Granulocytic Sarcoma of Ovary Associated with Chronic Myelogenous Leukaemia Mimicking Carcinoma: A Rare Case Report

Diptirani Samanta *

Department of Medical Oncology, Aharya Harihara Regional Cancer Centre, Cuttack, Odisha, India

Tapan Kumar Sahoo

Department of Radiation Oncology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India

K. Roopesh

Department of Radiation Oncology, Apollo Cancer Hospital, Jubilee Hills, Hyderabad, India

Kirti Ranjan Mohanty

Department of Radiation Oncology, TATA Memorial Hospital, Mumbai, India

Chaitali Bose

Department of Radiation Oncology, Aharya Harihara Regional Cancer Centre, Cuttack, Odisha, India

Surendra Nath Senapati

Department of Radiation Oncology, Aharya Harihara Regional Cancer Centre, Cuttack, Odisha, India

*Author to whom correspondence should be addressed.


Abstract

Granulocytic sarcoma is a rare haematological neoplasm due to extramedullary leukemic deposits. Granulocytic Sarcoma of ovary is even rare associated with chronic myeloid leukaemia and responds to imatinib treatment. A strong vigilance is required. Here we report a case of granulocytic sarcoma of ovary in a 31 year old female with primary infertility being provisionally diagnosed as ovarian tumour. Later on, after complete haematological investigation and fine needle aspiration cytology of ovarian tumour, the case is found to be of granulocytic sarcoma associated with chronic myeloid leukaemia. The aim of documenting this case report is to establish the possibility of granulocytic sarcoma in unusual site which was initially thought to be of nonhematological malignancy and proved by tissue diagnosis to be of haematological malignancy.

 

Keywords: Chronic myeloid leukaemia, extramedullary, fine needle aspiration cytology, granulocytic sarcoma


How to Cite

Samanta, Diptirani, Tapan Kumar Sahoo, K. Roopesh, Kirti Ranjan Mohanty, Chaitali Bose, and Surendra Nath Senapati. 2015. “Granulocytic Sarcoma of Ovary Associated With Chronic Myelogenous Leukaemia Mimicking Carcinoma: A Rare Case Report”. Journal of Cancer and Tumor International 3 (2):1-5. https://doi.org/10.9734/JCTI/2016/22486.

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