A5080689131- Tuberous Sclerosis Complex Research
- Renal cell carcinoma treatment
- Urologic and reproductive health conditions
- Peripheral Neuropathies and Disorders
- Genetic Syndromes and Imprinting
- Lung Cancer Diagnosis and Treatment
- SARS-CoV-2 and COVID-19 Research
- Bone and Joint Diseases
- Histiocytic Disorders and Treatments
- Long-Term Effects of COVID-19
- Gestational Trophoblastic Disease Studies
- Prenatal Screening and Diagnostics
- Infectious Disease Case Reports and Treatments
- Lung Cancer Treatments and Mutations
- COVID-19 Clinical Research Studies
- Cancer Genomics and Diagnostics
- CNS Lymphoma Diagnosis and Treatment
- PI3K/AKT/mTOR signaling in cancer
- Renal and related cancers
Sir Ganga Ram Hospital
2024
All India Institute of Medical Sciences Raipur
2019
All India Institute of Medical Sciences
2019
All India Institute of Medical Sciences Bhopal
2019
Low-grade oncocytic tumour (LOT) of the kidney has recently emerged as a potential novel type. Despite similarity to oncocytoma or eosinophilic chromophobe renal cell carcinoma, it shows diffuse keratin 7 immunohistochemistry (IHC) and negative KIT (CD117), which differs from both. We aimed identify molecular characteristics these tumours. Seventeen tumours (one male, 16 female, nine previously published) fitting original description this entity (solid morphology, often with areas cells...
Xanthogranulomatous inflammation is a rare, destructive pattern of inflammation, affecting different organs, that often produces mass-like lesion, simulating malignancy. Although benign, it can coexist with We, herein, report the case 60-year-old male patient, who presented testicular mass was partly necrotic and showed heterogeneous enhancement on contrast study. Testicular tumor markers were normal. In view clinicoradiological suspicion malignant cause, high inguinal orchidectomy...
A BSTRACT Hydatidiform mole is a condition characterised by abnormal trophoblastic hyperplasia and failure of embryonic tissue development. The risk recurrence seen to be associated with biallelic maternal mutations in NLRP7 , KHDC3 L PAD16 genes. Women such have major reproductive normal pregnancy only 1.8%. We report the case 31-year-old woman previous three molar pregnancies who on genetic testing was found compound heterozygous for pathogenic variants gene (c.2738A>G c.2078G>C)....
We present the clinicopathologic conference of a 34-year-old lady with history facial palsy 14 years ago who developed new deficits mononeuritis multiplex, maculopapular rash, pancytopenia, splenomegaly, lung involvement and cognitive decline rapidly over three years. Investigations revealed reversal albumin globulin ratio, mediastinal adenopathy, ANA positivity, low C3 levels CSF being inflammatory MRI showing extensive hemorrhagic lesions mass effect. She had progressive fatal course...