Multiple Yellow-Brown Papules on the Penis

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Multiple Yellow-Brown Papules on the Penis

The Diagnosis: Eruptive Syringoma 

A punch biopsy of a lesion on the penis was performed. Histopathologic examination revealed many tadpole-shaped cords of epithelial cells and small ducts in the dermis (Figure). Based on clinical and histopathological findings, a diagnosis of eruptive syringoma was made. The patient declined treatment.  

Multiple epithelial cell nests with tadpolelike eccrine ductal structures and several calcium deposits in the dermis (H&E, original magnification ×100).

Syringomas are common benign eccrine neoplasms. They present clinically as small flesh-colored to brownish papules symmetrically distributed on the face, neck, trunk, pubic area, arms, and legs.1-3 Classic syringoma occurs more frequently in young adult women.1 Eruptive syringoma is a rare variant, and the age of onset ranges from 3 to 50 years.1-13  Eruptive syringoma is the term for multiple lesions that occur synchronously in any part of the body.1,4,13 The term eruptive is not the opposite of localized and refers to the time of onset of the lesion. There may be both a generalized eruptive syringoma or a localized eruptive syringoma depending on the distribution of the lesions.1 The most common site for syringoma occurrence is the eyelid; penile syringoma is extremely rare. Several cases of penile syringoma have been reported, but eruptive penile syringoma is rare.3,5-10,12,13  

Histopathology is essential for the diagnosis of syringoma. Hematoxylin and eosin stain shows multiple small cystic ducts and epithelial cell nests in the dermis. Ductal structures sometimes appear tadpolelike or comma shaped depending on the section.1,2,7,12 

The clinical differential diagnosis of syringoma includes sebaceous hyperplasia, verruca plana, molluscum contagiosum, bowenoid papulosis, condyloma acuminatum, lichen planus, lichen nitidus, milia, angiofibroma, epidermal cyst, calcinosis cutis, granuloma annulare, and sarcoidosis.3,8,12 

Because syringoma is benign, treatment is not necessary unless there is a cosmetic problem.3,5,7,8,12 There is no satisfactory treatment of eruptive penile syringoma. Treatment options include topical tretinoin and adapalene, oral isotretinoin, cryotherapy, microelectrodesiccation with an epilating needle, dermabrasion, CO2 laser, and surgical excision.2,3,7,8,12  

Adult patients with penile syringoma may be concerned about sexually transmitted diseases due to the appearance of the papules. If cosmesis is not an issue, clinicians should reassure the patient after a biopsy that the lesions are benign and self-limiting without recommending treatment.  

References
  1. Ghanadan A, Khosravi M. Cutaneous syringoma: a clinicopathologic study of 34 new cases and review of the literature. Indian J Dermatol. 2013;58:326. 
  2. Soler-Carrillo J, Estrach T, Mascaro JM. Eruptive syringoma: 27 new cases and review of the literature. J Eur Acad Dermatol Venereol. 2001;15:242-246. 
  3. Baek JO, Jee HJ, Kim TK, et al. Eruptive penile syringomas spreading to the pubic area and lower abdomen. Ann Dermatol. 2013;25:116-118. 
  4. Pruzan DL, Esterly NB, Prose NS. Eruptive syringoma. Arch Dermatol. 1989;125:1119-1120. 
  5. Olson JM, Robles DT, Argenyi ZB, et al. Multiple penile syringomas. J Am Acad Dermatol. 2008;59(2 suppl 1):S46-S47. 
  6. Petersson F, Mjornberg PA, Kazakov DV, et al. Eruptive syringoma of the penis. a report of 2 cases and a review of the literature. Am J Dermatopathol. 2009;31:436-438. 
  7. Huang C, Wang W, Wu B. Multiple brownish papules on the penile shaft. Indian J Dermatol Venereol Leprol. 2011;77:404. 
  8. Cohen PR, Tschen JA, Rapini RP. Penile syringoma: reports and review of patients with syringoma located on the penis. J Clin Aesthet Dermatol. 2013;6:38-42. 
  9. Vaca EE, Mundinger GS, Zelken JA, et al. Surgical excision of multiple penile syringomas with scrotal flap reconstruction. Eplasty. 2014;14:E21. 
  10. Mitkov M, Balagula Y, Taube JM, et al. Plaque-like syringoma with involvement of deep reticular dermis. J Am Acad Dermatol. 2014;71:e206-207. 
  11. Vaca EE, Mundinger GS, Zelken JA, et al. Surgical excision of multiple penile syringomas with scrotal flap reconstruction. Eplasty. 2014;14:e21. 
  12. Dhossche JM, Brodell RT, Al Hmada Y, et al. Skin-colored papules of the penis. Pediatr Dermatol. 2015;32:145-146. 
  13. Todd PS, Gordon SC, Rovner RL, et al. Eruptive penile syringomas in an adolescent: novel approach with serial microexcisions and suture-adhesive repair. Pediatr Dermatol. 2016;33:E57-E60.
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The authors report no conflict of interest.

