51 research outputs found

    Cyclooxygenase-2 and Vascular Endothelial Growth Factor Expression and Their Correlation with Angiogenesis in Gastric Carcinomas

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    Amaç: Bu çalışmanın amacı, mide karsinomları ile bunların lenf nodu metastazlarında siklooksijenaz-2 (COX-2) ve vasküler endotelyal büyüme (growth) faktörü (VEGF) immün reaktivitelerini belirlemek, bunların anjiyogenezle ve histopatolojik prognostik parametrelerle olan ilişkisini araştırmaktır.Gereç ve Yöntemler: Otuz üç gastrik karsinom olgusunda immünhistokimyasal yöntemlerle COX-2, VEGF ekspresyonu ve CD34 ile belirlenen mikrodamar dansitesi (MVD) derecesi incelendi.Bulgular: COX-2 ile normal mukoza %96,9, karsinom grubu %87,8 oranında pozitif boyandı. Tümördeki COX-2 boyanma derecesi ile mukozadaki COX-2 boyanma derecesi arasında istatistiksel olarak anlamlı bir fark izlenmedi. Damar invazyonu pozitif olguların COX-2 ile lenf nodu boyanma derecesi anlamlı olarak daha yüksek idi (p<0,01). VEGF ile normal mukoza %100, karsinom grubu %93,9 oranında pozitif boyandı. Normal mukoza karsinom grubuna kıyasla VEGF ile anlamlı olarak daha yüksek oranda pozitiflik gösterdi (p=0,05). MVD derecesi tümöre kıyasla mukozada daha fazla idi (p<0,01). Kötü diferansiye karsinomlar, iyi ve orta derecede diferansiye karsinomlara göre anlamlı olarak daha yüksek MVD derecesine sahipti (p<0,05). Tümörde ve metastatik lenf nodlarında COX-2 ve VEGF ekspresyonu ile MVD derecesi arasında herhangi bir ilişki tespit edilmedi. COX-2, VEGF ve MVD derecesinin klinikopatolojik parametrelerle ilişkisi istatistiksel olarak anlamlı bulunmadı.Sonuç: Bu bulgulara göre gastrik karsinomlarda MVD derecesi artarken, tümör diferansiasyonu azalıyor olabilir, fakat COX-2 ve VEGF'nin gastrik karsinom gelişimindeki rolü henüz tam olarak anlaşılamamıştır. COX-2, VEGF ve MVD derecesinin gastrik karsinogenezis sürecindeki yerini tam olarak açığa kavuşturabilmek için daha geniş serilerle ileri çalışmalara gereksinim vardır.Objective: The aim of this study was to investigate the expression of cyclooxygenase-2 (COX-2) and vascular endothelial growth factor (VEGF) in gastric carcinomas and lymph node metastasis and their relationship with angiogenesis and prognostic histopathological parameters.Materials and Methods: COX-2 and VEGF expression and microvessel density (MVD) grade identified by antibodies against CD34 were investigated immunohistochemically in 33 patients with gastric carcinoma. Results: The expression of COX-2 was 96.9% in normal mucosa and 87.8% in gastric carcinoma. Although COX-2 expression in mucosa was higher than in carcinoma, the difference was not statistically significant. The COX-2 positivity rates in lymph nodes were significantly higher in patients with vascular invasion (p&lt;0.01). The expression of VEGF was 100% in normal mucosa and 93.9% in gastric carcinoma. VEGF levels in mucosa were significantly higher than in carcinoma (p=0.05). MVD grade in mucosa was significantly higher than in gastric carcinoma (p&lt;0.01). MVD values were significantly higher in poorly differentiated carcinomas than in well and moderately differentiated carcinomas (p&lt;0.05). There was no association between COX-2 and VEGF expression and MVD grade in tumor tissues and metastatic lymph nodes. There was no correlation of clinicopathological parameters with COX-2 and VEGF expression and MVD grade.Conclusion: Our results suggest that the MVD in gastric carcinoma may correlate with tumor grade, but the precise roles of COX-2 and VEGF in gastric cancers are not yet fully understood. Further studies with large series are needed to clarify the importance of COX-2, VEGF and MVD in cancer progression

    Cyclooxygenase-2 and Vascular Endothelial Growth Factor Expression and Their Correlation with Angiogenesis in Gastric Carcinomas

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    Objective: The aim of this study was to investigate the expression of cyclooxygenase-2 (COX-2) and vascular endothelial growth factor (VEGF) in gastric carcinomas and lymph node metastasis and their relationship with angiogenesis and prognostic histopathological parameters. Materials and Methods: COX-2 and VEGF expression and microvessel density (MVD) grade identified by antibodies against CD34 were investigated immunohistochemically in 33 patients with gastric carcinoma. Results: The expression of COX-2 was 96.9% in normal mucosa and 87.8% in gastric carcinoma. Although COX-2 expression in mucosa was higher than in carcinoma, the difference was not statistically significant. The COX-2 positivity rates in lymph nodes were significantly higher in patients with vascular invasion (p<0.01). The expression of VEGF was 100% in normal mucosa and 93.9% in gastric carcinoma. VEGF levels in mucosa were significantly higher than in carcinoma (p=0.05). MVD grade in mucosa was significantly higher than in gastric carcinoma (p<0.01). MVD values were significantly higher in poorly differentiated carcinomas than in well and moderately differentiated carcinomas (p<0.05). There was no association between COX-2 and VEGF expression and MVD grade in tumor tissues and metastatic lymph nodes. There was no correlation of clinicopathological parameters with COX-2 and VEGF expression and MVD grade. Conclusion: Our results suggest that the MVD in gastric carcinoma may correlate with tumor grade, but the precise roles of COX-2 and VEGF in gastric cancers are not yet fully understood. Further studies with large series are needed to clarify the importance of COX-2, VEGF and MVD in cancer progression

