Sudeep Khera
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Sudeep Khera has a total of 89 co-authors. Here are the top co-authors by number of shared publications:
- Poonam Elhence
Department of Pathology, AIIMS Jodhpur, Jodhpur, India
6 shared publications Rashim Sharma
Department of Pathology and Lab Medicine, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India
3 shared publications- Taruna Yadav
Department of Diagnostic and Interventional Radiology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India
3 shared publications - Vikas Meshram
Department of Forensic Medicine and Toxicology, All India Institute of Medical Sciences, Jodhpur, 342005, India
3 shared publications - Aasma Nalwa
Department of Pathology and Lab Medicine, All India Institute of Medical Sciences, Jodhpur, India
2 shared publications - Deepak Kumar Jha
Department of Neurosurgery, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India
2 shared publications
Latest Publications
- Open Access
- 12 August 2026
- Published by Georg Thieme Verlag KG in Indian Journal of Neurosurgery
IDH1 Immunoexpression and Ki-67 Labeling Index in Glioma and Their Correlation with Clinicopathological Parameters
The most common primary malignant tumors of the central nervous system are gliomas, and the most frequent isocitrate dehydrogenase (IDH) mutation in gliomas is IDH1 R132H, rather than IDH2 mutations. The proliferative marker Ki-67 has been widely studied in gliomas; however, its relationship with IDH1 status and clinicopathological parameters remains incompletely understood. This study evaluated the immunohistochemical expression of IDH1 and Ki-67 labeling index (LI) in astrocytic tumors and their correlation with clinicopathological parameters. The present study is an ambispective hospital-based observational study that included 56 histologically diagnosed glioma cases evaluated over a 5-year period. Immunohistochemical expressions of IDH1 and Ki-67 LI were assessed and correlated with clinicopathological parameters. There was a significant positive correlation between Ki-67 LI and age (Pearson's r = 0.306, p = 0.022) and histopathological grade (p < 0.001). Advanced age at diagnosis, male gender, and absence of IDH1 immunoexpression were associated with higher Ki-67 LI. The observed association between IDH1 status and proliferative activity warrants further investigation in larger studies with multivariate analysis and outcome data.
- 12 August 2026
- Published by Georg Thieme Verlag KG in Indian Journal of Neurosurgery
Open AccessIDH1 Immunoexpression and Ki-67 Labeling Index in Glioma and Their Correlation with Clinicopathological Parameters
The most common primary malignant tumors of the central nervous system are gliomas, and the most frequent isocitrate dehydrogenase (IDH) mutation in gliomas is IDH1 R132H, rather than IDH2 mutations. The proliferative marker Ki-67 has been widely studied in gliomas; however, its relationship with IDH1 status and clinicopathological parameters remains incompletely understood. This study evaluated the immunohistochemical expression of IDH1 and Ki-67 labeling index (LI) in astrocytic tumors and their correlation with clinicopathological parameters. The present study is an ambispective hospital-based observational study that included 56 histologically diagnosed glioma cases evaluated over a 5-year period. Immunohistochemical expressions of IDH1 and Ki-67 LI were assessed and correlated with clinicopathological parameters. There was a significant positive correlation between Ki-67 LI and age (Pearson's r = 0.306, p = 0.022) and histopathological grade (p < 0.001). Advanced age at diagnosis, male gender, and absence of IDH1 immunoexpression were associated with higher Ki-67 LI. The observed association between IDH1 status and proliferative activity warrants further investigation in larger studies with multivariate analysis and outcome data.
