Ann Dermatol.  2015 Apr;27(2):133-141. 10.5021/ad.2015.27.2.133.

Periadnexal Mucin as an Additional Histopathologic Feature of Chronic Eczematous Dermatitis

Affiliations
  • 1Department of Dermatology, Yonsei University Wonju College of Medicine, Wonju, Korea. ahnsk@yonsei.ac.kr
  • 2Institute of Lifestyle Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.

Abstract

BACKGROUND
Cutaneous mucinoses are a heterogeneous group of disorders characterized by an abnormal amount of mucin in the skin. However, the pathomechanism of an excessive mucin deposition in the skin is still unknown. Eczematous dermatitis is sub-classified histologically into acute, subacute, and chronic variants. The characteristic histopathologic findings for chronic eczema are variable. However, periadnexal mucin deposition is not known as a feature of chronic eczema.
OBJECTIVE
To evaluate the presence of periadnexal mucin deposition in chronic eczematous dermatitis.
METHODS
We analyzed the skin biopsy specimens from 36 patients who were pathologically diagnosed with chronic eczematous dermatitis. Alcian blue, colloidal iron, and periodic acid-Schiff stains were used to evaluate the mucin deposition in histologic sections. Two dermatologists and two dermatopathologists evaluated the degree of mucin deposition using a 4-point scale.
RESULTS
Various amounts of mucin deposition were observed in the periadnexal area of patients who were diagnosed with chronic eczema. Mucin deposition was more visible after staining with mucin-specific stains. Evaluation of the staining analysis scores revealed that the staining intensities were significantly higher in patients with chronic eczema than age- and site-matched controls (normal, acute to subacute eczema, and psoriasis vulgaris).
CONCLUSION
Periadnexal mucin (secondary mucinoses) may be an additional finding of chronic eczematous dermatitis.

Keyword

Eczema; Periadnexal mucin; Mucinoses

MeSH Terms

Alcian Blue
Biopsy
Colloids
Coloring Agents
Eczema*
Humans
Iron
Mucinoses
Mucins*
Psoriasis
Skin
Alcian Blue
Colloids
Coloring Agents
Iron
Mucins

Figure

  • Fig. 1 Pathology of a 56-year-old male who is diagnosed with chronic eczema. (A) Periadnexal mucin deposition (H&E, ×40), (B) mucin deposition is more visible when the slide is stained with colloidal iron (×40), and (C) the periodic acid-Schiff (PAS) staining is negative. These findings indicate that the mucin around the periadnexal area is dermal mucin, not epithelial mucin (PAS, ×40).

  • Fig. 2 Pathology of a 61-year-old male who is diagnosed with lichen simplex chronicus. (A) Chronic eczema showing periadnexal mucin deposition (H&E, ×40), (B) the mucin deposition is clearly visible after staining with colloidal iron and (C) Alcian blue (×40), and (D) the periodic acid-Schiff (PAS) staining is negative (×40).

  • Fig. 3 Pathology of a 5-year-old male who is diagnosed with atopic dermatitis. (A) Chronic eczema showing periadnexal mucin deposition (H&E, ×40), (B) the mucin deposition is more prominent after staining with colloidal iron, and (C) Alcian blue (×200).

  • Fig. 4 Pathology of the control samples that are diagnosed with normal skin or acute eczema. Mucin deposition is less visible in the control samples. (A) Normal skin (H&E, ×40), (B) normal skin (colloidal iron, ×40), (C) acute eczema (H&E, ×40), and (D) acute eczema (colloidal iron, ×40).

  • Fig. 5 Pathology of the control samples that are diagnosed with psoriasis vulgaris. (A) H&E (×40), (B) periodic acid-Schiff (×40), (C) Alcian blue (×40), and (D) colloidal iron (×40) staining are negative.

  • Fig. 6 Pathology of the patients diagnosed with chronic eczema with their hair follicles in the specimen (colloidal iron, ×100). A, B: weak, C, D: moderate, E, F: strong.

