K. M. Mohandas
Tata Memorial Hospital
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Publication
Featured researches published by K. M. Mohandas.
Anz Journal of Surgery | 2009
Parul J. Shukla; Savio G. Barreto; K. M. Mohandas; Shailesh V. Shrikhande
Background: Although mortality rates following pancreatoduodenectomy have drastically reduced over the last few decades, high morbidity rates have continued to trouble pancreatic surgeons across the world. Interventional radiology has reduced the need for re‐exploration for complications following pancreatoduodenectomy. There remain specific indications for re‐exploration in such scenarios. It is thus pertinent to identify those clinical scenarios where surgery still has a role in managing complications of pancreatoduodenectomy. The aim of the study was to define the role of surgery for dealing with complications following pancreatoduodenectomy.
Journal of Cancer Research and Therapeutics | 2010
Navin Krishnamoorthy; Munita Bal; Mukta Ramadwar; Kedar Deodhar; K. M. Mohandas
Primary plasmacytoma of the gastrointestinal tract is a rare entity. We report a case of a primary gastric plasmacytoma in a 57-year-old man who presented with upper-gastrointestinal bleeding. Endoscopy showed a nodular gastric mass with central umblication. Histological examination of the gastrectomy specimen revealed a monoclonal lambda-chain extramedullary plasmacytoma. Further staging was found to be negative for multiple myeloma. As other more common pathologic processes at this site may also be endowed with numerous plasma cells, awareness of this entity and distinction using immunohistochemistry are extremely crucial. Because systemic disease ultimately develops in many patients with localized plasmacytoma, such patients should be followed closely for the appearance of clinical, biochemical, and roentgenologic evidence of multiple myeloma.
Hpb | 2008
Parul J. Shukla; Savio G. Barreto; Shailesh V. Shrikhande; Mukta Ramadwar; Kedar Deodhar; Shaesta Mehta; Prachi Patil; K. M. Mohandas
The pathogenesis of gallbladder cancer presenting synchronously with malignancy of the bile duct has not been clearly understood. The possible causes for the simultaneous presence of these tumors could be due to local spread, metastases, de novo multifocal origin, or as part of a field change in the extrahepatic biliary apparatus. In this article, we discuss the cases of four patients with simultaneous gallbladder and bile duct malignancies and analyze their individual pathologies to provide an explanation into the mechanisms that may play a role in such conditions.
Hpb | 2007
Parul J. Shukla; Savio G. Barreto; Piyush Gupta; R. Neve; Mukta Ramadwar; Kedar Deodhar; Shaesta Mehta; Shailesh V. Shrikhande; K. M. Mohandas
BACKGROUND/AIMS The concept of metaplastic and non-metaplastic types of gall bladder cancer and the likelihood of hormone receptor expression in the nuclei of tumour cells raised the possibility of a potential role for anti-estrogen therapy in gall bladder cancer. This study was carried out to determine the hormone receptors (ER/PR) expression level in gall bladder cancer using specific immunohistochemical assays and correlate it with patient and tumour histopathological characteristics. PATIENTS AND METHODS Histopathological tumour specimens of 62 patients who underwent a radical cholecystectomy were analysed. Pronase pretreatment and primary monoclonal antibodies were used to perform immunohistochemical analysis for ER and PR. RESULTS The histology was adenocarcinoma--predominantly, moderately to poorly differentiated (91%). Gallstones were present in 90% of the individuals. Of the 62 specimens analysed, 62 (100%) and 61 (98%) were negative for ER and PR, respectively. CONCLUSION The high incidence of gallstone-related gall bladder cancer in India is associated with metaplasia and a tendency to poorer differentiation in the tumour histology. These tumours are consequently less likely to express hormone receptors. Thus, there does not seem to be a role for anti-hormone therapy in patients with histogenesis similar to that seen in India.
International Journal of Colorectal Disease | 2013
K. M. Mohandas; Parul J. Shukla; Shailesh V. Shrikhande; Umesh Mahantshetty; S. Chopra; Mahesh Goel; Shaesta Mehta; Prachi Patil; Mukta Ramadwar; Kedar Deodhar; Supreeta Arya; Shyam Kishore Shrivastava
PurposeThis trial was undertaken to compare the rates of resectability between patients treated with neoadjuvant concurrent chemoradiation vs. boosted radiotherapy alone.Materials and methodsPatients with clinically unresectable rectal cancer were randomized to receive external beam radiation therapy (EBRT) to pelvis (45 Gy) with concurrent oral Capecitabine (CRT group; Arm 1) or EBRT to pelvis (45 Gy) alone followed by 20 Gy dose of localized radiotherapy boost to the primary tumor site (RT with boost group, Arm 2). All patients were assessed for resectability after 6 weeks by clinical examination and by CT scan and those deemed resectable underwent surgery.ResultsA total of 90 patients were randomized, 46 to Arm 1 and 44 to Arm 2. Eighty seven patients (44 in Arm 1 and 41 in Arm 2) completed the prescribed treatment protocol. Overall resectability rate was low in both the groups; R0 resection was achieved in 20 (43 %) patients in Arm 1 vs. 15 (34 %) in Arm 2. Adverse factors that significantly affected the resectability rate in both the groups were extension of tumor to pelvic bones and signet ring cell pathology. Complete pathological response was seen in 7 and 11 %, respectively. There was greater morbidity such as wound infection and delayed wound healing in Arm 2 (16 vs. 40 %; p = 0.03).ConclusionEscalated radiation dose without chemotherapy does not achieve higher complete (R0) tumor resectability in locally advanced inoperable rectal cancers, compared to concurrent chemoradiation.
Annals of Surgical Oncology | 2008
Parul J. Shukla; R. Neve; Savio G. Barreto; Rohini Hawaldar; Mandar S. Nadkarni; K. M. Mohandas; Shailesh V. Shrikhande
Indian Journal of Gastroenterology | 2003
R. Neve; Biswas S; Dhir; K. M. Mohandas; Kelkar R; Parul J. Shukla; Jagannath P
World Journal of Surgery | 2012
Shailesh V. Shrikhande; Sachin S. Marda; Kunal Suradkar; Supreeta Arya; Guruprasad Shetty; Munita Bal; Parul J. Shukla; Mahesh Goel; K. M. Mohandas
Indian Journal of Gastroenterology | 2005
Parul J. Shukla; Durgatosh Pandey; Pramod P Rao; Shailesh V. Shrikhande; Meenakshi Thakur; Supreeta Arya; Subhash Ramani; Shaesta Mehta; K. M. Mohandas
Indian Journal of Gastroenterology | 2003
Hegde; K. M. Mohandas; Mukta Ramadwar; Parul J. Shukla; Shaesta Mehta