Results 131 to 140 of about 42,023 (285)

A Middle-Aged Female with Multiple Brownish Plaques and Nodules: A Case Report of Multiple Cutaneous Reticulohistiocytomas

open access: yesNepal Journal of Dermatology, Venereology & Leprology, 2018
Non-Langerhans-Cell histiocytosis spectrum of disorders includes multicentric reticulohistiocytosis (MR) and multiple cutaneous reticulohistiocytomas (MCR), which are very uncommon granulomatous conditions. In reticulohistiocytoma, the most common sites
Karuna Singh Sijapati   +2 more
doaj  

Histiocitosis de células de Langerhans en el raquis infantil [PDF]

open access: yes, 2006
Introducción: la Histiocitosis de células de Langerhans incluye un amplio espectro de enfermedades de etiología desconocida, observada preponderantemente en niños.
Fernández, Claudio A.   +2 more
core  

Histiocytosis-X [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1962
J S, Pegum, P, Wallis
openaire   +2 more sources

Cellular distribution of mutations and association with disease risk in Langerhans cell histiocytosis without BRAFV600E [PDF]

open access: gold, 2022
Paul Milne   +6 more
openalex   +1 more source

New cases expand the genotype, phenotype and therapeutic landscape of H syndrome

open access: yes
British Journal of Haematology, Volume 208, Issue 1, Page 363-366, January 2026.
Clément Triaille   +10 more
wiley   +1 more source

Gastrointestinal Langerhans cell histiocytosis responding to cladribine and imatinib mesylate [PDF]

open access: yes, 2010
Gastrointestinal involvement in Langerhans cells histiocytosis (LCH) is extremely rare. An optimal treatment regimen is not defined yet and its prognosis is relatively poor.
Agreda Vásquez, Gladys Patricia   +4 more
core  

Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis [PDF]

open access: gold, 2014
Vincent Grobost   +4 more
openalex   +1 more source

A neonatal pustule:Langerhans cell histiocytosis [PDF]

open access: yes, 2019
Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia   +4 more
core  

Sinus Histiocytosis with Massive Lymphadenopathy (Rosai Dorfman Disease) and Anaplastic Large Cell Lymphoma [PDF]

open access: yes
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare and benign source of lymphadenopathy first described in 1969. This disease commonly presents in children and young adults with supra-diaphragmatic lymphadenopathy mainly at cervical nodal ...
Garg, Kapil Kumar, Singh, Harpreet
core   +1 more source

Home - About - Disclaimer - Privacy