| Literature DB >> 24596759 |
Sathish Selva Kumar1, Padmini Ramachandran2, Veena G2, Napa Madhusudhan3, Uday Kumbhar4.
Abstract
Desmoid Tumour (DT) is a rare benign, myofibroblastic tumour originating from muscle fascia with tendency to recur but, it rarely metastasizes. We are reporting here a case of DT that presented as an intra-abdominal mass with pelvic extension in a patient who underwent hysterectomy for fibroid uterus seventeen years ago. A clinical diagnosis of ovarian malignancy was made. Ovarian tumour markers for surface epithelial and germ cell tumours were negative. Imaging studies suggested DT and the same was excised surgically. A histopathological diagnosis of DT was made and confirmed with immunohistochemistry (IHC) markers. DT should always be considered especially in female patients with previous history of surgery. A complete surgical excision is the treatment of choice with recurrent cases requiring radiotherapy. A differential diagnosis like sarcoma and further toxic chemotherapy can be avoided with careful histopathological evaluation and IHC confirmation of DTs.Entities:
Keywords: Desmoid tumour; Myofibroblast tumour
Year: 2013 PMID: 24596759 PMCID: PMC3939539 DOI: 10.7860/JCDR/2014/7358.3901
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X