Browsing by Author "Kotan, C"
Now showing 1 - 7 of 7
- Results Per Page
- Sort Options
Conference Object Clinical Characteristics and Genetic Screening of an Extended Family With Men2a(Editrice Kurtis S R L, 2002) Algün, E; Abaci, N; Kösem, M; Kotan, C; Köseoglu, B; Boztepe, H; Aksoy, HMEN-2A is characterized by medullary thyroid carcinoma (MTC) with pheochromocytoma and sometimes parathyroid adenoma. In affected members of the family, the risk of MTC is about 100%. Biochemical screening allows tumors to be detected early but even at this stage treatment is not always curative. Missense mutations in exon 10 and 11 of the RET proto-oncogene are associated with MEN2A. Early detection of this mutation by DNA analysis allows the identification of the carriers of the gene. We performed genetic screening in 88 members of an extended family with MEN2A and found 18 members positive for RET mutation (Cys634Gly). Only three of these 18 RET positive cases had a previous diagnosis of medullary cancer and/or pheochromocytoma. Up to now, 12 of the RET positive cases have undergone thyroidectomy. There was extended disease with cervical lymph node metastasis in 6 of them, bilateral medullary microcancer in 3 and c-cell hyperplasia in the remaining 3. Three of the 18 RET positive patients had also pheochromocytoma. Primary hyperparathyroidism was present in only one patient. The mean age of diagnosis of medullary cancer was between 25-50 yr and mean age of death was between 35-95 yr in affected members of the family. The family had many other affected members in other cities in Turkey and in other countries throughout the world from Australia to the Netherlands. So this family is perhaps one of the most extended families with MEN2A. (C) 2002, Editrice Kurtis.Article Extrahepatic Biliary Obstruction Caused by Small-Cell Lung Cancer(Taylor & Francis Ltd, 2001) Kotan, C; Er, M; Özbay, B; Uzun, K; Barut, I; Ozgoren, EThe pancreas is a rare site of metastasis from small-cell lung cancer (SCLC). We present the case of a pancreatic metastasis of small-cell lung, cancer associated with jaundice, in which, initially, the case was evaluated as a primary pancreatic carcinoma and pancreaticoduodenectomy was performed. We also review the reported cases of pancreatic metastases from SCLC.Article A Human Fasciolosis Presenting With Cholelithiasis and Choledocholithiasis in Van, Turkey(Saudi Med J, 2004) Yilmaz, H; Kotan, C; Soylemez, O; Arslanturk, HArticle Mri Findings of Hepatic Alveolar Echinococcosis(Elsevier Science inc, 2003) Harman, M; Arslan, H; Kotan, C; Etlik, O; Kayan, M; Deveci, ADiagnosis of liver infestation by alveolar echinococcosis (AE) is based on serologic, sonographic and computed tomography (CT) findings. Experience with magnetic resonance imaging (MRI) demonstrates that features of this disease are limited. CT and MRI findings of 14 cases with hepatic AE were compared in this report. We have described the MRI appearance of hepatic AE, which exhibits variable signal intensities on T1- and T2-weighted images. Fibrous and parasitic tissue showed low signal both on T1- and, generally, on T2-weighted images. In a few cases, a high signal on T2-weighted images may be observed, due either to central necrotic zones or to small peripheral cyst. MRI than by CT was more easily identified central necrosis. However, MRI seemed to be less effective than CT in allowing us to reach a positive diagnosis, due to its inability to show microcalcifications. In addition, MRI may not reveal small lesions. In most cases, T1-weighted images revealed more clearly than CT did the margins of the lesions and the hepatic extension, especially to hepatic veins, vena cava and perihepatic spaces. (C) 2003 Elsevier Inc. All rights reserved.Article Mucinous Appendicular Cystadenocarcinoma During Pregnancy - a Case Report(Sci Printers & Publ inc, 2003) Zeteroglu, S; Kotan, C; Ozen, S; Goktolga, UBACKGROUND: Primary appendicular adenocarcinoma is a rare type of appendicular carcinoma. We report mucinous appendicular adenocarcinoma during pregnancy. To our knowledge, this is the third reported case. CASE: A 35-year-old woman at 21 weeks of gestation presented with acute abdominal symptoms for the previous 10 days and underwent appendectomy. Histopathologically, examination of the appendectomy material was reported as "mucinous appendicular cystadenocarcinoma." The pregnancy was terminated by misoprostol induction. A right hemicolectomy and staging procedure were performed on the third postpartum day with relaparotomy. CONCLUSION. Although it rarely coexists with pregnancy, primary appendicular adenocarcinoma should be considered in pregnant women with atypical acute abdominal symptoms of long duration. Primary adenocarcinoma of the appendix should be treated with right hemicolectomy even if it is a secondary procedure. Termination of pregnancy is not essential to the surgical procedure, and the decision on the outcome of the pregnancy should be made with the patient.Article Peritoneal Hydatid Cyst: an Unusual Cause of Abdominal Pain in a Haemodialysis Patient(Oxford Univ Press, 2006) Sayarlioglu, H; Erkoc, R; Soyoral, Y; Etlik, O; Dogan, E; Kotan, CArticle Primary Malignant Fibrous Histiocytoma Presenting as an Intussusception: Report of the Small Intestine of a Case(Springer, 2002) Kotan, C; Kosem, M; Alici, S; Ilhan, M; Tuncer, I; Harman, MMalignant fibrous histiocytoma occurs most commonly in the extremities and trunk, but rarely in the visceral organs. Malignant fibrous histiocytoma of the small intestine is an extremely rare condition. To our knowledge, only ten cases of primary tumors involving the small intestine have been described up to now. Among them only one case has been reported to lead to intussusception. This case report documents the appearance of a storiform-pleomorphic type primary malignant fibrous histiocytoma of the ileum, which led to intussusception, in a 58-year-old man with a 3-month history of dyspepsia, weight loss, general fatigue, and nonspecific abdominal pain. The patient was well with no sign of disease at 8 months after surgery. The clinical and pathologic characteristics of malignant fibrous histiocytoma of the small intestine as found in the literature are also reviewed.