A5046270689- Autoimmune Bullous Skin Diseases
- Autoimmune and Inflammatory Disorders
- Eosinophilic Disorders and Syndromes
- Drug-Induced Adverse Reactions
- Thyroid Cancer Diagnosis and Treatment
- Vascular Malformations and Hemangiomas
- Syphilis Diagnosis and Treatment
- Herpesvirus Infections and Treatments
- Leprosy Research and Treatment
- Chronic Myeloid Leukemia Treatments
- Amoebic Infections and Treatments
- Cutaneous lymphoproliferative disorders research
- Infectious Diseases and Tuberculosis
- Head and Neck Anomalies
- Pancreatitis Pathology and Treatment
- Bartonella species infections research
- Genomics and Rare Diseases
- Glycosylation and Glycoproteins Research
- COVID-19 Clinical Research Studies
- Histiocytic Disorders and Treatments
- BRCA gene mutations in cancer
- Abdominal Trauma and Injuries
- COVID-19 and healthcare impacts
- Cytomegalovirus and herpesvirus research
- Mycobacterium research and diagnosis
University of Florida
2023-2024
Florida College
2023-2024
Edward Via College of Osteopathic Medicine
2020-2021
Jacksonville College
2020
Mayo Clinic in Florida
2020
Addenbrooke's Hospital
1980
Cambridge School
1980
University of Cambridge
1980
Classically, secondary syphilis presents as a generalized nonpruritic papulosquamous eruption, which may include the palms and soles, typically occuring 3 to 10 weeks after initial spirochete inoculation.1,2 Numerous unusual presentations have been reported, including but not limited to, annular or figurative plaques, “moth-eaten” alopecia, polymorphic papules, granulomatous nodules, crusted nail changes.3 Typical histologic findings superficial deep perivascular lymphocytic infiltrate with...
Without tissue biopsy and holistic review of presentation, histology, immunohistochemistry, lymphocytoma cutis (LC) can often be misdiagnosed as other benign conditions or malignant pathologies such cutaneous B cell lymphoma (CBCL). A 36-year-old female presented with a two-year history progressive indurated, edematous plaque in the preauricular area. At patient also had labs significant for thrombocytopenia eosinophilia. Original treatment topical steroids did not lead to clinical...
Antecedentes: La enfermedad de Gaucher es causada por la acumulación del glicolípido glucosilceramidasa en el sistema macrofagocítico debido a deficiencia enzima glucocerebrosidasa. Se han descrito tres formas clínicas enfermedad. prevalencia mundial 1 caso 40,000- 100,000 nacimientos, aunque poblaciones ascendencia judío askenazi puede ser tan alta como 850 individuos. El diagnóstico definitivo se obtiene través observación directa células médula ósea y confirmación diagnóstica las...
In the earliest cases of COVID-19, a higher percentage severe and fatal was observed in patients with cancer, including those haematological malignancies. However, chronic myeloid leukaemia (CML) had better prognoses, suggesting that tyrosine kinase inhibitors (TKIs) may have therapeutic effect against SARS-CoV-2. This study describes clinical epidemiological characteristics CML receiving TKIs tested for SARS-CoV-2 Tegucigalpa, Honduras.An Analytical cross-sectional conducted. The sample...
Acute Generalized Exanthematous Pustulosis is a rare drug-induced skin disorder that can present at any age. It typically noted by swelling and erythema, with numerous facial and/or anogenital nonfollicular pustules quickly disseminate. Staphylococcal scalded syndrome presents erythema similarly favor the head intertriginous sites subsequent bullae formation. We case of four-year-old female who presented SSSS complicated development AGEP discuss course her condition treatment.