Cargando…

Xanthomatous nevus: A potential new entity

Detalles Bibliográficos
Autores principales:	Corbeddu, Marialuisa, El Hachem, May, Stracuzzi, Alessandra, Carnevale, Claudia, Alaggio, Rita, Diociaiuti, Andrea
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081870/ https://www.ncbi.nlm.nih.gov/pubmed/33948475 http://dx.doi.org/10.1016/j.jdcr.2021.03.041

Ejemplares similares

First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses
por: Diociaiuti, Andrea, et al.
Publicado: (2020)

Xanthomatous pleuritis
por: Singh, Ranjit Kumar, et al.
Publicado: (2018)

Monomorphic xanthomatous type of xanthogranuloma: a rare entity
por: Devi Nivean, Pratheeba, et al.
Publicado: (2017)

Urinary bladder xanthomatous cystitis
por: Shah, Shrenik J., et al.
Publicado: (2017)

PIK3CA-related overgrowth with an uncommon phenotype: case report
por: Rotunno, Roberta, et al.
Publicado: (2022)

A Rare Case of Xanthomatous Meningioma
por: Altindag, Sultan Deniz, et al.
Publicado: (2022)

Multidisciplinary care for patients with epidermolysis bullosa from birth to adolescence: experience of one Italian reference center
por: Retrosi, Chiara, et al.
Publicado: (2022)

Management of Upper Airway Infantile Hemangiomas: Experience of One Italian Multidisciplinary Center
por: Corbeddu, Marialuisa, et al.
Publicado: (2021)

Vascular Birthmarks as a Clue for Complex and Syndromic Vascular Anomalies
por: Diociaiuti, Andrea, et al.
Publicado: (2021)

Giant congenital exophytic strawberry‐like mass in a newborn
por: Carnevale, C., et al.
Publicado: (2021)

Woolly Hair Nevus: A Rare Entity
por: Venugopal, V, et al.
Publicado: (2012)

Brauer Nevus of Eyebrow: A Rare Entity
por: Kumar, Sumir, et al.
Publicado: (2020)

A case report of palmar xanthoma with xanthomatous neuropathy
por: Lee, Hyun Yi, et al.
Publicado: (2021)

Epidermolysis Bullosa in children: the central role of the pediatrician
por: Marchili, Maria Rosaria, et al.
Publicado: (2022)

Woolly Hair Nevus Type 2: Rare Entity
por: Taj, Farhana Tahseen, et al.
Publicado: (2019)

Congenital self-healing reticulohistiocytosis in a newborn: unusual oral and cutaneous manifestations
por: Rizzoli, Alessandra, et al.
Publicado: (2021)

Xanthomatous Hypophysitis Mimicking a Pituitary Adenoma: Case Report and Review of the Literature
por: Aste, Laura, et al.
Publicado: (2010)

Steroid Responsive Xanthomatous Hypophysitis Associated with Autoimmune Thyroiditis: A Case Report
por: Joung, Ji Young, et al.
Publicado: (2013)

Rectal Blue Nevus: Distinguishing Features of a Rare Entity
por: Mohan, Neena, et al.
Publicado: (2016)

Xanthomatous Pleuritis Associated With Pancreaticopleural Fistula
por: Nakashima, Koki, et al.
Publicado: (2022)

Microcystic Adnexal Carcinoma with Xanthomatous Reaction
por: FUJII, Kazuyasu, et al.
Publicado: (2021)

Xanthomatous Hypophysitis Secondary to a Ruptured Rathke’s Cleft Cyst: A Case Report
por: Gezer, Emre, et al.
Publicado: (2022)

Angioma serpiginosum: a case report and review of the literature
por: Diociaiuti, Andrea, et al.
Publicado: (2019)

Bilateral Systematized Epidermolytic Verrucous Epidermal Nevus: A Rare Entity
por: Mishra, Vivek, et al.
Publicado: (2015)

Xanthomatous cutaneous Rosai-Dorfman disease with overlapping features of IgG4-related disease
por: Gitin, Alexander, et al.
Publicado: (2022)

Cutaneous Infantile Haemangiomas with Intracranial and Intraspinal Involvement: A European Multicentre Experience and Review
por: DIOCIAIUTI, Andrea, et al.
Publicado: (2020)

Xanthomatous sialadenitis: Autoimmune- or treatment-induced lesions?
por: Handra-Luca, Adriana
Publicado: (2017)

Prominent Follicular Keratosis in Multiple Intestinal Atresia with Combined Immune Deficiency Caused by a TTC7A Homozygous Mutation
por: Diociaiuti, Andrea, et al.
Publicado: (2022)

Juvenile idiopathic arthritis in infants with Harlequin Ichthyosis: two cases report and literature review
por: Auriti, Cinzia, et al.
Publicado: (2020)

Multi-drugs resistant acne rosacea in a child affected by Ataxia-Telangiectasia: successful treatment with Isotretinoin
por: Cantarutti, Nicoletta, et al.
Publicado: (2015)

Paraneoplastic pemphigus and Castleman’s disease: a case report and a revision of the literature
por: Irrera, Mariangela, et al.
Publicado: (2023)

Xanthomatous Hypophysitis Presenting in an Adolescent Girl: A Long-Term Follow-Up of a Rare Case and Review of the Literature
por: Wong, Jeanne Sze Lyn, et al.
Publicado: (2021)

Xanthomatous Hypophysitis: A Case Report and Comprehensive Literature Review
por: Zhu, Jianyu, et al.
Publicado: (2021)

A Xanthomatous Eruption in a Patient with Jaundice and Constitutional Symptoms
por: Serra-García, Laura, et al.
Publicado: (2022)

Xanthomatous sypophysitis secondary to a ruptured Rathke's cleft cyst
por: Gezer, Emre, et al.
Publicado: (2023)

Two Italian Patients with ELOVL4-Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization
por: Diociaiuti, Andrea, et al.
Publicado: (2021)

Patient with giant Becker's nevus and epidermal nevus
por: Issa, George, et al.
Publicado: (2011)

Pagetoid reticulosis (Woringer-Kolopp disease) in a 2-year-old girl—Case report and review of the literature
por: Corbeddu, Marialuisa, et al.
Publicado: (2018)

Melorheostosis: a rare entity: a case report
por: Kherfani, Abdelhakim, et al.
Publicado: (2014)

Becker's Nevus with Recurrent Eczema Limited to the Nevus Lesion
por: Lee, Ji Su, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_e6h2g3coq37bgsu7ed89519ff1