Results 61 to 70 of about 287,512 (253)

Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]

open access: yes, 2016
Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco   +4 more
core  

Neurosurgical interventions for patients with nasopharyngeal carcinoma: a single institution experience [PDF]

open access: yes, 2013
BACKGROUND: Nasopharyngeal carcinoma (NPC) is a frequent head and neck cancer in southern China and Southeast Asia. The majority of NPC patients are managed by radiation oncologists, medical oncologists and head and neck surgeons. Actually, neurosurgical
Chao Ke   +11 more
core   +1 more source

Rosai Dorfman Disease: A Rare Cause of Cervical Lymphadenopathy [PDF]

open access: yesNational Journal of Laboratory Medicine, 2018
Rosai Dorfman disease, a sinus histiocytosis, is rare to find and difficult to diagnose. It may masquerade as commoner diseases including infections and malignancies.
Sreenath Sreenivasan   +4 more
doaj   +1 more source

Granulocytic sarcoma (chloroma) of the oral cavity: Report of a case and literature review [PDF]

open access: yes, 2003
SummaryA case of granulocytic sarcoma (chloroma) of the palatal mucosa is reported. Granulocytic sarcomas are composed of a localized collection of immature myeloid cells and are considered to be specific lesions of AML or the onset of a blast crisis in ...
M.J. Koudstaal   +55 more
core   +1 more source

Thoracotomies in Children in Low to Middle Income Countries: The Indications for Surgery

open access: yesPediatric Pulmonology, Volume 60, Issue 10, October 2025.
ABSTRACT Introduction There is a scarcity of data on the utilization of thoracotomy for lung pathology in children in low‐ and middle‐income countries (LMICs). These countries have high burdens of infectious diseases, especially tuberculosis, hydatic disease and Human immunodeficiency virus (HIV).
Jacobus Botha   +10 more
wiley   +1 more source

Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature

open access: yesJournal of the Belgian Society of Radiology, 2014
Rosai-Dorman disease (RDD) is a rare disorder of proliferative histiocytes with an unknown etiology. It is also known as sinus histiocytosis with massive lymphadenopathy. Most patients present with painless cervical lymphadenopathy due to accumulation of
H M Duijsens   +4 more
doaj   +1 more source

Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement

open access: yesSouth African Journal of Radiology, 2023
Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented.
Smily Sharma   +3 more
doaj   +1 more source

Childhood Cancer Survivors in Latin America: Insights Into Health Outcomes and Information Needs

open access: yesPediatric Blood &Cancer, Volume 72, Issue 9, September 2025.
ABSTRACT Background Childhood cancer survivors (CCSs) face long‐term health challenges, yet the health and specific needs of Latin American survivors remain underexplored. This study aimed to describe the health‐related, psychosocial late effects, and information needs among CCSs in the region. Methods This mixed‐method study combined quantitative data
Ana Carolina Izurieta‐Pacheco   +17 more
wiley   +1 more source

Pulsatile tinnitus —a review of 84 patients [PDF]

open access: yes, 2018
Pulsatile tinnitus can be annoying for a patient and can also be the only clue to a potentially devastating and life-threatening disease. In order to understand its clinical spectrum and management better we analysed the files of 84 patients seen at our ...
Mattle, Heinrich   +3 more
core  

Differential Diagnoses of Systemic Mastocytosis in Routinely Processed Bone Marrow Biopsy Specimens: A Review [PDF]

open access: yes, 2010
Diagnosis of systemic mastocytosis (SM) is mainly based on the morphological demonstration of compact mast cell infiltrates in various tissue sites. In almost all patients such infiltrates are detected in the bone marrow.
Horny, H. -P., Sotlar, K., Valent, P.
core   +1 more source

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