AI Summary & Key Takeaways
AI InsightHerein, we aimed to report a case of malignant fibrous histiocytoma, a rare cause of rectal mass, who was treated with abdominoperineal resection + end colostomy.
📌 3 Key Takeaways
Abstract
Malignant fibrous histiocytoma is a type of soft tissue sarcoma that originates from mesenchymal tissues and that mostly affects extremities. Abdominal malignant fibrous histiocytoma usually has a poor prognosis and is rarely seen in the rectum. A 52-year-old female patient presented with rectal bleeding, tenesmus and anemia. She was operated for an obstructive rectal mass and postoperative pathology was reported as malignant fibrous histiocytoma. Herein, we aimed to report a case of malignant fibrous histiocytoma, a rare cause of rectal mass, who was treated with abdominoperineal resection + end colostomy.
Özet
Malign fibröz histiyositom, sıklıkla uyluk, kalça ve ekstemitelerde görülen bir yumuşak doku sarkomu tipi olup, mezenkimal dokulardan kaynaklanır. Abdominal kaynaklı malign fibröz histiyositom genellikle kötü prognozlu olup, rektumda da çok nadiren gözlenir. Elli iki yaşında kadın hasta, rektal kanama, tenesmus ve anemi semptomları ile başvurdu. Obstruktif rektal kitle nedeniyle opere edilen hastanın postoperatif patolojisi malign fibröz histiositom olarak raporlandı. Biz burada abdominoperineal rezeksiyon + uç kolostomi ile tedavi ettiğimiz, nadir görülen rektal kitlenin bir sebebi olan malign fibröz histiositom olgusunu liteatür eşliğinde sunmayı planladık.