Temat: Granulomatosis with polyangiitis - Katalog OPAC zbiorów

Skocz do pozycji: 1.

Tytuł:: Diagnosis and treatment of corneal ulcers in the course of systemic autoimmune diseases
Owrzodzenia rogówki w przebiegu układowych chorób o podłożu autoimmunologicznym. Rozpoznanie i leczenie
Autorzy:: Czarnacka, Kinga
Chmura-Hołyst, Alicja
Alsoubie, Ismael
Cwalina, Oliwia
Pandey, Ada
Prokop, Dominika
Gawlak, Małgorzata
Kuźlik, Bartosz
Guzek, Katarzyna
Sajak-Hydzik, Katarzyna
Pawlicka, Ilona
Piskorz, Agnieszka
Kozak, Maciej
Roszkowska, Anna
Powiązania:: https://bibliotekanauki.pl/articles/6567720.pdf
Data publikacji:: 2021-03-31
Wydawca:: Medical Education
Tematy:: peripheral ulcerative keratitis
corneal damage
rheumatoid arthritis
systemic lupus erythematosus
granulomatosis with polyangiitis
obwodowe wrzodziejące zapalenie rogówki
uszkodzenie rogówki
reumatoidalne zapalenie stawów
toczeń rumieniowaty układowy
ziarniniakowatość z zapaleniem naczyń
Opis:: Peripheral ulcerative keratitis is an inflammatory condition, usually crescent shaped and occurring in the corneal stromal region, where it is always associated with corneal stromal thinning. Peripheral ulcerative keratitis often occurs in the course of rheumatic diseases but is most commonly associated with rheumatoid arthritis. Peripheral ulcerative keratitis is also seen in granulomatosis with polyangiitis, polyarteritis nodosa, relapsing chondritis, and systemic lupus erythematosus. These diseases are analyzed in the article in relation to peripheral ulcerative keratitis with a discussion of individual treatment methods in specific cases.
Obwodowe wrzodziejące zapalenie rogówki jest stanem zapalnym, zwykle w kształcie półksiężyca, występującym w okolicy rąbka rogówki, gdzie zawsze wiąże się ze ścieńczeniem zrębu rogówki. Niejednokrotnie występuje w przebiegu chorób reumatoidalnych, natomiast najczęściej związane jest z reumatoidalnym zapaleniem stawów. Obwodowe wrzodziejące zapalenie rogówki obserwuje się także w: ziarniniakowatości z zapaleniem naczyń, guzkowatym zapaleniu tętnic, nawracającym zapaleniu chrząstek oraz w toczniu rumieniowatym układowym. Wymienione choroby opisano w odniesieniu do obwodowego wrzodziejącego zapalenia rogówki, z omówieniem poszczególnych metod leczenia w określonych przypadkach.
Źródło:: OphthaTherapy; 2023, 10, 1; 43-47
2353-7175
2543-9987
Pojawia się w:: OphthaTherapy
Dostawca treści:: Biblioteka Nauki

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Tytuł:: Indications and Long-term Outcomes of Open Augmentation Rhinoplasty with Autogenous L-shaped Costal Cartilage Strut Grafts – A Single Plastic Surgeon’s Experience
Autorzy:: Leach, Laura
Shamil, Eamon
Malata, Charles M
Powiązania:: https://bibliotekanauki.pl/articles/1398127.pdf
Data publikacji:: 2018
Wydawca:: Index Copernicus International
Tematy:: augmentation rhinoplasty
costal cartilage grafts
autoimmune inflammatory disease
granulomatosis with polyangiitis
relapsing polychondritis
screw fixation of grafts
Opis:: Introduction: We present a single surgeon’s experience of open augmentation rhinoplasty with autogenous L-shaped costal cartilage grafts, with long-term patient-reported outcome data. We highlight the salient operative steps and outline the peri-operative care required to optimise outcomes. Materials and Methods: A retrospective review of eleven such augmentation rhinoplasties performed between 2008 and 2016 was undertaken. Indications included saddle nose deformity [granulomatosis with polyangiitis (n=7) and relapsing polychondritis (n=1)], post-traumatic nasal collapse (n=1) and advanced cosmetic westernisation of the nose (n=2). Long-term patient-reported outcome was assessed with a patient questionnaire. Results: All patients achieved marked improvement in nasal position, shape and function. There was no cartilage exposure, warping or resorption and no recurrent deformities. One patient’s dorsal graft was fractured two years later during an ophthalmological procedure and the deformity was re-corrected successfully, again with the above technique. Average follow up was 5.2 years. Of the nine patients who responded to the follow-up questionnaire, 100% were satisfied with their nasal appearance. 100% of responders at follow-up reported that they have had no problems relating to their nose (n=9). Discussion: L-shaped costal cartilage grafts provided a reliable, reproducible approach in augmentation rhinoplasty for disparate indications (inflammatory, traumatic and cosmetic) in the hands of a low-volume operator. With careful patient selection and planning, this technique can provide pleasing aesthetic outcomes and high patient satisfaction, with good long-term outcomes.
Źródło:: Polish Journal of Otolaryngology; 2018, 72, 3; 26-32
0030-6657
2300-8423
Pojawia się w:: Polish Journal of Otolaryngology
Dostawca treści:: Biblioteka Nauki

