CONTROVERSE DIAGNOSTICE ȘI TERAPEUTICE ÎN PNEUMOPATIILE INTERSTIȚIALE ASOCIATE CU ANCA
DOI:
https://doi.org/10.52692/1857-0011.2025.3-83.35Cuvinte cheie:
Vasculite ANCA, Pneumopatii interstițiale, terapie antifibroticăRezumat
Vasculitele asociate cu ANCA (AAV) sunt boli rare, dar cu impact prognostic major. Tot mai multe date arată că acestea nu se limitează la inflamația vasculară, ci pot asocia boală interstițială pulmonară (PID), frecvent cu pattern UIP, asociat cu mortalitate crescută. Situația este deosebit de relevantă deoarece PID poate preceda diagnosticul de vasculită, fiind adesea confundată cu fibroză pulmonară izolată, ceea ce crește riscul de subdiagnostic. Tratamentele standard pentru vasculite s-au dovedit ineficiente în controlul fibrozei și au amplificat riscul infecțios, în timp ce agenții antifibrotici deschid noi perspective, dar dovezile rămân limitate. Lipsa unor ghiduri și a studiilor dedicate generează incertitudine clinică, iar AAV-PID se conturează ca un domeniu emergent în pneumologie și reumatologie, unde nevoia de cercetare este urgentă și potențialul de a îmbunătăți prognosticul este considerabil.
Referințe
Watts R.A., Scott D.G. ANCA vasculitis: to lump or split? Why we should study MPA and GPA separately. Rheumatology (Oxford), 2012; 51(12): p. 2115-7.
Qasim A., Patel J.B. ANCA-Associated Vasculitis. 2025. https://doi.org/ NBK554372 [bookaccession]
Doliner B., Rodriguez K., Montesi S.B., et al. Interstitial lung disease in ANCA-associated vasculitis: associated factors, radiographic features and mortality. Rheumatology (Oxford), 2023; 62(2): p. 716-725.
Alba M.A., Flores-Suarez L.F., Henderson A.G., et al. Interstital lung disease in ANCA vasculitis. Autoimmun Rev, 2017; 16(7): p. 722-729.
Schirmer J.H., Wright M.N., et al. Clinical presentation and long-term outcome of 144 patients with microscopic polyangiitis in a monocentric German cohort. Rheumatology (Oxford), 2016; 55(1): p. 71-9.
Fernandez Casares M., Gonzalez A., et al. Microscopic polyangiitis associated with pulmonary fibrosis. Clin Rheumatol, 2015; 34(7): p. 1273-7.
Kagiyama N., Takayanagi N., et al. Antineutrophil cytoplasmic antibody-positive conversion and microscopic polyangiitis development in patients with idiopathic pulmonary fibrosis. BMJ Open Respir Res, 2015; 2(1): p. e000058.
Eleftheriou D., Katsenos,S. et al. Pulmonary fibrosis presenting as an early manifestation of microscopic polyangiitis. Monaldi Arch Chest Dis, 2012; 77(3-4): p. 141-4.
Tanaka T., Otani K., Egashira R., et al. Interstitial pneumonia associated with MPO-ANCA: clinicopathological features of nine patients. Respir Med, 2012; 106(12): p. 1765-70.
Kono M., Nakamura Y., et al. Usual interstitial pneumonia preceding collagen vascular disease: a retrospective case control study of patients initially diagnosed with idiopathic pulmonary fibrosis. PLoS One, 2014; 9(4): p. e94775.
Nozu T., Kondo M., Suzuki K., et al. A comparison of the clinical features of ANCA-positive and ANCA-negative idiopathic pulmonary fibrosis patients. Respiration, 2009; 77(4): p. 407-15.
Ando M., Miyazaki E., Ishii T., et al. Incidence of myeloperoxidase anti-neutrophil cytoplasmic antibody positivity and microscopic polyangitis in the course of idiopathic pulmonary fibrosis. Respir Med, 2013; 107(4): p. 608-15.
Huang H., Wang Y.X., Jiang C.G., et al. A retrospective study of microscopic polyangiitis patients presenting with pulmonary fibrosis in China. BMC Pulm Med, 2014; 14: p. 8.
Comarmond C., Crestani B., Tazi A., et al. Pulmonary fibrosis in antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis: a series of 49 patients and review of the literature. Medicine (Baltimore), 2014; 93(24): p. 340-349.
Yamagata M., Ikeda K., Tsushima K., et al. Prevalence and Responsiveness to Treatment of Lung Abnormalities on Chest Computed Tomography in Patients With Microscopic Polyangiitis: A Multicenter, Longitudinal, Retrospective Study of One Hundred Fifty Consecutive Hospital-Based Japanese Patients. Arthritis Rheumatol, 2016; 68(3): p. 713-23.
Maillet T., Goletto T., Beltramo G., et al. Usual interstitial pneumonia in ANCA-associated vasculitis: A poor prognostic factor. J Autoimmun, 2020; 106: p. 102338.
Imokawa S., Uehara M., Uto T., et al. Organizing pneumonia associated with myeloperoxidase anti- neutrophil cytoplasmic antibody. Respirol Case Rep, 2015; 3(4): p. 122-4.
Takada K., Miyamoto A., Nakahama H., et al. Myeloperoxidase anti-neutrophil cytoplasmic antibody- associated vasculitis with a unique imaging presentation of organizing pneumonia: A case report. Respir Med Case Rep, 2020; 31: p. 101294.
Yates M., Watts R.A., Bajema I.M., et al. EULAR/ ERA-EDTA recommendations for the management of ANCA-associated vasculitis. Ann Rheum Dis, 2016; 75(9): p. 1583-94.
Hellmich B., Sanchez-Alamo B., Schirmer J.H., et al. EULAR recommendations for the management of ANCA-associated vasculitis: 2022 update. Ann Rheum Dis, 2024; 83(1): p. 30-47.
Xu C., Xu Z., Ren J. Use of rituximab in connective tissue disease-associated interstitial lung disease: a narrative review. Front Med (Lausanne), 2025; 12: p. 1555442.
Vacchi C., Manfredi A., Cassone G., et al. Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease. Drugs Context, 2021; 10.
Shi J., Shen Q., Chen X.M., et al. Clinical characteristics and outcomes in microscopic polyangiitis patients with renal involvement: a study of 124 Chinese patients. BMC Nephrol, 2019; 20(1): p. 339.
Ono N., Inoue Y., Miyamura T., et al. The Association of Airway Comorbidities With the Clinical
Phenotypes and Outcomes of Patients With Antineutrophil Cytoplasmic Autoantibody-associated Vasculitis. J Rheumatol, 2021; 48(3): p. 417-425.
Zhao W., Dai H., Liu Y., et al. Clinical features and prognosis of microscopic polyangiitis with usual interstitial pneumonia compared with idiopathic pulmonary fibrosis. Clin Respir J, 2019; 13(7): p. 460-466.
Flaherty K.R., Wells A.U., Cottin V., et al. Nintedanib in Progressive Fibrosing Interstitial Lung Diseases. N Engl J Med, 2019; 381(18): p. 1718-1727.
Descărcări
Publicat
Număr
Secțiune
##category.category##
Licență
Copyright (c) 2026 Buletinul Academiei de Științe a Moldovei. Științe medicale

Această lucrare este licențiată în temeiul Creative Commons Attribution 4.0 International License.