    Evaluation of amniotic fluid as a skin graft storage media compared with RPMI and saline

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    We aimed to assess and compare the histological changes of grafts stored in Roswell Park Memorial Institute-1640 solution (RPMI), amniotic fluid (AF), and saline. Amniotic fluid which has abundant nutrients, proteins, and growth factors, and antimicrobial features may be an easily achievable and cheap alternative for the short term preservation of skin grafts. Discarded surgical skin pieces obtained from 15 trauma patients were divided into three groups as RPMI, AF, and saline. The specimens were evaluated at days 7, 14, 21, and 28 for histological alterations by a 3-point scoring scale. Histological scores in the grafts stored in amniotic fluid and RPMI were found significantly lower than those stored in saline (p < 0.01). No significant difference was detected between AF and RPMI stored grafts. AF may be a good alternative for skin graft preservation as demonstrated by histological changes. New studies with multiple AF donators and repeated experiments will be worthwhile. Besides, restrictions of some ethical and legal issues for AF use should be solved. (C) 2010 Elsevier Ltd and ISBI. All rights reserved

    Pancreatic tumor metastasis to the navel in a case with three primary tumors – case report and review of the literature

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    Introduction. Sister Mary Joseph nodule (SMJN) is a metastasis that can occur in the umbilical region due to many tumors in the abdomen. Most of the cases are of gastrointestinal system origin and are often an indicator of poor prognosis. It can be seen in 1-3% of intraabdominal and pelvic malignancies. In the literature, around 300 studies are presented, mostly in the form of case reports. Very few (7-9%) of the cases with SMJN are from pancreatic origin. In our literature review, we found that in the majority (>90%) of SMJN cases due to pancreatic tumors, the lesions originated from the pancreatic tail and/or body, and tumor marker Ca-19.9 was very high in most cases (>90%). Aim. Here, the case of SMJN seen in a patient with three different primary tumors was discussed in the light of the literature data. Description of the case. Here, our case, whose third primary malignancy was detected in the pancreas in the PET/CT examination performed to investigate the origin of SMJN in a 68-year-old female patient who had undergone surgery due to breast in 2011 and endometrium cancers in 2018 and came with umbilical metastasis, is presented in the light of the literature data. Conclusion. As a result, in our case, which was followed up due to two primary tumors, it became important to know the origin of the SMJN that occurred due to the third primary tumor detected during the CT and PET/CT examination due to the newly emerging SMJN. It is important to know the origin and histopathological features of the SMJN in order to determine the treatment to the patien

    Proliferative fasciitis: A case report

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    Proliferatif fasiitis, fasiaları ve subkutanöz dokuyu tutan, sık görülmeyen benign, bir bağ doku lezyonudur. Genellikle yetişkinlerde, erkek ve kadınlarda eşit oranda, 40-70 yaş arasında sık görülür. Özellikle ön kol ve uyluk olmak üzere ekstremitelerde sık yerleşir. Histopatolojik olarak lezyon fibroblast benzeri hücreler ile ganglion benzeri büyük dev hücrelerden oluşur. Klinik olarak hızlı bü- yümesi, infiltratif büyüme paterni, hücreden zengin olması, mitoz oranının yüksek olabilmesi, dev hücrelerin varlı- ğı nedeniyle malign mezenkimal tümörlerle karışabilmektedir. Kırk beş yaşında erkek hastanın göğüs duvarı üzerinde saptanan bir kitle proliferatif fasiitis tanısı aldı. İmmunhistokimyasal olarak düz kas aktini, CD68, S-100 proteini ve CD34 ile boyanma izlenmedi. Spindle ve dev hücreler vimentin ile pozitif reaksiyon verdi.Proliferative fasciitis is a rare, benign connective tissue lesion arising from fascia and subcutaneus adipose tissue. Proliferative fasciitis is a lesion of adult life, with a peak incidence between ages 40 and 70 years. Males and females are equally affected. The majority of the lesions occurred in the extremities, especially in the forearm and the thigh. Histologically, the characteristic features of lesion are fibroblast-like cells and ganglionlike giant cells. The diffuse infiltrative growth, high cellularity, mitotic activity and presence of ganglion cell-like giant cells have led to the misinterpretation of malignant neoplasms. A 45 year-old man who developed a nodule on the chest wall diagnosed as proliferative fasciitis. The immunohistochemical study showed negativity CD68, S-100 protein, CD34 and smooth muscle actin in the cells. Vimentin immunoreactivity was detected in the spindle and giant cells
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