Phakomatosis pigmento vascularis with bulbar melanosis and oral changes in an Indian male patient - A rare case report
| Autor: | Mysore K Sunil, Anudeep Raina, Geetanjali Jina, SV Ravindra |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
lcsh:Medical physics. Medical radiology. Nuclear medicine
medicine.medical_specialty Capillary malformation lcsh:R895-920 Sturge–Weber syndrome Phakomatosis nevus of ota Medicine Radiology Nuclear Medicine and imaging General Dentistry phakomatosis Vasomotor business.industry Neural crest Melanocytic nevus medicine.disease Dermatology Nevus of Ota Melanosis melanosis lcsh:RK1-715 sturge-weber syndrome Otorhinolaryngology lcsh:Dentistry nevi business |
| Zdroj: | Journal of Indian Academy of Oral Medicine and Radiology, Vol 32, Iss 2, Pp 182-185 (2020) |
| ISSN: | 0972-1363 |
| Popis: | Phakomatosis Pigmento Vascularis (PPV) refers to a developmental abnormality characterized by concurrence of pigmented and capillary malformation with or without systemic manifestations. Abnormal development of melanocytic nevus cells and vasomotor neural cells arising from the neural crest has been attributed in the pathogenesis of PPV. It is classified into 5 major subtypes. Although there is no sex predilection, a preponderance of these cases has been noted in Japan. Through this rare case report, we describe the oral changes of PPV type II b in a 28 year old Indian male patient. |
| Databáze: | OpenAIRE |
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