Results 1 to 10 of about 46,210 (204)

Paradigm shift in vertebral eosinophilic granuloma [PDF]

open access: yesUkrainian Neurosurgical Journal, 2023
Objective: Eosinophilic granuloma is the most common type of Langerhans cell histiocytosis. Vertebral bone involvement of eosinophilic granuloma is a rare disease.
Muhammet Arif Ozbek   +2 more
doaj   +2 more sources

Diagnosis of solitary eosinophilic granuloma by CT, MRI, and 18F-FDG PET/CT: two clinical cases [PDF]

open access: yesDigital Diagnostics, 2021
This paper presents two clinical cases of eosinophilic granuloma of bone diagnosed by CT, MRI, and 18F-FDG PET/CT. In both cases the patients were admitted to the clinic with suspected primary malignant bone tumor and the diagnosis of a solitary ...
Pavel B. Gelezhe, Dmitriy V. Bulanov
doaj   +1 more source

Multifocal Eosinophilic Granuloma of Jaws and Skull with Classical and Unusual Radiographic/Imaging Findings [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Eosinophilic granuloma is basically a disorder of reticuloendothelial system and is one of the variants of langerhans cell histiocytosis. Multifocal eosinophilic granuloma affecting jaws and skull is relatively a rare disorder.
Jayam Raviraj   +4 more
doaj   +1 more source

Eosinophilic Granuloma: A Rare and Often Benign Condition Presenting as a Lump on the Head, which was Easily Treated

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2021
Eosinophilic granuloma is a localized, non-invasive form of Langerhans cell histiocytosis. It usually develops in the long bones and is more frequent in children under the age of 10 years. It is very rare in adults.
Tatiana Pires   +5 more
doaj   +1 more source

Recurrent eosinophilic granuloma of the maxilla in an adult female: About a rare case report

open access: yesAdvances in Oral and Maxillofacial Surgery, 2022
Langerhans cell histiocytosis (LCH) is a rare idiopathic disorder of the reticulo-endothelial system with abnormal proliferation of the bone marrow derived from Langerhans cells.LCH mainly affects children and young adults, with a slight male ...
Salma Adnane   +3 more
doaj   +1 more source

Benign orbital tumors with bone destruction in children. [PDF]

open access: yesPLoS ONE, 2012
PurposeTo present rare benign orbital tumors with bone destruction in children who could not be diagnosed pre-surgically and may simulate malignant ones.MethodsA retrospective review of cases.
Jianhua Yan, Sheng Zhou, Yongping Li
doaj   +1 more source

Eosinophilic granuloma of the mandible

open access: yesAnnals of Maxillofacial Surgery, 2020
Eosinophilic granuloma (EG) is a rare histiocytic disorder resulting from clonal proliferation of Langerhans cells. Eosinophilic granuloma, the most benign of the three entities of Langerhans cell histiocytosis, may be multiple or solitary. This lesion can affect any bones but commonly involves the mandible when the jaws are affected.
Prathap, Akhilesh   +4 more
openaire   +3 more sources

Necrobiotic granuloma: An update

open access: yesIndian Journal of Dermatopathology and Diagnostic Dermatology, 2018
Granulomatous disorders comprise a large family sharing the common histological denominator of granuloma formation. Collagenolytic or necrobiotic granuloma is one in which a granulomatous infiltrate develops around a central area of altered collagen and ...
Achyut Pokharel, Isha Poudel Koirala
doaj   +1 more source

Eosinophilic ulcer of the tongue - Case report [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2015
Eosinophilic ulcer of the oral mucosa is a rare, self-limiting, chronic and benign lesion of unknown pathogenesis that affects the oral mucosa. We present the case of a 65 year-old Caucasian female with a fivemonth history of a painful ulcer on the ...
Dario Didona   +4 more
doaj   +1 more source

Eosinophil granuloma due to parasite treated by laparoscopic and endoscopic cooperative surgery: a case report

open access: yesSurgical Case Reports, 2020
Background Gastric eosinophilic granuloma caused by parasitic infection is rare. It is often suspected to be a malignant disease and it is difficult to diagnose.
Toshikatsu Tsuji, Noriyuki Inaki
doaj   +1 more source

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