Results 11 to 20 of about 4,922,335 (121)

Indeterminate cell histiocytosis that presented clinically as benign cephalic histiocytosis [PDF]

open access: yesDermatology Online Journal, 2015
Indeterminate cell histiocytosis (ICH) is a rare, heterogeneous disorder that is characterized by immunophenotypic features of both Langerhans cell histiocytosis (LCH) and non-LCH. We describe a 12-month-old boy with a four-month history of asymptomatic, small, pink-tan papules on his face.
Haimovic, Adele   +4 more
openaire   +6 more sources

Indeterminate cell histiocytosis successfully treated with narrowband UVB [PDF]

open access: yesDermatology Online Journal, 2013
We present a 47-year-old man with a sudden eruption of more than 100 reddish-brown papules, which histologically exhibited a dense dermal proliferation of large mononuclear cells with vesicular nuclei and abundant pale cytoplasm. Electron microscopy and immunohistochemistry revealed findings consistent with indeterminate cell histiocytosis and the ...
Logemann, Nicholas   +2 more
openaire   +6 more sources

A Case of Indeterminate Cell Histiocytosis

open access: yesNishinihon Journal of Dermatology, 2020
Seisho Sato   +2 more
exaly   +3 more sources

Indeterminate Cell Histiocytosis Mimicking Rosacea [PDF]

open access: yesCureus, 2021
Indeterminate cell histiocytosis (ICH) is a rare proliferative disorder of histiocytes, which display morphologic and immunophenotypic characteristics of both Langerhans cell histiocytosis (LCH) and non-Langerhans cell histiocytosis (NLCH). We describe an unusual clinical presentation of ICH mimicking rosacea and provide a relevant review of the ...
Fischer, Andrew S   +4 more
openaire   +2 more sources

Indeterminate dendritic cell tumor (IDCT) [PDF]

open access: yesVestnik Dermatologii i Venerologii, 2023
Indeterminate dendritic cell tumor (IDCT) is rare histiocytic tumor characterized by the proliferation of indeterminate dendritic cells. It is more often diagnosed in middle-aged people, in approximately equal proportions in men and women.
Evgenia V. Okladnikova   +4 more
doaj   +1 more source

Intermediate-dose cytarabine is an effective therapy for adults with non-Langerhans cell histiocytosis

open access: yesOrphanet Journal of Rare Diseases, 2022
Background Non-Langerhans cell histiocytosis, including Erdheim–Chester disease (ECD), Rosai–Dorfman disease (RDD), indeterminate cell histiocytosis (ICH), and unclassified histiocytosis, is a rare disorder lacking a standard treatment strategy.
Ting Liu   +7 more
doaj   +1 more source

CD1a-positive dendritic cell-enriched pigmented purpuric dermatosis in association with dyslipidemia

open access: yesJournal of Dermatology and Dermatologic Surgery, 2022
Indeterminate cells (ICs) are dendritic cells (DCs) that share the histologic features of Langerhans cells and macrophages but lack Birbeck granules. It remains unclear whether IC histiocytosis is a separate disease entity or a reactive process.
Tiffany Hinojosa   +3 more
doaj   +1 more source

CURRENT THERAPIES PRIMARY LANGERHANS CELL HYSTIOCYTOSIS

open access: yesHematology, Transfusion and Cell Therapy, 2023
Langerhans cell histiocytosis (LCH) is a neoplastic histiocytic disorder that most commonly affects bones and skin, but it can also involve the bone marrow, liver, spleen, lungs, pituitary gland/central nervous system, and other organs.
Deniz Tuğcu
doaj   +1 more source

A case report of a blueberry muffin baby caused by congenital self-healing indeterminate cell histiocytosis

open access: yesBMC Pediatrics, 2023
Background Blueberry muffin is a descriptive term for a neonate with multiple purpuric skin lesions. Many causes are known, amongst them life-threatening diseases like congenital infections or leukemia.
S. B. L. Koster   +6 more
doaj   +1 more source

Erratum: Indeterminate Cell Histiocytosis: Report of a Case

open access: yesActa Medica Iranica, 2015
Alireza Ghanadan   +8 more
doaj   +1 more source

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