Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ulku, Kucuk"'
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 1, Pp 7-10 (2019)
Background: Tumor budding was defined as a single cancer cell or a cluster of fewer than five cancer cells in the stroma of the invasive tumor margin. It has been suggested as a prognostic factor in various cancers, such as esophageal, lung, colorect
Externí odkaz:
https://doaj.org/article/bd57203abaf04946938327df597bd188
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 61, Iss 3, Pp 319-322 (2018)
Background: Investigation of morphological differences in relation with serological variables between primary versus secondary Sjögren's syndrome associated with systemic scleroderma (Scl-SS). Materials and Methods: A total of 69 primary Sjögren's
Externí odkaz:
https://doaj.org/article/0ee891a944894d0b96b892913207d605
Autor:
Salih Budak, Cem Yücel, Mehmet Zeynel Keskin, Mehmet Yoldas, Erdem Kısa, Ertan Can, Ulku Kucuk, Zafer Kozacıoğlu
Publikováno v:
Archivio Italiano di Urologia e Andrologia, Vol 90, Iss 1, Pp 8-10 (2018)
Objectives: Transurethral bladder tumour resection (TURBT) is the common surgical method used in the diagnosis, staging and treatment of patients with bladder tumour. Most of the rare tumours other than the urothelial carcinomas of the bladder are in
Externí odkaz:
https://doaj.org/article/512740e65284401e8e8728b5ef5404b3
Autor:
Ebru Cakir, Ulku Kucuk, Ayca Ersen, Emel E Pala, Mehmet Senoglu, Ali O Binatli, Zubeyde Yildirim
Publikováno v:
Journal of Cytology, Vol 34, Iss 1, Pp 63-65 (2017)
Giant cell ependymomas (GCE) are extremely rare tumors, with 24 cases described in the literature. Squash cytology is a rapid, reliable, simple technique for intraoperative consultation in neurosurgical practice. We describe a rare case of GCE arisin
Externí odkaz:
https://doaj.org/article/1c58e06ff81145dcacb15a944abdc000
Publikováno v:
Indian Journal of Neurosurgery, Vol 03, Iss 03, Pp 154-157 (2014)
Synchronous presentation of multiple primary central nervous system tumors is extremely rare. Meningioma is the most commonly reported tumor in association with other intracranial neoplasms. Review of the literature revealed only 17 cases of meningio
Externí odkaz:
https://doaj.org/article/c0b710fcf6074c2c91ebb2117858a4d5
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 56, Iss 2, Pp 129-134 (2013)
Background: Conventionally growth pattern, stromal overgrowth, stromal cellularity and stromal mitotic activity are the main parameters in the grading of phyllodes tumors (PTs). Recent studies revealed that both p53 and Ki-67 expressions are correlat
Externí odkaz:
https://doaj.org/article/66c3537e1b2841fb875c1a687a6e183b
Autor:
Ozgur Cakmak, Cemal Selcuk Isoglu, Ercument Aziz Peker, Huseyin Tarhan, Ulku Kucuk, Orcun Celik, Ferruh Zorlu, Yusuf Ozlem Ilbey
Publikováno v:
Archivio Italiano di Urologia e Andrologia, Vol 87, Iss 4, Pp 330-331 (2016)
Primary renal cell carcinomas have rarely been reported in patients with crossed fused renal ectopia. We presented a patient with right to left crossed fused kidney harbouring renal tumor. The most frequent tumor encountered in crossed fused renal ec
Externí odkaz:
https://doaj.org/article/19a0a8b0000843bb800951bed29eaa08
Publikováno v:
Case Reports in Urology, Vol 2014 (2014)
Urothelial carcinoma developing in orthotopic ileal neobladder is an extremely rare entity. Fewer than 10 cases have been reported in the literature describing urothelial carcinoma recurrence in orthotopic ileal neobladder. We report a case of transi
Externí odkaz:
https://doaj.org/article/0f086ed29dd240f0ab26aa81eed19765
Publikováno v:
Case Reports in Pathology, Vol 2012 (2012)
Giant cell angiofibroma (GCA) was initially described as a potentially recurrent tumor in the orbit of adults. However, it is now recognized that it can also present in other locations. The morphological hallmark is a richly vascularized patternless
Externí odkaz:
https://doaj.org/article/3b1db34b6477418f885908fe46e889e5
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 55, Iss 3, Pp 375-376 (2012)
Lipoid proteinosis is a rare autosomal recessive disorder of variable severity that may involve the skin, mucous membranes of the upper respiratory tract and internal organs that may display different clinical manifestations based on the site of invo
Externí odkaz:
https://doaj.org/article/739f6c3824ef4b23b1cad5788af335f5