Results 11 to 20 of about 29,211 (229)

Xanthogranulomatous Inflammation of Colon: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Xanthogranulomatous Inflammation (XGI) is a rare pathological condition that can affect various organs, such as lungs, endometrium, vagina, fallopian tube, ovary, testis, stomach, colon, appendix and pancreas.
Ramya Lakshminarayanan   +3 more
doaj   +1 more source

Xanthogranulomatous Cholecystitis: CT and USG Characteristics [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2019
Cholecystitis is a common finding in everyday practice of ultrasound. The diagnosis of Xanthogranulomatous Cholecystitis (XGC) is however an uncommon entity and every radiologist should be aware of the characteristic ultrasound and CT findings to ...
Siddarth Ragupathi, Sahadevan Vijay
doaj   +1 more source

Comparative Immunopathology of Cetacean morbillivirus Infection in Free-Ranging Dolphins From Western Mediterranean, Northeast-Central, and Southwestern Atlantic

open access: yesFrontiers in Immunology, 2019
Cetacean morbillivirus (CeMV; Paramyxoviridae) causes epizootic and interepizootic fatalities in odontocetes and mysticetes worldwide. Studies suggest there is different species-specific susceptibility to CeMV infection, with striped dolphins (Stenella ...
Josué Díaz-Delgado   +24 more
doaj   +1 more source

Histiocytic sarcoma [PDF]

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2010
A 59-year-old white woman, SC, after being treated for pneumonia, presented with an increase in the size of lymph nodes. The immunohistochemical examination diagnosed histiocytic sarcoma. Relapse occurred 12 months after starting chemotherapy. The patient evolved with febrile neutropenia, septic shock and death.
Eduardo Silva Machado   +4 more
openaire   +3 more sources

Histiocyte disorders [PDF]

open access: yesBritish Medical Bulletin, 1996
Histiocyte disorders are characterised by tissue infiltration with cells of monocyte/macrophage lineage, with two disorders, Langerhans' cell histiocytosis (LCH) and haemophagocytic lymphohistiocytosis (HLH) accounting for the overwhelming majority of cases in childhood and, apart from monocyte variants of acute myeloid leukaemia, histiocytic ...
openaire   +2 more sources

Malakoplakia of Bone Presenting as Bilateral Septic Arthritis: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Malakoplakia is an uncommon chronic inflammatory disorder that usually involves an abnormal immunological response to underlying infection. Though it is reported in almost every organ system, involvement of bone is extremely rare, where it usually ...
S Supriya, B Krishnamoorthi Adiga
doaj   +1 more source

Histiocytic sarcoma of the oesophagus

open access: yesRevista Española de Enfermedades Digestivas, 2022
A 20-year-old male with no medical history of interest who goes to the emergency room because of retrosternal pain, odynophagia, dysphagia, and fever. On physical examination: 37.7ºC axillary temperature, bad general condition, and central chest pain on palpation.
Carlos, Comesaña Castellar   +7 more
openaire   +2 more sources

Os histiócitos e as histiocitoses não Langerhans em dermatologia Histiocytes and non-Langerhans cell histiocytoses in dermatology

open access: yesAnais Brasileiros de Dermatologia, 2003
Atualmente, os histiócitos não são mais compreendidos como células únicas, mas como um grupo heterogêneo de células com o mesmo aspecto histológico, mas com características e funções distintas entre si.
Flávio Barbosa Luz   +3 more
doaj   +1 more source

Benign fibrohistiocytic tumour of the palate

open access: yesIndian Journal of Dermatopathology and Diagnostic Dermatology, 2020
Benign fibrous histiocytomas of soft tissue are composed of spindled fibroblasts admixed with secondary elements including histiocytes, foam cells, and inflammatory cells. These tumors occur equally in males and females and most often arise in the dermis
Nilima Sharma, Mohammad Jaseem Hassan
doaj   +1 more source

Erdheim–Chester Disease Involving the Biliary System and Mimicking Immunoglobulin G4-Related Disease: A Case Report

open access: yesJournal of the Korean Society of Radiology, 2023
First described in 1930 as a lipoid granulomatosis, Erdheim-Chester disease (ECD) is a rare histiocytosis encompassing a group of disorders caused by overproduction of histiocytes, a subtype of white blood cells. This disease most commonly involves the
Hyuk Gi Hong   +3 more
doaj   +1 more source

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