Results 221 to 230 of about 10,082 (250)
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Lymphocyte sub-populations and non-Langerhans’ cell monocytoid cells in pulmonary Langerhans’ cell histiocytosis

Pathology - Research and Practice, 2008
Pulmonary Langerhans' cell histiocytosis (PLCH) is a disease characterized by the occurrence of complex fibro-cellular interstitial lesions dominated by Langerhans' cells (LC), which occurs predominantly in young adult smokers. We undertook this retrospective study to better define the lymphohistiocytic cell populations in PLCH in order to obtain a ...
R, Nagarjun Rao   +2 more
openaire   +2 more sources

Successful treatment of Erdheim-Chester disease, a non–Langerhans-cell histiocytosis, with interferon-α

Blood, 2005
AbstractErdheim-Chester disease is a rare non-Langerhans histiocytosis with multisystem involvement. To date, there is no standard treatment for this disorder, and more than half of the patients succumb within 3 years. Because interferon-α promotes the terminal differentiation of histiocytes and dendritic cells, we hypothesized that this molecule would
Fadi, Braiteh   +3 more
openaire   +2 more sources

[Acquired regressive cutaneous non-Langerhans-cell histiocytosis in an infant].

Annales de dermatologie et de venereologie, 1998
Cutaneous histiocytosis of childhood often regresses spontaneously without treatment. In some cases however, it is difficult to differentiate aggressive forms and electron microscopy and immunohistochemistry can be a valuable help. We report a case of cutaneous histiocytosis in a child which illustrates the difficulties encountered in the ...
M, Campourcy   +6 more
openaire   +1 more source

A Rare Presentation of a Rare Non-Langerhans Cell Histiocytosis

A74. RARE CASES IN THORACIC ONCOLOGY, 2023
A.A. Velthottam Rathinam   +2 more
openaire   +1 more source

Non-langerhans Cell Histiocytosis-Including Erdheim-Chester Disease- and the Lung

2014
Erdheim-Chester disease (ECD) is a rare form of non–Langerhans’ cell histiocytosis that may present with pulmonary involvement. The disease was first described as the “lipoid granulomatose” in 1930. Between then and 2013, more than 500 cases have been reported.
Julien Haroche   +5 more
openaire   +1 more source

[Clinicopathological study of non-Langerhans cell histiocytosis in central nervous system].

Zhonghua nei ke za zhi, 2016
To explore the clinicopathological features and imaging characteristics of non-Langerhans cell histiocytosis in central nerve system, thus to facilitate the diagnosis and differential diagnosis.A total of ten cases were enrolled in the study, with seven cases of Rosai-Dorfman disease (RDD) and three cases of xanthoma disseminatum (XD).
Tingting, Zhang   +4 more
openaire   +1 more source

Langerhans cell and non Langerhans cell histiocytosis: So different?

2007
The Author reports the clinical and laboratory criteria that do not support the strict distinction between Langerhans cell and non Langerhans cell histiocytosis as reported in the relevant literature.
openaire   +1 more source

Cutaneous Erythrodermatic Non-Langerhans Cell Histiocytosis in Childhood.

The American Journal of Dermatopathology, 1997
K. Bosler, R. Linsc, K. Jung
openaire   +1 more source

Retinal Manifestations in a Patient with Xanthoma Disseminatum (Non-Langerhans Cell Histiocytosis)

Klinische Monatsblätter für Augenheilkunde, 2011
Konstantinidis L   +4 more
openaire   +3 more sources

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