22 results on '"Çomunoğlu N"'
Search Results
2. Suprascapular nerve compression due to rib osteochondroma: MR imaging features
- Author
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Dikici, A.S., Bakan, S., Kandemirli, S.G., Sonmez, S., Ersen, E., Comunoglu, N., and Kantarci, F.
- Published
- 2016
- Full Text
- View/download PDF
3. Age-related histopathological changes in the cardiac conducting system in the Turkish population: an evaluation of 202 autopsy cases.
- Author
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Çomunoğlu, C., Çomunoğlu, N., Eren, B., Tanrlöver, Ö., Türkmen, N., Gündoğmuş, Ü.N., and Eren, F.
- Abstract
Background: Histopathological features of the cardiac conducting system (CCS) in the Turkish population have not been investigated previously. Material and methods: We examined CCS of 202 autopsy heart specimens dissected between the years 2004 and 2005 in Bursa Forensic Medicine Institution. Of the 202 cases from all age groups, 154 were males and 48 were females. Results: In our cases, an increase in fibrous and adipose tissue concordant with age, indicating an age-related nature, were detected. Fibrous and fatty tissue infiltration appeared at the age of 35. Fatty infiltration started between the ages 20 and 34 years at the sinoatrial node (SAN). There was no relationship between obesity and fatty tissue infiltration in SAN and atrioventricular node (AVN). In 4 cases calcification and in 19 cases inflammation was observed. Amyloid accumulation was not present. In 7 cases myocardial infarction not involving CCS was seen. In 1 case fibroelastoma was detected. Conclusions: In the Turkish population age-related fibrosis and fatty infiltration in CCS appeared at the age of 35 years and increased with age. Fatty infiltration in the SAN started at a younger age than that reported in the literature. In cases where the cause of death could not be determined, we could not detect lethal pathological features. However, we think that examination of the CCS will improve the quality of autopsy diagnosis. [ABSTRACT FROM AUTHOR]
- Published
- 2012
4. Prognostic significance of proliferative markers and apoptosis in oral dysplasia
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Tore, G., Sencift, K., Comunoglu, N., Guler, N., and Cologlu, S.
- Published
- 2007
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5. Baş-boyun spesimenleri patolojik değerlendirme ve raporlama rehberi
- Author
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CİNEL, ZELİHA LEYLA and Cinel Z. L., Gökcan M. K., Veral A., Çomunoğlu N., Soluk Tekkeşin M.
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Health Sciences ,Klinik Tıp (MED) ,Sağlık Bilimleri ,Clinical Medicine (MED) - Published
- 2021
6. The importance of hemosiderin deposition in the infant brain: an autopsy study.
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Türkmen İnanır, N., Eren, F., Akgöz, S., Eren, B., Çetin, S., Gündoğmuş, U. N., Çomunoğlu, N., and Çomunoğlu, C.
- Subjects
- *
HEMOSIDERIN , *BLOOD pigments , *BRAIN physiology , *AUTOPSY , *INFANTS - Abstract
Background/aim: Iron is an essential element involved in many metabolic processes. Presence and accumulation of iron in various body systems can result in different outcomes. Its accumulation in the central nervous system (CNS) cannot be detected routinely by application of hematoxylin-eosin staining. Detection of the presence of hemosiderin in the brain and cerebellum by application of Perls' dye is of importance in cases of infant deaths. Material and Methods: In this study, brain and cerebellar specimens obtained from 52 eligible infants (aged 0-1 years) autopsied in our institute between the y ears 2010 and 2013, independent of the cause of death, were analyzed in order to detect possible presence of hemosiderin. Perls' dye was used to detect histopathological staining intensity and distribution of hemosiderin in the brain and cerebellum. Results: Cases did not differ significantly as for the patients' age and gender (p =0.473), type of the culprit trauma (p =0.414), death/crime scene (p =0.587), and diagnosis groups (p =0.550). In this autopsy study blue colored hemosiderin granulations, stained with Perls' dye were detected in the brain (n: 39, 75%), and cerebellum (n: 35, 67.3%). A weakly negative, but significant correlation was detected between the postmortem interval and intensity values of cerebellar hemosiderin (Spearman's correlation coefficient: -0.381, p =0.024). A statistically significant difference was found between the distribution scores of cerebral hemosiderin in cases with and without trauma history (p =0.03). Median cerebral hemosiderin distribution scores were 2.5 and 2, respectively. Conclusions: The detection of a correlation between the presence of cerebral and cerebellar hemosiderin, and postmortem interval in the age group of 0-1 years, should be interpreted as an important finding in the analysis of cerebral iron. The presence of hemosiderin in the CNS may be a significant finding in the elucidation of infant deaths and this procedure should be carried out on a routine basis. [ABSTRACT FROM AUTHOR]
- Published
- 2015
7. The impact of the tumor immune microenvironment and tumor-infiltrating lymphocyte subgroups on laryngeal cancer prognosis.
