As per Dr. Sachin Jadhav, Group Head of Hematology and Bone Marrow Transplant, HCG Cancer Hospital, “This was an extremely challenging and complex case as the patient was suffering from a rare condition ‘Congenital Hemophilia’. In people with hemophilia, there is a deficiency of plasma products which helps in stopping blood loss. Factor 8 and factor 9 help in clotting the blood so that they do not suffer excess blood loss. In a hemophilic patient, this product is absent. So, in case of an injury, these patients may experience excessive bleeding or may even bleed to death. Factor replacement is created to artificially supplement what is not there in the body. Once these factors are diagnosed and the patient is known for a factor deficiency, then according to their bleeding tendencies, the factors are replaced so that the patient does not bleed abnormally.”
Dr. Pramod S Chinder, Director & Head of the Department- Orthopedic Oncology, HCG Cancer Hospital says, “This is the biggest tumor we have operated of this hemophilia condition. It was a huge tumor that kept on bleeding to itself and led to the decrease in hemoglobin which was highly challenging while operating the patient. The bleeding was uncontrollable and was threat to life of the patient. We were extra cautious and prepared during the surgery to face any complications. With the support of Dr. Sachin and multidisciplinary team approach we were able to successfully perform the surgery.”