Hybrid Clinical and Histopathological Pattern in Annular Lesions: An Overlap between Annular Elastolytic Giant Cell Granuloma and Granuloma Annulare?
- Felipe Ladeira de Oliveira, Luisa Kelmer Côrtes de Barros Silveira, A. M. Machado, J. Nery
- MedicineCase Reports in Dermatological Medicine
- 15 October 2012
A rare hybrid pattern in histopathology demonstrating coexistence of AEGCG and GA is described, and an endocrine disease, such as diabetes mellitus (DM), could contribute to the coexistence.
The Therapeutic Benefit of Allopurinol in the Treatment of Foreign Body Granulomas Caused by Polymethylmethacrylate Microspheres
- Luisa Kelmer Côrtes de Barros Silveira, Felipe Ladeira de Oliveira, F. Barbosa
- MedicineCase Reports in Dermatological Medicine
- 27 December 2012
The objective of this case report is to describe the successful treatment of foreign body granulomas caused by polymethylmethacrylate microspheres using allopurinol, an innovative therapy for this condition.
A Unique Dermoscopy Pattern of Solitary Cutaneous Reticulohistiocytosis
- Felipe Ladeira de Oliveira, Letycia Lopes Chagas Nogueira, C. Meotti
- MedicineCase Reports in Dermatological Medicine
- 6 February 2013
A case of SCR is reported in an 11-year-old child and a unique dermoscopy pattern of this lesion is emphasized and its correlation with clinical and histopathological aspects in the diagnosis is emphasized.
Localized Scleroderma Associated with Chronic Hepatitis C
- Felipe Ladeira de Oliveira, Luisa Kelmer Côrtes de Barros Silveira, M. Rambaldi, F. Barbosa
- MedicineCase Reports in Dermatological Medicine
- 21 November 2012
The objective of this paper is based on the description of a case of localized morphea, which came years after the discovery of hepatitis C, as well as a discussion of possible relations between both diseases.
Netherton’s syndrome and lepromatous leprosy: a mere coincidence?
- Felipe Ladeira de Oliveira, Bruna Obeica Vasconcellos, L. Azulay-Abulafia
- MedicineInternational Journal of Dermatology
- 1 February 2013
Netherton’s syndrome is a rare autosomal recessive condition which involves a complex immunological dysfunction, ichthyosiform dermatitis, and erythroderma, characteristic defects of the hair shaft and atopy.