A5011598942- Sarcoma Diagnosis and Treatment
- Bone Tumor Diagnosis and Treatments
- Vascular Tumors and Angiosarcomas
- Kidney Stones and Urolithiasis Treatments
- Salivary Gland Tumors Diagnosis and Treatment
- Ear and Head Tumors
- Urinary and Genital Oncology Studies
- Gastrointestinal Tumor Research and Treatment
- Pediatric Urology and Nephrology Studies
- AI in cancer detection
- Pancreatic and Hepatic Oncology Research
- Management of metastatic bone disease
- Cancer and Skin Lesions
- Ureteral procedures and complications
- Gallbladder and Bile Duct Disorders
- Lipid metabolism and disorders
- Bladder and Urothelial Cancer Treatments
- Tumors and Oncological Cases
- Urological Disorders and Treatments
- Social Media in Health Education
- Cardiac tumors and thrombi
- Vascular Malformations and Hemangiomas
- Head and Neck Cancer Studies
- Nasal Surgery and Airway Studies
- Soft tissue tumors and treatment
SUNY Upstate Medical University
2018-2021
Hospital Universitario Ramón y Cajal
2013-2019
Low-grade fibromyxoid sarcoma, also known as Evans tumor, is a low-grade sarcoma that most commonly arises in the deep soft tissue of proximal extremities or trunk young adults. It very rare viscera primary site, with only few cases reported literature. Here, we present case tumor occurring an unusual and rarely location; intrathoracic mass arising from diaphragmatic pleura.
Background: In the era of personalized medicine, there has been an increase in demand on cytopathology service to perform rapid onsite evaluation touch imprints (ROSETIs) needle core biopsies (NCBs) ensure sample adequacy and provide preliminary diagnosis. Limited publications have addressed use telecytopathology for ROSETIs. We present our experience with telecytopathology-guided ROSETIs NCBs. Materials Methods: Cytotechnologist transmitted real-time images Diff-QUIK stained NCBs using...
To evaluate histologic changes in middle ear and eustachian tube (ET) mucosa of mice after exposure to tobacco or electronic cigarette (e-cigarette) smoke. determine whether there were any mitigating effects application anti-IL-13 the epidermal growth factor receptor antagonist AG1478 on noted within ET mucosa.Controlled animal study.Fifty BALB/cJ randomly assigned one five groups: A control group with no smoke exposure, two groups exposed smoke, e-cigarette vapor. Within 4 weeks was...
Clear Cell Carcinomas of Müllerian origin are extremely rare within the upper urinary system. Their morphology is identical to that female genital tract. When they arise in tract, it thought be due ectopic embryogenesis. Here, we present a case 21-year-old woman with Carcinoma, type, arising from renal pelvis. Histologically, consisted tubulopapillary architecture associated foamy macrophages and mucinous background. The neoplastic cells exhibited variably sized round nuclei prominent...
Abstract Introduction Low-grade fibromyxoid sarcoma, also known as Evans tumor, is a low-grade sarcoma that most commonly arises in the deep soft tissue of proximal extremities or trunk young adults. It very rare viscera primary site with only few cases reported literature. Here we present case tumor occurring an unusual and rarely location: mediastinum. Method A 32-year-old male presented history persistent cough, subsequent imaging revealed left diaphragmatic measuring around 11 cm...
Abstract: Transducin-like enhancer of split 1 (TLE1) is a transcription factor known for its strong overexpression and immunopositivity in synovial sarcoma. Several studies have revealed that not always specific to sarcoma, with several cases showing positivity peripheral nerve sheath tumors solitary fibrous tumors. Occasional weak staining TLE1 has also been described clear cell high-grade chondrosarcoma, Ewing rhabdomyosarcoma, GIST, myxofibrosarcoma, leiomyosarcoma. Here we present the...
Abstract Epithelial‐myoepithelial carcinoma (EMCa) is a rare neoplasm that most frequently afflicts the parotid gland. Histologically, dual layer of inner, luminal epithelial cells and outer myoepithelial with associated background hyalinization characterize these tumors. Several variants EMCa have been described, including more recent description apocrine variant. We present here case 71‐year‐old male mass diagnosed on FNA as an epithelial‐myoepithelial carcinoma. To our knowledge, this...
Introduction: Metastatic bone lesions are sometimes managed with en bloc resection that creates defects often requiring reconstruction. Reconstructive options for intercalary segmental dependent on defect site and size. The radius is a rare of metastatic disease even rarer to require resection. While vascularized or nonvascularized fibular autografts have been used in this setting, there no prior report detailing the use large autogenous iliac crest graft. We structural autograft...