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Year : 2009  |  Volume : 46  |  Issue : 1  |  Page : 34--39

Desmoid tumors: Experience of 32 cases and review of the literature

V Kumar1, S Khanna2, AK Khanna2, R Khanna2 
1 Department of Surgical Oncology, Institute of Medical Sciences, Banaras Hindu University, Varanasi-221 005, UP, India
2 Department of General Surgery, Institute of Medical Sciences, Banaras Hindu University, Varanasi-221 005, UP, India

Correspondence Address:
V Kumar
Department of Surgical Oncology, Institute of Medical Sciences, Banaras Hindu University, Varanasi-221 005, UP
India

Background: Desmoids are infiltrative, locally destructive, soft tissue tumors. Although they do not metastasize, the incidence of local recurrence is quite high. Aim : Present study aimed at reporting the 10-year experience of 32 desmoid cases and reviewing some facts with symptoms, investigation, and treatment of the disease. Materials and Methods : Thirty two cases of desmoid tumors were reviewed over a 10-year span. Surgical resection and adjuvant radiotherapy were the treatments of choice whenever histological margins were positive . Results : Multiparous women in reproductive age were the most commonly afflicted. The commonest site of presentation was the abdominal wall. Ninety one percent (20/22) were infraumbilical. The tumors were found in the rectus sheath in 14 patients (64%) and were laterally situated in 8 patients (36%). Local infiltration was found in six patients and the urinary bladder was most commonly involved (3/6). Locally recurrent desmoids were seen in eight patients (25%). Conclusions : In our experience, 25% of the desmoid tumors (8/32) were recurrent and postoperative radiotherapy did not seem to influence the local recurrence rate. The most important predictor for recurrence was tumors of >5 cm.


How to cite this article:
Kumar V, Khanna S, Khanna A K, Khanna R. Desmoid tumors: Experience of 32 cases and review of the literature.Indian J Cancer 2009;46:34-39


How to cite this URL:
Kumar V, Khanna S, Khanna A K, Khanna R. Desmoid tumors: Experience of 32 cases and review of the literature. Indian J Cancer [serial online] 2009 [cited 2020 Apr 6 ];46:34-39
Available from: http://www.indianjcancer.com/article.asp?issn=0019-509X;year=2009;volume=46;issue=1;spage=34;epage=39;aulast=Kumar;type=0