نتایج جستجو برای: chronic sialadenitis

تعداد نتایج: 497561  

Journal: :Archives of Otolaryngology–Head & Neck Surgery 2012

Journal: :Der Pathologe 1989
J O Dreyer Y Sakuma G Seifert

The course of radiation-induced sialadenitis in 58 cases in the salivary gland registry (Institute for Pathology of the University of Hamburg 1965-1987) was subjected to pathohistological and immunohistochemical analysis. The pathohistological changes may be classified by severity into 3 stages. Stage I is characterized by mild inflammatory interstitial changes and moderate atrophy of individua...

2006
Maik Ellies Rainer Laskawi

BACKGROUND Diseases of the salivary glands are rare in infants and children (with the exception of diseases such as parotitis epidemica and cytomegaly) and the therapeutic regimen differs from that in adults. It is therefore all the more important to gain exact and extensive insight into general and special aspects of pathological changes of the salivary glands in these age groups. Etiology and...

Journal: :The hematology journal : the official journal of the European Haematology Association 2002
Francesco Bertoni Franco Cavalli Finbarr E Cotter Emanuele Zucca

Extranodal marginal zone B-cell lymphoma is a discrete clinicopathologic entity arising in mucosaassociated lymphoid tissue (MALT), characterised by unique pathogenic, histologic and clinical features. MALT B-cell lymphoma occurs more frequently in organs, such as stomach, salivary glands, or thyroid, which acquire lymphoid tissue only after chronic phlogistic events. This occurs in response to...

2015
Wei Li Yan Chen Zhi-Peng Sun Zhi-Gang Cai Tong-Tong Li Lei Zhang Min-Xian Huang Hong Hua Mei Li Xia Hong Jia-Zeng Su Zhu-Yan Zhang Yan-Ying Liu Jing He Zhan-Guo Li Yan Gao Guang-Yan Yu

INTRODUCTION Immunoglobulin G4-related disease (IgG4-RD) is a newly recognized fibro-inflammatory condition. Forty-two cases with immunoglobulin G4-related sialadenitis (IgG4-RS) confirmed by histopathological and immunohistochemical assessment were studied to clarify the clinicopathologic characteristics of the salivary glands involved in IgG4-RS, especially the relationship between the histop...

Journal: :Developmental period medicine 2016
Elwira Kołodziejczyk Karolina Wejnarska Grzegorz Oracz

Autoimmune pancreatitis (AIP) is a rare chronic inflammatory autoimmune disease of the pancreas. It is estimated that it accounts for 2-6% of all the chronic pancreatitis (CP) cases in adult patients. AIP is usually characterized by sudden onset. The presenting symptoms most commonly include painless jaundice, general weakness and loss of weight. Imaging studies often reveal diffuse enlargement...

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