Hyperkeratosis Lenticularis Perstans (Flegel Disease)

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Background

Flegel originally described hyperkeratosis lenticularis perstans (HLP) in 1958 as red-brown papules with horny scales of irregular outline measuring 1-5 mm in diameter and up to 1 mm in depth.[1] Lesions are located primarily on the dorsal feet and lower legs, with a decreasing likelihood of manifestation proximally. Most cases have been reported in Europe.

Pathophysiology

No instigating factor has been identified clearly; some investigators have implicated UV light. However, in one case report, evidence of Borrelia infection (Borrelia burgdorferi and Borrelia garinii) was found using DNA sequencing in fresh tissue and blood from a patient with hyperkeratosis lenticularis perstans, without clinical evidence of Lyme borreliosis.[2] Ultrastructurally, a loss or decreased number of membrane-coating granules (also termed Odland bodies) has been reported. Membrane-coating granules are influential in the normal process of desquamation. A decrease, malformation, or absence of these membrane-coating granules may result in decreased desquamation of the stratum corneum, retention hyperkeratosis, and clinically keratotic hyperkeratosis lenticularis perstans lesions. Some authors have suggested that a cell-mediated cytotoxicity against epithelial cells may be involved in the pathogenesis of hyperkeratosis lenticularis perstans.

Epidemiology

Frequency

United States

No data exist on incidence or prevalence of this disease. Hyperkeratosis lenticularis perstans (Flegel disease) likely has both a familial and nonfamilial variant, since several reports have postulated both an autosomal dominant and a sporadic mode of inheritance.[3]

International

Most cases have been reported in Europe. International incidence is similar to that seen in the United States.

Race

Hyperkeratosis lenticularis perstans does not have a race predilection, although it has mostly been reported in the white population.

Sex

No sex predilection is apparent.

Age

Hyperkeratosis lenticularis perstans reportedly occurs most commonly in mid-to-older age groups; however, reports exist of hyperkeratosis lenticularis perstans occurring in patients as young as 13 years.

Prognosis

Except for the possibility that lesions may progress slowly and involve more proximal sites, prognosis for hyperkeratosis lenticularis perstans (Flegel disease) is excellent. No mortality has been reported.

History

Small keratotic papules typically begin to develop symmetrically on the lower extremities (see the images below).



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Clinical photograph of the upper thigh showing numerous red-brown papules with sparing of the inguinal crease.



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A higher-powered view of the patient seen in the previous image. Photograph of the upper thigh demonstrates 1- to 4-mm, noncoalescing keratotic papule....

Papules spread proximally at a slow rate. Hyperkeratosis lenticularis perstans usually is an asymptomatic condition.

Physical Examination

Small, red-brown, hyperkeratotic, 1-5 mm papules on the lower extremities are the most frequent and characteristic presentation of hyperkeratosis lenticularis perstans.[4, 5] Involvement of the eyes, ear pinnae, arms, axillae, palms, soles, and the oral mucosa has been reported, although these reports are rare. Involvement of the trunk has been reported but remains an unusual variant.[6, 7]

Dermatoscopic findings suggest a brown, structureless center with peripheral scaly, white areas enhanced by polarized light.[8]

Removal of the scale reveals a bright-red base, often with pinpoint bleeding. A localized unilateral variant has been reported.[9, 10] The trunk tends to be spared; absence of axial lesions is characteristic.

Causes

To date, the causes of hyperkeratosis lenticularis perstans (Flegel disease) are unknown. Some authors suggest that exposure to the sun may be involved.

Other Tests

Since several reports have associated hyperkeratosis lenticularis perstans (Flegel disease) with an endocrinopathy, obtain a thorough and complete systems review, as well as social and family histories. Laboratory, radiographic, or surgical tests are not needed, unless indicated by information gleaned from these sources.

Procedures

Skin biopsy with hematoxylin and eosin staining shows characteristic findings of hyperkeratosis lenticularis perstans (Flegel disease). Electron microscopy is not essential.

Histologic Findings

A discrete area of hyperkeratosis occurs (with areas of parakeratosis) overlying a thinned stratum malpighii and thinned-to-absent granular layer. Irregular acanthosis and some vascular dilatation are peripheral. A lymphoid infiltrate with occasional histiocytes in a bandlike pattern in the papillary dermis typically is seen. See the images below.



