Results 31 to 40 of about 21,961 (244)

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

open access: yes, 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,
Hale, Christopher S   +4 more
core   +1 more source

Pulmonary Langerhans cell histiocytosis causing spontaneous bilateral pneumothorax in a child

open access: yesThe Egyptian Journal of Internal Medicine, 2015
Bilateral pneumothorax is very rare in childhood. Moreover, if it is due to pulmonary involvement of Langerhans cell histiocytosis, it is even rarer in childhood.
Anupam Patra   +3 more
doaj   +1 more source

Cerebral manifestation and diagnostic dilemma of Rosai-Dorfman disease

open access: yesCNS Oncology, 2023
Rosai-Dorfman disease (RDD) is a rare, S100-positive histiocytic proliferation, that can cause both nodal and extranodal illness. We present a case of a 53-year-old male patient.
Szintia Almási   +3 more
doaj   +1 more source

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

Swelling of bilateral parotid glands: An unusual symptom of multisystem Langerhans cell histiocytosis

open access: yesSAGE Open Medical Case Reports, 2014
Objective: Langerhans cell histiocytosis is an unusual disorder of unknown etiology with heterogeneous clinical behaviors and variable outcomes. It can involve one or more organs or systems, but to our best knowledge, parotid glands involvement in ...
Xiaojun Yuan   +4 more
doaj   +1 more source

Langerhans cell histiocytosis (histiocytosis x) – in the mandible

open access: yesBrazilian Dental Science, 2013
This article reports a case of 65 year-old man consultedin a private radiology dental clinic for a panoramicradiography, where was indicated a radiolucent area,extending into the periapical region of the teeth 35 to 43 to the base of the mandible ...
Angela Jordão Camargo   +5 more
doaj   +1 more source

Manganese overload as a co-factor of neurological symptoms in a patient with sclerosing cholangitis due to Langerhans cell histiocytosis

open access: yesHaematologica
Not available.
Jerome Razanamahery   +7 more
doaj   +1 more source

Hand-Schüller-Christian disease

open access: yesIndian Journal of Dental Research, 2012
Langerhan cell histiocytosis, formerly known as histiocytosis X, traditionally denotes a group of diseases that stem from proliferative reticuloendothelial disturbances.The etiology and pathogenesis of the disease remain debatable.
Deepak Bhargava   +3 more
doaj   +1 more source

Puzzle histiocytosis (solitary mononuclear xanthogranuloma with LCH component). A case report*

open access: yes, 2017
We report a case of 40-year-old Caucasian man presented with an asymptomatic nodule localized on his arm. The puzzle histiocytosis composed of juvenile xanthogranuloma and Langerhans cell histiocytosis was diagnosed.
Katarzyna Woszczyna-Mleczko   +5 more
core   +1 more source

Hemophagocytic lymphohistiocytosis associated with extranodal NK/T cell lymphoma, nasal type or aggressive NK cell leukemia: a retrospective multicenter study of Jiangsu Cooperative Lymphoma Group (JCLG)

open access: yesAnnals of Hematology
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory syndrome, among which NK-cell malignancy-associated HLH represents a clinically rare entity that has not been systematically investigated.
Yongle Li   +23 more
doaj   +1 more source

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