Isolated Langerhans Cell Histiocytosis of the Thyroid: A very rare case report.

Autor: Erol, Ali, Gözden, Hilmi Erdem, Koç, Sinan, Kuzular, Hatice

Publikováno v: Turkish Journal of Internal Medicine; 2024, Vol. 6 Issue 4, p163-166, 4p

Erdheim–Chester Disease of the Breast: First Review and First Case of Isolated Severe Gynecomastia.

Autor: Giardino, Francesco Ruben¹ (AUTHOR) f.ruben.giardino@gmail.com, Cuomo, Roberto¹ (AUTHOR), Pozzi, Mirco¹ (AUTHOR), Marcaccini, Gianluca¹ (AUTHOR), Bacchini, Stefano¹ (AUTHOR), Marzouk El Araby, Mohamed¹ (AUTHOR), Grimaldi, Luca¹ (AUTHOR), Nisi, Giuseppe¹ (AUTHOR)

Publikováno v: Diagnostics (2075-4418). Apr2023, Vol. 13 Issue 7, p1239. 14p.

Expression and Clinical Correlation of PD-1/PD-L1 and VE1(BRAFp.V600E) in Pediatric Langerhans Cell Histiocytosis.

Autor: Tandon, Sneha¹ sneha.tandon@nhs.net, Weitzman, Sheila², Joyce, Brooklyn², Mcguire, Bryan³, Stephens, Derek³, Whitlock, James², Hawkins, Cynthia⁴, Bo Yee Ngan⁴, Abla, Oussama²

Publikováno v: Mediterranean Journal of Hematology & Infectious Diseases. 2023, Vol. 15 Issue 1, p1-9. 9p.

Liquid biopsy of cerebrospinal fluid enabling the detection and therapeutic targeting of the BRAF^V600E mutation in a patient with overlapping Erdheim-Chester/Rosai-Dorfman disease.

Autor: Pieri, Valentina, Berzero, Giulia, Paterra, Rosina, Ferré, Laura, Tomelleri, Alessandro, Campochiaro, Corrado, Esposito, Federica, Calimeri, Teresa, Cangi, Maria Giulia, Tenace, Nazario Pio, Ferreri, Andrés José María, Castellano, Antonella, Barbera, Maurizio, Anzalone, Nicoletta, Gay, Lorenzo Gabriel, Bello, Lorenzo, Colecchia, Maurizio, Ponzoni, Maurilio, Finocchiaro, Gaetano, Filippi, Massimo

Publikováno v: Journal of Neurology; Jan2024, Vol. 271 Issue 1, p575-579, 5p

Childhood Langerhans cell histiocytosis with severe lung involvement: a nationwide cohort study.

Autor: Le Louet, Solenne¹ (AUTHOR) solennelelouet@gmail.com, Barkaoui, Mohamed-Aziz¹ (AUTHOR), Miron, Jean¹ (AUTHOR), Galambrun, Claire² (AUTHOR), Aladjidi, Nathalie³ (AUTHOR), Chastagner, Pascal⁴ (AUTHOR), Kebaili, Kamila⁵ (AUTHOR), Armari-Alla, Corinne⁶ (AUTHOR), Lambilliotte, Anne⁷ (AUTHOR), Lejeune, Julien⁸ (AUTHOR), Moshous, Despina^9,10 (AUTHOR), Della Valle, Valeria¹¹ (AUTHOR), Sileo, Chiara¹¹ (AUTHOR), Ducou Le Pointe, Hubert¹¹ (AUTHOR), Chateil, Jean-François¹² (AUTHOR), Renolleau, Sylvain¹³ (AUTHOR), Piloquet, Jean-Eudes¹⁴ (AUTHOR), Portefaix, Aurelie¹⁵ (AUTHOR), Epaud, Ralph¹⁶ (AUTHOR), Chiron, Raphaël¹⁷ (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 9/9/2020, Vol. 15 Issue 1, p1-11. 11p.