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Öğe Auricular mucormycosis: a case report.(2007) Oktay M.F.; Askar I.; Kilinç N.; Tuzcu A.; Topçu I.Mucormycosis is a rare, saprophytic, invasive, and fulminant fungal disease. It occurs in immunocompromised patients such as those with diabetes mellitus or blood dyscrasia, or in patients under immunosuppressive therapy. A 17-year-old female patient with diabetic ketoacidosis presented with a black-colored lesion in the auricle and external ear canal. Physical examination showed necrosis of the auricle, external ear canal, and neighboring skin. She also had facial paralysis. Debridement of the necrotic tissues was performed and the samples were submitted for microbiologic and histopathologic examination, which showed nonseptate hyphae. Postoperatively, systemic amphotericin B was empirically administered. The patient died on the seventh day.Öğe A case of solitary angiokeratoma circumscriptum of the tongue.(2007) Yildirim M.; Kilinç N.; Oktay M.F.; Topçu I.Angiokeratoma circumscriptum is an uncommon vascular entity. The lesion is present at birth and usually involves the lower extremities. A 9-year-old girl presented with multiple pink-colored, small-raised lesions in the dorsal part of her tongue, which had been present since birth. There was no history of trauma, cold injury, or similar lesions elsewhere in her body. She complained of pain and rare bleeding from the lesions after eating hard foods. Physical examination showed multiple, grouped, erythematous, shiny papules mostly in the dorsal aspect of the tongue. There were no other lesions in other parts of the oral mucosa. After an incisional biopsy of the lesion, the diagnosis was made as solitary angiokeratoma circumscriptum.Öğe Cavernous hemangioma of the uterus: (A case report)(2002) Uzunlar A.K.; Yilmaz F.; Kilinç N.; Arslan A.Cavernous hemangioma of the uterus is an extremely rare lesion. We report a postmenopausal patient with abnormal uterine bleeding due to hemangioma and simple endometrial hyperplasia.Öğe Fraser syndrome: Two cases report(2007) Kilinç N.; Etem H.Fraser syndrome (cryptophthalmos syndactyly syndrome) is a rare autosomal recessive disorder. The main features are cryptophthalmos (hidden eye), ear, nose and skeletal malformations, syndactyly, laryngeal stenosis and malformation of the uro-genital system, lungs, liver and central nervous system. Renal anomalies (uni-or bilateral agenesis) occur in 85 per cent. These anomalies were first documented by Fraser in 1962. Two Fraser syndrome cases diagnosed as normal spontan vaginal post delivery without prenatal following were presented rarely in the light of the literature knowledge.Öğe Massive hemolysis due to dacron patch leakage following repair of ventricular septal defect(2006) Göz M.; Çakir Ö.; Kilinç N.; Eren M.N.Massive hemolysis following closure of a ventricular septal defect (VSD) is rarely encountered complication. In this article, a case of 30 years-old male developed a severe degree of intravascular hemolysis within 24 hours due to residual shunt after a Dacron patch closure of ventricular septal defect. In early period, corticosteroid treatment was effective. To report, we discussed that corticosteroid therapy can be attempted before early reoperation.Öğe Mucinous tumors of the ovary: Analysis of 38 cases(2001) Yaldiz M.; Uzunlar A.K.; Kilinç N.; Yalinkaya A.; Akkuş M.; Tunik S.Ovarian mucinous tumors stem from ovarian surface epithelium and are divided into benign, borderline and malignant. It is difficult to differentiate borderline and malignant mucinous tumors. Thirty-eight cases of ovarian mucinous tumors which were diagnosed at the Pathology Department of Dicle University Medical Faculty were reviewed. Of these, 18 (47.3%), six (15.7%) and 14 (36.8%) were benign, borderline and malignant, respectively. The patients' ages ranged from 18 to 67 (average 44.5) years. Bilaterality was detected in 1/18 (5.5%), 0/6 and 4/14 (28.5%) of benign, borderline and malignant mucinous tumors, respectively. Mean tumor size was 26.4 cm. Microscopically, there was no stratification in the benign tumors. The borderline tumors had papillary infoldings and 2-3 layers of atypical epithelial cells but no invasion of the stroma. Malignant tumors had four or more layers of atypical epithelial cells and stromal invasion.