- Author
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Tevetoğlu F, Çomunoğlu N, and Yener HM
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- Humans, Prognosis, Male, Female, Middle Aged, Aged, Disease-Free Survival, Carcinoma, Squamous Cell immunology, Carcinoma, Squamous Cell pathology, Carcinoma, Squamous Cell surgery, Forkhead Transcription Factors metabolism, Adult, Tumor Microenvironment immunology, Lymphocytes, Tumor-Infiltrating immunology, Lymphocytes, Tumor-Infiltrating pathology, Laryngeal Neoplasms immunology, Laryngeal Neoplasms pathology
- Abstract
The absence of improvement in survival rates across various cancers, including laryngeal cancer, has led to an increasing interest in understanding the immune response to cancer. In head and neck cancers, immune modulatory mechanisms such as immune microenvironment and immune infiltration are important in cancer pathogenesis. This study aims to explore the distribution of tumor-infiltrating lymphocyte (TIL) subgroups in the immune microenvironment and evaluate their impact on tumor histopathological characteristics and prognosis. The study included 50 patients who underwent laryngectomy for laryngeal squamous cell carcinoma, in Istanbul University - Cerrahpaşa, Faculty of Medicine Department of Otorhinolaryngology, between January 2016 and January 2018. Pathology specimens were evaluated using immunohistochemistry to assess the expressions of the CD3, CD20, CD8, CD4, CD25, and FoxP3 markers, identifying subgroups of TILs. The investigation aimed to uncover how these subgroups influence tumor histopathological features and survival outcomes. The high infiltration of CD3, CD20, and CD4 had a positive impact on disease-specific survival, disease-free survival, and recurrence-free survival. In addition, overall survival was positively affected by high CD3 and CD4 infiltrations. However, no significant relationship was observed between the expressions of CD8, FoxP3, and CD25 and any of the survival parameters. The infiltration of CD3, CD20, and CD4 positive cells indicative of a robust antitumoral immune response-emerged as favorable prognostic factors in laryngeal cancer. These findings suggest that enhancing the infiltration of CD3, CD20, and CD4 lymphocytes could be a therapeutic strategy worth exploring in clinical trials., Competing Interests: Declaration of conflicting interestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
- Published
- 2024
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8. Comparison of MRI findings of hypothalamic-optic chiasmatic gliomas and craniopharyngiomas.
- Author
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Karaman AK, Özgen KH, Korkmazer B, Hamid R, Kübra Yıldırım H, Kemerdere R, Çomunoğlu N, Tanrıöver N, Arslan S, and Kızılkılıç O
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- Humans, Male, Female, Adult, Middle Aged, Retrospective Studies, Diagnosis, Differential, Adolescent, Young Adult, Child, Aged, Hypothalamic Neoplasms diagnostic imaging, Child, Preschool, Contrast Media, Craniopharyngioma diagnostic imaging, Magnetic Resonance Imaging methods, Pituitary Neoplasms diagnostic imaging, Pituitary Neoplasms pathology, Glioma diagnostic imaging, Glioma pathology, Optic Chiasm diagnostic imaging, Optic Chiasm pathology
- Abstract
Background: Differential diagnosis of hypothalamic-optic chiasmatic gliomas (HOCGs) and craniopharyngiomas on magnetic resonance imaging (MRI) can be quite challenging., Purpose: To compare the MRI features of HOCGs and cranipharyngiomas., Material and Methods: Patients diagnosed with HOCG or craniopharyngioma in histopathological evaluation between 2012 and 2022 and who underwent preoperative contrast-enhanced brain MRI were included. Various MRI features were retrospectively evaluated for each lesion: T2-weighted imaging and fluid attenuation inversion recovery hyperintensity, calcification, cystic change, T1-weighted (T1W) imaging hyperintensity of the cystic component, hemorrhage, involvement of sellar, suprasellar or other adjacent structures, lobulated appearance, presence of hydrocephalus, and contrast enhancement pattern. Apparent diffusion coefficient (ADC) values were also evaluated and compared., Results: Among 38 patients included, 13 (34%) had HOCG and 25 (66%) had craniopharyngioma. Craniopharyngiomas had a significantly higher rate of cystic changes, calcification, and T1W imaging hyperintensity of the cystic component than HOCGs ( P <0.05). Of HOCGs, 92% had chiasm involvement, 23% had optic nerve involvement, and 31% had brain stem involvement. On the other hand, chiasm involvement was observed in 8% of craniopharyngiomas, but none had optic nerve and/or brain stem involvement ( P <0.05). While 62% (8/13) of HOCGs had diffuse homogeneous enhancement, 80% (20/25) of craniopharyngiomas had a diffuse heterogeneous enhancement pattern. Mean ADC values were significantly higher in craniopharyngiomas compared to HOCGs (2.1 vs. 1.6 ×10
