Results 191 to 200 of about 14,204,460 (231)

New entity of an isolated pulmonary non-Langerhans cell histiocytosis

European Respiratory Journal, 2013
Background: Histiocytic disorders are rare, heterogeneous diseases with abnormal tissue infiltration by histiocytes. So far, pulmonary manifestation in Non-Langerhans cell histiocytoses (NLCH) occurred only as a part of a systemic disease. Case: A 37 year old male stonesculptor suffered from progressive dyspnea and thoracic tightness.
Michael Kreuter, Claus Peter Heussel, Christian Nagel, Richard P. Baum, Philipp A. Schnabel, Felix J.F. Herth, Dirk Theegarten   +6 more
openaire   +1 more source

Suprasellar non-Langerhans cell histiocytosis (Erdheim–Chester disease)—a case report

Clinical Imaging, 2013
Erdheim-Chester disease (ECD) is an uncommon non-Langerhans cell histiocytosis that affects multiple body systems and can present clinically in a myriad of ways. An adult onset is most common with bony involvement and constitutional symptoms. We report the case of a 52-year-old female presenting with diabetes insipidus and a suprasellar mass on imaging,
Manas, Sharma, Beth, Vettiyil, Eric, Bartlett, Eugene, Yu   +3 more
openaire   +2 more sources

Efficacy and Tolerance of Cladribine for Non‐Langerhans Cell Histiocytosis

European Journal of Haematology
ABSTRACT Background Erdheim‐Chester Disease ( ECD ) and Rosai‐Dorfman Disease ( RDD ) Are Rare Non‐Langerhans Cell Histiocytoses That Share Several Clinical and Histological Features ...
Quentin Riller, Thouraya Ben Salem, Jean‐François Emile, Frédéric Charlotte, Ahmed Idbaih, Benoît Faucher, Sébastien De Almeida, Guillaume Martin‐Blondel, Abdellatif Tazi, Jean Donadieu, Etienne Riviere, Maxime Samson, Camille Souffir, Zahir Amoura, Julien Haroche, Fleur Cohen‐Aubart   +15 more
openaire   +1 more source

GENERALIZED NON‐LANGERHANS CELL HISTIOCYTOSIS: FOUR CASES ILLUSTRATE A SPECTRUM OF DISEASE

International Journal of Dermatology, 1995
Abstract Background. The proliferation of non‐Langerhans cell histiocytes is a poorly understood process of unknown cause. Variation in the clinical features and/or histopathology of histiocytic proliferation has led to subclassification of the general category of non‐Langerhans cell histiocytes.
E A, Mullans, T N, Helm, J S, Taylor, K F, Helm, J W, Olin, W F, Bergfeld   +5 more
openaire   +2 more sources

Intracranial findings of Non-Langerhans-Cell Histiocytosis

2019
Learning objectives Background Findings and procedure details Conclusion Personal information ...
openaire   +1 more source

A unique non-Langerhans cell histiocytosis with some features of generalized eruptive histiocytoma

Journal of the American Academy of Dermatology, 1994
A symmetric eruption of hundreds of coalescent small red macules and a few slightly elevated papules sparing the flexures was observed in a 73-year-old man. Light microscopic examination showed loose aggregates of small and large histiocytic cells. Electron microscopy showed an absence of Langerhans cell granules and lipid droplets.
S, Goerdt, G, Bonsmann, C, Sunderkötter, S, Grabbe, T, Luger, G, Kolde   +5 more
openaire   +2 more sources

Non–Langerhans Cell Histiocytosis with Involvement of the Optic Disc and Retina

Ophthalmology Retina, 2022
Vipin Rana, Renu Suthar, Deeksha Katoch
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, Cynthia, Boxrud, Bita, Esmaeli, Razelle, Kurzrock   +3 more
openaire   +2 more sources

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, Anne-Laure Brun, Frédérique Capron, Frédéric Charlotte, Philippe A. Grenier, Zahir Amoura   +5 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, R. Khanam, T. Sahai   +2 more
openaire   +1 more source