Results 21 to 30 of about 18,484 (199)

Indeterminate Cell Histiocytosis [PDF]

open access: closedArchives of Pathology & Laboratory Medicine, 2003
Abstract Indeterminate cell histiocytosis is a rare disorder involving altered homing mechanisms of the cutaneous histiocytic/dendritic system. It has been described predominantly in adults, with less than a dozen cases in children. A 13-year-old adolescent girl presented with a 4-year history of asymptomatic erythematous nodules and ...
Rodolfo Rodrı́guez-Jurado   +3 more
openalex   +2 more sources

Post‐scabietic nodules: Mimicker of infantile indeterminate cell histiocytosis and potential diagnostic pitfall [PDF]

open access: bronzeJournal of cutaneous pathology, 2019
Indeterminate cell histiocytosis (ICH) is an extremely rare disease and little is known about its etiology. Patients usually present with nodular, dermal proliferations of indeterminate cells, which characteristically resemble Langerhans cells but lack ...
Kristen N. Ruby   +3 more
openalex   +2 more sources

ETV3-NCOA2 in indeterminate cell histiocytosis: clonal translocation supports sui generis [PDF]

open access: bronzeBlood, 2015
Ryanne A. Brown   +8 more
openalex   +2 more sources

Indeterminate Cell Histiocytosis in a Pediatric Patient: Successful Treatment with Thalidomide

open access: yesPathology & Oncology Research, 2011
The 15-year-old male patient presented several 2-6 mm large livid reddish-yellowish, shiny, compact papules on the head, trunk and extremities, which had developed within the last 4 months. Histology showed normal epidermis with dense dermal infiltrate of histiocytes accompanied by few eosinophils, Touton or foamy giant cells. The histiocytes were S100
Mária Katona   +5 more
openaire   +4 more sources

Indeterminate Cell Histiocytosis: Report of a Case

open access: closedActa Medica Iranica, 2014
Indeterminate cell histiocytosis is a very rare disorder of histiocytes proliferation. It has both Langerhans and non-Langerhans cell histiocytosis immunophenotypic features.
Alireza Ghanadan   +8 more
doaj   +1 more source

Sequential occurrence of primary cutaneous indeterminate cell histiocytosis after oesophageal cancer and subsequent bullous pemphigoid: a case report

open access: hybridBritish journal of hospital medicine
Aims/Background Indeterminate cell histiocytosis is a rare proliferative histiocytic disease with an unknown aetiology, which shares immunophenotypic features of both Langerhans cells and macrophages.
Xiaoxiao Jia   +3 more
openalex   +2 more sources

Assessment of Hemophagocytic Lympho-Histiocytosis (HLH) in the Setting of Adult Acute Liver Failure. [PDF]

open access: yesJ Viral Hepat
ABSTRACT Hemophagocytic lympho‐histiocytosis (HLH) is a life‐threatening disease, only occasionally presenting as acute liver failure (ALF) in adults. HLH is challenging to diagnose. We reviewed the ALF Study Group (ALFSG) registry for suspected HLH subjects, as well as 184 with other ALF etiologies for cases that might have been missed, assessing ...
Anouti A   +5 more
europepmc   +2 more sources

Indeterminate cell histiocytosis. Clinical and pathologic study in a pediatric patient.

open access: closedArchives of pathology & laboratory medicine, 2003
Indeterminate cell histiocytosis is a rare disorder involving altered homing mechanisms of the cutaneous histiocytic/dendritic system. It has been described predominantly in adults, with less than a dozen cases in children. A 13-year-old adolescent girl presented with a 4-year history of asymptomatic erythematous nodules and plaques, measuring from 1 ...
Rodolfo Rodrı́guez-Jurado   +3 more
openalex   +4 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

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