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Mycetoma: A Common Yet Unrecognized Health Burden in Central India
Context: Mycetoma is a chronic suppurative infective disorder of skin, subcutaneous tissue, fascia, and bones caused by the traumatic inoculation of either fungal (eumycotic) or bacterialExpand
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Subcutaneous Fat Necrosis of the Newborn Secondary to Sepsis: A Case Report
Subcutaneous fat necrosis of the newborn (SCFN) is a rare noninfectious type of panniculitis, which primarily affects term and postterm infants. It is usually a benign, self-limiting condition, butExpand
Angina Bullosa Hemorrhagica
© 2019 Indian Dermatology Online Journal | Published by Wolters Kluwer Medknow A 48‐year‐old male, a known case of hypertension and diabetes mellitus, presented with asymptomatic, single blood‐filledExpand
Angina bullosa hemorrhagica: A rare case report in known asthmatic on inhaled corticosteroids
Angina bullosa hemorrhagica (ABH) is characterized by development of acute onset of painless solitary or multiple blood-filled vesicles or bullae in oral mucosa which are not attributed to bloodExpand
Dermatological changes in pregnancy in central India: a cross sectional study
Background: Pregnancy is a period of profound endocrine and metabolic alterations which make the pregnant woman susceptible to changes in the skin and its appendages. These changes in pregnancy canExpand
Bardet–Biedl Syndrome with Café-au-Lait Macule: Association or Coincidence?
An 8‐year‐old male child, born out of nonconsanguineous marriage, presented with dark‐colored skin lesion over the neck and abdomen. The parents of the child gave history of diminished vision andExpand
Sorafenib Induced Hand-Foot Skin Reaction at Low Dose
© 2020 Indian Dermatology Online Journal | Published by Wolters Kluwer Medknow Sir, Sorafenib, a small multikinase inhibitor, is the Food and Drug Administration (FDA) approved for the treatment ofExpand
Segmental giant café au lait macule in neurofibromatosis 1
A 2-year-old male child born of third degree consanguineous marriage was brought to dermatology outpatient department with multiple dark colored flat lesions over body and one large dark colored flatExpand
Klippel–Trenaunay Syndrome with Arterio-veno-lymphatic Malformation: A Rare Presentation
Klippel–Trenaunay syndrome (KTS) is a rare disorder characterized by triad of vascular malformations, varicose veins, and bony or soft tissue hypertrophy involving an extremity. Port wine stain isExpand