Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Histopathological aspects of usual interstitial pneumonia in patients with systemic connective tissue diseases

M. Makovická, B. Durcová, A. Vrbenská, P. Makovický, P. Michalčová, K. Kráľová, J. Muri

. 2025 ; 40 (1) : 49-56. [pub] 20240610

Jazyk angličtina Země Španělsko

Typ dokumentu časopisecké články, kazuistiky

Perzistentní odkaz   https://www.medvik.cz/link/bmc25002949

Five cases of patients with systemic connective tissue diseases (CTD) who developed connective tissue disease-associated interstitial lung disease (CTD-ILD) with progressive pulmonary fibrosis (PPF) are reported here. Unspecified ILD was diagnosed using high-resolution computed tomography (HRCT). Histologically, all cases were usual interstitial pneumonia (UIP) with findings of advanced (3/5) to diffuse (2/5) fibrosis, with a partially (4/5) to completely (1/5) formed image of a honeycomb lung. The fibrosis itself spread subpleurally and periseptally to more central parts (2/5) of the lung, around the alveolar ducts (2/5), or even without predisposition (1/5). Simultaneously, there was architectural reconstruction based on the mutual fusion of fibrosis without compression of the surrounding lung parenchyma (1/5), or with its compression (4/5). The whole process was accompanied by multifocal (1/5), dispersed (2/5), or organized inflammation in aggregates and lymphoid follicles (2/5). As a result of continuous fibroproduction and maturation of the connective tissue, the alveolar septa thickened, delimiting groups of alveoli that merged into air bullae. Few indistinctly visible (2/5), few clearly visible (1/5), multiple indistinctly visible (1/5), and multiple clearly visible (1/5) fibroblastic foci were present. Among the concomitant changes, areas of emphysema, bronchioloectasia, and bronchiectasis, as well as bronchial and vessel wall hypertrophy, and mucostasis in the alveoli and edema were observed. The differences in the histological appearance of usual interstitial pneumonia associated with systemic connective tissue diseases (CTD-UIP) versus the pattern associated with idiopathic pulmonary fibrosis (IPF-UIP) are discussed here. The main differences lie in spreading lung fibrosis, architectural lung remodeling, fibroblastic foci, and inflammatory infiltrates.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc25002949
003      
CZ-PrNML
005      
20250206103953.0
007      
ta
008      
250121s2025 sp f 000 0|eng||
009      
AR
024    7_
$a 10.14670/HH-18-777 $2 doi
035    __
$a (PubMed)38934227
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sp
100    1_
$a Makovická, Mária $u Department of Histology and Embryology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic $u Cancer Research Institute, Biomedical Research Centre of the Slovak Academy of Sciences, Bratislava, Slovak Republic
245    10
$a Histopathological aspects of usual interstitial pneumonia in patients with systemic connective tissue diseases / $c M. Makovická, B. Durcová, A. Vrbenská, P. Makovický, P. Michalčová, K. Kráľová, J. Muri
520    9_
$a Five cases of patients with systemic connective tissue diseases (CTD) who developed connective tissue disease-associated interstitial lung disease (CTD-ILD) with progressive pulmonary fibrosis (PPF) are reported here. Unspecified ILD was diagnosed using high-resolution computed tomography (HRCT). Histologically, all cases were usual interstitial pneumonia (UIP) with findings of advanced (3/5) to diffuse (2/5) fibrosis, with a partially (4/5) to completely (1/5) formed image of a honeycomb lung. The fibrosis itself spread subpleurally and periseptally to more central parts (2/5) of the lung, around the alveolar ducts (2/5), or even without predisposition (1/5). Simultaneously, there was architectural reconstruction based on the mutual fusion of fibrosis without compression of the surrounding lung parenchyma (1/5), or with its compression (4/5). The whole process was accompanied by multifocal (1/5), dispersed (2/5), or organized inflammation in aggregates and lymphoid follicles (2/5). As a result of continuous fibroproduction and maturation of the connective tissue, the alveolar septa thickened, delimiting groups of alveoli that merged into air bullae. Few indistinctly visible (2/5), few clearly visible (1/5), multiple indistinctly visible (1/5), and multiple clearly visible (1/5) fibroblastic foci were present. Among the concomitant changes, areas of emphysema, bronchioloectasia, and bronchiectasis, as well as bronchial and vessel wall hypertrophy, and mucostasis in the alveoli and edema were observed. The differences in the histological appearance of usual interstitial pneumonia associated with systemic connective tissue diseases (CTD-UIP) versus the pattern associated with idiopathic pulmonary fibrosis (IPF-UIP) are discussed here. The main differences lie in spreading lung fibrosis, architectural lung remodeling, fibroblastic foci, and inflammatory infiltrates.
650    _2
$a lidé $7 D006801
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé středního věku $7 D008875
650    12
$a nemoci pojiva $x patologie $x komplikace $7 D003240
650    _2
$a mužské pohlaví $7 D008297
650    12
$a intersticiální plicní nemoci $x patologie $x komplikace $7 D017563
650    _2
$a senioři $7 D000368
650    _2
$a počítačová rentgenová tomografie $7 D014057
650    _2
$a idiopatická plicní fibróza $x patologie $x komplikace $7 D054990
650    _2
$a plíce $x patologie $x diagnostické zobrazování $7 D008168
650    _2
$a dospělí $7 D000328
655    _2
$a časopisecké články $7 D016428
655    _2
$a kazuistiky $7 D002363
700    1_
$a Durcová, Barbora $u Department of Pneumology, National Institute for Tuberculosis, Lung Diseases and Thoracic Surgery in Vyšné Hágy, Slovak Republic
700    1_
$a Vrbenská, Adela $u Department of Pathology, National Institute for Tuberculosis, Lung Diseases and Thoracic Surgery in Vyšné Hágy, Slovak Republic
700    1_
$a Makovický, Peter $u Department of Histology and Embryology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic $u Cancer Research Institute, Biomedical Research Centre of the Slovak Academy of Sciences, Bratislava, Slovak Republic
700    1_
$a Michalčová, Patricie $u Department of Histology and Embryology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic $u Department of Clinical Neurosciences, Ostrava University Hospital, Ostrava-Poruba, Czech Republic
700    1_
$a Kráľová, Klaudia $u Cancer Research Institute, Biomedical Research Centre of the Slovak Academy of Sciences, Bratislava, Slovak Republic $u Department of Zoology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovak Republic
700    1_
$a Muri, Jozef $u Department of Histology and Embryology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic $u Centre of Chest Surgery, National Institute for Tuberculosis, Lung Diseases and Thoracic Surgery in Vyšné Hágy, Slovak Republic. muri.jozef@gmail.com
773    0_
$w MED00005439 $t Histology and histopathology $x 1699-5848 $g Roč. 40, č. 1 (2025), s. 49-56
856    41
$u https://pubmed.ncbi.nlm.nih.gov/38934227 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20250121 $b ABA008
991    __
$a 20250206103948 $b ABA008
999    __
$a ok $b bmc $g 2263005 $s 1238956
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2025 $b 40 $c 1 $d 49-56 $e 20240610 $i 1699-5848 $m Histology and histopathology $n Histol Histopathol $x MED00005439
LZP    __
$a Pubmed-20250121

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...