoid tissue (MALT) lymphoma is rare and is known to be associated with Sjögren’s syndrome (SjS). SjS is rarely accompanied by serositis. Here, we describe the first case of postoperative cardiac tam
Externí odkaz:
https://doaj.org/article/d49e33064fad4f6a90579ece77be5ff6
Autor:
Yuto Kato, Kentaro Fukunaga, Aya Ooka, Shunichi Tokuoka, Yoko Kataoka, Takuya Fujita, Hiroyuki Sugihara, Masafumi Yamaguchi
Publikováno v:
Respirology Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract Immunoglobulin G4 (IgG4)‐related disease is a chronic inflammatory condition often characterized by exudative pleural effusions. However, transudative pleural effusions, like in the presented case of an 80‐year‐old man with multiple co
Externí odkaz:
https://doaj.org/article/fd6e6d2c78104d07b337057fb468e675
Publikováno v:
Infectious Disease Reports, Vol 15, Iss 6, Pp 795-805 (2023)
A large number of monkeypox (MPOX) cases have been reported in Europe and North America in 2022, and a new outbreak of this disease was declared. We describe a case of a patient with probable monkeypox during the height of this epidemic in Poland. Th
Externí odkaz:
https://doaj.org/article/7818350ec10949fd8e53a50869627df9
Publikováno v:
Respiratory Medicine Case Reports, Vol 50, Iss , Pp 102065- (2024)
Xanthogranulomatous pleuritis is an extremely rare pathological entity, characterized by the infiltration of foamy cells and multinucleated giant cells within the pleural space. This condition often mimics infectious and neoplastic processes, present
Externí odkaz:
https://doaj.org/article/f24041a531904248843114c1d2fd3883
Publikováno v:
Respiratory Medicine Case Reports, Vol 50, Iss , Pp 102030- (2024)
Extrapulmonary tuberculosis could affect many organs beside lung airway and parenchyma. The mycobacterium tuberculosis can invade area such as the pleural and pericardium by lymphogenic, hematogenic, or direct infection. Patient with history exposure
Externí odkaz:
https://doaj.org/article/eb749f4435ab4029b10ffd421d0957c6
Autor:
Jeerawat Kaewwinud, Sireethorn Pienchitlertkajorn, Kamolphop Koomtanapat, Lalita Lumkul, Pakpoom Wongyikul, Phichayut Phinyo
Publikováno v:
Heliyon, Vol 10, Iss 1, Pp e23440- (2024)
Background: Diagnosing tuberculous pleural effusion (TPE) in patients presenting with Lymphocyte-Predominant Exudative pleural effusion (LPE) is challenging, due to the poor clinical utility of TB culture. Adenosine deaminase (ADA) has been recommend
Externí odkaz:
https://doaj.org/article/627370cfa5f541eda0e8fce995047521
Publikováno v:
Revista Methodo, Vol 8, Iss 4 (2023)
La enfermedad relacionada con IgG4 (ER-IgG4) es una entidad multisistémica poco frecuente, caracterizada por lesiones con un denso infiltrado linfoplasmocítico con abundantes células positivas para inmunoglobulina G (IgG)4, fibrosis estoriforme, f
Externí odkaz:
https://doaj.org/article/d35eda2fafc5461baa52d96c012cdacd