Results 61 to 70 of about 10,193 (191)

Chronic Pruritic Papular Eruption in an Elderly Man

JEADV Clinical Practice, EarlyView.
Filipe Monteiro, Inês Tribolet‐Abreu, Gustavo Almeida‐Silva, Inês Amaral, Ivânia Soares, Sónia Fernandes, Joana Antunes   +6 more
wiley   +1 more source

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

PAMJ 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, Nisrine Khoubila, Siham Cherkaoui, Mohamed Rachid, Mouna Lamchahab, Meryem Qachouh, Abdellah Madani, Asmaa Quessar   +7 more
doaj   +1 more source

Dermoscopy in the diagnosis of juvenile xanthogranuloma [PDF]

Anais 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, Roberto Gomes Tarlé, Lismary Aparecida de Forville Mesquita   +2 more
doaj   +1 more source

Uncommon variants of Non-Langerhans Cell Histiocytosis [PDF]

, 2019
Background: Histiocytosis are rare disorders of the mononuclear phagocyte system, characterized by a derangement in differentiation, proliferation or function of monocytes and dendritic cells.
Chiara Moltrasio, Arturo Bonometti, Emanuela Passoni, Emanuela De Juli, Gianluca Nazzaro, Marco Paulli, Silvia Alberti-Violetti, Filippo Bagnoli, Emilio Berti, Jessica Gliozzo   +9 more
core  

Perineurioma‐like EMA‐positive calvarial neoplasms: clinicopathological study of eight cases

Histopathology, EarlyView.
Perineurioma‐like, EMA‐positive calvarial neoplasms (PLECN) are a rare group of intraosseous spindle cell tumours that demonstrate overlapping morphologic features of perineurioma and fibroblastic meningioma. These lesions tend to behave indolently but show a propensity for progressive growth.
Raheel Rizwan, Yingting Mok, Josephine K Dermawan, Alexandra Isaacson, Veronica Ulici, Scott E Kilpatrick, John D Reith, Gabrielle Yeaney, Hakan Ilaslan, Karen J Fritchie   +9 more
wiley   +1 more source

The various clinical spectra of juvenile xanthogranuloma: imaging for two case reports and review of the literature

BMC Pediatrics, 2019
Background Juvenile xanthogranuloma (JXG) belongs to the heterogeneous group of non-Langerhans cell histiocytosis and is caused by an accumulation and proliferation of macrophages.
Michaela Höck, Bernhard Zelger, Gisela Schweigmann, Barbara Brunner, Bettina Zelger, Gabriele Kropshofer, Ursula Kiechl-Kohlendorfer   +6 more
doaj   +1 more source

Non-Langerhans cell histiocytosis associated with lymphocyte-predominant Hodgkin's disease

, 1999
We report a 74-year-old man who presented with a rash on the trunk showing clinical and histological features of non-Langerhans cell histiocytosis. Two years after presentation he developed weight loss, lymphadenopathy and hepatosplenomegaly; a diagnosis
Sviland, L., Ibbotson, S. H., Slater, D. N., Reynolds, N. J.   +3 more
core   +1 more source

Langerhans cell histiocytosis (histiocytosis X) [PDF]

, 1997
There has been a renewed interest in Langerhans cell histiocytosis in recent years due both to advances in basic research and to improvements in diagnostic and treatment approaches.
K Y Lam, Lam, KY
core   +1 more source

Histiocytes: Multifaceted Regulators of Health and Disease

Veterinary Clinical Pathology, EarlyView.
ABSTRACT The mononuclear phagocyte system encompasses macrophages, dendritic cells (DCs), and monocytes. Tissue‐resident macrophages and dendritic cells arise during embryogenesis and are replenished either through self‐renewal or by monocytes during inflammation.
Erika J. Gruber
wiley   +1 more source

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

Case 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, Hania Shakeri, Niloofar Nobakht, Anjay Rastogi, Mohammad Kamgar   +4 more
doaj   +1 more source