BIOMAT Database Logo BIOMAT Database Logo

[Apropos of papulous mucinosis: acral persistent papular mucinosis or minor form of scleromyxedema]. 1992

O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Clinique Dermatologique B, Hôpital Claude-Huriez, CHU, Lille.

UI MeSH Term Description Entries
D008854 Microscopy, Electron Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen. Electron Microscopy
D009230 Myxedema A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips. Myxedemas
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000169 Acrodermatitis Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome. Gianotti-Crosti Syndrome,Infantile Papular Acrodermatitis,Acrodermatitis Papulosa Infantum,Acropapulo-Vesicular Syndrome,Erythemato-Vesiculo-Papulous Eruptive Syndrome,Papular Acrodermatitis of Childhood,Papulovesicular Acrolocated Syndrome,Acrodermatitides,Acrodermatitis Papulosa Infantums,Acropapulo Vesicular Syndrome,Acropapulo-Vesicular Syndromes,Childhood Papular Acrodermatitides,Childhood Papular Acrodermatitis,Erythemato Vesiculo Papulous Eruptive Syndrome,Erythemato-Vesiculo-Papulous Eruptive Syndromes,Gianotti Crosti Syndrome,Infantile Papular Acrodermatitides,Papular Acrodermatitides, Infantile,Papular Acrodermatitis, Infantile,Papulovesicular Acrolocated Syndromes,Syndrome, Acropapulo-Vesicular,Syndrome, Erythemato-Vesiculo-Papulous Eruptive,Syndrome, Gianotti-Crosti,Syndromes, Acropapulo-Vesicular,Syndromes, Erythemato-Vesiculo-Papulous Eruptive,Syndromes, Papulovesicular Acrolocated
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D017520 Mucinoses Mucoid states characterized by the elevated deposition and accumulation of mucin (mucopolysaccharides) in dermal tissue. The fibroblasts are responsible for the production of acid mucopolysaccharides (GLYCOSAMINOGLYCANS) in the ground substance of the connective tissue system. When fibroblasts produce abnormally large quantities of mucopolysaccharides as hyaluronic acid, chondroitin sulfate, or heparin, they accumulate in large amounts in the dermis. Mucinosis

Related Publications

O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
[Persistent acral papulous mucinosis].
January 1996, Annales de dermatologie et de venereologie,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Acral persistent papular mucinosis.
March 1992, The British journal of dermatology,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Acral persistent papular mucinosis.
August 1993, International journal of dermatology,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Acral persistent papular mucinosis.
July 1990, Journal of the American Academy of Dermatology,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Acral persistent papular mucinosis.
December 1992, Journal of the American Academy of Dermatology,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
[Acral persistent papular mucinosis].
October 2006, Actas dermo-sifiliograficas,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Acral persistent papular mucinosis.
December 2004, Journal of the American Academy of Dermatology,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Acral persistent papular mucinosis.
January 2021, Clinics in dermatology,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Acral persistent papular mucinosis.
August 1989, Journal of the American Academy of Dermatology,
O Podglajen-Wecxsteen, and E Ehrsam, and C Mailfer, and G Rotteleur, and M Lecomte-Houcke, and P Thomas
Atypical acral persistent papular mucinosis.
June 1999, International journal of dermatology,
Copied contents to your clipboard!