نتایج جستجو برای: dyskeratotic acantholysis

تعداد نتایج: 294  

2011
Zoran Jukić Iva Ledinsky Monika Ulamec Mario Ledinsky Božo Krušlin Davor Tomas

BACKGROUND Acantholytic squamous cell carcinoma (ASCC) is an uncommon histopathologic variant of SCC, characterized by marked acantholysis, wherein the tumor cells demonstrate defective cohesion to one another in the cancer nest leading to a pseudoglandular or pseudovascular appearance. The most common site of ASCC is the sun-exposed areas of the skin. Sporadic cases of ASCC have also been repo...

Journal: :Endoscopy 2015
Paolo Cecinato Liboria Laterza Loredana De Marco Annamaria Casali Magda Zanelli Romano Sassatelli

resulting in dysphagia A 44-year-old man was admitted to our institution because of the appearance of painful cutaneous, oral, and genital vesicles. His previous medical history was unremarkable. He had had pharyngitis treated with amoxicillin 1 month before the hospitalization. On physical examination, symmetrically erythematous plaques, covered with vesicles, were seen. Because of subsequent ...

Journal: :The Journal of Cell Biology 1997
Peter J. Koch M G. Mahoney Hiroyasu Ishikawa Leena Pulkkinen Jouni Uitto Leonard Shultz George F. Murphy Diana Whitaker-Menezes John R. Stanley

In patients with pemphigus vulgaris (PV), autoantibodies against desmoglein 3 (Dsg3) cause loss of cell-cell adhesion of keratinocytes in the basal and immediate suprabasal layers of stratified squamous epithelia. The pathology, at least partially, may depend on protease release from keratinocytes, but might also result from antibodies interfering with an adhesion function of Dsg3. However, a d...

2015
Camille Luyet Katja Schulze Beyza S. Sayar Denise Howald Eliane J. Müller Arnaud Galichet

The majority of pemphigus vulgaris (PV) patients suffer from a live-threatening loss of intercellular adhesion between keratinocytes (acantholysis). The disease is caused by auto-antibodies that bind to desmosomal cadherins desmoglein (Dsg) 3 or Dsg3 and Dsg1 in mucous membranes and skin. A currently unresolved controversy in PV is whether apoptosis is involved in the pathogenic process. The ob...

Journal: :Acta dermato-venereologica 2000
M Roger C Valence J M Bressieux P Bernard A Fur

A 52-year-old man who had had WaldenstroÈm's disease for 5 years presented to our department with clinical manifestations of hyperviscosity syndrome including headaches and paresthesias of the extremities. All treatments for the haemopathy had been withdrawn 6 months earlier because of drug resistance. Besides splenomegaly, physical examination showed 2 types of cutaneous lesions: nonfollicular...

2012
Thierry Olivry Keith E. Linder Ping Wang Petra Bizikova Joseph A. Bernstein Stanley M. Dunston Judy S. Paps Margret L. Casal

In humans, congenital and hereditary skin diseases associated with epidermal cell-cell separation (acantholysis) are very rare, and spontaneous animal models of these diseases are exceptional. Our objectives are to report a novel congenital acantholytic dermatosis that developed in Chesapeake Bay retriever dogs. Nine affected puppies in four different litters were born to eight closely related ...

Journal: :Case reports in gastrointestinal medicine 2021

Pemphigus vulgaris (PV) is an autoimmune blistering disorder of the skin and mucosal surfaces characterized by acantholysis (loss adhesion between epidermal cells). Esophageal involvement PV underdiagnosed entity as routine diagnostic endoscopy not recommended in asymptomatic patients. Dysphagia odynophagia are common presenting symptoms; however, upper gastrointestinal bleeding (UGIB) associat...

Journal: :Indian Journal of Dermatology, Venereology and Leprology 2017

Journal: :International Journal of Immunopathology and Pharmacology 2007

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