Results 141 to 150 of about 19,037 (201)

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

open access: closedBritish 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   +3 more
openaire   +3 more sources

Ocular Involvement in a Case of Systemic Indeterminate Cell Histiocytosis

open access: closedCornea, 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   +5 more
openaire   +3 more sources

Indeterminate cell histiocytosis: fact or fiction?

open access: closedJournal of Cutaneous Pathology, 2005
Abstract:  Indeterminate cell histiocytosis is a rare disorder, in which the predominant cells have the characteristics of both Langerhans cells and macrophages. We, in this study, describe 18 patients and compare them with those previously published. Most patients were adults with either solitary or multiple red‐brown papules or nodules.
Gudrun, Ratzinger   +4 more
openaire   +3 more sources

A case of COVID‐19‐associated generalized indeterminate cell histiocytosis successfully treated with systemic PUVA

open access: closedJournal of the European Academy of Dermatology and Venereology, 2023
Finn Abeck   +5 more
semanticscholar   +2 more sources

A Case of Solitary Indeterminate Cell Histiocytosis

open access: closedThe Journal of Dermatology, 2003
Yasuyuki, Amo   +3 more
openaire   +3 more sources

Indeterminate Cell Histiocytosis and a Review of Current Treatment.

Cutis
P. Sulejmani   +5 more
semanticscholar   +3 more sources

Indeterminate Dendritic Cell Histiocytosis Harboring ETV3::NCOA2 Translocation with Complete Metabolic Response to MEK Inhibition.

open access: closedBritish Journal of Dermatology
Indeterminate dendritic cell histiocytosis (IDCH) is a rare condition that usually has cutaneous involvement. Recent studies have revealed that ETV3::NCOA2 translocations are unique to IDCH; however, there are currently no standard treatment options for ...
Vyshnavi Rallapalle   +11 more
semanticscholar   +2 more sources

Indeterminate cell histiocytosis: A systematic review of the literature with a comprehensive revision of clinical, histopathological, and molecular features

Journal of the European Academy of Dermatology and Venereology, 2023
Indeterminate cell histiocytosis (ICH) is a very rare histiocytic disorder, primarily involving the skin. It affects more frequently adults, often presenting with a generalized papular eruption, and needs to be differentiated from other neoplastic ...
Simone Zanella, E. Berti, A. Bonometti
semanticscholar   +1 more source

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

open access: closedMedical 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   +5 more
openaire   +3 more sources

An Atypical Myelomonocytic Cell Infiltrate: Use of Next-Generation Sequencing to Diagnose Indeterminate Cell Histiocytosis.

American journal of dermatopathology, 2022
Indeterminant cell histiocytosis (ICH) is a rare lymphoproliferative disorder that demonstrates features of Langerhans and non-Langerhans cell histiocytoses and diagnosis can be challenging.
M. E. Belina   +3 more
semanticscholar   +1 more source

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