-3 mm2 /s, P <0.05)., Conclusion: Although some neuroimaging findings may overlap, features such as presence of cyst and calcification, brain stem and optic pathway involvement, different enhancement patterns, and ADC values may be helpful in the differential diagnosis of HOCGs and craniopharyngiomas., Competing Interests: Declaration of conflicting interestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.- Published
- 2024
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9. The Effect of the Ganglionic Segment Inflammatory Response to Postoperative Enterocolitis in Hirschsprung Disease.
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Benibol Y, Önenerk Men AM, Hakalmaz AE, Çomunoğlu N, Topuzlu Tekant G, and Özcan R
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- Humans, Infant, Tumor Necrosis Factor-alpha, Inflammation, Risk Factors, Hirschsprung Disease complications, Hirschsprung Disease surgery, Hirschsprung Disease pathology, Enterocolitis etiology, Enterocolitis pathology, Enterocolitis surgery
- Abstract
Introduction: We examined the relationship between proinflammatory cytokines that occur in the inflammatory reaction in the intestine in Hirschsprung disease (HD) and Hirschsprung-associated enterocolitis (HAEC)., Methods: Thirty cases (M:27, F:3) operated on due to HD. The cases were divided into three groups: group 1 with pre and post operative EC, group 2 with post-operative, and group 3 with pre-operative EC. The intestinal segments were evaluated by immunohistochemistry for interleukin 1 beta (IL-1ß), tumor necrosis factor-alpha (TNF-α), and interleukin 6 (IL-6)., Results: IL-1β staining was significantly higher in the ganglionic zone of groups with enterocolitis compared to the control group ( p = 0.012). TNF-α staining in the transitional zone of Group 3 and IL-1β staining in the ganglionic zone of Group 1 was significantly higher than the control group ( p = 0.030, p = 0.020)., Conclusion: In our study, older age at diagnosis and more than 20% IL-1ß staining in the ganglionic segment were found to be risk factors for HAEC. It is noteworthy that the increase in IL-1ß can be associated with HAEC.
- Published
- 2024
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10. Germinoma Misdiagnosed as Lymphocytic Hypophysitis
- Author
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Şahin S, Başkurt O, Çomunoğlu N, Kadıoğlu P, and Gazioğlu N
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- Humans, Diagnostic Errors, Autoimmune Hypophysitis, Hypopituitarism, Germinoma diagnosis
- Published
- 2023
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11. Ewing Sarcoma Displaying Extensive Well Differentiated Neuroblastomatous Differentiation: A Case Report.
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Çomunoğlu N, Çomunoğlu C, Özcan R, and Ocak S
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- Female, Humans, Child, RNA-Binding Protein EWS genetics, Cell Differentiation, Biopsy, Biomarkers, Tumor analysis, Sarcoma, Ewing diagnosis, Sarcoma
- Abstract
Introduction: A tumor with EWSR1/FLI fusion displaying extensive well differentiated neuroblastomatous differentiation is presented., Case Report: A nine-year-old female patient had a thoracic vertebra 8 paraspinal mass. The lesion was resected incompletely. Histopathologically, a small round cell tumor with gangliomatous differentiation was seen. This was initially diagnosed as an intermixed ganglioneuroblastoma. In the completion surgery biopsy material, the small round cell component was more prominent. Immunohistochemistry for both samples showed membrane positivity for CD99 and nuclear positivity for NKX2.2 in the small round cell component of the tumor. Molecular analysis revealed EWSR1/FLI fusion. The diagnosis then considered a "Ewing Sarcoma Displaying Extensive Well Differentiated Neuroblastomatous Differentiation"., Conclusion: Tumors with the EWSR1/FLI fusion may show neuroblastomatous differentiation. We chose to treat this as an Ewing Sarcoma (ES). Recognition of this phenomenon in ES cases may prevent a possible misinterpretation and a failure in oncologic treatment.
