Results 141 to 150 of about 6,359 (165)

A Child with Both Langerhans and Non‐Langerhans Cell Histiocytosis

Pediatric Dermatology, 2002
Abstract: The histiocytic syndromes consist of a group of disorders that share in common the proliferation of cells of the monocytic/macrophage lineage. It has been conventional to divide the histiocytoses into two separate groups: Langerhans cell histiocytosis (LCH) and non‐LCH.
Ayelet, Shani-Adir, Pauline, Chou, Elaine, Morgan, Anthony J, Mancini   +3 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, Beth, Vettiyil, Eric, Bartlett, Eugene, Yu   +3 more
openaire   +2 more sources

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

Clinical and Experimental Dermatology, 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 of lymphocyte-predominant Hodgkin's disease was made on lymph node biopsy.
null Ibbotson, null Sviland, null Slater, null Reynolds   +3 more
openaire   +4 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

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

Erdheim- Chester Disease (Non-Langerhans Cell Histiocytosis)

Journal of Cancer Research Reviews & Reports
52 years old female with recurrent admission for myalgias, inflammatory arthritis, rash around the eyes and abdomen (A, B). Routine blood tests were either normal or negative apart from low C4 level. Pan CT of the body was unremarkable.
Yousef Gulnaz, Adel Ekladious
openaire   +1 more source

Intracranial findings of Non-Langerhans-Cell Histiocytosis

2019
Learning objectives Background Findings and procedure details Conclusion Personal information ...
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

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, Chung-Che, Chang, Joseph F, Tomashefski   +2 more
openaire   +2 more sources