نتایج جستجو برای: hyperkeratosis

تعداد نتایج: 1721  

Journal: :Acta dermatovenerologica Croatica : ADC 2009
Angel Fernandez-Flores Jose A Manjon

We present a case of hyperkeratosis lenticularis perstans (Flegel's disease) in a 71-year-old-woman. Apart from all the typical morphological features of the disease, we evidenced mounds of parakeratosis that contained neutrophils, alternating with other strata of the horny layers in which no infiltrate was seen. Such a pattern has been described in association with diseases that show a periodi...

Journal: :Neurology 2012
James Collins A Reghan Foley Volker Straub Carsten G Bönnemann

A 32-year-old woman and a 50-year-old man with clinically typical Bethlem myopathy developed seemingly spontaneous keloids on their shoulder region (figure). The patients did not recall any significant trauma to the skin of this region. Bethlem myopathy (MIM #158810) is caused by dominant and recessive mutations in the collagen VI genes: COL6A1, COL6A2, and COL6A3. Skin manifestations include h...

2014
Tae-Hyoun Kim Dong-Su Kim Ju-Hee Han Seo-Na Chang Kyung-Sul Kim Seung-Hyeok Seok Dong-Jae Kim Jong-Hwan Park Jae-Hak Park

Corynebacterium (C.) bovis infection in nude mice causes hyperkeratosis and weight loss and has been reported worldwide but not in Korea. In 2011, nude mice from an animal facility in Korea were found to have white flakes on their dorsal skin. Histopathological testing revealed that the mice had hyperkeratosis and Gram-positive bacteria were found in the skin. We identified isolated bacteria fr...

ژورنال: مجله دندانپزشکی 2002
لطف آذر, مهرداد ,

Papillon Lefevre Syndrome (PLS) is a rare recessive autosomal disease, which is associated with palm and sole hyperkeratosis and early periodontium break down of deciduouse and permanent dentition. In the differential diagnosis of PLS, congenital form of palm and sole hyperkeratosis should be considered.Recently, mutation in catepesin C gene has been recognized as a genetic basis for PLS diseas...

2012
Hande Kaba Yesim Bakar Özlem Çinar Özdemir Seda Sertel

Lymphedema is a chronic, progressive, and often debilitating condition. Primary lymphedema is a lymphatic malformation developing during the later stage of lymph angiogenesis. Secondary lymphedema is the result of obstruction or disruption of the lymphatic system, which can occur as a consequence of tumors, surgery, trauma, infection, inflammation, and radiation therapy. Here, we report a 64-ye...

Journal: :Dental materials journal 2001
S Fujisawa N Okada E Muraoka

The purpose of this study was to evaluate the histopathological effect of eugenol and bis-eugenol on oral mucous membranes at the tissue organ level. Oral mucous membranes of mice were applied with three reagents, eugenol, bis-eugenol, and acetone (as the control). The control group showed a normal architecture. The eugenol group showed severe hyperkeratosis, parakeratosis, cellular edema, patc...

2016
Anup Kumar Tiwary Dharmendra Kumar Mishra

PC is commonly described as a rare genodermatosis characteristically manifesting as massive subungual hyperkeratosis with nail thickening, focal palmoplantar keratoderma alongwith deep f issur ing and blistering, oral leukokeratosis and discrete follicular hyperkeratosis [1,2]. Other features including abnormalities of teeth, hairs and larynx can also be seen depending on the clinical types. On...

Journal: :Archives of dermatology 2001
A Mehanna J A Malak A G Kibbi

BACKGROUND To date, approximately 43 cases of hyperkeratosis of the nipple and areola have been reported, most of which have been sporadic. OBSERVATION We describe 3 patients with this dermatosis who were encountered in the outpatient clinic of the Department of Dermatology at the American University of Beirut Medical Center, Beirut, Lebanon, within a 1-year period. CONCLUSION Hyperkeratosi...

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