Results 51 to 60 of about 74,348 (167)

Coordinate anatomy of the upper parts of urinary tract at ontogenesis stages: II mature age [PDF]

open access: yes, 2016
The research was aimed at study of the renal hilum normal anatomy with validation of system of morphometric indices of renal hilum morphotype at the stages of human postnatal ontogenesis.
Danylchenko, S.I., Shklar, A.S.
core   +2 more sources

Rheumatoid neutrophilic dermatitis

open access: yesJEADV Clinical Practice, Volume 3, Issue 5, Page 1364-1380, December 2024.
Rheumatoid neutrophilic dermatitis (RND) is a rare dermatological condition typically associated with rheumatoid arthritis (RA). Overall, 54 cases of RND were reviewed from a Medline (via PubMed) and Scopus databases. Majority of patients were female (72.3%) with a median (IQR) age at the time of diagnosis of 58 years‐old (65‐45).
Biagio Scotti   +6 more
wiley   +1 more source

Characterization of multinucleated giant cells in synovium and subchondral bone in knee osteoarthritis and rheumatoid arthritis [PDF]

open access: yes, 2015
Background: Multinucleated giant cells have been noticed in diverse arthritic conditions since their first description in rheumatoid synovium. However, their role in the pathogenesis of osteoarthritis (OA) or rheumatoid arthritis (RA) still remains ...
A Consolaro   +61 more
core   +4 more sources

Histiocyte‐rich ROS1‐rearranged inflammatory myofibroblastic tumour of the trachea: A rare neoplasm presenting with asthma‐like symptoms

open access: yesRespirology Case Reports, Volume 12, Issue 12, December 2024.
A flow volume loop demonstrated classical upper airway obstruction pattern. Abstract Inflammatory myofibroblastic tumour is a rare tumour. We present an atypical case of Inflammatory myofibroblastic tumour which was trachea in location, histocyte rich and ROS1 rearranged.
Chin Tong Kwok   +5 more
wiley   +1 more source

Multinucleated Giant Cells Polymorphism in Epulis [PDF]

open access: yes, 2015
In the present study we investigated multinucleated giant cells (MGCs) presence, density and morphology in epulis. Histopathological examination performed on specimens excised from two patients and stained using Goldner’s trichrome method revealed MGCs
Boșca, Adina Bianca   +7 more
core   +2 more sources

Formation, etiology and pathogenesis of giant cells [PDF]

open access: yes, 2016
Introduction: Giant cells are the cells that superior to their size common cell types. They can be as in normal so in pathological conditions. Cells that are encountered in normal conditions are divided into two types: megakaryocytes and multinucleate ...
Avdyeyev, S., Diachenko, O.
core  

Manifestação Incomum de uma Entidade Rara: Doença de Erdheim-Chester [PDF]

open access: yes, 2019
A 69-year-old woman presented with sudden left hemiparesis. Computed tomography (CT) scan excluded acute brain injuries. Patient was admitted with acute ischemic stroke of right hemisphere. There was full recovery within 24 hours and etiologic studies
Achega, M   +3 more
core   +1 more source

Neoadjuvant intralesional methotrexate for juvenile xanthogranuloma in an adult [PDF]

open access: yes, 2021
Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis usually occurring in infants and typically located in the head or neck.1 Clinically, solitary skin lesions are found in 60%–82% of patients and the most common variant is characterized
Antoñanzas, J. (Javier)   +6 more
core   +1 more source

Erdheim–Chester disease: An elusive diagnosis in a 50‐year‐old Ethiopian man presenting with diffuse sclerotic bone lesion

open access: yesClinical Case Reports, Volume 12, Issue 9, September 2024.
Key Clinical Message Diagnosis of Erdheim–Chester disease (ECD) requires the clinician to be familiar with its various manifestations, classic radiologic and histologic features. This case highlights the significance of considering ECD in any patient presenting with bone pain and symmetric osteosclerosis of long bones of extremities to allow for early ...
Semir Abdi Usmael   +7 more
wiley   +1 more source

Erdheim‑Chester disease of multisystem involvement with delayed diagnosis: A case report and literature review

open access: yesExperimental and Therapeutic Medicine
Erdheim-Chester disease (ECD) is a rare tumor of histiocytic origin, characterized by foamy or lipid-laden histiocytes mixed or surrounded by fibrosis that infiltrate multiple organs. Misdiagnosis is common due to the diversity of clinical presentations.
Xiaotong Shi   +6 more
semanticscholar   +1 more source

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