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Öğe Congenital fibrous epulis in the infant(Yonsei Univ Coll Medicine, 2002) Inan, M; Yalçin, Ö; Pul, MCongenital fibrous epulis is an extremely rare tumor of infancy. It is a benign gingival tumor and generally seen in maxillary alveolar crest and its etiology remains the subject of debate. Congenital fibrous epulis could be considered a hamartomatous lesion. Histologically it does not show the closely packed large granular cells necessary for the diagnosis of an ordinary congenital epulis. Instead, it consists of irregular bundles of collagenous connective tissue, varying numbers of fusiform cells with oval or fusiform shaped nuclei and mild subepithelial inflammatory infiltration with tiny blood vessels and in this case a woven bone spicule in the deep area. Recommended treatment for this tumor is simple excision. We report upon a case of congenital fibrous epulis in a male infant and discuss the clinical features, histopathologic findings, and surgical treatment.Öğe Lipoblastoma: a rare cervical mass in childhood(Elsevier Sci Ireland Ltd, 2001) Basaran, UN; Inan, M; Bilgi, S; Pul, MA 4-year-old girl had a left side cervical swelling for three months. The mass was free from surrounding tissues and excised completely. Histopathologic diagnosis of the specimen was lipoblastoma. Cervical lipoblastoma is a rapidly growing neoplasm. Only two cases of cervical lipoblastomas caused airway obstruction have been reported. Recurrence is rare in cases of lipoblastoma. Complete excision of the tumor is the treatment of choice. Seventeen cases of cervical lipoblastoma have been reported until now in the literature. but we think that lipoblastoma is more frequent than reported. Lipoblastoma must be remembered as a rare cause of cervical masses in childhood. (C) 2001 Elsevier Science Ireland Ltd, All rights reserved.Öğe Prenatally closed gastroschisis with midgut atresia(Springer-Verlag, 2002) Basaran, UN; Inan, M; Gücer, F; Yardim, T; Pul, MSpontaneous prenatal closure of gastroschisis (GS) is rare and usually associated with atresia of the midgut. We describe a case of GS diagnosed at 20 weeks' gestation that resolved spontaneously in utero. At delivery the infant had an ileus. A laparotomy with a jejunocolostomy was performed, but she died at 2 months of age due to complications of total parenteral nutrition.Öğe The Rapunzel syndrome (trichohezoar) causing gastric perforation in a child: A case report(Springer Verlag, 1996) Pul, N; Pul, MThe Rapunzel syndrome (RS), is a rare form of gastric trichobezoar extending throughout the bowel. We report on a patient with RS causing gastric perforation and discuss the aetiology, pathogenesis, diagnosis and treatment of this unusual syndrome. RS is found characteristically in girls with varying gastro-intestinal symptoms. The recommended treatment for large or complicated trichobezoars is surgery. Psychiatric follow up is essential to diminish the frequency of reccurrence. Conclusion Symptoms of trichobezoars are nonspecific and may mimic those of other pathological gastro-intestinal conditions. Early diagnosis and treatment of this condition is of prime importance and may avoid later fatal complications.Öğe Waugh's syndrome: Report of two cases(W B Saunders Co-Elsevier Inc, 2004) Inan, M; Basaran, UN; Ayvaz, S; Pul, MThe association of intussusception and intestinal malrotation has been reported rarely in the literature. This association is called Waugh's syndrome. The authors report 2 cases of Waugh's syndrome and discuss diagnostic features and treatment methods. (C) 2004 Elsevier Inc. All rights reserved.
