Results 111 to 120 of about 1,062 (154)

A Case of Folliculotropic Mycosis Fungoides Initially Misleading as a Poikilodermatous Rash: The Importance of Gene Rearrangement Testing in Early-Stage Disease (Folliculotropic T-Cell Lymphocytosis). [PDF]

Cureus
Moreno BA, Lutwak M, Sherkin S, Kerdel F.   +3 more
europepmc   +1 more source

Connective tissue nevi: A case report of a uniquely presenting eyelid collagenoma. [PDF]

Am J Ophthalmol Case Rep
Srikumar S, Krassilnik N, Mehta MP.
europepmc   +1 more source

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Childhood cutaneous mucinosis

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.
G C, Velho, M, Oliveira, R, Alves, F, Silvestre, A, Massa, A P, Baptista   +5 more
exaly   +4 more sources

[Cutaneous mucinosis of infancy]. [PDF]

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 2021
Cutaneous mucinosis of infancy is a rare skin disease with just a few reported cases in the literature. We report the case of an 11-year-old boy with asymptomatic, skin-coloured papules and plaques on his right arm that had appeared 9 months prior to presentation.
Lisa, Eholzer, Ilske, Oschlies, Mark, Berneburg, Sigrid, Karrer   +3 more
openaire   +3 more sources

Cutaneous Mucinosis of Infancy

Pediatric Dermatology, 1994
Abstract: 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, L G, Rabinowitz, A D, Segura, N B, Esterly   +3 more
openaire   +2 more sources

Perforating Cutaneous Mucinosis

Dermatologica, 2009
A case is described in which a papulonodular eruption developed all over the body. Histologic examination of one of the lesions revealed the dermis to contain mucin (hyaluronic acid). In some areas there was perforation through the epidermis of the mucinous material.
S, Brenner, B, Ilie, A, Krakowski
openaire   +2 more sources

Cutaneous focal mucinosis

British Journal of Dermatology, 1989
A 39-year-old man had typical cutaneous focal mucinosis on the left forearm. The fibroblasts in the myxomatous lesion had many cytoplasmic vesicles, and on electron microscopy, these were compatible with condensing vacuoles or secretory granules. The fibroblasts in this case were considered to be mucoblasts involved in the over-production of the ground
S, Nishiura, M, Mihara, S, Shimao, H, Ogawa, Y, Kawamura   +4 more
openaire   +2 more sources

Self Healing Cutaneous Mucinosis

Dermatology, 2009
Self-healing juvenile cutaneous mucinosis is a new entity distinct from previously described forms of cutaneous mucinosis. We present a new case in a 26-year-old female patient who began abruptly with a papular eruption, involving the scalp, face, neck and trunk, accompanied by periarticular papules on the hands and arthralgias.
M E, de las Heras, B, Pérez, J M, Arrazola, A, Rocamora, A, Ledo   +4 more
openaire   +2 more sources

Cutaneous lymphadenoma with focal mucinosis

Journal of Cutaneous Pathology, 1992
Cutaneous lymphadenoma of the eyebrow occurred in a 72‐year‐old man. The nodular tumor was well circumscribed but non encapsulated and invaded the reticular dermis and superficial hypodermis without any connection with the epidermis. Tumor cells had a basal‐like appearance and were arranged in small lobules and islands with peripheral palisading and ...
J, Wechsler, G, Fromont, J M, André, E S, Zafrani   +3 more
openaire   +2 more sources

Self-healing Juvenile Cutaneous Mucinosis

Archives of Dermatology, 1995
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
openaire   +3 more sources