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Tytuł:: Sinusogenes orbital complication as the first symptom of refractory granulomatosis with polyangiitis and the use of rituximab in treatment. A case report
Autorzy:: Mielcarek-Kuchta, D.
Lembicz, M.
Puszczewicz, M.
Rzymkowska, M.
Nowicka, A.
Kopeć, T.
Leszczyńska, M.
Szyfter, W.
Powiązania:: https://bibliotekanauki.pl/articles/1917276.pdf
Data publikacji:: 2015
Wydawca:: Uniwersytet Medyczny w Białymstoku
Tematy:: Granulomatosis with polyangiitis
refractory GPA
rituximab
Opis:: Granulomatosis with polyangiitis (GPA) is a rare disease involving multiple organs and systems, characterized by necrotizing inflammation of small and medium-sized vessels and formation of granulomas. There are several forms of the disease. In the generalized form (including severe one), cyclophosphamide in combination with steroids is usually used. There are also cases of a particularly severe and refractory course of the disease, which do not respond to the standard treatment. In such cases some other methods of treatment are recommended, including biological agents such as rituximab - anti-CD20 monoclonal antibody. We described a case of a 17-year-old patient with refractory GPA, resistant to standard remission induction therapy. In case of this patient, advanced lesions were mainly localized in the lungs, sinuses and middle ear. The disease progressed despite standard therapy. Therefore, it was decided to use an alternative treatment with a biological agent – rituximab. In the assessment after therapy we observed a significant clinical recovery as well as the improvement in laboratory tests, pulmonary function tests and radiological imaging. Within six months after the administration of rituximab, progression of the disease was not observed, which was evidenced in radiological imaging and pulmonary function tests. The case illustrates how biological agents, including rituximab, are extending the therapeutic options for patients with GPA, especially with severe forms of the disease.
Źródło:: Progress in Health Sciences; 2015, 5, 1; 265-270
2083-1617
Pojawia się w:: Progress in Health Sciences
Dostawca treści:: Biblioteka Nauki

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Skocz do pozycji: 4.

Tytuł:: Unmasking the nature of granulomatosis with polyangiitis – a diagnostic odyssey revealed through a compelling case report
Autorzy:: Sajdak, Piotr
Krużel, Aleksandra
Stodolak, Marcel
Bednarski, Artur
Ziajor, Seweryn
Turski, Mikołaj
Żurowska, Klaudia
Kłos, Kamil
Tomasik, Justyna
Dębik, Marika
Szydłowski, Łukasz
Powiązania:: https://bibliotekanauki.pl/articles/40614541.pdf
Data publikacji:: 2024-06-30
Wydawca:: Uniwersytet Rzeszowski. Wydawnictwo Uniwersytetu Rzeszowskiego
Tematy:: autoimmune diseases
granulomatosis with polyangiitis
vasculitis
Opis:: Introduction and aim. Granulomatosis with polyangiitis (GPA), formerly known as Wegener’s granulomatosis, presents a formidable challenge in the realm of autoimmune diseases. Granulomatosis, characterized by vasculitis and granuloma formation, exhibits diverse clinical manifestations. The rarity of GPA is evident, with an estimated incidence between 0.4 and 11.9 cases per 1 million person-years. The aim of this report is to show the complex diagnostic challenges inherent in GPA, demonstrating the diagnostic process from initial symptoms. Description of the case. This case report unfolds the diagnostic journey of a 52-year-old Caucasian male. The presented case, initially suspected as a respiratory infection, led to a comprehensive investigation owing to persistent symptoms, abnormal blood counts, and elevated inflammatory markers. This narrative aims to depict the patient’s diagnostic journey. Key diagnostic tools include ANCA testing, imaging studies, and tissue biopsy. Pulmonary nodules, lymphangitic changes, and renal involvement culminating in a GPA diagnosis confirmed by positive ANCA and anti-PR3 antibodies. The successful management of this case involved a tailored therapeutic regimen, including cyclophosphamide and methylprednisolone, addressing both vasculitic and renal components. Conclusion. This case contributes to the understanding of atypical presentations of GPA, emphasizing the importance of a holistic and dynamic diagnostic approach.
Źródło:: European Journal of Clinical and Experimental Medicine; 2024, 22, 2; 462-468
2544-2406
2544-1361
Pojawia się w:: European Journal of Clinical and Experimental Medicine
Dostawca treści:: Biblioteka Nauki

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