Results 51 to 60 of about 18,028 (178)

Indeterminate Cell Histiocytosis: Report of a Case

open access: yesActa Medica Iranica, 2014
Indeterminate cell histiocytosis is a very rare disorder of histiocytes proliferation. It has both Langerhans and non-Langerhans cell histiocytosis immunophenotypic features.
Alireza Ghanadan   +8 more
doaj  

The clinicopathological characteristics and differential diagnosis of histiocytosis

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2015
The histiocytosis is divided into Langerhans' cell histiocytosis (histiocytosis X) and non-Langerhans' cell histiocytosis (NLCH). The former mainly occurs in lymphatic hematopoietic tissue and often involves central nervous system (CNS).
Shi-zhu YU
doaj  

Pericardial Effusion and Tamponade as the Manifestation of Erdheim–Chester Disease

open access: yesAnnals of Internal Medicine: Clinical Cases
We hereby report the case of a 77-year-old man hospitalized due to pericardial effusion and tamponade. Upon investigating potential etiologies of the pericardial effusion, we diagnosed him with non-Langerhans cell histiocytosis, also known as Erdheim ...
María Andreo Galera   +6 more
doaj   +1 more source

Indeterminate Cell Histiocytosis in Association with Acute Myeloid Leukemia

open access: yesDermatology Research and Practice, 2010
Indeterminate cell histiocytosis (ICH) is a rare proliferative disorder, in which the predominant cells share morphologic and immunophenotypic features from both Langerhans and non-Langerhans cell histiocytosis. We describe a 62-year-old man presenting a
Filipa Ventura   +5 more
doaj   +1 more source

Dermoscopy in the diagnosis of juvenile xanthogranuloma [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2018
: Juvenile xanthogranuloma is the most common form of non-Langerhans cell histiocytosis. It manifests clinically as a red-yellow papule, usually showing spontaneous remission. The diagnosis is based on clinical and histological findings.
Thaís Erance de Oliveira   +2 more
doaj   +1 more source

Changes in multi‐gene cancer panels for children: A 4‐year retrospective review

open access: yesJournal of Genetic Counseling, Volume 34, Issue 4, August 2025.
Abstract The multi‐gene panel is the most utilized genetic test to evaluate for germline cancer predisposition syndromes. However, the rate of change of commercial multigene panels is not well understood, and its value as a standalone test has also not been investigated.
Elise G. Williams   +4 more
wiley   +1 more source

Langerhans cell histiocytosis in children: a case report and brief review of the literature

open access: yesPAMJ Clinical Medicine, 2019
Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, is a non-malignant disease involving clonal proliferation of Langerhans cells. It is an orphan disease affecting mainly the child and the young adult.
Zakaria El Ouali   +7 more
doaj   +1 more source

Erdheim-Chester Disease Presenting with Secondary Hypertension as a Result of Bilateral, Proximal Renal Artery Stenosis: A Case Report

open access: yesCase Reports in Nephrology and Dialysis, 2017
Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis presenting most commonly with bone and central nervous system symptoms, including but not limited to bone pain and diabetes insipidus.
Farid Arman   +4 more
doaj   +1 more source

Erdheim-Chester Disease: Utility of 18F-FDG Positron Emission Tomography [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2018
Erdheim-Chester Disease (ECD) is a rare non Langerhans cell histiocytosis of unknown origin with multiorgan involvement. We report a case of a man who presented to us with haematuria, asthenia, fever, nausea and malleolar oedema.
Angelina Cistaro   +4 more
doaj   +1 more source

A young man with multifocal brainstem leptomeningeal disease

open access: yes
Brain Pathology, EarlyView.
Burana Khiankaew   +7 more
wiley   +1 more source

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