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Skin Diseases Caused by Disorders in Mucopolysaccharide Metabolism

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Dermatology

Abstract

The mesenchymal ground substance is an amorphous material that constitutes the matrix of the dermal and subcutaneous connective tissue, together with collagen and elastic fibers. This ground substance contains substantial amounts of glycosaminoglycans, which are rich in acid mucopolysaccharides as well as water, salts, and glycoproteins. The mucopolysaccharide part constitutes about 0.5–1.0 mg per gram dry weight in the skin. The acid mucopolysaccharides are mainly hyaluronic acid, dermatan sulfate, and chondroitin-6-sulfate, as well as smaller amounts of heparitin sulfate. The exact composition of the acid mucopolysaccharides in the skin varies from one region to another and also with age and sex. Wharton’s substance in the umbilical cord contains a preponderance of hyaluronic acid and relatively little sulfated mucopolysaccharides, whereas the skin in an adult contains little hyaluronic acid but more sulfated acid mucopolysaccharides of the type of dermatan sulfate and chondroitin-6-sulfate. The acid mucopolysaccharides in the ground substance are important to balance the water and salt metabolism within the skin. Probably, the salt-extractable hyaluronic acid is particularly important for the water-binding capacity of the connective tissue ground substance, while the sulfated muco-polysaccharides play a special role in the production of the collagen and elastic fibers.

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Bibliography:Skin Diseases Caused by Disorders in Mucopolysaccharide Metabolism

  • Horwitz AL (1979) The mucopolysaccharidoses: clinical and biochemical correlations. Am J Ment Defic 84: 113–123

    PubMed  CAS  Google Scholar 

  • Kamp JJP van de, Niermeijer MF, von Figura K et al. (1981) Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C ). Clin Genet 20: 152–160

    Google Scholar 

  • McKusick VA, Neufeld EF (1983) The mucopolysaccharide storage disorders. In: Stanbury JB, Wyngaarden JB, Fredrickson DS et al. (eds) The metabolic basis of inherited disease, 4th edn. McGraw-Hill, New York, pp 751–777

    Google Scholar 

  • Spranger JW, Wiedemann HR (1970) The genetic mucolipidoses. Diagnosis and differential diagnosis. Hum Genet 9: 113–139

    Google Scholar 

  • Spranger JW (1975) Morphological aspects of the mucopolysaccharidoses. In: Holten JB, Ireland JT (eds) Inborn errors of skin, hair, and connective tissue. MTP, Lancaster, pp 39–60

    Google Scholar 

  • Carney JA, Headington JT, Su WPD (1986) Cutaneous myxomas: a major component of the complex of myxomas, spotty pigmentation, and endocrine overactivity. Arch Dermatol 122: 790–798

    Article  PubMed  CAS  Google Scholar 

  • Johnson WC, Helwig EB (1966) Cutaneous focal mucinosis. Arch Dermatol 93: 13–20

    Article  PubMed  CAS  Google Scholar 

  • Lum D (1980) Cutaneous mucinosis of infancy. Arch Dermatol 116: 198–200

    Article  PubMed  CAS  Google Scholar 

  • Cawley EP, Lupton CH, Wheeler CE et al. (1957) Examination of normal and myxedematous skin. Use of Mowry’s alcian blue-periodic acid-Schiff technique. Arch Dermatol 76: 537–544

    Google Scholar 

  • Gottron HA, Korting GW (1953) Zur Pathogenese des Myxoedema circumscriptum tuberosum. Arch Dermatol Syph 195: 625–649

    PubMed  CAS  Google Scholar 

  • Reuter MJ (1931) Histopathology of the skin in myxedema. Arch Dermatol Syph 24: 55–71

    Article  Google Scholar 

  • Braun-Falco O, Petzoldt D (1967) E.M.O.-Syndrom. Exophthalmus, Myxoedema circumscriptum praetibiale und Osteoarthropathia hypertrophicans (E.M.0.-Syndrom). Münchn Med Wochenschr 79: 1523–1529

    Google Scholar 

  • Kind R, Hornstein OP (1976) Klinik des prätibialen Myxödems und neue Aspekte zur Diagnostik und Pathogenese. Hautarzt 27: 375–381

    PubMed  CAS  Google Scholar 

  • Konrad K, Brenner W, Pehamberger H (1980) Ultrastructural and immunological findings in Graves’ disease with pretibial myxedema. J Cutan Pathol 7: 99–108

    Article  PubMed  CAS  Google Scholar 

  • Korting GW, Nürnberger F, Müller G (1967) Zur Ultrastruktur der Bindegewebszellen beim Myxoedema circumscriptum praetibiale. Arch Klin Exp Dermatol 229: 381–389