Correspondence: Ji Hyun Lee, MD, PhD, 222 Banpo-daero, Seocho-gu, Seoul, 137-701, Korea ([email protected]).

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From the Department of Dermatology, Seoul St. Mary’s Hospital, College of Medicine, Catholic University of Korea.

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The Diagnosis: Eruptive Syringoma 

A punch biopsy of a lesion on the penis was performed. Histopathologic examination revealed many tadpole-shaped cords of epithelial cells and small ducts in the dermis (Figure). Based on clinical and histopathological findings, a diagnosis of eruptive syringoma was made. The patient declined treatment.  

Multiple epithelial cell nests with tadpolelike eccrine ductal structures and several calcium deposits in the dermis (H&E, original magnification ×100).

Syringomas are common benign eccrine neoplasms. They present clinically as small flesh-colored to brownish papules symmetrically distributed on the face, neck, trunk, pubic area, arms, and legs.1-3 Classic syringoma occurs more frequently in young adult women.1 Eruptive syringoma is a rare variant, and the age of onset ranges from 3 to 50 years.1-13  Eruptive syringoma is the term for multiple lesions that occur synchronously in any part of the body.1,4,13 The term eruptive is not the opposite of localized and refers to the time of onset of the lesion. There may be both a generalized eruptive syringoma or a localized eruptive syringoma depending on the distribution of the lesions.1 The most common site for syringoma occurrence is the eyelid; penile syringoma is extremely rare. Several cases of penile syringoma have been reported, but eruptive penile syringoma is rare.3,5-10,12,13  

Histopathology is essential for the diagnosis of syringoma. Hematoxylin and eosin stain shows multiple small cystic ducts and epithelial cell nests in the dermis. Ductal structures sometimes appear tadpolelike or comma shaped depending on the section.1,2,7,12 

The clinical differential diagnosis of syringoma includes sebaceous hyperplasia, verruca plana, molluscum contagiosum, bowenoid papulosis, condyloma acuminatum, lichen planus, lichen nitidus, milia, angiofibroma, epidermal cyst, calcinosis cutis, granuloma annulare, and sarcoidosis.3,8,12 

Because syringoma is benign, treatment is not necessary unless there is a cosmetic problem.3,5,7,8,12 There is no satisfactory treatment of eruptive penile syringoma. Treatment options include topical tretinoin and adapalene, oral isotretinoin, cryotherapy, microelectrodesiccation with an epilating needle, dermabrasion, CO2 laser, and surgical excision.2,3,7,8,12  

Adult patients with penile syringoma may be concerned about sexually transmitted diseases due to the appearance of the papules. If cosmesis is not an issue, clinicians should reassure the patient after a biopsy that the lesions are benign and self-limiting without recommending treatment.  

The Diagnosis: Eruptive Syringoma 

A punch biopsy of a lesion on the penis was performed. Histopathologic examination revealed many tadpole-shaped cords of epithelial cells and small ducts in the dermis (Figure). Based on clinical and histopathological findings, a diagnosis of eruptive syringoma was made. The patient declined treatment.  