- Published
- 2023
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12. Machine learning as a clinical decision support tool for patients with acromegaly.
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Sulu C, Bektaş AB, Şahin S, Durcan E, Kara Z, Demir AN, Özkaya HM, Tanrıöver N, Çomunoğlu N, Kızılkılıç O, Gazioğlu N, Gönen M, and Kadıoğlu P
- Subjects
- Humans, Insulin-Like Growth Factor I metabolism, Machine Learning, Retrospective Studies, Treatment Outcome, Acromegaly metabolism, Acromegaly surgery, Adenoma metabolism, Adenoma surgery, Decision Support Systems, Clinical, Growth Hormone-Secreting Pituitary Adenoma metabolism, Growth Hormone-Secreting Pituitary Adenoma surgery, Human Growth Hormone
- Abstract
Objective: To develop machine learning (ML) models that predict postoperative remission, remission at last visit, and resistance to somatostatin receptor ligands (SRL) in patients with acromegaly and to determine the clinical features associated with the prognosis., Methods: We studied outcomes using the area under the receiver operating characteristics (AUROC) values, which were reported as the performance metric. To determine the importance of each feature and easy interpretation, Shapley Additive explanations (SHAP) values, which help explain the outputs of ML models, are used., Results: One-hundred fifty-two patients with acromegaly were included in the final analysis. The mean AUROC values resulting from 100 independent replications were 0.728 for postoperative 3 months remission status classification, 0.879 for remission at last visit classification, and 0.753 for SRL resistance status classification. Extreme gradient boosting model demonstrated that preoperative growth hormone (GH) level, age at operation, and preoperative tumor size were the most important predictors for early remission; resistance to SRL and preoperative tumor size represented the most important predictors of remission at last visit, and postoperative 3-month insulin-like growth factor 1 (IGF1) and GH levels (random and nadir) together with the sparsely granulated somatotroph adenoma subtype served as the most important predictors of SRL resistance., Conclusions: ML models may serve as valuable tools in the prediction of remission and SRL resistance., (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Published
- 2022
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13. Role of Immunohistochemistry in the Differential Diagnosis of Pediatric Renal Tumors: Expression of Cyclin D1, Beta-Catenin , PDGFR-Alpha, and PTEN.
- Author
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Kepil N, Batur Ş, Kain ZE, Özcan G, Emre Ş, Özcan R, Celkan TT, and Çomunoğlu N
- Subjects
- Biomarkers, Tumor metabolism, Child, Cyclin D1 metabolism, Diagnosis, Differential, Female, Humans, Immunohistochemistry, Male, PTEN Phosphohydrolase, Receptor, Platelet-Derived Growth Factor alpha, beta Catenin metabolism, Kidney Neoplasms pathology, Sarcoma, Clear Cell pathology, Wilms Tumor diagnosis
- Abstract
Objective: Pediatric renal tumors overlap histomorphologically and may cause misdiagnosis. We aimed to determine the role of immunohistochemical staining of Cyclin D1, PTEN, beta-catenin and PDGFR-alpha on pediatric renal tumors., Material and Method: Thirty-six cases of 8 different tumors were included in the study. Four blocks of paraffin tissue microarray were constructed. Cyclin D1, PTEN, beta-catenin and PDGFR-alpha were used in all cases. Staining intensity and extent were graded., Results: All cases of clear cell sarcoma (CCS) and epithelial components of Wilms tumor (WT) showed immunopositivity for Cyclin D1 but blastemal and stromal components of WT were negative. All cases of CCS and most cases of WT consisting of blastemal and stromal components demonstrated loss of expression with PTEN., Conclusion: Cyclin D1 is not a specific immunohistochemical marker due to its strong and diffuse positivity in CCS cases. It may be useful to differentiate CCS from blastemal and stromal components of WT. Other markers except cyclin D1 do not have a role in the differential diagnosis.
- Published
- 2022
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14. Primitive neuroectodermal tumor in a child with Currarino syndrome.