  • Fig. 7 Physician assessment of the mucin deposition using a 4-point scale. The staining intensities are significantly higher in patients with chronic eczema compared to those with acute eczema, psoriasis, or normal skin (**p<0.01).


Reference

1. Wintroub B, Arndt K, Robinson J, Leboit P. The cutaneous mucinosis. In : Arndt KA, LeBoit PE, Robinson JK, Wintroub BU, editors. Cutaneous medicine and surgery: an integrated program in dermatology. Philadelphia: WB Saunders Co.;1996. p. 1832–1840.
2. Rongioletti F, Rebora A. Cutaneous mucinoses: microscopic criteria for diagnosis. Am J Dermatopathol. 2001; 23:257–267.
3. Pandya AG, Sontheimer RD, Cockerell CJ, Takashima A, Piepkorn M. Papulonodular mucinosis associated with systemic lupus erythematosus: possible mechanisms of increased glycosaminoglycan accumulation. J Am Acad Dermatol. 1995; 32:199–205.
Article
4. Wu H, Brandling-Bennett HA, Harrist TJ. Noninfectious vesiculobullous and vesiculopustular diseases. In : Elder DE, Elenitsas R, Johnson BL, Murphy GF, Xu X, editors. Lever's histopathology of the skin. Philadelphia: Lippincott Williams & Wilkins;2009. p. 237.
5. Rebora A, Rongioletti F. Mucinosis. In : Bolognia JL, Jorrizo JL, Rapini RR, editors. Dermatology. Mosby: Elsevier Limited;2003. p. 647.
6. Edward M, Fitzgerald L, Thind C, Leman J, Burden AD. Cutaneous mucinosis associated with dermatomyositis and nephrogenic fibrosing dermopathy: fibroblast hyaluronan synthesis and the effect of patient serum. Br J Dermatol. 2007; 156:473–479.
Article
7. Harper RA, Rispler J. Lichen myxedematosus serum stimulates human skin fibroblast proliferation. Science. 1978; 199:545–547.
Article
8. Cheung HS, Nicoloff JT, Kamiel MB, Spolter L, Nimni ME. Stimulation of fibroblast biosynthetic activity by serum of patients with pretibial myxedema. J Invest Dermatol. 1978; 71:12–17.
Article
9. Duncan MR, Berman B. Differential regulation of collagen, glycosaminoglycan, fibronectin, and collagenase activity production in cultured human adult dermal fibroblasts by interleukin 1-alpha and beta and tumor necrosis factoralpha and beta. J Invest Dermatol. 1989; 92:699–706.
Article
10. Falanga V, Tiegs SL, Alstadt SP, Roberts AB, Sporn MB. Transforming growth factor-beta: selective increase in glycosaminoglycan synthesis by cultures of fibroblasts from patients with progressive systemic sclerosis. J Invest Dermatol. 1987; 89:100–104.
Article
11. Vakirlis E, Lazaridou E, Tzellos TG, Gerou S, Chatzidimitriou D, Ioannides D. Investigation of cytokine levels and their association with SCORAD index in adults with acute atopic dermatitis. J Eur Acad Dermatol Venereol. 2011; 25:409–416.
Article
12. Villagomez MT, Bae SJ, Ogawa I, Takenaka M, Katayama I. Tumour necrosis factor-alpha but not interferon-gamma is the main inducer of inducible protein-10 in skin fibroblasts from patients with atopic dermatitis. Br J Dermatol. 2004; 150:910–916.
Article
13. Ackermann L, Harvima IT. Mast cells of psoriatic and atopic dermatitis skin are positive for TNF-alpha and their degranulation is associated with expression of ICAM-1 in the epidermis. Arch Dermatol Res. 1998; 290:353–359.
Article
14. Junqueira LC, Montes GS, Martins JE, Joazeiro PP. Dermal collagen distribution. A histochemical and ultrastructural study. Histochemistry. 1983; 79:397–403.
Full Text Links
  • AD
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr