Fahriye Kılınç

Dr. Fahriye Kılınç

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 November 2023 in Journal of Neuro-Oncology
Verified
Journal Article
Closed access
PDF file
BYBerrin Benli Yavuz
Berrin Benli Yavuz
FKFahriye Kılınç
Fahriye Kılınç
GKGul Kanyilmaz
Gul Kanyilmaz
MAMeryem Aktan
Meryem Aktan

1 August 2021 in Journal of Pediatric Urology
Verified
Journal Article
Closed access
AAArif AYDIN
Arif AYDIN
MSMehmet Giray Sönmez
Mehmet Giray Sönmez
GEGökhan Ecer
Gökhan Ecer
FKFahriye Kılınç
Fahriye Kılınç
RKRahim Kocabas
Rahim Kocabas
MBMehmet Balasar
Mehmet Balasar

1 May 2021 in Clinics and Research in Hepatology and Gastroenterology
Verified
Journal Article
Closed access
MAMurat Araz
Murat Araz
FKFahriye Kılınç
Fahriye Kılınç
UKUlku Kerimoglu
Ulku Kerimoglu
MKMuharrem Keskin
Muharrem Keskin
TKTevfik Kucukkartallar
Tevfik Kucukkartallar

1 January 2020 in Tuberk Toraks
Verified
Journal Article
Closed access
NPNecdet Poyraz
Necdet Poyraz
MYMehmet Emin Yazar
Mehmet Emin Yazar
FKFahriye Kılınç
Fahriye Kılınç
CKCelalettin Korkmaz
Celalettin Korkmaz
TATamer Altınok
Tamer Altınok
Inflammatory myofibroblastic tumor is a neoplasia of unknown clinical etiology that clinically and radiologically tends to mimic a malignant neoplasm. The tumor is histologically composed of a mixture of inflammatory cells, myofibroblastic spindle cells and plasma cells. It can occur in any part of the body. Although pulmonary inflammatory myofibroblastic tumor is the most common primary lung mass especially in childhood, this entity is usually not considered in differential diagnosis of lung nodules or masses. In this article, we aimed to disscus the pathology and imaging findings of the pulmonary inflammatory myofibroblastic tumor and increase the familiarity of radiologists and clinicians to this entity.

1 December 2022 in Selcuk Tip Dergisi
Verified
Journal Article
Closed access
DODoç.Dr. Pembe OLTULU
Doç.Dr. Pembe OLTULU
MTMahmut Tekecik
Mahmut Tekecik
ZTZulal Taflioglu Tekecik
Zulal Taflioglu Tekecik
FKFahriye Kılınç
Fahriye Kılınç
BIBilsev Ince
Bilsev Ince
Amaç: Bu çalışmanın amacı, yüzün altı farklı bölgesinin epidermis, dermis ve toplam deri kalınlıklarının belirlenerek cilt kalınlığı haritası oluşturmaktır. Hastalar ve Yöntem: Yaşları 30-80 arasında değişen 90 kadın ve 90 erkek hastanın yüz derisi, saçlı deri, alın, yanak, kulak, burun ve dudak bölgelerinden 9-10 mm sağlıklı doku içeren örnekler retrospektif olarak çalışmaya dahil edildi. Örnekler incelendi ve ışık mikroskobu altında mikrometre ile epidermis ve dermis kalınlıkları ölçüldü. Bulgular: Çalışmaya alınan 90 kadın katılımcının 6 yüz bölgesinin epidermis kalınlıkları 65,91±14,44 μm ile 120,91 ±44,74 μm, dermis kalınlıkları 1150±217,43 μm ile 1498,33±388,56 μm ve toplam deri kalınlıkları 1234,83± 217,6 μm ve 1599,33±492,2 μm idi. Çalışmaya alınan 90 erkek katılımcının 6 yüz bölgesinin epidermis kalınlıkları 79,08±13,88 μm ile 122,75±32,5 μm, dermis kalınlıkları 1106,66±389,82 μm ile 1942,5±464,06 μm ve toplam deri kalınlıkları 1756±503,75 μm ve 2022,5±460,24 μm arasında bulundu. Sonuç: Kadın hastalarda en ince epidermis saçlı deriden, erkek hastalarda ise en ince epidermis yanaktan ölçüldü. En kalın epidermis kadın ve erkek hastalarda üst dudak üstü bölgedeydi. Ancak dermis kalınlığının en ince ve kalın olduğu bölgeler cinsiyete göre farklılık gösterdi. Daha ileri çalışmalarda, daha çok merkezli, çok ırklı materyaller kullanılarak yüzün daha fazla alt birime bölünmesiyle yüz derisi kalınlığının tam bir haritası elde edilebilir.

30 September 2024 in Archives of Rheumatology
Verified
Journal Article
Open access
MEMustafa Çağrı Ergün
Mustafa Çağrı Ergün
OYOkancan Yılmaz
Okancan Yılmaz
HBHakan Bilgen
Hakan Bilgen
DODoç.Dr. Pembe OLTULU
Doç.Dr. Pembe OLTULU
FKFahriye Kılınç
Fahriye Kılınç
RTRecep Tunç
Recep Tunç
Objectives: This study aimed to investigate the relationship between patients with and without extraglandular involvement in Sjögren's syndrome (SS) by analyzing ANA (antinuclear antibody) and ENA (extractable nuclear antigen) results and minor salivary gland pathology findings. Patients and methods: A total of 265 (245 females; 20 males; mean age: 50.4±12.4; range, 19 to 79 years) patients diagnosed with SS were included in the retrospective cohort study between March 1, 2011, and December 1, 2021. Detailed documentation was performed, capturing demographic characteristics, clinical information, laboratory findings, medication usage, and manifestations of the syndrome. The patients were divided into two groups, with (78 females; 8 males; mean age: 52.7±11.5; range, 22 to 78 years or without (167 females; 12 males; mean age: 49.3±12.8; range, 19 to 79 years extraglandular involvement. Results: The mean follow-up duration was 63.1±31.9 months. Extraganular involvement, including joint involvement, lung involvement, central nervous system involvement, hematological involvement, hepatitis, and lymphoma, was observed in 32.5% of the patients. Patients with extraglandular involvement required multiple medications, while those with only glandular involvement predominantly used hydroxychloroquine. The mean duration from SS diagnosis to extraglandular involvement was 15.2±27.8 months. The comparison between patients with and without extraglandular involvement revealed a significant association between higher focus scores (FS) and extraglandular manifestations. However, no significant differences were observed in terms of ANA positivity, ANA titers, or ENA positivity. Regression analysis indicated that age and FS were linked to systemic involvement. Conclusion: This study highlights the importance of FS as a predictive indicator for extraglandular manifestations in SS. Advanced age was found to be associated with an increased likelihood of extraglandular involvement. Assessing FS and age can aid in predicting extraglandular manifestations.