Results 91 to 100 of about 4,922,335 (121)

Indeterminate cell histiocytosis—a clinicopathological entity with features of both X- and non-X histiocytosis

British Journal of Dermatology, 1996
An otherwise healthy 50-year-old woman presented with a 6-month history of having developed more than 100 generalized, non-confluent, reddish-brown, partially yellow-coloured papules. A non-epidemotropic, monomorphous infiltrate of vacuolated mononuclear, and occasionally multinuclear, histiocytes, positive for factor XIIIa and macrophage markers HAM56
A, Sidoroff, B, Zelger, H, Steiner, N, Smith   +3 more
openaire   +2 more sources

Indeterminate cell histiocytosis successfully treated with ultraviolet B phototherapy

Clinical and Experimental Dermatology, 2008
Indeterminate cell histiocytosis (ICH) is a rare disorder, characterized by infiltration of the skin by neoplastic cells that are characteristically positive for S-100 and CD1a, but lack Birbeck's granules. A 75-year-old man presented with a 4-year history of multiple papules on the trunk, limbs, face and neck.
M, Ishibashi, T, Ouchi, A, Tanikawa, A, Ishiko   +3 more
openaire   +2 more sources

Ocular Involvement in a Case of Systemic Indeterminate Cell Histiocytosis

Cornea, 2001
To describe ocular involvement in a case of systemic indeterminate cell histiocytosis, a rare disease characterized by the proliferation of indistinct histiocytes. These histiocytes resemble Langerhans cells but lack Birbeck granules. The disease usually occurs in adults, with no predisposition for either sex.
M, Calatayud, J L, Güell, O, Gris, J, Puig, E, Arrondo, P, Huguet   +5 more
openaire   +2 more sources

Generalized Indeterminate Cell Histiocytosis Presenting as Eroded Papules and Crusts

The American Journal of Dermatopathology, 2017
Abstract: Indeterminate cell histiocytosis (ICH) is a very rare histiocytic disease. We reported a case of generalized ICH presenting as eroded papules and crusts, accompanied with intermittent fever, pulmonary disorder, lymphadenectasis in the mediastinum, and the retroperitoneum.
Yaping, Li, Harrison Xiao, Bai, Chang, Su, Guiying, Zhang   +3 more
openaire   +2 more sources

INDETERMINATE CELL HISTIOCYTOSIS WITH OCULAR INVOLVEMENT IN A NEONATE: A CASE REPORT

RETINAL Cases & Brief Reports
Purpose: The authors describe a case of Indeterminate cell histiocytosis, a rare disease of histiocytic proliferation on the spectrum of Langerhans cell histiocytosis. Methods: Data were collected through retrospective chart review. Results:
Alexis Kassotis, Lauren Yeager, Dmitry Bogomolny, Brian Marr   +3 more
openaire   +2 more sources

Indeterminate-cell histiocytosis: immunophenotypic and cytogenetic findings in an infant.

Medical and pediatric oncology, 1999
The authors report the immunohistochemical, ultrastructural, and cytogenetic findings in a case of malignant histiocytic proliferation in an infant.The patient presented initially with bone lesions without skin or systemic involvement. Multiple biopsies were studied extensively by immunohistochemistry and electron microscopy.
E, Martin Flores-Stadler, F, Gonzalez-Crussi, M, Greene, M, Thangavelu, M, Kletzel, P M, Chou   +5 more
openaire   +1 more source

Expression of CD1 molecules and colony‐stimulating factor 1 receptor in indeterminate cell histiocytosis

Journal of Dermatology, 2021
Naoki Oishi, Tetsuo Kondo, Youichi Ogawa   +2 more
exaly  

Chemotherapeutic experience in indeterminate cell histiocytosis

British Journal of Dermatology, 2005
R. Caputo, A.V. Marzano, E. Passoni, M. Bellinvia   +3 more
openaire   +2 more sources

Treatment of indeterminate cell histiocytosis with pravastatin

Journal of the American Academy of Dermatology, 2011
Molly V. Burns, Ammar Ahmed, Gabriela Blanco Callahan, Lu Q. Le, Clay Cockerell   +4 more
openaire   +1 more source

Case 51. Indeterminate dendritic cell histiocytosis

2021
E. Akufo-Tetteh, B. Vydianath, J. Scarisbrick   +2 more
openaire   +1 more source