María Paz Rollán

ORCID: 0000-0003-0282-9288
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About
Contact & Profiles
Research Areas
  • Genetic and rare skin diseases.
  • Helicobacter pylori-related gastroenterology studies
  • Cutaneous Melanoma Detection and Management
  • Soft tissue tumor case studies
  • Eosinophilic Esophagitis
  • Viral-associated cancers and disorders
  • Dermatologic Treatments and Research
  • Cytomegalovirus and herpesvirus research
  • Gastrointestinal disorders and treatments
  • Hedgehog Signaling Pathway Studies
  • Vascular Malformations and Hemangiomas
  • Autoimmune Bullous Skin Diseases
  • Eosinophilic Disorders and Syndromes
  • Polyomavirus and related diseases
  • Gastric Cancer Management and Outcomes
  • Tumors and Oncological Cases
  • Veterinary medicine and infectious diseases
  • Immunodeficiency and Autoimmune Disorders

Clínica Alemana
2021-2022

Universidad del Desarrollo
2021-2022

Darier disease is an uncommon autosomal dominant inherited disease, caused by a mutation in the ATP2A2 gene. The clinical findings are hyperkeratotic papules on trunk, scalp, face, and neck, maceration of intertriginous areas, palmar pits, whitish oral mucosa nail abnormalities. main histopathologic acantholysis dyskeratotic keratinocytes. Dermatoscopic features comedo-like openings with central polygonal yellowish/brownish structure, surrounded halo. First-line treatment includes acitretin....

10.1016/j.abd.2021.05.021 article EN cc-by Anais Brasileiros de Dermatologia 2022-07-16

Abstract We present a 12‐year‐old girl with multiple geographic capillary malformations in segmental distribution over the left trunk and arm that were at birth evolved years ulceration, atrophy, subsequent scarring. Our case is clinically consistent recently described entity “multifocal malformation central atrophy.” To our knowledge, patient oldest reported to date.

10.1111/pde.14622 article EN Pediatric Dermatology 2021-06-21

El lupus eritematoso sistémico buloso (LESB) es una enfermedad ampollar subepidérmica autoinmune secundaria a la presencia de autoanticuerpos contra el colágeno VII membrana basal. Es considerada variante (LES), siendo infrecuente en población pediátrica.Objetivo: Describir caso paciente pediátrica con erupción compatible LESB.Caso Clínico: Paciente sexo femenino 16 años ascendencia mapuche, antecedentes LES diagnosticado los 10 edad, tratamiento. Consultó por vesiculobulosa generalizada 6...

10.32641/andespediatr.v92i3.2729 article ES cc-by Andes pediatrica 2021-06-22
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