- 20 March 2026
- Published by Springer Nature in Forensic Science, Medicine and Pathology
- Vol. 22 (3) , 1-6
Fatal intracerebral hemorrhage in a pregnant woman following varicella zoster virus infection: a rare neurological complication
- 20 March 2026
- Published by Springer Nature in Forensic Science, Medicine and Pathology
- Vol. 22 (3) , 1-6
Fatal intracerebral hemorrhage in a pregnant woman following varicella zoster virus infection: a rare neurological complication
- 24 February 2026
- Published by Springer Nature in Indian Journal of Otolaryngology and Head & Neck Surgery
- Vol. 78 (4) , 2398-2401
A Case Report and Literature Review on a Rare Differential Diagnosis of Palatal Swelling: Palatal Schwannoma
- 24 February 2026
- Published by Springer Nature in Indian Journal of Otolaryngology and Head & Neck Surgery
- Vol. 78 (4) , 2398-2401
A Case Report and Literature Review on a Rare Differential Diagnosis of Palatal Swelling: Palatal Schwannoma
- 16 October 2025
- Published by Springer Nature in SN Comprehensive Clinical Medicine
- Vol. 7 (1) , 1-4
When Small Cells Matter: A Unique Variant of Medullary Thyroid Carcinoma, A Case Report
- 16 October 2025
- Published by Springer Nature in SN Comprehensive Clinical Medicine
- Vol. 7 (1) , 1-4
When Small Cells Matter: A Unique Variant of Medullary Thyroid Carcinoma, A Case Report
- 28 August 2025
- Published by Springer Nature in Indian Journal of Hematology and Blood Transfusion
- Vol. 42 (3) , 1032-1036
Expression of Anti-parietal Cell Antibody (APCA) and Intrinsic Factor Blocking Antibody (IFBA) in Individuals with Vitamin B12 Deficiency: Experience from a Tertiary Care Centre from India
Vitamin B12 deficiency is a worldwide public health issue, with its prevalence high in the developing countries. It is a micronutrient synthesized by microorganisms and obtained through diet and its deficiency can lead to megaloblastic anaemia and neurological deficits. The elderly are more prone to it. Pernicious anaemia is a prevalent cause of megaloblastic anaemia, which is associated with autoimmune destruction of parietal cells and intrinsic factor deficiency by APCA and AIFA antibodies. These antibodies can cause mucosal damage and hinder vitamin B12 absorption. The present prospective observational study included 166 patients with severe vitamin B12 deficiency (defined by Vitamin B12 levels ≤ 150 pg/mL) who were treated at a tertiary care centre in western Rajasthan. Expression of AIFA and APCA were assessed and their association with different parameters were evaluated. The present study didnot find any significant association between APCA and AIFA impressions, indicating that the absence or presence of one antibody did not strongly predict the presence or absence of the other antibody. This suggests that these autoantibodies may have distinct roles or mechanisms in PA and further research is needed to understand their relationship.
- 28 August 2025
- Published by Springer Nature in Indian Journal of Hematology and Blood Transfusion
- Vol. 42 (3) , 1032-1036
Expression of Anti-parietal Cell Antibody (APCA) and Intrinsic Factor Blocking Antibody (IFBA) in Individuals with Vitamin B12 Deficiency: Experience from a Tertiary Care Centre from India
Vitamin B12 deficiency is a worldwide public health issue, with its prevalence high in the developing countries. It is a micronutrient synthesized by microorganisms and obtained through diet and its deficiency can lead to megaloblastic anaemia and neurological deficits. The elderly are more prone to it. Pernicious anaemia is a prevalent cause of megaloblastic anaemia, which is associated with autoimmune destruction of parietal cells and intrinsic factor deficiency by APCA and AIFA antibodies. These antibodies can cause mucosal damage and hinder vitamin B12 absorption. The present prospective observational study included 166 patients with severe vitamin B12 deficiency (defined by Vitamin B12 levels ≤ 150 pg/mL) who were treated at a tertiary care centre in western Rajasthan. Expression of AIFA and APCA were assessed and their association with different parameters were evaluated. The present study didnot find any significant association between APCA and AIFA impressions, indicating that the absence or presence of one antibody did not strongly predict the presence or absence of the other antibody. This suggests that these autoantibodies may have distinct roles or mechanisms in PA and further research is needed to understand their relationship.
