Volume 15 (2020)
Volume 14 (2019)
Volume 13 (2018)
Volume 12 (2017)
Volume 11 (2016)
Volume 10 (2015)
Volume 9 (2014)
Volume 8 (2013)
Volume 7 (2012)
Volume 6 (2011)
Volume 5 (2010)
Volume 4 (2009)
Volume 3 (2008)
Volume 2 (2007)
Volume 1 (2006)
1. Secondary Malignant Transformation of Giant Cell Tumor of Bone: Is It a Fate?

Sajjadeh Movahedinia; Tina Shooshtarizadeh; Hassan Mostafavi

Volume 14, Issue 2 , Spring 2019, , Pages 165-174

http://dx.doi.org/10.30699/ijp.14.2.165

Abstract
  The malignant transformation of conventional giant cell tumor of bone (GCTOB) is rare and usually occurs with irradiation. Here we report two neglected cases of conventional GCTOB with spontaneous malignant transformation at 11 and 16 years after initial diagnosis. In the former case, the patient refused ...  Read More

2. Osteocartilaginous Choriostoma of Palatine Tonsil: a Rare Hidden Entity

Shilpa Bairwa; Bhawna Sethi; Pawan Singh; Ashok Sangwaiya; Shivani Kalhan

Volume 13, Issue 4 , Autumn 2018, , Pages 471-473

Abstract
  A choriostoma is an aggregate of microscopically normal cells or tissues which occurs in an aberrant location. It follows a benign course, rarely seen in head and neck region. A choriostoma of the palatine tonsil is very rare; less than 10 cases were reported till date. A 11-year-old male referred to ...  Read More

Oral Pathology
3. A Bizarre Presentation of Osteoid Osteoma of Maxilla

Tanya Khaitan; Pachigolla Ramaswamy; Uday Ginjupally; Arpita Kabiraj

Volume 11, Issue 5 , Autumn 2016, , Pages 431-434

Abstract
  Osteoid osteoma (OO) is a benign osteogenic lesion that is extremely rare in jaws. It is characterized by proliferation of either cancellous or compact bone and can be central, peripheral or extraskeletal. Pain is a distinctive feature of this lesion accompanied by vasomotor disturbances, which occur ...  Read More

4. A Case of Bone Angiosarcoma

Mahmood Akhavan Tafti; Najmeh Jafari; Jalil Zare; Mohamad Jalal Jafari

Volume 11, Issue 5 , Autumn 2016, , Pages 465-468

Abstract
  Primary angiosarcoma of bone is very rare.It occurs more commonly in middle-age and later life, with a male predominance in the ratio of 2:1. Angiosarcoma of bone has a tendency to involve the long tubular bones, and multifocal involvement is common. Here, we present a case of a 69-yr-old man in Shahid ...  Read More

5. Nonfunctional Adrenocortical Carcinoma with Foci of Osseous Metaplasia in a Young Girl

Srilatha Parampalli Srinivas; Alfred Roy; Vijay kumar

Volume 7, Issue 2 , Spring 2012, , Pages 130-134

Abstract
  Nonfunctional adrenocortical carcinoma is an extremely rare malignant tumor in children. Unlike the functional tumor which is detected early due to its hormonal presentation, nonfunctional tumor is detected at a later stage. Here we report a case of a 10 year old girl who presented with abdominal mass ...  Read More