Öğe Nevoid hyperkeratosis of the nipple and areola: Case report(2001) Kilinç N.; Yaldiz M.; Yilmaz F.; Akdeniz S.; Özekinci S.Nevoid hyperkeratosis of the nipple and areola is a rare benign condition of unknown etiology, Its characteristic properties are verrucous thickening and brownish discoloration of the nipple and areola. In microscopic examination, hyperkeratosis, papillomatosis and acanthosis with keratotic plugging were observed and nevoid hyperkeratosis was diagnosed. We discussed this rare condition in the light of current literature.Öğe Nondecidualized and decidualized endometriosis of the abdominal wall: A report of two cases secondary to cesarean section(2002) Kilinç N.; Yalinkaya A.; Özaydin M.[No abstract available]Öğe p53, c-erbB-2 expression and steroid hormone receptors in breast carcinoma: Correlations with histopathological parameters(2004) Kilinç N.; Yaldiz M.Objective: The aim of the study was to evaluate the p53 tumor suppressor gene, c-erbB-2 and steroid hormone receptor expression in breast carcinoma by immunohistochemistry and to correlate them with different histopathologic parameters. Materials and Methods: p53, c-erbB-2, steroid hormone receptors and their correlation with age, tumor size, histological grade, axillary lymph-node status, and menopausal status were investigated in 65 breast carcinoma cases. All markers were measured immunohistochemically on paraffin sections. Association between estrogen receptor (ER), progesterone receptor (PgR), p53 and c-erbB-2 expression and clinicopathologic variables were assessed by the chi-square test for qualitative parameters. Results: c-erbB-2 staining was found in 35.3% of breast carcinomas and was associated with ductal subtype and age under 35 (p = 0.022, p = 0.003, respectively); p53 staining was seen in 27.6% of cases and was associated with high histological grade and postmenapausal status (p = 0.038, p = 0.002, respectively). Progesterone receptor expression was associated with positive axillary status (p = 0.003). Conclusion: We concluded that expressions of c-erbB-2, p53, ER, and PgR may be used in the evaluation of breast carcinoma. Therefore the present study suggests that p53 expression is a marker of high histological grade in postmenopausal status, and that c-erbB-2 expression is associated with histologically ductal subtype.Öğe Pleomorfic carcinoma: A rare case of lung cancer(2008) Özçelik C.; Avci A.; Kilinç N.; Onat S.Pleomorphic carcinoma is a rare epithelial malignant tumor. Pulmonary pleomorphic carcinoma was introduced by the 1999 World Health Organization classification as a new peculiar type of lung carcinoma showing concurrent malignant epithelial and sarcomatoid spindle cell elements. Rarely seening, advange age, male sex dominance, upper lobe involvement, big sized (more than 7 cm.) at time of diagnosis , and poor prognosis are the characteristics of it. We are reporting 63-year-old man with pleomorfic carcinoma in the left lower lobe who was treated by left pneumonectomy.Öğe Post cesarean section necrotizing fasciitis: Case report(2006) Demir B.; Kilinç N.; Gul? T.Necrotizing fasciitis is a rare severe, acute, rapidly progressive, and potentially life threatening condition caused by bacterial infection of the soft tissued. This infection is characterized by extensive necrosis of superficial fascia and subcutaneous tissue and extreme systemic toxicity. Treatment of this lethal infection includes broad spectrum antiobitics and extensive surgicial debridement. As it is a rare condition, a case of necrotizing fasciitis which appeared post cesarian section is reported with a review of the literature.Öğe Primary gastric choriocarcinoma: Case report(2000) Bayhan G.; Yaldiz M.; Yalinkaya A.; Kilinç N.; Gül T.; Erden A.C.[No abstract available]