    PubMed  CAS  Google Scholar 

  • Lubach D, Freyschmidt J (1981) Das EMO-Syndrom. Klinische und röntgenologische Zeichen. Hautarzt 32: 91–93

    Google Scholar 

  • Lynch PJ, Maize JC, Sisson JC (1973) Pretibial myxedema and nonthyrotoxic thyroid disease. Arch Dermatol 107: 107–111

    Article  PubMed  CAS  Google Scholar 

  • Schermer DR, Roenigk HH Jr, Schumacher OP et al. (1970) Relationship of long-acting thyroid stimulator to pretibial myxedema. Arch Dermatol 102: 62–67

    Article  PubMed  CAS  Google Scholar 

  • Archibald GC, Calvert HT (1977) Hypothyroidism and li- chen myxoedematosus. Arch Dermatol 113: 684–685

    Article  PubMed  CAS  Google Scholar 

  • Dalton JE, Seidell MA (1953) Studies on lichen myxedema- tosus (papular mucinosis). Arch Dermatol 67: 194–209

    Article  CAS  Google Scholar 

  • Hardie RA, Hunter JAA, Urbaniak S et al. (1979) Spontaneous resolution of lichen myxoedematosus. Br J Dermatol 100: 727–730

    Article  PubMed  CAS  Google Scholar 

  • Hill TG, Crawford JN, Rogers CC (1976) Successful management of lichen myxedematosus. Arch Dermatol 112: 67–69

    Article  PubMed  CAS  Google Scholar 

  • Howsden SM, Herndon JH Jr, Freeman RG (1975) Lichen myxedematosus. A dermal infiltrative disorder responsive to cyclophosphamide therapy. Arch Dermatol 111: 1325–1330

    Google Scholar 

  • Krebs A, Müller A (1980) Lichen myxoedematosus and multiples Myelom vom Typ IgG/kappa. Hautarzt 31: 649–653

    PubMed  CAS  Google Scholar 

  • Braun-Falco O, Weidner I (1970) Skleromyxödem ArndtGottron mit Knochenmarks-Plasmocytose und Myositis. Arch Belg Dermatol (Suppl) 26: 193–217

    CAS  Google Scholar 

  • Chanda JJ (1979) Scleromyxedema. Cutis 24: 549–552

    CAS  Google Scholar 

  • Feldman P, Shapiro L, Pick AI et al. (1969) Scleromyxede-ma. A dramatic response to melphalan. Arch Dermatol 99: 51–56

    Google Scholar 

  • Gottron HA (1954) Skleromyxödem (eine eigenartige Erscheinungsform von Myxothesaurodermie). Arch Dermatol Syph 199: 71–91

    CAS  Google Scholar 

  • Hardmeier T, Vogel A (1970) Elektronenmikroskopische Befunde bei Skleromyxödem Arndt-Gottron. Arch Klin Exp Dermatol 237: 722–736

    PubMed  CAS  Google Scholar 

  • Harris RB, Perry HO, Kyle RA et al. (1979) Treatment of scleromyxedema with melphalan. Arch Dermatol 115: 295–299

    Article  PubMed  CAS  Google Scholar 

  • Kantor GR, Bergfeld WF, Katzin WE et al. (1986) Scleromyxedema associated with scleroderma, renal disease and acute psychosis. J Am Acad Dermatol 14: 879–888

    Article  PubMed  CAS  Google Scholar 

  • Keining E, Braun-Falco O (1956) Zur Klinik und Pathogenese des Skleromyxoedems. Acta Derm Venereol (Stockh) 36: 37–71

    CAS  Google Scholar 

  • Kövary PM, Vakilzadeh F, Zaun H (1980) Skleromyxödem Arndt-Gottron — eine paraproteinämische Dermatose. Aktuel Dermatol 6: 155–113

    Google Scholar 

  • Lang E, Zabel M, Schmidt H (1984) Skleromyxoedem Arndt-Gottron und assoziierte Phänomene. Dermatologica 168: 29–35

    Article  Google Scholar 

  • Lowe NJ, Dufton PA, Hunter RD et al. (1982) Electron-beam treatment of scleromyxoedema. Br J Dermatol 106: 449–454

    Article  PubMed  CAS  Google Scholar 

  • Milam CP, Cohen LE, Fenske NA et al. (1988) Scleromyxedema: therapeutic response to isotretinoin in three patients. J Am Acad Dermatol 19: 469–477

    Article  PubMed  CAS  Google Scholar 

  • Proppe A, Becker V, Hardmeier T (1969) Skleromyxödem Arndt-Gottron und Plasmocytom. Hautarzt 20: 53–59

