A5028598959- Dermatological and Skeletal Disorders
- Genetic and rare skin diseases.
- Immunodeficiency and Autoimmune Disorders
- Vascular Tumors and Angiosarcomas
- Oral and Maxillofacial Pathology
- Genital Health and Disease
- Skin and Cellular Biology Research
- Cancer and Skin Lesions
- Nail Diseases and Treatments
- Salivary Gland Tumors Diagnosis and Treatment
- Cellular transport and secretion
- Reproductive tract infections research
- Female Genital Mutilation/Cutting Issues
- Urinary Tract Infections Management
- Cervical Cancer and HPV Research
- Pneumocystis jirovecii pneumonia detection and treatment
- Elbow and Forearm Trauma Treatment
- Soft tissue tumor case studies
- Musculoskeletal synovial abnormalities and treatments
- Nonmelanoma Skin Cancer Studies
- Hedgehog Signaling Pathway Studies
- Dermatological and COVID-19 studies
- Urological Disorders and Treatments
- melanin and skin pigmentation
- Vasculitis and related conditions
Bangalore Medical College and Research Institute
2024-2025
Christian Medical College & Hospital
2020-2025
Sri Venkateswara Medical College and Ruia Hospital
2024
Christie's
2021
BACKGROUND Treatment of ingrown toenail includes various nonsurgical and surgical treatments. However, there is no consensus on the ideal first-choice treatment. OBJECTIVE To compare phenolization versus matricectomy (SM) after lateral nail plate avulsion in terms efficacy, recurrence rates, postoperative outcomes, cosmesis. METHODS The authors enrolled 45 consenting patients randomized them into 2 groups (Group 1 = Group SM) using stratified block randomization followed up at week, month, 6...
The authors declare no conflicts of interest.
A wide range of inherited and acquired conditions can manifest as infantile erythroderma, among which CARD14 -associated papulosquamous eruption (CAPE) is a rare cause. An infant boy presented with psoriasiform rash that progressed to erythroderma was unresponsive topical steroids cyclosporine. The early onset the disease, its severity resistance conventional treatment were suggestive genetic Genetic evaluation revealed homozygous variant uncertain significance establishing diagnosis CAPE,...
Click here for the corresponding questions to this CME article.
Epidermolytic ichthyosis (EI) is a rare inherited related to heterozygous mutations in the Keratin 1 or 10 genes. Because of broad phenotypic spectrum, it sometimes difficult differentiate from other keratinopathic ichthyoses (KI) clinical practice. We report an intriguing case KI presenting as generalized reticulate pattern surrounding islands normal skin, epidermolytic hyperkeratosis and binucleate cells on histopathology, mutation KRT10. Through this case, we would like demonstrate...
Abstract Sorafenib is a multikinase inhibitor used in the treatment of various solid tumors. Mucocutaneous adverse events are experienced by 70 to 90% patients receiving sorafenib, underscoring importance awareness among oncologists and dermatologists. Spiny follicular hyperkeratosis (SFH) benign rarely reported skin reaction linked sorafenib. It characterized flesh-colored or white, hyperkeratotic spicules, preferentially involving face, scalp, upper trunk, arms. Besides being acknowledged...
Question A 76-year-old female came to us for evaluation of gradually progressing hyperpigmented papules over her abdomen 10 years duration. There was occasional discharge and few lesions healed spontaneously with scarring hyperpigmentation. She reported minimal improvement topical tretinoin 0.05% used previously. Her medical history included tuberculous ascites treated 11 back, diabetes uncontrolled blood sugars, chronic liver disease secondary non-alcoholic fatty disease, complete heart...