Results 191 to 200 of about 10,817 (231)

Endolymphatic Non-Langerhans Cell Histiocytosis of the Larynx

Journal of Pediatric Hematology/Oncology, 2010
We report on an uncommon laryngeal non-Langerhans cell histiocytosis. An 11-year-old boy presented with a 6 months history of progressive breath inhibition. Magnetic resonance imaging showed diffuse laryngeal and local lymph node swelling. Histology first resembled sarcoidosis, however, corticosteroids were ineffective.
Carl Friedrich, Classen, Dieter, Haffner, Horst, Nizze, Peter, Möller, Friedrich, Prall   +4 more
openaire   +2 more sources

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
exaly   +3 more sources

Fibroblastic rheumatism: fibromatosis rather than non‐Langerhans cell histiocytosis

Journal of Cutaneous Pathology, 2010
Background: Fibroblastic rheumatism is a unique fibro‐proliferative disease affecting the skin and joints. It is characterized by distinctive clinical and histological features related to benign spindle‐shaped cells proliferation. Pediatric reports are scarce in the literature.
Nicolas, Kluger, Alexandra, Dumas-Tesici, Dominique, Hamel, Nicole, Brousse, Sylvie, Fraitag   +4 more
openaire   +2 more sources

Intracranial non-Langerhans cell histiocytosis presenting as an isolated intraparenchymal lesion

Pediatric Radiology, 2010
Non-Langerhans cell histiocytosis in the absence of cutaneous or other organ involvement is very rare. A Caucasian boy age 3 years 11 months presented with episodes of recurrent right-side seizures over 2 weeks. Brain CT and MR imaging showed a single enhancing left frontal lobe lesion.
Smitha, Rajaram, Stephen B, Wharton, Fiona, Shackley, Ashok, Raghavan, Daniel J A, Connolly   +4 more
openaire   +2 more sources

Non Langerhans Cell Histiocytosis of the Rectum: Case Report and Review of the Literature

Japanese Journal of Gastroenterology and Hepatology, 2022
Histiocytosis is a condition resulting from the abnormal proliferation of dentritic cells of the mononuclear phagocytic system. Previously classified as Langerhans cell histiocytosis and non-Langerhans cell histiocytosis, and recently into 5 categories (L, C, R, M and H), it can be localized to an organ or have a systemic manifestation, affecting most ...
Bouhairie MM, Mansour J, El Naderi S, Abou Rached A   +3 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

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

Intracranial findings of Non-Langerhans-Cell Histiocytosis

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

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

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