Adem YÜKSEL, Gülşah Şafak ÖR, Gökmen Umut ERDEM, Kübra BOZKURT, Esma TÜRKMEN BEKMEZ, Dinçer AYDIN

İnvajinasyonla Pesente Olan İnflamatuar Fibroid Polip: Olgu Sunumu

ÖZ İnflamatuar fibroid polipler tüm gastrik poliplerin içinde oldukça nadir görülürler Genellikle submukozadan köken alırlar ve boyutları sıklıkla 1-3 cm' dir. İmmünhistokimyasal boyamada da dendritik hücre kökenli olduğunu düşünülmektedir. Patogenezi bilinmemektedir. Ayırıcı tanıda diğer mezenkimal tümörlerle ve gastrointestinal stromal tümörlerle karışabilmektedir. En sık mide antrumundan köken almakla birlikte gastrointestinal sistemin her yerinde görüIülebilir. Tanı obstrüksiyona bağlı yakınmalarla veya genellikle rastlantısal olarak konulmaktadır. Özellikle ince barsak yerleşimli poliplerin bir komplikasyon gelişmeden tespit edilmesi oldukça zordur. Biz de burada invajinasyona neden olan bir inflamatuar fibroid polip olgusunu sunmayı amaçladık

Inflammatory Fibroid Polyp Which is Presented with Invagination: Case Report

ABSTRACTInflammatory fibroid polyp is a rare polypoid lesion of the gastrointestinal tract that generally originates from the submucosa. It is 1-3 cm in size. Immunohistochemical staining is also thought to be of dendritic cell origin. Pathogenesis of inflammatory fibroid polyp is unknown. In differential diagnosis may be confused with other mesenchymal tumors and gastrointestinal stromal tumors. Although it originatesmostly from the stomach antrum, it can also be found elsewhere throughout the gastrointestinal tract. Diagnosis is complaints related with obstructions or usually detected coincidentally by complaints. Especially, it is difficult to detect in small intestine located polyps without developing a complication. We aimed to present a case of inflammatory fibroid polyp causing invagination. Arnold-Chiari malformation (ACM) is a congenital defect and some of the cases are accompanied by syringomyelia. There are four types of the malformation, type 1 being the most common in adults. Diagnosis of the malformation is usually difficult and therefore delayed. In this case report, we present our experience of anesthesia in a 4-year-old patient with ACM Type I with syringomyelia

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