- Author
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Çebi MN, Yılmaz G, Çelikdemir G, Özcan R, Ocak S, Celkan TT, and Çomunoğlu N
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- Anal Canal abnormalities, Anal Canal pathology, Anal Canal surgery, Child, Female, Humans, Infant, Rectum abnormalities, Rectum pathology, Sacrum abnormalities, Syringomyelia, Digestive System Abnormalities diagnosis, Digestive System Abnormalities surgery, Neuroectodermal Tumors, Primitive diagnosis, Neuroectodermal Tumors, Primitive surgery, Teratoma diagnosis
- Abstract
Background: Curarino syndrome is a rare and complex anomaly with the triad of anorectal malformation, presacral mass and sacral bone deformation. The most common cause of the presacral mass is meningioma, but teratoma is the diagnosis in about one-third of the cases. Malignant transformation of teratoma in the form of carcinoma, rhabdomyosarcoma and leukemia have previously been reported on rare occasions., Case: A 19 month-old-girl was referred with a presacral mass of 29mm x 23mm x 24mm. She was diagnosed as Currarino syndrome. The presacral mass was surgically resected and pathological examination revealed a foci of primitive neurectodermal tumor., Conclusions: This is the first case of Currarino syndrome with a primitive neuroectodermal tumor (PNET) foci in the presacral mass. Considering the risk of malignant transformation, the accurate pathological examination is important for complete systemic evaluation and treatment plan in these children.
- Published
- 2022
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15. The Use of Three-Dimensional Printed Technology for Mandibular Reconstruction in a Rare Case of Giant Odontogenic Myxofibroma.
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Yilmaz YZ, Elkhatroushi T, Erdur ZB, Karaaltin MV, Çomunoğlu N, and Batioğlu-Karaaltin A
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- Fibula, Humans, Mandible, Technology, Fibroma, Free Tissue Flaps, Mandibular Neoplasms diagnostic imaging, Mandibular Neoplasms surgery, Mandibular Reconstruction, Odontogenic Tumors diagnostic imaging, Odontogenic Tumors surgery
- Abstract
Abstract: Odontogenic myxofibroma is a benign odontogenic tumor of mesenchymal tissue that generally originates from the mandible. It is an extremely rare tumor accounting for approximately 2% of all odontogenic tumors. In this report, the authors presented a giant right mandibular mass that extends to the angle of the mandible and displacing the tongue laterally caused significant malocclusion, pain, and impaired oral intake. The tumoral involvement of the mandibula required a partial mandibulectomy with the resection of right mandibular ramus, body, and bilateral parasymphysis. Right mandibular condyle was preserved. The mandibular defect was reconstructed with a fibula free flap. Three-dimensional printed maxillofacial bone model of the patient was used as contour modeling and guide. Histopathologic examination confirmed the diagnosis as odontogenic myxofibroma.The purpose of the report is to present a very rare case of odontogenic myxofibroma and its general characteristics, radiological features, differential diagnosis, surgical management, and the use of three-dimensional printing technology in the field of mandibular reconstruction., Competing Interests: The authors report no conflicts of interest., (Copyright © 2021 by Mutaz B. Habal, MD.)
- Published
- 2021
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16. Bilateral Synchronous Testicular Germ Cell Tumors in Children: Case Report and Review of the Literature.