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Hematoxylin and eosin-stained section, low magnification. Epidermal hyperplasia with rete elongation surmounted by a thickened, compact, hyperkeratoti....



View Image

Hematoxylin and eosin-stained section, medium magnification. The lateral edge of the lesion demonstrates abrupt hyperkeratosis and a combination of ep....



View Image

Hematoxylin and eosin-stained section, high magnification. The section shows mostly orthokeratotic scale, thinning of the epidermis with a diminished ....

Some evidence has indicated that older lesions may show some histologic differences compared with newer ones.[11] Older lesions can show absence of epidermal atrophy and may infiltrate the upper dermis. Ultrastructural studies also reveal the presence of many normal-appearing, membrane-coating granules in the keratinocytes of an old lesion, whereas these normal organelles were not found in the keratinocytes of earlier hyperkeratotic skin lesions.[12]

Electron microscopy

Several authors have reported an absence or decrease in the number of membrane-coating granules, or Odland bodies, within lesional keratinocytes. Although other authors have found Odland bodies to be present, most suggest that the membrane-coating granules may undergo some alterations in number or morphology. Perilesional skin uniformly shows normal keratinocyte differentiation.

Medical Care

A variety of topical agents have been used to treat this disease, but none is universally effective.

Reports on the effectiveness of tacalcitol and calcipotriol conflict with another report stating they are not effective,[13] and yet another report saying calcipotriol is effective.[14]

Topical 5% fluorouracil and a synthetic vitamin D-3 derivative have been used together with effective results.[14]

The most consistently successful therapies have been the topical application of 5% fluorouracil cream (over several months), local excision, and dermabrasion (see Surgical Care).[15, 16]

In 1986, Gabrielsen reported that hyperkeratosis lenticularis perstans (Flegel disease) was effectively treated with etretinate. Initially, treatment aggravated the condition; however, after 10 weeks of treatment, the papules of hyperkeratosis lenticularis perstans (Flegel disease) nearly all resolved.[17]

Oral retinoids have been successful with continuous therapy. However, short-coarse oral retinoid therapy has also shown success in one case.[7] Patients tend to relapse when therapy is discontinued.

Tretinoin, emollients, psoralen with ultraviolet A (PUVA), and keratolytics have shown varying, but mostly unrewarding, results, even in combination.[18, 19, 20] Topical steroids have similarly shown mixed results, although betamethasone dipropionate showed a response in a 2008 case study.[21]

Surgical Care

Dermabrasion is a possible surgical modality. However, a large number of lesions, as well as lesion location, make this an impractical approach. Local excision may be successful, especially if the number of lesions is small. Cryotherapy is an additional possibility.

Medication Summary

These medications have proven the most efficacious for the treatment of hyperkeratosis lenticularis perstans (Flegel disease).

Fluorouracil topical (Efudex, Fluoroplex)

Clinical Context:  Fluorouracil has been in clinical use since the 1960s. Systemic absorption is limited to approximately 6% of the applied dose and is selectively higher in abnormal skin. Fluorouracil interferes with pyrimidine metabolism by inhibiting thymidylate synthetase, thus inhibiting DNA synthesis.

It is available as 5% (Efudex) or 1% (Fluoroplex) cream, 2% or 5% solution (both Efudex), or 1% solution (Fluoroplex).

If applied with the fingers, wash hands immediately after application.

Fluorouracil is FDA approved for the treatment of actinic keratosis and superficial basal cell carcinomas.

Class Summary

Inhibit cell growth and proliferation.

Calcipotriene (Dovonex)

Clinical Context:  Calcipotriene is a  synthetic vitamin D-3 derivative that possesses therapeutic properties similar to vitamin D-3, including inhibition of epidermal proliferation, induction of differentiation, and anti-inflammatory effects.

Class Summary

Essential for normal DNA synthesis.

Author

Daniel Roling, MD, Associate Clinical Professor, Department of Dermatology, Hospital of the University of Pennsylvania

Disclosure: Nothing to disclose.

Coauthor(s)

Jacqueline M Junkins-Hopkins, MD, Associate Professor, Director, Division of Dermatopathology and Oral Pathology, Department of Dermatology, Johns Hopkins Medical Institutions

Disclosure: Nothing to disclose.