Multiple epithelial cell nests with tadpolelike eccrine ductal structures and several calcium deposits in the dermis (H&E, original magnification ×100).

Syringomas are common benign eccrine neoplasms. They present clinically as small flesh-colored to brownish papules symmetrically distributed on the face, neck, trunk, pubic area, arms, and legs.1-3 Classic syringoma occurs more frequently in young adult women.1 Eruptive syringoma is a rare variant, and the age of onset ranges from 3 to 50 years.1-13  Eruptive syringoma is the term for multiple lesions that occur synchronously in any part of the body.1,4,13 The term eruptive is not the opposite of localized and refers to the time of onset of the lesion. There may be both a generalized eruptive syringoma or a localized eruptive syringoma depending on the distribution of the lesions.1 The most common site for syringoma occurrence is the eyelid; penile syringoma is extremely rare. Several cases of penile syringoma have been reported, but eruptive penile syringoma is rare.3,5-10,12,13  

Histopathology is essential for the diagnosis of syringoma. Hematoxylin and eosin stain shows multiple small cystic ducts and epithelial cell nests in the dermis. Ductal structures sometimes appear tadpolelike or comma shaped depending on the section.1,2,7,12 

The clinical differential diagnosis of syringoma includes sebaceous hyperplasia, verruca plana, molluscum contagiosum, bowenoid papulosis, condyloma acuminatum, lichen planus, lichen nitidus, milia, angiofibroma, epidermal cyst, calcinosis cutis, granuloma annulare, and sarcoidosis.3,8,12 

Because syringoma is benign, treatment is not necessary unless there is a cosmetic problem.3,5,7,8,12 There is no satisfactory treatment of eruptive penile syringoma. Treatment options include topical tretinoin and adapalene, oral isotretinoin, cryotherapy, microelectrodesiccation with an epilating needle, dermabrasion, CO2 laser, and surgical excision.2,3,7,8,12  

Adult patients with penile syringoma may be concerned about sexually transmitted diseases due to the appearance of the papules. If cosmesis is not an issue, clinicians should reassure the patient after a biopsy that the lesions are benign and self-limiting without recommending treatment.  

