A5111811606- Renal Diseases and Glomerulopathies
- Vasculitis and related conditions
- Renal Transplantation Outcomes and Treatments
- Neuroendocrine Tumor Research Advances
- Urologic and reproductive health conditions
- Pituitary Gland Disorders and Treatments
- Urinary and Genital Oncology Studies
- Lymphoma Diagnosis and Treatment
- Neuroblastoma Research and Treatments
- Chronic Lymphocytic Leukemia Research
- Organ Transplantation Techniques and Outcomes
- Systemic Sclerosis and Related Diseases
- Infectious Diseases and Mycology
- Thyroid Cancer Diagnosis and Treatment
- Bone Tumor Diagnosis and Treatments
- Congenital Anomalies and Fetal Surgery
- Thyroid and Parathyroid Surgery
- Ovarian cancer diagnosis and treatment
- Lung Cancer Research Studies
- Cancer Genomics and Diagnostics
- Antifungal resistance and susceptibility
- Renal and related cancers
- Fungal Infections and Studies
- Pediatric Hepatobiliary Diseases and Treatments
- Urological Disorders and Treatments
Sir Ganga Ram Hospital
2021-2025
Army Hospital Research and Referral
2007-2024
Arkana Laboratories
2007-2020
Jaipur National University
2020
Armed Forces Medical College
2011-2016
Marymount University
2016
Command Hospital
2015
Southern Command Hospital
2014
Sanjay Gandhi Post Graduate Institute of Medical Sciences
2005-2012
Cystic lesions of the adrenal glands are relatively uncommon and most them clinically silent. Though rarely associated with malignant changes, they may carry detrimental consequences if misdiagnosed. exhibit a broad histomorphological spectrum, ranging from pseudocysts, endothelial cysts, epithelial cysts parasitic cysts. Here we present case young woman left-sided abdominal pain contrast-enhanced CT showing 10.4×7.7×7.8 cm fluid-filled left suprarenal lesion. The patient underwent...
Introduction Pancreaticoduodenectomy is the standard treatment for resectable pancreatic head malignancies and other ampullary/peri-ampullary lesions. It also of care symptomatic relief in chronic pancreatitis. However, despite advancements diagnostic modalities, some lesions that are clinically suspicious malignancy may reveal a surprising benign pathology. Thus, various neoplastic non-neoplastic encountered pancreaticoduodenectomy specimens. Methods specimens received at our institute over...
Reticulate hyperpigmentary disorders are a group of rare genetic pigmentary abnormalities which includes reticulate acropigmentation Kitamura (RAPK), Dowling-Degos disease (DD), Dohi (RAPD), Haber's syndrome, and Galli-Galli disease. A 25-year-old male presented with asymptomatic dark-colored lesions on his hands feet light-colored skin involving the trunk since three years. Dermatological examination revealed hyperpigmented macules in pattern dorsa feet, front sides neck, axillae,...
The pituitary develops as a result of complex, intricate, and precise neuro-embryological events in the sixth to eighth weeks gestation. Some ectopic cell rests can become adenomatous. Rarely, these clivus be site formation adenoma. Our patient, 35-year-old parous woman, was being treated for acromegaly, imaging studies revealed clival mass lesion. Trans-sphenoidal excision done immunohistochemistry tumor growth hormone-secreting tumor.
The incidence, risk factors and outcome of graft pyelonephritis are variably described in literature. All patients who had been transplanted at our center between January 2002 November 2006 presented with acute dysfunction were subjected to biopsy. Those neutrophilic casts interstitial inflammation predominant neutrophils included the study. Out 265 patients, 110 period underwent biopsy for dysfunction. 26 proven (AGPN). Nine early AGPN (within 6 months) other 17 late AGPN. Nearly 19%...
Abstract: The development of post‐transplant lymphoproliferative disorders (PTLD) is a well‐recognized complication solid organ transplantation in patients receiving immunosuppressive therapy. literature on PTLD live renal allograft recipients scarce and most the data pertains to cadaveric transplants. As donor grafts form mainstay programme India, this study was carried out define profile recipients. On retrospective evaluation, nine cases amongst 1700 from January 1989 August 2004, were...
Hypospadias is a common congenital abnormality typified by proximally placed ectopic urethral meatus along the ventral surface of penis. Androgen receptor (AR) and estrogen (ER) expression in hypospadias tissues may be altered hypospadias.We evaluated immunohistochemistry AR ER 75 from repair, compared this to that tissue patients undergoing circumcision. We also intensity between different severities hypospadias.AR quantitative grading score decreased with severity hypospadias, while...
Chordomas are most commonly of extradural origin and associated with bone destruction. Extra-osseous intradural chordomas extremely rare the cases described located near clivus. We report an case multiple extra-osseous intraspinal in a 36-year-old male patient autopsy findings. This highlights that behaviour spinal is not universally low grade, but variable aggressive.
Renal Involvement in scleroderma is a known problem and the manifestations are well described. involvement systemic lupus erythematosus (SLE) also known. However, SLE overlap syndrome, renal findings may vary being combination of features immune complex mediated glomerulonephritis as thrombotic microangiopathy. We report case which manifestation such situation was focal necrotising pauci-immune with crescents, anti-neutrophil cytoplasmic antibody negative. To best our knowledge, have not...
Malignant melanoma is an aggressive, notorious tumor showing great variability in morphological and immunohistochemical expression, thus commonly leading to erroneous diagnosis. Within the group, amelanotic melanoma, with its wide clinical presentations, lack of pigmentation, varied histological appearances, has taken on a new persona as master masquerader. Use immunohistochemistry diagnosis malignant tumors, including primordial indispensable. However, problem gets compounded scenario...
Scleroderma renal crises (SRC) is a serious complication of systemic sclerosis whose prognosis remains despite management with angiotensin-converting enzyme inhibitors, antihypertensives and dialysis. Pulmonary syndrome (PRS), characterised by diffuse alveolar hemorrhage (DAH) SRC, rare carries grave prognosis. This case report discusses the clinicopathological features 43-year-old male presenting severe hypertension rapidly progressive failure who subsequently developed DAH died. The...
Uterine neuroendocrine carcinomas are rare, accounting for <1% of endometrial carcinomas, and include both large cell small types.[1][1] Prognosis is distinctly worse, even in early stage tumors, with strong propensity rapid recurrence distant metastasis.[2 3][2] Accurate diagnosis