Results 21 to 30 of about 12,716 (134)

Novel actionable ROS1::GIT2 fusion in non-Langerhans cell histiocytosis with central nervous system involvement [PDF]

Acta Neuropathologica, 2022
Gábor Bedics, Monika Csóka, Lilla Reiniger, Edit Varga, Zoltán Liptai, Gergő Papp, Anna Bekő, Catherine Cervi, Csaba Bödör, Bálint Scheich   +9 more
openaire   +3 more sources

Clinical features and outcomes of non-pulmonary unifocal adult Langerhans cell histiocytosis [PDF]

Blood Cancer Journal, 2022
Dear Editor, Langerhans cell histiocytosis (LCH) is a rare hematologic disorder affecting adults with an estimated incidence of 1 – 2 cases per million [1].
Marie Hu, Gaurav Goyal, Jithma P. Abeykoon, Aldo A. Acosta‐Medina, Gordan J. Ruan, Jason R. Young, Aishwarya Ravindran, N. Nora Bennani, Mithun Vinod Shah, Robert Vassallo, Jay H. Ryu, Caroline Davidge‐Pitts, Matthew J. Koster, W. Oliver Tobin, Julio C. Sartori‐Valinotti, Karen L. Rech, Ronald S. Go   +16 more
openalex   +2 more sources

Isolated Bone Marrow Non–Langerhans Cell Histiocytosis Preceding RUNX1-Mutated Acute Myeloid Leukemia: Case Report and Literature Review [PDF]

American Journal of Clinical Pathology, 2019
OBJECTIVES The prevalence of concomitant myeloid neoplasms was recently reported to be unexpectedly high among adults without non-Langerhans cell histiocytosis (non-LCH); however, the coexistence of non-LCH with RUNX1 genetic aberration has not been ...
Areej Al Mugairi, Saeed Al Turki, Hind Salama, Khlood Al Ahmadi, Khadega A. Abuelgasim, Moussab Damlaj   +5 more
openalex   +2 more sources

Cutaneous sinus histiocytosis of face of the non-Langerhans cell histiocytoses type (cutaneous Rosai — Dorfman disease)

Vestnik Dermatologii i Venerologii, 2018
An extremely rare case of sinus histiocytosis of the non-Langerhans cell histiocytoses type is described in 55-year-old patient with isolated localization of cutanious lesion on the right cheek without involvement of nodular structures.
Е. V. Sokolovsky, Г. Н. Михеев, Rybakova Mg, Е. B. Manasheva, V. A. Seredina   +4 more
openalex   +3 more sources

Renovascular Hypertension: Unraveling a Case of Mixed Histiocytosis

Annals of Internal Medicine: Clinical Cases, 2023
Renovascular hypertension is a cause of secondary hypertension. Atherosclerotic renal artery stenosis and fibromuscular dysplasia are the main causes, but other rare entities can involve the renal arteries.
Pedro Marques, Joana Tender Vieira, Inês M. de Sá, André Carvalho, João Rocha-Neves, Irene Gullo, Edite Pereira, José Manuel Lopes, Jorge Almeida   +8 more
doaj   +1 more source

The use of topical Rapamycin in successfully treating non-Langerhans cell histiocytosis in a pediatric patient

Journal of Skin and Sexually Transmitted Diseases
Non-Langerhans cell histiocytosis (non-LCH) refers to a collection of medical conditions distinguished by the excessive growth of histiocytes in bodily tissues. It is important to note that these conditions do not meet the established diagnostic criteria
David Pudukadan, Jeevana Mary Jose
openalex   +2 more sources

Adult-onset of Langerhans cell histiocytosis: a clinical case

Alʹmanah Kliničeskoj Mediciny, 2021
Langerhans cell histiocytosis is mainly diagnosed in children, and its manifestation in adult age is quite uncommon. Skin rashes may be non-specific and mimic a number of dermatoses.
Olga V. Chernysheva, Olga V. Dorokhina, Albina N. Khlebnikova, Elena V. Selezneva   +3 more
doaj   +1 more source

A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations

Journal of Cutaneous Immunology and Allergy, 2023
Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito, Akihiko Uchiyama, Yayoi Shibusawa, Sei‐ichiro Motegi   +3 more
doaj   +1 more source

Relapse of Non-Gastrointestinal Langerhans Cell Histiocytosis in the Rectum in a Child: A Case Report

Clinical Medicine Insights: Case Reports, 2023
Langerhans cell histiocytosis (LCH) is a rare disorder most commonly involving skin, bone and lung. The gastrointestinal tract (GIT) is an uncommon site of disease and only a handful of case reports exist.
Saad Muhammad Saeed, Sundus Bilal, Asif Loya, Muhammed Aasim Yusuf   +3 more
openalex   +2 more sources

Adult Langerhans cell histiocytosis with pulmonary and colorectoanal involvement: a case report

Journal of Medical Case Reports, 2017
Background Langerhans cell histiocytosis is a rare systemic disease characterized by the abnormal overproduction of histiocytes that tend to infiltrate single or multiple organ systems leading to significant tissue damage. It mainly affects – by order of
Mohamad Jihad Mansour, Elias Mokbel, Eddy Fares, Janah Maddah, Fadi Nasr   +4 more
doaj   +1 more source