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Kebudi R, Sezer A, Eliçevik M, Ocak S, Çomunoğlu N, Birgen D, Kervancıoğlu ME, and Kuruğoğlu S
- Subjects
- Humans, Infant, Male, Tissue Preservation methods, Treatment Outcome, Ultrasonography methods, alpha-Fetoproteins analysis, Cryopreservation methods, Neoplasms, Germ Cell and Embryonal blood, Neoplasms, Germ Cell and Embryonal pathology, Neoplasms, Germ Cell and Embryonal surgery, Neoplasms, Multiple Primary blood, Neoplasms, Multiple Primary pathology, Neoplasms, Multiple Primary surgery, Orchiectomy methods, Organ Sparing Treatments methods, Teratoma blood, Teratoma pathology, Teratoma surgery, Testicular Neoplasms blood, Testicular Neoplasms pathology, Testicular Neoplasms surgery, Testis diagnostic imaging, Testis pathology, Testis surgery
- Abstract
Bilateral testicular tumors are very rare in pediatric patients and only a few case reports have been reported. These patients have a high risk of sterility due to bilateral orchiectomy and subsequent gonadotoxic treatments. Therefore, if possible, testis-sparing surgery should be performed in patients with benign masses and testicular tissue preservation may be recommended in order to maintain fertility in later life. We present a 23 months old boy with synchronous bilateral testicular tumor managed with unilateral orchiectomy and testis-sparing surgery and testicular tissue cryopreservation performed to the controlateral side. We also review the literature on bilateral testis tumors in children., (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Published
- 2020
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17. An Unusual Presentation of Carney Complex
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Dağdeviren Çakır A, Turan H, Celkan T, Çomunoğlu N, Ercan O, and Evliyaoğlu O
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- Child, Humans, Male, Bone Neoplasms diagnosis, Bone Neoplasms etiology, Bone Neoplasms genetics, Carney Complex complications, Carney Complex diagnosis, Carney Complex genetics, Cyclic AMP-Dependent Protein Kinase RIalpha Subunit genetics, Osteochondroma diagnosis, Osteochondroma etiology, Osteochondroma genetics, Sertoli Cell Tumor diagnosis, Sertoli Cell Tumor etiology, Sertoli Cell Tumor genetics, Testicular Neoplasms diagnosis, Testicular Neoplasms etiology, Testicular Neoplasms genetics
- Abstract
Carney complex (CNC) is a multiple neoplasia syndrome, characterized by pigmented lesions of the skin and mucosa, cardiac, cutaneous and other myxomas and multiple endocrine and non-endocrine tumors. Most of the cases have an inactivating mutation in the PRKAR1A gene. Osteochondromyxoma (OMX) is an extremely rare myxomatous tumor of bone, affecting 1% of CNC patients. Large cell calcifying Sertoli cell tumor (LCCSCT) is a testicular tumor affecting more than 75% of males with CNC. Here, we report an atypical case of CNC without typical pigmented skin lesions, presenting with a bone based tumor as the first manifestation. Initial presentation was for a recurrent, locally invasive intranasal tumor without definite diagnosis. Further clinical developments during follow up, central precocious puberty and testicular tumor with calcification, led to the diagnosis of LCCSCT, a CNC-related tumor. Histopathologic examination of the intranasal tumor was re-evaluated with this knowledge and OMX was diagnosed. Coexistence of OMX and LCCSCT suggested CNC. Genetic analysis revealed a heterozygous non-sense p.Trp 224* (c.672G>A) in the PRKAR1A gene. In our case, the diagnosis of OMX was delayed, because it is extremely rare and little is known about this tumor. Thus the aim of this report was to alert other clinicians to consider CNC if OMX is diagnosed.
- Published
- 2020
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18. Adrenal masses in children: Imaging, surgical treatment and outcome.
- Author
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Emre Ş, Özcan R, Bakır AC, Kuruğoğlu S, Çomunoğlu N, Şen HS, Celkan T, and Tekant GT
- Subjects
- Adolescent, Adrenal Cortex Neoplasms diagnostic imaging, Adrenal Cortex Neoplasms pathology, Adrenal Gland Diseases diagnostic imaging, Adrenal Gland Diseases pathology, Adrenal Gland Neoplasms diagnostic imaging, Adrenal Gland Neoplasms pathology, Animals, Child, Child, Preschool, Female, Ganglioneuroblastoma diagnostic imaging, Ganglioneuroblastoma pathology, Ganglioneuroma diagnostic imaging, Ganglioneuroma pathology, Hematoma diagnostic imaging, Hematoma pathology, Hemiptera, Humans, Infant, Male, Neuroblastoma diagnostic imaging, Neuroblastoma pathology, Pheochromocytoma diagnostic imaging, Pheochromocytoma pathology, Retrospective Studies, Risk Factors, Adrenal Cortex Neoplasms surgery, Adrenal Gland Diseases surgery, Adrenal Gland Neoplasms surgery, Ganglioneuroblastoma surgery, Ganglioneuroma surgery, Hematoma surgery, Neuroblastoma surgery, Pheochromocytoma surgery
- Abstract
Background/objective: This study aims to evaluate the current surgical approach to adrenal masses in the pediatric age group., Methods: We retrospectively analyzed cases that underwent surgery for adrenal masses between 2007 and 2017. Patients were assessed regarding age, sex, primary diagnosis, image defined risk factors (IDRF), surgical treatment method, complications, duration of hospital stay, and follow-up., Results: We examined 50 patients who underwent surgery for adrenal mass (mean age: 4.8 years; range: 5 days-14 years). For IDRF assessment, Ultrasonography was used in 42, Computed Tomography in 36, and Magnetic Resonance Imaging in 36 patients. Lesions were present on the right in 25, left in 21, and bilateral in 4 patients. Histopathological findings were neuroblastoma (n = 29), ganglioneuroma (n = 6), adrenal cortex tumor (n = 5), ganglioneuroblastoma (n = 4), pheochromocytoma (n = 3), cyst (n = 1), and adrenal hematoma (n = 2). Laparotomy was performed on 37 patients, and laparoscopy on 13 patients. None of the cases had any operative complications., Conclusion: The crucial factors determining the surgical approach to adrenal masses in pediatric cases are the histopathology of the mass, volume, and IDRF. Minimally invasive procedures could be reliably performed in appropriate cases., (Copyright © 2019. Published by Elsevier Taiwan LLC.)