- 29 May 2025
- Published by Springer Nature in Indian Journal of Surgery
- Vol. 88 (1) , 146-149
Unusual Scrotal Swelling: A Rare Case of Paratesticular Liposarcoma and Literature Review
- 29 May 2025
- Published by Springer Nature in Indian Journal of Surgery
- Vol. 88 (1) , 146-149
Unusual Scrotal Swelling: A Rare Case of Paratesticular Liposarcoma and Literature Review
- 22 February 2024
- Published by BMJ in BMJ Case Reports
- Vol. 17 (2) , e255750
Primary soft tissue sarcoma breast with multiphenotypic differentiation
Primary soft tissue sarcomas of the breast are rare aggressive neoplasms. These often are misdiagnosed with other more common neoplasms like fibroepithelial malignancies, namely phyllodes tumour and metaplastic carcinoma. Being uncommon, chances of being misdiagnosed are higher leading to early mortality. A multidisciplinary team incorporating surgery, pathology, chemotherapy and radiotherapy is required to formulate an approach to primary soft tissue sarcoma. Generally, these tumours may show single or dual phenotype; we present one rare case report showing multiphenotypic differentiation.
- 22 February 2024
- Published by BMJ in BMJ Case Reports
- Vol. 17 (2) , e255750
Primary soft tissue sarcoma breast with multiphenotypic differentiation
Primary soft tissue sarcomas of the breast are rare aggressive neoplasms. These often are misdiagnosed with other more common neoplasms like fibroepithelial malignancies, namely phyllodes tumour and metaplastic carcinoma. Being uncommon, chances of being misdiagnosed are higher leading to early mortality. A multidisciplinary team incorporating surgery, pathology, chemotherapy and radiotherapy is required to formulate an approach to primary soft tissue sarcoma. Generally, these tumours may show single or dual phenotype; we present one rare case report showing multiphenotypic differentiation.
- Open Access
- 13 November 2023
- Published by The Korean Association of Hepato-Biliary-Pancreatic Surgery in Annals of Hepato-Biliary-Pancreatic Surgery
- Vol. 27 (4) , 329-341
Vascular tumors of the liver: A brief review
Sujata Sarangi, Balamurugan Thirunavukkarasu, Sudeep Khera, Selvakumar B, Taruna Yadav. Ann Hepatobiliary Pancreat Surg 2023;27:329-41. https://doi.org/10.14701/ahbps.23-046
- 13 November 2023
- Published by The Korean Association of Hepato-Biliary-Pancreatic Surgery in Annals of Hepato-Biliary-Pancreatic Surgery
- Vol. 27 (4) , 329-341
Open AccessVascular tumors of the liver: A brief review
Sujata Sarangi, Balamurugan Thirunavukkarasu, Sudeep Khera, Selvakumar B, Taruna Yadav. Ann Hepatobiliary Pancreat Surg 2023;27:329-41. https://doi.org/10.14701/ahbps.23-046
- Open Access
- 3 May 2023
- Published by Wolters Kluwer Health in Journal of Cancer Research and Therapeutics
- Vol. 20 (5) , 1611-1614
Pleomorphic adenoma: Indeed, a versatile tumor
Pleomorphic adenoma is the most common and well-studied salivary gland neoplasm. It is a benign tumor most commonly occurring in the parotid gland although it can be seen in other major and minor salivary glands. There is a variety of metaplasia seen in Pleomorphic adenoma most commonly squamous metaplasia, others noted are osseous metaplasia, oncocytic metaplasia, sebaceous metaplasia, and adipocytic metaplasia. Also, at times tyrosine crystalloids are seen. This study discusses a few of the metaplasia and the presence of tyrosine crystals in pleomorphic adenoma. Indeed, this tumor proves true to its name.
- 3 May 2023
- Published by Wolters Kluwer Health in Journal of Cancer Research and Therapeutics
- Vol. 20 (5) , 1611-1614
Open AccessPleomorphic adenoma: Indeed, a versatile tumor
Pleomorphic adenoma is the most common and well-studied salivary gland neoplasm. It is a benign tumor most commonly occurring in the parotid gland although it can be seen in other major and minor salivary glands. There is a variety of metaplasia seen in Pleomorphic adenoma most commonly squamous metaplasia, others noted are osseous metaplasia, oncocytic metaplasia, sebaceous metaplasia, and adipocytic metaplasia. Also, at times tyrosine crystalloids are seen. This study discusses a few of the metaplasia and the presence of tyrosine crystals in pleomorphic adenoma. Indeed, this tumor proves true to its name.