Results 131 to 140 of about 1,291 (187)
Papular lesions on the forearms in a 56-year-old woman. [PDF]
Öner S, Avcı C, Lebe B.
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Merkel Cell Carcinoma Presenting as a Solitary Facial Nodule in a 59-Year-Old Woman. [PDF]
Almutairi R +6 more
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A rare presentation of the diffuse dermal mucinosis in adenocarcinoma of the lungs treated with pembrolizumab and pemetrexed. [PDF]
Koch K, Solanki K, Zhu J.
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Eosinophilic Folliculitis Presenting as Persistent Pruritic Facial Papules: A Diagnostic Challenge. [PDF]
Bai JQA, Mahmood MN, Chow EY.
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Connective tissue nevi: A case report of a uniquely presenting eyelid collagenoma. [PDF]
Srikumar S, Krassilnik N, Mehta MP.
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The nomenclature and classification of cutaneous mucinosis is quite complex. An updated classification of idiopathic cutaneous mucinosis (lichen myxoedematosus), included three clinicopathological subsets: a generalized papular and sclerodermoid form, a localized papular form, and an atypical or intermediate form.
C-W, Chen +4 more
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Journal of the European Academy of Dermatology and Venereology, 1998
AbstractA case of childhood cutaneous mucinosis is described. This is a clinical condition that is rarely seen and has only recently been included in the group of primary mucinosis.
A Massa
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AbstractA case of childhood cutaneous mucinosis is described. This is a clinical condition that is rarely seen and has only recently been included in the group of primary mucinosis.
A Massa
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Self-healing Juvenile Cutaneous Mucinosis
Mucinoses represent a puzzling and heterogeneous group of rare diseases, and self-healing juvenile cutaneous mucinosis is an extremely rare disease among them.A scleroedematous condition of the face, associated with papular lesions and arthropathies, had occurred in a 5-year-old boy 10 days after onset of fever, arthralgia, muscle tenderness, and ...
R. Caputo, R. Grimalt, C. Gelmetti
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Cutaneous Mucinosis of Infancy
Pediatric Dermatology, 1994Abstract: Cutaneous mucinosis of infancy has been reported only rarely in the literature. We describe a case occurring in a black infant giri. Although no associated abnormalities have been described previously, our patient had a history of developmental delay, congenital cataracts, bilateral inguinal hernias, and an accessory tragus. The significance
K S, Stokes +3 more
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