Results 31 to 40 of about 63,443 (241)

Eosinophilic granuloma

open access: yes, 2002
Localised Langerhans-cell histiocytosis of bone (eosinophilic granuloma) is a benign tumour-like condition with a variable clinical course. Different forms of treatment have been reported to give satisfactory results.
B. A. Alman   +5 more
core   +1 more source

Eosinophilic Granuloma in Jaw Bone: A Pare Pediatric Case Report. [PDF]

open access: yesEthiop J Health Sci, 2016
Background: Eosinophilic granuloma (EG), one of the three clinical forms of Langerhans cell histiocytosis (LCH), is a benign inflammatory reaction to an unknown etiologic agent. It most commonly occurs in children and young adults.
Kannan K   +5 more
europepmc   +2 more sources

A Case of Angioleiomyoma with Epithelioid Granuloma

open access: yesCase Reports in Dermatology, 2011
We describe a 61-year-old Japanese woman who had been aware of a lesion on her left thigh for 10 years. Pathological examination demonstrated a well-circumscribed encapsulated nodule at the dermal-subcutaneous boundary, composed of eosinophilic spindle ...
Masazumi Onishi   +4 more
doaj   +1 more source

Nasal fibrosis: long-term follow up of four cases of eosinophilic angiocentric fibrosis [PDF]

open access: yes, 2005
Eosinophilic angiocentric fibrosis is a rare, benign cause of submucosal thickening and fibrosis within the upper respiratory tract. It predominantly affects the nose although cases have been reported in the subglottis.
Gallimore, A, Paun, S, Lund, VJ
core  

Eosinophilic Granuloma of the Ishium [PDF]

open access: yes, 1963
Eosinophilic granuloma of the bone characterized by marked infiltration of eosinophilic cells was first reported by Finzi in 1929. Since that time nearly 200 papers appeared in literature on this disease by the present time. We have found this disease in
Hongo, Hiroshi   +3 more
core   +2 more sources

Old disease, new twist

open access: yesJournal of Hospital Medicine, EarlyView.
Abstract An 81‐year‐old man with a history of high‐grade urothelial carcinoma of the bladder and ureter on treatment with atezolizumab and tiragolumab presented to the emergency department with 5 months of malaise, generalized weakness, and fatigue and 2 weeks of subjective fevers. One month prior to presentation, he received an empiric 9‐day course of
Hadi Roudsari   +4 more
wiley   +1 more source

Eosinophilic granuloma with metachronous actinomycosis – A case report with literature review

open access: yesIndian Journal of Health Sciences and Biomedical Research KLEU, 2022
Eosinophilic granuloma (EG) is a type of histiocytosis X with uncertain etiology. The lesion manifests as single or multiple areas of bone destruction with mild-to-severe pain or may be asymptomatic in some cases.
Kavya Soundararajan   +3 more
doaj   +1 more source

A hepatic enigma: Pediatric presentation of primary biliary cholangitis

open access: yesJPGN Reports, EarlyView.
Abstract Primary biliary cholangitis (PBC) is a chronic autoimmune condition characterized by destruction of intrahepatic bile ducts, leading to fibrosis and cirrhosis of the liver. It is an extremely rare pediatric disease with very few pediatric cases reported to date. Here, we report the case of a 14‐year‐old female who presented with elevated liver
Sindhura Kasturi   +3 more
wiley   +1 more source

Eosinophilic granuloma of the orbit: Report of two cases

open access: yes, 2007
We present clinical, radiological, and histopathological findings and treatment results of two infants with orbital eosinophilic granuloma. Both patients presented at 1 year of age with unilateral proptosis, periorbital edema, and a superotemporally ...
Kuzu, Isinsu   +3 more
core   +1 more source

Histiocytosis x: Recurrent isolated mandibular lesion (case report) [PDF]

open access: yesStomatološki glasnik Srbije, 2003
Histiocytosis X usually affects children and adolescents. In our case, a 54-year-old woman was admitted to hospital for evaluating and treatment of an isolated, painless swelling of the left side of the mandible.
Basta-Jovanović Gordana M.   +3 more
doaj   +1 more source

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