    PubMed  CAS  Google Scholar 

  • Schnyder UW, Kaufmann J (1979) Skleromyxoedema Arndt-Gottron, Plasmozytom ( IgG-Kappa-Typ ). Dermatologica 159: 407–409

    Google Scholar 

  • Winkelmann RK (1976) Pathogenesis and staging of scleroderma. Acta Derm Venereol (Stockh) 56: 83–92

    CAS  Google Scholar 

  • Bleehen SS, Slater DN, Mahood J et al. (1982) Reticular erythematous mucinosis: light and electron microscopy, immunofluorescence and histochemical findings. Br J Dermatol 106: 9–18

    Article  PubMed  CAS  Google Scholar 

  • Dijkmans BAC, Bergman W, Eulderink F et al. (1986) Reticular erythematous mucinosis syndrome in a patient with polyarthritis. Acta Derm Venereol (Stockh) 66: 442–445

    CAS  Google Scholar 

  • Herzberg J (1981) Das REM-Syndrom. Z Hautkr 56: 1317–1325

    PubMed  CAS  Google Scholar 

  • Morison WL, Shea CR, Parrish JA (1979) Reticular erythematous mucinosis syndrome: report of two cases. Arch Dermatol 115: 1340–1342

    Article  PubMed  CAS  Google Scholar 

  • Perry HO, Kierland RR, Montgomery H (1960) Plaque-like form of cutaneous mucinosis. Arch Dermatol 82: 980–985

    Article  PubMed  CAS  Google Scholar 

  • Przybilla B, Landthaler M (1987) Photoprovozierbare plaqueartige kutane Muzinose. In: Braun-Falco O, Schill WB (eds) Fortschritte der praktischen Dermatologie und Venerologie, vol 11. Springer, Berlin, pp 530–532

    Google Scholar 

  • Steigleder GK (1975) Plaque-artige Form der cutanen Mucinose (PCM) und Retikuläre erythematöse Mucinosis (REM-Syndrom). Z Hautkr 50: 25–32

    PubMed  CAS  Google Scholar 

  • Steigleder GK, Gartmann H, Linker U (1974) REM-Syndrom. Retikuläre erythematöse Mucinosis ( Rundzellenerythematosis ). Z Hautkr 49: 235–238

    Google Scholar 

  • Steigleder GK, Gartmann H, Linker U (1974) REM syndrome: reticular erythematous mucinosis (round-cell erythematosis), a new entity? Br J Dermatol 91: 191–199

    Article  PubMed  CAS  Google Scholar 

  • Braun-Falco O (1957) Mucophanerosis intrafollicularis et seboglandularis. Dermatol Wochenschr 136: 1289–1303

    Google Scholar 

  • Cabré J, Korting GW (1964) Zum symptomatischen Charakter der “Mucinosis follicularis”: Ihr Vorkommen beim Lupus erythematodes chronicus. Dermatol Wochenschr 149: 513–518

    Google Scholar 

  • Emmerson RW (1969) Follicular mucinosis. A study of 47 patients. Br J Dermatol 81: 395–413

    Article  PubMed  CAS  Google Scholar 

  • Ishibashi A (1976) Histogenesis of mucin in follicular mucinosis. An electron microscopic study. Acta Derm Venereol (Stockh) 56: 163–171

    CAS  Google Scholar 

  • Jablonska St, Chorzelski T, Lancucki J (1959) Mucinosis follicularis. Hautarzt 10: 27–33

    Google Scholar 

  • Kim R, Winkelmann RK (1962) Follicular mucinosis (alopecia mucinosa). Arch Dermatol 85: 490–498

    Article  PubMed  CAS  Google Scholar 

  • Lancer HA, Bronstein BR, Nakagawa H et al. (1984) Follicular mucinoses: a detailed morphologic and immunopathologic study. J Am Acad Dermatol 10: 760–768

    Article  PubMed  CAS  Google Scholar 

  • Pinkus H (1957) Alopecia mucinosa. Arch Dermatol 76: 419–426

    Article  CAS  Google Scholar 

  • Wolff HH, Kinney J, Ackerman AB (1978) Angiolymphoid hyperplasia with follicular mucinosis. Arch Dermatol 114: 229–232

    Article  PubMed  CAS  Google Scholar 

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© 1991 Springer-Verlag Berlin Heidelberg

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Braun-Falco, O., Plewig, G., Wolff, H.H., Winkelmann, R.K. (1991). Skin Diseases Caused by Disorders in Mucopolysaccharide Metabolism. In: Dermatology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-00181-3_43

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  • DOI: https://doi.org/10.1007/978-3-662-00181-3_43

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-00183-7

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