大肠腺瘤性息肉病全结肠切除术后累发腹壁纤维瘤病1例
摘要
<正>家族性腺瘤性息肉病(familial adenomatous polyposis,FAP)是一种以大肠多发息肉样病变为主要特征的常染色体显性遗传的综合征,FAP包括肠内表现和肠外表现:肠内表现主要为多发腺瘤样息肉,肠外表现主要为腹外、腹壁及腹内侵袭性纤维瘤病(aggressive fibromatosis,AF)等。本院近期接诊一名FAP术后累发AF患者,现结合相关文献报道如下。
引文
[1]Kim PS,Han DS,Han HS,et al.Intra-abdominal fibromatosis after gastrectomy for gastric cancer[J].Annals of Surgical Treatment&Research,2014,87(6):331.
[2]沈俊俊,潘月芬.结肠癌术后转移合并腹壁韧带样纤维瘤1例[J].浙江医学,2017,39(10):856.
[3]Campos FG,Martinez CAR,Novaes M,et al.Desmoid tumors:clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis[J].Familial Cancer,2015,14(2):211.
[4]Torres JC,Xin C.An unusual finding in a desmoid-type fibromatosis of the pancreas:a case report and review of the literature[J].Journal of Medical Case Reports,2018,12(1):123.
[5]徐一宁,朱建明,杨乐.家族性腺瘤性息肉病术后并发小肠纤维瘤病一例[J].临床外科杂志,2013,21(11):865.
[6]朱斌,谢海伟,杨小兵.腹壁侵袭性纤维瘤病11例的临床特征及外科诊疗[J].江苏医药,2016,42(23):2636.
[7]李海燕,钟海烽,张大伟,等.肠系膜侵袭性纤维瘤病11例临床分析[J].中华胃肠外科杂志,2017,20(9).
[8]徐晓东,于恩达,刘连杰,等.家族性腺瘤性息肉病伴发硬纤维瘤的诊治探讨[J].中华普通外科杂志,2010,25(7):596.
[9]CreuzéM,Afchain P,Munck A,et al.Desmoid tumors in an adolescent girl with familial adenomatous polyposis[J].Arch Pediatr,2013,9(11):232.
[10]侯丽娜,杨晓棠,张建新,等.腹外型侵袭性纤维瘤病的CT及磁共振成像表现[J].中国药物与临床,2017,17(8):1142.
[11]罗振东,陈卫国,贾铭,等.侵袭性纤维瘤病CT表现及鉴别诊断[J].中国医学影像学杂志,2012,20(6):405.
[12]洪睿霞,赵怀,罗丽,等.侵袭性纤维瘤病的超声表现及误诊分析[J].中国介入影像与治疗学,2017,14(6):374.
[13]彭季兰.下腹壁纤维瘤病超声误诊1例[J].中国超声诊断杂志,2006,7(7):500.
[14]王军燕,孙延豹.侵袭性纤维瘤病的影像学表现[J].医学影像学杂志,2017(12):2315.
[15]韩方海,周声宁.侵袭性纤维瘤病的诊治体会[J].中华胃肠外科杂志,2017,20(11).
[16]Kallam AR,Ramakrishna BV,Roy GK,et al.Desmoid tumours:our experience of six cases and review of literature[J].Journal of Clinical&Diagnostic Research Jcdr,2014,8(10):01.
[17]Desurmont T,Lefèvre JH,Shields C,et al.Desmoid tumour in familial adenomatous polyposis patients:responses to treatments[J].Familial Cancer,2015,14(1):31.
[18]Li W,Zhou Y,Li Q,et al.Intestinal perforation during chemotherapeutic treatment of intra-abdominal desmoid tumor in patients with Gardner’s syndrome:report of two cases[J].World Journal of Surgical Oncology,2016,14(1):178.
[19]Yoon GW,Kim J D,Chung SH.The Analysis of Treatment of Aggressive Fibromatosis Using Oral Methotrexate Chemotherapy[J].Clinics in Orthopedic Surgery,2014,6(4):439.
[20]Sugrue JJ,Cohen SB,Marshall RM,et al.Palliative Resection of a Giant Mesenteric Desmoid Tumor[J].Ochsner Journal,2015,15(4):468.
[21]Santos M,Rocha A,Martins V,et al.Desmoid Tumours in Familial Adenomatous Polyposis:Review of 17Patients from a Portuguese Tertiary Center[J].Journal of Clinical&Diagnostic Research Jcdr,2016,10(10):01.
