Results 31 to 40 of about 13,327 (249)

Oral manifestation of Langerhans cell histiocytosis: a case report

open access: yesBMC Oral Health, 2018
Background Bone necrosis of the jaw is a serious condition with a broad differential diagnosis of pathologies such as cutaneous histiocytosis, bone metastases or malignant tumours. In addition to the most common cause, medication related osteonecrosis of
Julia Luz   +5 more
doaj   +1 more source

Langerhans Cell Histiocytosis of the Thyroid with Multiple Cervical Lymph Node Involvement Accompanying Metastatic Thyroid Papillary Carcinoma

open access: yesCase Reports in Pathology, 2014
A 37-year-old male case was admitted with goiter. Ultrasonography of thyroid showed a 5 cm cystic nodule in the left lobe with a 1.5 cm solid component. Fine needle aspiration biopsy revealed atypia of undetermined significance or follicular lesion.
A. Bahar Ceyran   +5 more
doaj   +1 more source

Diagnostic Challenge in Rapidly Growing Langerhans Cell Histiocytosis with Aneurysmal Bone Cyst in the Maxilla: A Case Report

open access: yesDiagnostics, 2022
Langerhans cell histiocytosis (LCH) is a rare neoplastic disorder characterized by the clonal proliferation of CD1a +/CD 207 + dendritic cells, whose features are similar to those of epidermal Langerhans cells.
Ye Rin Hwang   +3 more
doaj   +1 more source

Common Acute Lymphoblastic Leukemia Ph+ Following Langerhans Cell Histiocytosis in a Multi-Malformed Child with INV (9) (p12;q13) (mat):Case Report [PDF]

open access: yes, 2010
The occurrence of Langerhans cell histiocytosis (LCH) and another malignancy in the same patient is infrequent but has been recognized. The genetic changes that could be responsible for LCH and/or concomitant leukemia development are obscure. To the best
Pavelić, Jasminka   +2 more
core   +1 more source

Blindness in a patient with malignant histiocytosis [PDF]

open access: yesCancer, 1977
Malignant histiocytosis (MH) is a rapidly fatal systemic disease for which there is no adequate therapy. A case of MH with involvement of both eyes resulting in bilateral blindness is presented. Infiltration with malignant cells was seen in the ciliary bodies at autopsy. Attempts at treatment for this complication are discussed.
David J. Klein   +6 more
openaire   +3 more sources

Clinicopathological characteristics of histiocytic sarcoma affecting the central nervous system in dogs. [PDF]

open access: yes, 2020
BackgroundHistiocytic sarcoma affecting the central nervous system (CNS HS) in dogs may present as primary or disseminated disease, often characterized by inflammation.
Crowe, Chelsea M   +10 more
core  

Langerhans cell histiocytosis [PDF]

open access: yes, 1998
The authors present a rare case of Langerhans cell histiocytosis in a 31 year old female patient with vulvar, peri-anal and oral lesions, diabetes insipidus, pulmonary skin and bone infiltrations.
Atallah, Álvaro Nagib   +10 more
core   +2 more sources

Chromosome abnormalities in malignant histiocytosis [PDF]

open access: yesCancer, 1985
Chromosome and pathologic studies were performed on two patients (a 12-year-old boy and a 62-year-old woman) with malignant histiocytosis (MH). Both patients had chromosome abnormalities in their neoplastic cells: the boy's karyotype was 45,Xp+,-Y,9p+,18q-, and the woman's 48,XX,+16, inv(1),mar(5),6p-,10p+,12q+,i(18q),+i(18q).
Yasuhiko Kaneko   +5 more
openaire   +3 more sources

A rare case of Rosai–Dorfman disease presenting as a pulmonary artery mass in a 33‐year‐old female with hypoxia

open access: yesPulmonary Circulation, 2023
Rosai–Dorfman disease (RDD) is a rare form of non‐Langerhans histiocytosis. It is often idiopathic in etiology, but has been associated with viral, autoimmune, and malignant disease.
Veena Dronamraju   +8 more
doaj   +1 more source

Dendritic Cells Cause Bone Lesions in a New Mouse Model of Histiocytosis. [PDF]

open access: yes, 2015
Langerhans cell histiocytosis (LCH) is a rare disease caused by the clonal accumulation of dendritic Langerhans cells, which is often accompanied by osteolytic lesions.
Acha-Orbea, H.   +11 more
core   +10 more sources

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