Specialty Editors

Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University Health Sciences Center, Paul L Foster School of Medicine; Consulting Staff, Mountain View Dermatology, PA

Disclosure: Nothing to disclose.

Rosalie Elenitsas, MD, Herman Beerman Professor of Dermatology, University of Pennsylvania School of Medicine; Director, Penn Cutaneous Pathology Services, Department of Dermatology, University of Pennsylvania Health System

Disclosure: Received royalty from Lippincott Williams Wilkins for textbook editor.

Chief Editor

William D James, MD, Paul R Gross Professor of Dermatology, Vice-Chairman, Residency Program Director, Department of Dermatology, University of Pennsylvania School of Medicine

Disclosure: Received income in an amount equal to or greater than $250 from: Elsevier; WebMD.

Additional Contributors

Noah S Scheinfeld, JD, MD, FAAD, † Assistant Clinical Professor, Department of Dermatology, Weil Cornell Medical College; Consulting Staff, Department of Dermatology, St Luke's Roosevelt Hospital Center, Beth Israel Medical Center, New York Eye and Ear Infirmary; Assistant Attending Dermatologist, New York Presbyterian Hospital; Assistant Attending Dermatologist, Lenox Hill Hospital, North Shore-LIJ Health System; Private Practice

Disclosure: Nothing to disclose.

References

  1. Flegel H. [Hyperkeratosis lenticularis perstans.]. Hautarzt. 1958 Aug. 9(8):363-4. [View Abstract]
  2. Schwarzova K, Kozub P, Szep Z, Golovchenko M, Rudenko N. Detection of Borrelia burgdorferi sensu stricto and Borrelia garinii DNAs in patient with Hyperkeratosis lenticularis perstans (Flegel disease). Folia Microbiol (Praha). 2016 Sep. 61 (5):359-63. [View Abstract]
  3. Bean SF. The genetics of hyperkeratosis lenticularis perstans. Arch Dermatol. 1972 Jul. 106(1):72. [View Abstract]
  4. Humphrey S, Crawford RI, Au S. Long-standing spiny papules on the lower extremities. Flegel disease, or hyperkeratosis lenticularis perstans (HLP). Arch Dermatol. 2008 Nov. 144(11):1509-14. [View Abstract]
  5. Li TH, Hsu CK, Chiu HC, Chang CH. Multiple asymptomatic hyperkeratotic papules on the lower part of the legs. Hyperkeratosis lenticularis perstans (HLP) (Flegel disease). Arch Dermatol. 1997 Jul. 133(7):910-1, 913-4. [View Abstract]
  6. Miljkovic J. An unusual generalized form of hyperkeratosis lenticularis perstans (Flegel's disease). Wien Klin Wochenschr. 2004. 116 Suppl 2:78-80. [View Abstract]
  7. Krishnan A, Kar S. Photoletter to the editor: Hyperkeratosis lenticularis perstans (Flegel's disease) with unusual clinical presentation. Response to isotretinoin therapy. J Dermatol Case Rep. 2012 Sep 28. 6(3):93-5. [View Abstract]
  8. Valdebran M, Terrero D, Xue R. Dermoscopic findings in hyperkeratosis lenticularis perstans. J Am Acad Dermatol. 2016 Dec. 75 (6):e211-e213. [View Abstract]
  9. Miranda-Romero A, Sanchez Sambucety P, Bajo del Pozo C, Martinez Fermandez M, Esquivias Gomez JI, Garcia Munoz M. Unilateral hyperkeratosis lenticularis perstans (Flegel's disease). J Am Acad Dermatol. 1998 Oct. 39(4 Pt 1):655-7. [View Abstract]
  10. Urbina F, Sudy E, Misad C. A case of localized, unilateral hyperkeratosis lenticularis perstans on a woman's breast. J Dtsch Dermatol Ges. 2016 Apr. 14 (4):416-8. [View Abstract]
  11. Ando K, Hattori H, Yamauchi Y. Histopathological differences between early and old lesions of hyperkeratosis Lenticularis Perstans (Flegel's disease). Am J Dermatopathol. 2006 Apr. 28(2):122-6. [View Abstract]
  12. Jang KA, Choi JH, Sung KJ, Moon KC, Koh JK. Hyperkeratosis lenticularis perstans (Flegel's disease): histologic, immunohistochemical, and ultrastructural features in a case. Am J Dermatopathol. 1999 Aug. 21(4):395-8. [View Abstract]
  13. Blaheta HJ, Metzler G, Rassner G, Garbe C. Hyperkeratosis lenticularis perstans (Flegel's disease)--lack of response to treatment with tacalcitol and calcipotriol. Dermatology. 2001. 202(3):255-8. [View Abstract]
  14. Metze D, Lubke D, Luger T. [Hyperkeratosis lenticularis perstans (Flegel's disease) - a complex disorder of epidermal differentiation with good response to a synthetic vitamin D3 derivate]. Hautarzt. 2000 Jan. 51(1):31-5. [View Abstract]
  15. Pearson LH, Smith JG Jr, Chalker DK. Hyperkeratosis lenticularis perstans (Flegel's disease). Case report and literature review. J Am Acad Dermatol. 1987 Jan. 16(1 Pt 2):190-5. [View Abstract]
  16. Wilson PD, Ive FA. Treatment of hyperkeratosis lenticularis perstans (Flegel) with topical fluorouracil. Dermatologica. 1980. 160(5):337-40. [View Abstract]
  17. Gabrielsen TO. [Tigason in hyperkeratosis lenticularis perstans (HLP)--a case report]. Z Hautkr. 1986 Feb 15. 61(4):214-7. [View Abstract]
  18. Cooper SM, George S. Flegel's disease treated with psoralen ultraviolet A. Br J Dermatol. 2000 Feb. 142(2):340-2. [View Abstract]
  19. Langer K, Zonzits E, Konrad K. Hyperkeratosis lenticularis perstans (Flegel's disease). Ultrastructural study of lesional and perilesional skin and therapeutic trial of topical tretinoin versus 5-fluorouracil. J Am Acad Dermatol. 1992 Nov. 27(5 Pt 2):812-6. [View Abstract]
  20. Lindsay E. Zinc paste bandages and the treatment of Flegel's disease. Br J Community Nurs. 2005 Mar. 10(3):S14-9. [View Abstract]
  21. Sterneberg-Vos H, van Marion AM, Frank J, Poblete-Gutierrez P. Hyperkeratosis lenticularis perstans (Flegel's disease) - successful treatment with topical corticosteroids. Int J Dermatol. 2008 Nov. 47 Suppl 1:38-41. [View Abstract]