[22]Desurmont T,Lefèvre JH,Shields C,et al.Desmoid tumour in familial adenomatous polyposis patients:responses to treatments[J].Familial Cancer,2015,14(1):31.
[23]Seinen JM,Niebling MG,Bastiaannet E,et al.Four different treatment strategies in aggressive fibromatosis:A systematic review[J].Clinical&Translational Radiation Oncology,2018,12:1.
[2]沈俊俊,潘月芬.结肠癌术后转移合并腹壁韧带样纤维瘤1例[J].浙江医学,2017,39(10):856.
[3]Campos FG,Martinez CAR,Novaes M,et al.Desmoid tumors:clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis[J].Familial Cancer,2015,14(2):211.
[4]Torres JC,Xin C.An unusual finding in a desmoid-type fibromatosis of the pancreas:a case report and review of the literature[J].Journal of Medical Case Reports,2018,12(1):123.
[5]徐一宁,朱建明,杨乐.家族性腺瘤性息肉病术后并发小肠纤维瘤病一例[J].临床外科杂志,2013,21(11):865.
[6]朱斌,谢海伟,杨小兵.腹壁侵袭性纤维瘤病11例的临床特征及外科诊疗[J].江苏医药,2016,42(23):2636.
[7]李海燕,钟海烽,张大伟,等.肠系膜侵袭性纤维瘤病11例临床分析[J].中华胃肠外科杂志,2017,20(9).
[8]徐晓东,于恩达,刘连杰,等.家族性腺瘤性息肉病伴发硬纤维瘤的诊治探讨[J].中华普通外科杂志,2010,25(7):596.
[9]CreuzéM,Afchain P,Munck A,et al.Desmoid tumors in an adolescent girl with familial adenomatous polyposis[J].Arch Pediatr,2013,9(11):232.
[10]侯丽娜,杨晓棠,张建新,等.腹外型侵袭性纤维瘤病的CT及磁共振成像表现[J].中国药物与临床,2017,17(8):1142.
[11]罗振东,陈卫国,贾铭,等.侵袭性纤维瘤病CT表现及鉴别诊断[J].中国医学影像学杂志,2012,20(6):405.
[12]洪睿霞,赵怀,罗丽,等.侵袭性纤维瘤病的超声表现及误诊分析[J].中国介入影像与治疗学,2017,14(6):374.
[13]彭季兰.下腹壁纤维瘤病超声误诊1例[J].中国超声诊断杂志,2006,7(7):500.
[14]王军燕,孙延豹.侵袭性纤维瘤病的影像学表现[J].医学影像学杂志,2017(12):2315.
[15]韩方海,周声宁.侵袭性纤维瘤病的诊治体会[J].中华胃肠外科杂志,2017,20(11).
[16]Kallam AR,Ramakrishna BV,Roy GK,et al.Desmoid tumours:our experience of six cases and review of literature[J].Journal of Clinical&Diagnostic Research Jcdr,2014,8(10):01.
[17]Desurmont T,Lefèvre JH,Shields C,et al.Desmoid tumour in familial adenomatous polyposis patients:responses to treatments[J].Familial Cancer,2015,14(1):31.
[18]Li W,Zhou Y,Li Q,et al.Intestinal perforation during chemotherapeutic treatment of intra-abdominal desmoid tumor in patients with Gardner’s syndrome:report of two cases[J].World Journal of Surgical Oncology,2016,14(1):178.
[19]Yoon GW,Kim J D,Chung SH.The Analysis of Treatment of Aggressive Fibromatosis Using Oral Methotrexate Chemotherapy[J].Clinics in Orthopedic Surgery,2014,6(4):439.
[20]Sugrue JJ,Cohen SB,Marshall RM,et al.Palliative Resection of a Giant Mesenteric Desmoid Tumor[J].Ochsner Journal,2015,15(4):468.
[21]Santos M,Rocha A,Martins V,et al.Desmoid Tumours in Familial Adenomatous Polyposis:Review of 17Patients from a Portuguese Tertiary Center[J].Journal of Clinical&Diagnostic Research Jcdr,2016,10(10):01.
[22]Desurmont T,Lefèvre JH,Shields C,et al.Desmoid tumour in familial adenomatous polyposis patients:responses to treatments[J].Familial Cancer,2015,14(1):31.
[23]Seinen JM,Niebling MG,Bastiaannet E,et al.Four different treatment strategies in aggressive fibromatosis:A systematic review[J].Clinical&Translational Radiation Oncology,2018,12:1.