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本文引用的文献

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Case report of an intra-abdominal desmoid tumour presenting with bowel perforation.一例以肠穿孔为表现的腹腔内硬纤维瘤病例报告。
Mcgill J Med. 2007 Jul;10(2):90-2.
2
Mesenteric fibromatosis: a rare cause of acute abdominal pain.肠系膜纤维瘤病:急性腹痛的罕见病因。
Ann R Coll Surg Engl. 2006 Mar;88(2):1-2. doi: 10.1308/147870806x95212.
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A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum.一项关于肠道息肉病的遗传学与临床研究,肠道息肉病是结肠癌和直肠癌的一个诱发因素。
Am J Hum Genet. 1951 Jun;3(2):167-76.
4
Follow-up study of a family group exhibiting dominant inheritance for a syndrome including intestinal polyps, osteomas, fibromas and epidermal cysts.对一个表现出综合征显性遗传的家族群体进行的随访研究,该综合征包括肠息肉、骨瘤、纤维瘤和表皮囊肿。
Am J Hum Genet. 1962 Dec;14(4):376-90.
5
Surgical management of intra-abdominal desmoid tumours.腹腔内硬纤维瘤的手术治疗
Br J Surg. 2000 May;87(5):608-13. doi: 10.1046/j.1365-2168.2000.01400.x.
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Intra-abdominal desmoid tumor.腹腔内硬纤维瘤
Cancer. 1971 May;27(5):1041-5. doi: 10.1002/1097-0142(197105)27:5<1041::aid-cncr2820270506>3.0.co;2-e.
7
The desmoid syndrome. New aspects in the cause, pathogenesis and treatment of the desmoid tumor.硬纤维瘤综合征。硬纤维瘤病因、发病机制及治疗的新进展。
Am J Surg. 1986 Feb;151(2):230-7. doi: 10.1016/0002-9610(86)90076-0.
8
Intra-abdominal fibromatosis. A pathologic analysis of 130 tumors with comparison of clinical subgroups.腹腔内纤维瘤病。130例肿瘤的病理分析及临床亚组比较
Am J Surg Pathol. 1990 Apr;14(4):335-41.

原发性肠系膜纤维瘤病:一例报告并文献简要回顾

Primary mesenteric fibromatosis: a case report with brief review of literature.

作者信息

Karbeet Radhakrishna Geeta, Bhat P R, Shenoy Rajgopal K, Pai Srinivas, Singh Harpreet

机构信息

Department of Surgery, Kasturba Medical College Hospital, Manipal University, Manipal, Karnataka India 576104.

出版信息

Indian J Surg. 2013 Jun;75(Suppl 1):131-3. doi: 10.1007/s12262-012-0515-7. Epub 2012 Jun 1.

DOI:10.1007/s12262-012-0515-7
PMID:24426540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3693259/
Abstract

Although fibromatosis of the mesentery is a very rare locally aggressive benign condition, the uncertain treatment modalities, the natural history of the disease, and the other common differential diagnosis of the condition along with inexperience of the general clinicians with this disease pose a challenge to the professionals. The prolonged periods of stability and even regression in size of the tumor offer a hope for treatment. Accounting for 0.03 % of all neoplasms, it is also known as deep fibromatosis and desmoid tumor. Here, we discuss one case of primary mesenteric fibromatosis in a young male patient who presented to us with chronic abdominal pain after he was treated for acid peptic disease for the same at a local hospital. This case shows how management of this disease can be delayed due to unfamiliarity among clinicians of this condition. In our patient, a palliative surgical management plan was undertaken due to symptomatic mass in the abdomen, owing to unresectability.

摘要

尽管肠系膜纤维瘤病是一种非常罕见的局部侵袭性良性疾病,但治疗方式不确定、疾病的自然史、该病症的其他常见鉴别诊断以及普通临床医生对这种疾病缺乏经验,给专业人员带来了挑战。肿瘤长时间保持稳定甚至体积缩小,为治疗带来了希望。它占所有肿瘤的0.03%,也被称为深部纤维瘤病和硬纤维瘤。在此,我们讨论一例年轻男性原发性肠系膜纤维瘤病病例,该患者在当地医院接受消化性溃疡疾病治疗后,因慢性腹痛前来就诊。该病例显示了由于临床医生对这种病症不熟悉,如何导致对该疾病的治疗延迟。在我们的患者中,由于腹部有症状性肿块且无法切除,因此采取了姑息性手术治疗方案。