Results 21 to 30 of about 1,612 (168)

Incidence, prevalence and survival in patients with Langerhans cell histiocytosis: A national registry study from England, 2013–2019

British Journal of Haematology, Volume 199, Issue 5, Page 728-738, December 2022., 2022
Summary This analysis is the largest population‐based study to date to provide contemporary and comprehensive epidemiological estimates of all third edition of the International Classification of Diseases for Oncology (ICD‐O‐3) coded Langerhans cell histiocytosis (LCH) from England.
Hanhua Liu, Charles A. Stiller, Colin J. Crooks, Brian Rous, Mary Bythell, John Broggio, Judith Rankin, Vasanta Nanduri, Peter Lanyon, Tim R. Card, Lu Ban, Lucy Elliss‐Brookes, Jennifer M. Broughan, Lizz Paley, Kwok Wong, Andrew Bacon, Mark Bishton, Joe West   +17 more
wiley   +1 more source

Children atopic dermatitis: Diagnosis, mimics, overlaps, and therapeutic implication

Dermatologic Therapy, Volume 35, Issue 12, December 2022., 2022
Abstract Atopic dermatitis (AD) is a chronic inflammatory, itching skin with a significant psychosocial impact on patients and relatives. In adults and adolescents besides flexural eczema, head and neck eczema, and hand eczema, which are the most frequent clinical phenotypes (84.9% and 84.2%, respectively), there are also other possible presentation ...
Maddalena Napolitano, Gabriella Fabbrocini, Fabrizio Martora, Lucia Genco, Matteo Noto, Cataldo Patruno   +5 more
wiley   +1 more source

A case of langerhans cell histiocytosis of the mandible that spontaneously regressed after biopsy in a child

Clinical Case Reports, Volume 9, Issue 6, June 2021., 2021
In younger patients of LCH, we should consider that the effectiveness of follow‐up without aggressive treatment for SS‐type LCH in the oral and maxillofacial bone. However, there are very rare case in which an SS‐type LCH recurred after showing a healing tendency.
Kisho Ono, Tatsuo Okui, Yuki Kunisada, Kyoichi Obata, Masanori Masui, Shoji Ryumon, Soichiro Ibaragi, Tomoya Nakamura, Akira Sasaki   +8 more
wiley   +1 more source

Solitary Langerhans cell histiocytosis of the sternum in a 21-year-old woman. [PDF]

Clin Case Rep
Key Clinical Message Children are more likely to develop Langerhans cell histiocytosis (LCH), a rare disorder with an unknown cause. LCH often invades skeletal systems, while it has occasionally been seen in the sternum or ribs. The best course of treatment for single‐site, skeletal LCH is yet unknown.
Soleimani N, Hosseinzadeh M, Amirian A, Hassani M, Mohammadzadeh S.   +4 more
europepmc   +2 more sources

Eosinophiel granuloom van het skelet en het verband met de ziekte van Hand Schüller-Christian en van Letterer-Siwe [PDF]

, 1948
De conclusie, dat eosinophiel granuloom, lipoid granulomatose en de ziekte van Letterer-Siwe uitingen van eenzelfde grondlijden zijn, werd in hoofdstuk VI besproken.
Hadders, Hendrik Nicolaas
core   +9 more sources

LANGERHANS CELLS HISTIOCYTOSIS IN ONE FAMILY [PDF]

Acta Medica Iranica, 2004
Histiocytosis of Langerhans cells (class 1 histiocytosis) consists of a range of clinical manifestations, including bone eosinophilic granuloma, Hand-Schüller-Christian syndrome, and Letterer-Siwe disease. These syndromes represent a spectrum of severity
Sh. Ansari, P. Vossough H. Haddad Deylami   +1 more
doaj   +1 more source

Histiocitose de células de Langerhans como causa de mielopatia: Relato de caso e revisão da literatura

Brazilian Neurosurgery, 2010
Histiocitose de células de Langerhans é uma doença uni ou multifocal que acomete osso, tecido mole ou ambos. Relativamente incomum, abrange entidades clínicas anteriormente conhecidas como doença de Hand-Schüller-Christian, Abt-Letterer-Siwe, Hashimoto ...
Fábio Teixeira Giovanetti Pontes, Adelmo Ferreira, Adriano Torres Antonucci, Johnathan de Sousa Parreira, Márcio Francisco Lehmann, Natally Marques Santiago, Luiz Henrique Garcia Lopes, Pedro Garcia Lopes, Wander Miguel Tamburus   +8 more
doaj   +1 more source

Erkennen – Der klinische Blick auf die kutane Tuberkulose [PDF]

J Dtsch Dermatol Ges
Zusammenfassung In vielen Ländern ist die Tuberkulose (TBC) bis heute eine der häufigsten Todesursachen und bleibt insbesondere durch Migrationsbewegungen auch in Deutschland von Bedeutung. Die Diagnose der seltenen kutanen Tuberkulose ist herausfordernd, da sie in vielfältigen klinischen Erscheinungsformen auftritt, die deutlich häufigeren ...
Gramminger C, Biedermann T.
europepmc   +2 more sources

Langerhans Cell Histiocytosis: Letterer - Siwe Disease Interest of Dermatological Signs for Diagnosis [PDF]

, 2017
Langerhans cell histiocytosis is defined as a clonal proliferation of Langerhans phenotypic-like cells. Letterer-Siwe disease is the most common and serious of these entities, affecting mainly infants up to two years of age.
Gallouj S, Lahlou A, Elmahi H, Mernissi FZ   +3 more
core   +1 more source

Letterer-Siwe disease

Health and Ecology Issues, 2018
The article describes a case of Letterer-Siwe disease (Langerhans cells histocytosis, histiocytosis X) in a 1-year-old infant, presents the authors` own observations focusing on the macroscopic and histological picture of skin lesions. The work also notes difficulties of diagnosis of this disease.
I. F. Shalyga, G. V. Tishchenko, L. A. Martemyanova, S. Yu. Turchenko, Yu. N. Avizhets   +4 more
openaire   +2 more sources