Clinical photograph of the upper thigh showing numerous red-brown papules with sparing of the inguinal crease.

A higher-powered view of the patient seen in the previous image. Photograph of the upper thigh demonstrates 1- to 4-mm, noncoalescing keratotic papules.

Hematoxylin and eosin-stained section, low magnification. Epidermal hyperplasia with rete elongation surmounted by a thickened, compact, hyperkeratotic scale. A bandlike lymphoid infiltrate expands the papillary dermis.

Hematoxylin and eosin-stained section, medium magnification. The lateral edge of the lesion demonstrates abrupt hyperkeratosis and a combination of epidermal atrophy and acanthosis.

Hematoxylin and eosin-stained section, high magnification. The section shows mostly orthokeratotic scale, thinning of the epidermis with a diminished granular cell layer, and an infiltrate of lymphocytes in the superficial dermis, which approximate the dermal-epidermal interface.

Clinical photograph of the upper thigh showing numerous red-brown papules with sparing of the inguinal crease.

A higher-powered view of the patient seen in the previous image. Photograph of the upper thigh demonstrates 1- to 4-mm, noncoalescing keratotic papules.

Hematoxylin and eosin-stained section, low magnification. Epidermal hyperplasia with rete elongation surmounted by a thickened, compact, hyperkeratotic scale. A bandlike lymphoid infiltrate expands the papillary dermis.

Hematoxylin and eosin-stained section, medium magnification. The lateral edge of the lesion demonstrates abrupt hyperkeratosis and a combination of epidermal atrophy and acanthosis.

Hematoxylin and eosin-stained section, high magnification. The section shows mostly orthokeratotic scale, thinning of the epidermis with a diminished granular cell layer, and an infiltrate of lymphocytes in the superficial dermis, which approximate the dermal-epidermal interface.