- Published
- 2020
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19. The investigation of hyaluronic acid and hyaluronidase-1 levels as tumour marker in larynx cancer.
- Author
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İnan HC, Yener M, Buyru N, Çelebi A, Yilmaz M, and Çomunoğlu N
- Subjects
- Adult, Aged, Aged, 80 and over, Biomarkers, Tumor metabolism, Carcinoma, Squamous Cell pathology, Female, Humans, Laryngeal Neoplasms pathology, Male, Middle Aged, Prospective Studies, Carcinoma, Squamous Cell metabolism, Hyaluronic Acid metabolism, Hyaluronoglucosaminidase metabolism, Laryngeal Neoplasms metabolism
- Abstract
Objective: The purpose of this study was to investigate the hyaluronic acid (HA) and hyaluronidase-1 (HYAL-1) levels in laryngeal cancer patients., Study Design: Prospective, controlled clinical trial., Setting: University Medical Center., Participants: Fifty laryngeal squamous cell carcinoma patients and 50 volunteers who gave saliva samples investigated prospectively between 2016 and 2017., Methods: Hyaluronidase-1 expression was measured by RT-PCR in normal and tumour tissue samples; hyaluronic acid values of saliva and tumour tissues were measured by ELISA method., Results: HYAL-1 expression increased 2.5-fold in tumour tissues compared to normal tissues, and the difference was statistically significant (P < 0.001).Mean saliva HA levels were 103.93 ± 69.04 ng/mL and 177.29 ± 98.44 ng/mL in the patients and controls' saliva specimens, respectively. The difference was not statistically significant (P = 0.657). HA levels were higher in tumour tissue samples than saliva samples, but there was not statistically significant difference between saliva and tumour tissue HA levels., Conclusion: HYAL-1 expression in laryngeal squamous cell carcinomas is elevated compared to normal tissues of same patients. Targeting this gene and HA catabolism products may use treatment of larynx cancer in the future., (© 2019 John Wiley & Sons Ltd.)
- Published
- 2019
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20. Histopathology of giant cell tumors of the bone: With special emphasis on fibrohistiocytic and aneurysmal bone cyst like components.
- Author
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Çomunoğlu N, Kepil N, and Dervişoğlu S
- Subjects
- Adult, Age Factors, Diagnosis, Differential, Female, Humans, Male, Neoplasm Staging, Orthopedic Procedures adverse effects, Orthopedic Procedures methods, Radiography methods, Retrospective Studies, Sex Factors, Turkey epidemiology, Bone Cysts, Aneurysmal diagnosis, Bone Cysts, Aneurysmal pathology, Bone Neoplasms diagnosis, Bone Neoplasms pathology, Femur diagnostic imaging, Femur pathology, Giant Cell Tumor of Bone diagnosis, Giant Cell Tumor of Bone pathology, Neoplasm Recurrence, Local epidemiology, Neoplasm Recurrence, Local pathology, Tibia diagnostic imaging, Tibia pathology
- Abstract
Objective: The aim of this study was to define histopathological features of giant cell tumor of bone, especially accompanying fibrohistiocytic or aneurysmal bone cyst like components, in the light of our institutions experience., Methods: A total of 120 cases (64 females and 56 males; mean age: 36.2 (12-80)) with 'GCT' diagnosed between the years 1996-2016 were included in this retrospective analysis. Cases were evaluated according to clinical features such as age, gender, localization, recurrence, metastasis and histopathological features., Results: Tumors were localized most frequently at proximal tibia and distal femur, respectively. In 11 cases areas rich in fibrohistiocytic component and in 20 cases aneurysmal bone cyst like component were observed. In 2 cases both components were present. Twenty three cases recurred. In 1 case which was primarily located at calcaneus, tumor metastasized to lung 4 years later during follow-up., Conclusion: GCT can be confused with other tumor or tumor-like lesions involving giant cells. Secondary changes such as fibrohistiocytic or aneurysmal bone cyst-like components and coagulation necrosis were frequently seen in conventional giant cell tumor of bone. For tumors having prominent fibrohistiocytic and/or aneurysmal bone cyst-like components, in order to detect characteristic areas representing GCT, additional sampling is essential. Although secondary histopathological changes do not appear to affect clinical outcome, these features are important in differential diagnosis. Approximately one fifth of GCT cases show recurrence and sacrum and foot bones were the most frequent sites for recurrence., Level of Evidence: Level IV, diagnostic study., (Copyright © 2018 Turkish Association of Orthopaedics and Traumatology. Production and hosting by Elsevier B.V. All rights reserved.)
