PDF(Pubmed)
Abstract：
UNASSIGNED: Desmoid tumor (DT) is a rare locally aggressive but non-metastatic mesenchymal soft tissue neoplasm that predominantly occurs in the abdominal wall, abdominal cavity, and extremities. Its occurrence in the mesentery is relatively uncommon.
UNASSIGNED: This article reports two cases of desmoid tumor treated at the Department of Gastrointestinal Surgery, Weifang People\'s Hospital. The first case was a 59-year-old male patient who had previously undergone surgery for esophagogastric junction cancer. Postoperatively, he developed an intra-abdominal mass that rapidly increased in size within three months. The second case was a 60-year-old male patient who incidentally discovered a mass in the left lower abdomen. Both patients underwent surgical treatment, and the postoperative pathological diagnosis was mesenteric desmoid tumor.
UNASSIGNED: The treatment of desmoid tumor remains challenging. Simple surgical resection often yields unsatisfactory outcomes, and the efficacy of adjuvant radiotherapy and chemotherapy is also limited. Further research and clinical practice are necessary to improve diagnostic and therapeutic strategies, aiming to enhance patient survival and quality of life.
UNASSIGNED: This article reports two cases of desmoid tumor treated at the Department of Gastrointestinal Surgery, Weifang People\'s Hospital. The first case was a 59-year-old male patient who had previously undergone surgery for esophagogastric junction cancer. Postoperatively, he developed an intra-abdominal mass that rapidly increased in size within three months. The second case was a 60-year-old male patient who incidentally discovered a mass in the left lower abdomen. Both patients underwent surgical treatment, and the postoperative pathological diagnosis was mesenteric desmoid tumor.
UNASSIGNED: The treatment of desmoid tumor remains challenging. Simple surgical resection often yields unsatisfactory outcomes, and the efficacy of adjuvant radiotherapy and chemotherapy is also limited. Further research and clinical practice are necessary to improve diagnostic and therapeutic strategies, aiming to enhance patient survival and quality of life.
摘要：
■纤维瘤（DT）是一种罕见的局部侵袭性但非转移性间充质软组织肿瘤，主要发生在腹壁，腹腔，和四肢。它在肠系膜的发生相对罕见。
■本文报道了胃肠外科治疗的两例硬纤维瘤，潍坊市人民医院.第一个病例是一名59岁的男性患者，他之前曾接受过食管胃结合部癌的手术。术后,他的腹内肿块在三个月内迅速增大。第二例是一名60岁的男性患者，偶然发现左下腹部有肿块。两名患者都接受了手术治疗，术后病理诊断为肠系膜纤维瘤。
■硬纤维瘤的治疗仍然具有挑战性。简单的手术切除通常会产生不令人满意的结果，辅助放疗和化疗的疗效也有限。进一步的研究和临床实践是必要的，以改善诊断和治疗策略，旨在提高患者的生存和生活质量。
■本文报道了胃肠外科治疗的两例硬纤维瘤，潍坊市人民医院.第一个病例是一名59岁的男性患者，他之前曾接受过食管胃结合部癌的手术。术后,他的腹内肿块在三个月内迅速增大。第二例是一名60岁的男性患者，偶然发现左下腹部有肿块。两名患者都接受了手术治疗，术后病理诊断为肠系膜纤维瘤。
■硬纤维瘤的治疗仍然具有挑战性。简单的手术切除通常会产生不令人满意的结果，辅助放疗和化疗的疗效也有限。进一步的研究和临床实践是必要的，以改善诊断和治疗策略，旨在提高患者的生存和生活质量。
