نتایج جستجو برای: atrophia maculosa varioliformis cutis

تعداد نتایج: 2604  

Journal: :Proceedings of the Royal Society of Medicine 1935

Journal: :Proceedings of the Royal Society of Medicine 1909

Journal: :Acta neurologica Taiwanica 2008
Tzu-Hui Li Tsung-Hwa Chen Hung-Sheng Lin Chia-Wei Liou Jia-Shou Liu Shun-Sheng Chen Wei-Hsi Chen

PURPOSE Cutis marmorata is a cutaneous livedoid disorder which can be differentiated from livedo reticularis in both clinical and pathological presentations. Unlike Sneddon syndrome, a detailed immunocoagulation profile has not yet been delineated for cutis marmorata in patients with cerebral ischemia. METHODS To analyze the immunocoagulation profile in cutis marmorata patients associated wit...

Journal: :Archives of disease in childhood 1993
J Verbov

Aplasia cutis and other scarring alopecias Congenital absence of skin (aplasia cutis) presents on the scalp as one or more noninflammatory well defined oval or circular ulcers, crusted areas (fig 1) or as scars. Lesions usually occur over the vertex in or adjacent to the midline and may involve skin only or occasionally may extend deeply to bone and dura. Complications include secondary infecti...

2011
Didem Didar Balcı Ebru Çelik Gökhan Sarıkaya Jülide Zehra Yenin Esin Atik

Calcinosis cutis is a condition characterized by the deposition of calcium salts in the skin and subcutaneous tissues, and patients suffering from it encounter various connective tissue disorders, such as dermatomyositis (DM), scleroderma, and systemic lupus erythematosus. Although calcinosis cutis is frequently accompanied by juvenile dermatomyositis, rare cases have been reported in adult pat...

2016
Luciana de Sales Caldato Juliana de Sousa Britto Ligia Niero-Melo Hélio Amante Miot

Bullous leukemia cutis is an uncommon clinical manifestation of cutaneous infiltration by leukemic cells, from B-cell chronic lymphocytic leukemia. We present the case of a 67-year-old, female, chronic lymphocytic leukemia patient. She was taking chlorambucil and developed facial edema with erythema and warmth, misjudged as facial cellulitis. Two days later, she developed bullous lesions in the...

Journal: :Dermatology online journal 2014
Burak Tekin Ayse Deniz Yucelten Yasar Bayri

Cutis tricolor was first described in a 17-year-old male patient by Happle et al. as a rare coexistence of circumscribed hyperpigmentation and hypopigmentation close to each other on a background of normally pigmented skin. Cutis tricolor has been reported as an isolated cutaneous finding or in various associations. To the best of our knowledge, cutis tricolor in association with teratoma and h...

Journal: :Acta dermato-venereologica 2001
A Benez S Metzger G Metzler G Fierlbeck

Aleukemic leukemia cutis is a rare condition characterized by the infiltration of the skin by leukemic cells before their appearance in the peripheral blood or bone marrow. We report here a 62-year-old seemingly healthy patient who presented with disseminated erythematous maculae. A skin biopsy showed leukemia cutis of monocytic type. No involvement of bone marrow or peripheral blood was found....

Journal: :acta medica iranica 0
farideh dehghani department of dermatology, shahid sadooghi university of medical sciences, yazd, iran. mohammad ebrahimzadeh department of dermatology, shahid sadooghi university of medical sciences, yazd, iran. mansour moghimi department of pathology, shahid sadooghi university of medical sciences, yazd, iran. mohammad taghi noorbala department of dermatology, shahid sadooghi university of medical sciences, yazd, iran.

amyloidosis cutis dyschromica (acd) is a rare form of macular amyloidosis characterized by hypo and hyperpigmented macules. here we described a 20 year old girl with diffuse hypo and hyperpigmentation since she was four years old. five other members of her family are also involved. biopsy of hyperpigmented lesions revealed increase of melanin in the basal layer, pigment incontinence and amorpho...

2013
Shusuke Uchida Naoki Oiso Tamio Suzuki Akira Kawada

Acanthosis nigricans is characterized by papillomatous brownish lesions mainly in the intertriginous areas. We used dermoscopy to examine such lesions in a family with acanthosis nigricans. The dermoscopic images showed an aberrant skin structure of linear crista cutis and sulcus cutis, and hyperpigmented dots in crista cutis. The hyperpigmented dots, which could not be seen with the naked eyes...

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