Cargando…

Facial Trichoepitheliomas Revealing the Rare Brooke–Spiegler Syndrome

Detalles Bibliográficos
Autores principales:	Gaudiello, F., Costanzo, Luca, Fabbrocini, Gabriella, Patri, Angela
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Letter to Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10075353/ https://www.ncbi.nlm.nih.gov/pubmed/37034546 http://dx.doi.org/10.4103/ijt.ijt_108_21

Ejemplares similares

Brooke-Spiegler Syndrome
por: Mohiuddin, Waseem, et al.
Publicado: (2018)

Giant Vascular Cylindroma in a Case of Brooke-Spiegler Syndrome
por: Watanabe, Yukina, et al.
Publicado: (2022)

<i>CYLD</i> GeneticTesting for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas
por: Dubois, Anna, et al.
Publicado: (2015)

Brooke-Spiegler Syndrome: A Rare Entity
por: Manchanda, Kajal, et al.
Publicado: (2012)

Brooke-Spiegler Syndrome: A Rare Entity
por: Rathi, Monika, et al.
Publicado: (2014)

Laser-assisted delivery of imiquimod in Brooke-Spiegler syndrome()
por: Botsali, Aysenur, et al.
Publicado: (2022)

Brooke-Spiegler Syndrome With Cervical Spine Lesion
por: Vasenina, Valentina, et al.
Publicado: (2020)

Brooke-Spiegler Syndrome: Age-Related Progression in a Family Group
por: Michelerio, Andrea, et al.
Publicado: (2023)

Malignant cylindroma in a patient with Brooke-Spiegler syndrome
por: Borik, Liliane, et al.
Publicado: (2015)

Brooke–Spiegler Syndrome: Familial Cylindromatosis, a Rare Variant of a Rare Familial Syndrome
por: Patel, Harsh, et al.
Publicado: (2021)

Turban Tumor: A Classical Presentation of Brooke–Spiegler Syndrome
por: Patra, Suman, et al.
Publicado: (2018)

Malignant eccrine spiradenocylindroma and parotid gland involvement in Brooke Spiegler syndrome
por: Merlo, Giulia, et al.
Publicado: (2022)

Brooke-Spiegler Syndrome with Multiple Scalp Cylindromas and Bilateral Parotid Gland Adenomas
por: Kalina, Peter, et al.
Publicado: (2012)

The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene
por: Farkas, Katalin, et al.
Publicado: (2016)

A rare case of Brooke-Spiegler syndrome: integrated surgical treatment of multiple giant eccrine spiradenomas of the head and neck in a young girl
por: Portincasa, A., et al.
Publicado: (2018)

Heterozygous Cylindromatosis Gene Mutation c.1628_1629delCT in a Family with Brook-Spiegler Syndrome
por: Aguilera, Cintia Arjona, et al.
Publicado: (2016)

A Case of Multiple Desmoplastic Trichoepithelioma
por: Moon, Seong Hun, et al.
Publicado: (2016)

Giant Solitary Trichoepithelioma: A Diagnosis of Exclusion
por: Patil, Nitin Krishna, et al.
Publicado: (2022)

Multiple Pigmented Trichoepitheliomas: A Case Report
por: Caccavale, Stefano, et al.
Publicado: (2023)

Trichoepithelioma and tattooing: a causal or casual relationship?
por: Fidanzi, Cristian, et al.
Publicado: (2023)

Multiple familial trichoepitheliomas in association with squamous cell carcinoma
por: Ganguly, Satyaki, et al.
Publicado: (2012)

Multiple Trichoepitheliomas: Cosmetic Improvement with Dermabrasion
por: Raghuveer, Chekuri, et al.
Publicado: (2011)

Immunologic skin signatures in SARS-CoV-2-negative patients with chilblain-like lesions
por: Vastarella, Maria, et al.
Publicado: (2021)

Gastrointestinal tract diseases as a risk factor for SARSCoV2 rectal shedding? An Italian report on 10 COVID-19 patients
por: Patrì, Angela, et al.
Publicado: (2021)

Multiple trichoepitheliomas: A rare occurrence
por: Karikal, Arvind, et al.
Publicado: (2013)

Metastatic trichoblastic carcinoma in the setting of trichoblastomatosis and multiple facial trichoepitheliomas
por: Janeczek, Monica, et al.
Publicado: (2021)

A rare case of sporadic multiple trichoepitheliomas
por: Sanaa, Krich, et al.
Publicado: (2015)

Trichoepithelioma: A Rare but Crucial Dermatologic Issue
por: Mohammadi, Ali Akbar, et al.
Publicado: (2014)

Repigmentation of White Forelock in a Familial Case of Piebaldism Reported via Teledermatology in the COVID-19 Era
por: Gaudiello, Francesca, et al.
Publicado: (2021)

Marin-Amat syndrome: A rare facial synkinesis
por: Jethani, Jitendra
Publicado: (2007)

Reply from George A. Brooks
por: Brooks, George A.
Publicado: (2022)

Giant solitary trichoepithelioma
por: Teli, Bhavuray, et al.
Publicado: (2015)

Inherited desmoplastic trichoepitheliomas
por: Lovgren, M.‐L., et al.
Publicado: (2019)

Solitary nasal trichoepithelioma
por: Patrocinio, Lucas Gomes, et al.
Publicado: (2015)

Hydroxychloroquine and ivermectin: A synergistic combination for COVID-19 chemoprophylaxis and treatment?
por: Patrì, Angela, et al.
Publicado: (2020)

Multiple Trichoepithelioma Syndrome: A Case Report
por: Guerreiro, Frederico P, et al.
Publicado: (2023)

Sexual transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): A new possible route of infection?
por: Patrì, Angela, et al.
Publicado: (2020)

The cytology of giant solitary trichoepithelioma
por: Krishnamurthy, Jayashree, et al.
Publicado: (2010)

Radiosurgical Ablation of Solitary Trichoepithelioma
por: Hanumanthiah, H C
Publicado: (2008)

Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
por: Vastarella, Marina, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_1fd5aj2kggc7uj73fk635uphpp