• Rare tumors · Jul 2014

    Case Reports

    Diffuse intestinal submucosal lipomatosis with incidental epidermal inclusion cyst of caecum clinically masquerading as carcinoma caecum.

    • Brijesh Thakur, Sanjeev Kishore, Aparna Bhardwaj, and Sandip Kudesia.
    • Department of Pathology, Shri Guru Ram Rai Institute of Medical and Health Sciences , Dehradun, India.
    • Rare Tumors. 2014 Jul 30; 6 (3): 5380.

    AbstractSymptomatic diffuse submucosal intestinal lipomatosis is a rare entity. Also few cases of epidermal inclusion cyst of caecum have been reported in literature. Here, we are presenting a rare case of intestinal submucosal lipomatosis with coincidence of epidermal inclusion cyst of caecum and presumptively diagnosed as carcinoma of ileocaecal region during surgery in a 55 years old male. Both are rare entity considering the location even they should be kept as a differential diagnosis in unusual cases of intestinal perforations with inconclusive radiological findings or clinical uncertainity.

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