نتایج جستجو برای: nodular prurigo

تعداد نتایج: 12129  

2009
Kun-Ying Tsai Chien-Chun Chiou Rosaline Chung-Yee Hui

Prurigo pigmentosa is a type of inflammatory dermatosis characterized by symmetrical pruritic erythematous papules that normally resolve with reticular pigmentation. In severe cases, edematous infi ltrative plaques may be found, but usually no vesicles or bullae. We presented a 32-year-old Taiwanese female, a case of insulin dependent diabetis mellitus with sudden onset of vesicobullae upon ery...

Journal: :Dermatology 2008
Tetsuya Higuchi Takahiro Satoh Hiroo Yokozeki

on his lower back and upper extremities. Each eruption was a bean-sized solitary papule ( fig. 1 a). Many of the papules had erosions or crusts due to excoriation. Some papules were arranged linearly or clustered to form small plaques. Steroid ointment was ineffective. He also had other cutaneous manifestations of dermatomyositis such as heliotrope rash, flagellate erythema of the upper back, p...

Journal: :Journal of Nippon Medical School = Nippon Ika Daigaku zasshi 2005
Hirotsugu Tashiro Harue Arai Takashi Hashimoto Shinichiro Takezaki Seiji Kawana

We report 45- and 61-year-old women with generalized prurigo nodularis-like eruption whose clinical, histologic and immunopathologic features were consistent with the diagnosis of pemphigoid nodularis. In one case, nodular lesions preceded the onset of generalized blistering by two years and in the other, no definite blister nor erosion was seen except for some appearing on the soles during the...

Journal: :Open Life Sciences 2019

Journal: :DMW - Deutsche Medizinische Wochenschrift 1902

Journal: :Proceedings of the Royal Society of Medicine 1935

Journal: :Archiv für Dermatologie und Syphilis 1916

Journal: :Clinical genetics 2006
B Drera D Castiglia N Zoppi R Gardella G Tadini G Floriddia N De Luca C Pedicelli S Barlati G Zambruno M Colombi

Dystrophic epidermolysis bullosa (DEB) pruriginosa (DEB-Pr) is a rare variant of DEB due to COL7A1 dominant and recessive mutations, which is characterized by severe itching and lichenoid or nodular prurigo-like lesions, mainly involving the extremities. Less than 30 patients have been described showing variable disease expression, and frequently, delayed age of onset. We report the clinical an...

Journal: :Proceedings of the Royal Society of Medicine 1924

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