- Published
- 2019
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21. Osteosarcoma of the Ethmoid Sinus.
- Author
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Erdur ZB, Gözen ED, Inan HC, Yener HM, Çomunoğlu N, Yol C, Papila Ç, and Cansiz H
- Subjects
- Adult, Bone Neoplasms diagnostic imaging, Bone Neoplasms pathology, Ethmoid Sinus diagnostic imaging, Ethmoid Sinus pathology, Female, Humans, Magnetic Resonance Imaging, Osteosarcoma diagnostic imaging, Osteosarcoma pathology, Paranasal Sinus Neoplasms diagnostic imaging, Paranasal Sinus Neoplasms pathology, Tomography, X-Ray Computed, Bone Neoplasms surgery, Ethmoid Sinus surgery, Osteosarcoma surgery, Paranasal Sinus Neoplasms surgery
- Abstract
Osteosarcoma (OS) is a malignant bone tumor and it is very rare in head and neck region. If it arises in this area, most common localizations of this tumor are mandible and maxilla and ethmoid sinus is very rare site for this malignancy. A 43-year-old female admitted to our clinic with the complaint of pain in the right half of the face and headache persisting for 2 months. According to the clinical symptoms and imaging studies, sinonasal ossifying fibroma was suspected. For this reason, patient was operated endoscopically and histopathological examination revealed that osteoid matrix producing atypical osteoblastic cells so these findings identified osteoblastic variant OS. This article is about a very rare case of OS of ethmoid sinus. The differential diagnosis, general characteristics, and classification of this tumor, radiological features, and surgical techniques are also presented.
- Published
- 2018
- Full Text
- View/download PDF
22. Simvastatin reduces VEGF and NO levels in acute stages of experimental traumatic brain injury.
- Author
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Yüksel H, Yavuz Ö, Iş M, Çomunoğlu N, Üzüm G, Akyüz F, and Yıldırım HA
- Subjects
- Acute Disease, Animals, Brain Injuries blood, Brain Injuries pathology, Male, Rats, Rats, Wistar, Anticholesteremic Agents therapeutic use, Brain Injuries drug therapy, Nitric Oxide blood, Simvastatin therapeutic use, Vascular Endothelial Growth Factor A blood
- Abstract
This study was undertaken to evaluate the effect of simvastatin, a cholesterol-lowering agent, on vascular endothelial growth factors (VEGFs), nitric oxide (NO) levels and neuroprotection, in rats with experimentally induced traumatic brain injury (TBI). Forty Wistar albino rats were categorized into four groups: sham operated (S), trauma (T), trauma + vehicle (T + V) and trauma + simvastatin (T + S). The T, T + V and T + S groups were subjected to TBI. The T + V group was administered vehicle [ethanol:saline (1/2)] and the T + S group was administered 1 mg/kg of simvastatin 3 h after the injury insult. Blood and brain tissue specimens were obtained 24 h after the trauma to measure VEGFs and NO levels and perform histopathological examinations. The histopathological injury scores of brain tissues were significantly higher in the T group, and simvastatin significantly prevented brain injury in the T + S group. In the T group, significant increases of VEGF levels in serum and brain tissues were noted, which were prevented with simvastatin treatment in the T + S group. The markedly high levels of NO in brain tissues of the T group were decreased by simvastatin treatment in the T + S group. It can be concluded that, as evidenced by histopathological findings, simvastatin treatment improves neuropathology in acute stages of TBI.
- Published
- 2013
- Full Text
- View/download PDF
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