References
  1. Ghanadan A, Khosravi M. Cutaneous syringoma: a clinicopathologic study of 34 new cases and review of the literature. Indian J Dermatol. 2013;58:326. 
  2. Soler-Carrillo J, Estrach T, Mascaro JM. Eruptive syringoma: 27 new cases and review of the literature. J Eur Acad Dermatol Venereol. 2001;15:242-246. 
  3. Baek JO, Jee HJ, Kim TK, et al. Eruptive penile syringomas spreading to the pubic area and lower abdomen. Ann Dermatol. 2013;25:116-118. 
  4. Pruzan DL, Esterly NB, Prose NS. Eruptive syringoma. Arch Dermatol. 1989;125:1119-1120. 
  5. Olson JM, Robles DT, Argenyi ZB, et al. Multiple penile syringomas. J Am Acad Dermatol. 2008;59(2 suppl 1):S46-S47. 
  6. Petersson F, Mjornberg PA, Kazakov DV, et al. Eruptive syringoma of the penis. a report of 2 cases and a review of the literature. Am J Dermatopathol. 2009;31:436-438. 
  7. Huang C, Wang W, Wu B. Multiple brownish papules on the penile shaft. Indian J Dermatol Venereol Leprol. 2011;77:404. 
  8. Cohen PR, Tschen JA, Rapini RP. Penile syringoma: reports and review of patients with syringoma located on the penis. J Clin Aesthet Dermatol. 2013;6:38-42. 
  9. Vaca EE, Mundinger GS, Zelken JA, et al. Surgical excision of multiple penile syringomas with scrotal flap reconstruction. Eplasty. 2014;14:E21. 
  10. Mitkov M, Balagula Y, Taube JM, et al. Plaque-like syringoma with involvement of deep reticular dermis. J Am Acad Dermatol. 2014;71:e206-207. 
  11. Vaca EE, Mundinger GS, Zelken JA, et al. Surgical excision of multiple penile syringomas with scrotal flap reconstruction. Eplasty. 2014;14:e21. 
  12. Dhossche JM, Brodell RT, Al Hmada Y, et al. Skin-colored papules of the penis. Pediatr Dermatol. 2015;32:145-146. 
  13. Todd PS, Gordon SC, Rovner RL, et al. Eruptive penile syringomas in an adolescent: novel approach with serial microexcisions and suture-adhesive repair. Pediatr Dermatol. 2016;33:E57-E60.
References
  1. Ghanadan A, Khosravi M. Cutaneous syringoma: a clinicopathologic study of 34 new cases and review of the literature. Indian J Dermatol. 2013;58:326. 
  2. Soler-Carrillo J, Estrach T, Mascaro JM. Eruptive syringoma: 27 new cases and review of the literature. J Eur Acad Dermatol Venereol. 2001;15:242-246. 
  3. Baek JO, Jee HJ, Kim TK, et al. Eruptive penile syringomas spreading to the pubic area and lower abdomen. Ann Dermatol. 2013;25:116-118. 
  4. Pruzan DL, Esterly NB, Prose NS. Eruptive syringoma. Arch Dermatol. 1989;125:1119-1120. 
  5. Olson JM, Robles DT, Argenyi ZB, et al. Multiple penile syringomas. J Am Acad Dermatol. 2008;59(2 suppl 1):S46-S47. 
  6. Petersson F, Mjornberg PA, Kazakov DV, et al. Eruptive syringoma of the penis. a report of 2 cases and a review of the literature. Am J Dermatopathol. 2009;31:436-438. 
  7. Huang C, Wang W, Wu B. Multiple brownish papules on the penile shaft. Indian J Dermatol Venereol Leprol. 2011;77:404. 
  8. Cohen PR, Tschen JA, Rapini RP. Penile syringoma: reports and review of patients with syringoma located on the penis. J Clin Aesthet Dermatol. 2013;6:38-42. 
  9. Vaca EE, Mundinger GS, Zelken JA, et al. Surgical excision of multiple penile syringomas with scrotal flap reconstruction. Eplasty. 2014;14:E21. 
  10. Mitkov M, Balagula Y, Taube JM, et al. Plaque-like syringoma with involvement of deep reticular dermis. J Am Acad Dermatol. 2014;71:e206-207. 
  11. Vaca EE, Mundinger GS, Zelken JA, et al. Surgical excision of multiple penile syringomas with scrotal flap reconstruction. Eplasty. 2014;14:e21. 
  12. Dhossche JM, Brodell RT, Al Hmada Y, et al. Skin-colored papules of the penis. Pediatr Dermatol. 2015;32:145-146. 
  13. Todd PS, Gordon SC, Rovner RL, et al. Eruptive penile syringomas in an adolescent: novel approach with serial microexcisions and suture-adhesive repair. Pediatr Dermatol. 2016;33:E57-E60.
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A 12-year-old boy presented with multiple asymptomatic, 0.1-cm, yellow-brown papules on the penile shaft of several years' duration. The lesions appeared suddenly. The patient had no history of trauma, injection, or an underlying disorder.  

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Brown Papules and a Plaque on the Calf

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Brown Papules and a Plaque on the Calf

The Diagnosis: Irritated Seborrheic Keratosis

Biopsies of one of the protruding papules and the underlying plaque were performed. The specimen from the papule showed hyperkeratosis, acanthosis, papillomatosis, and a flattened dermoepidermal junction with demarcated horizontal margin, which demonstrated apparent upward growth of the epidermis. Moderate lymphocytic infiltration in the upper dermis also was observed (Figure, A). The histologic findings of the plaque showed acanthosis, several pseudohorn cysts, hyperpigmentation of the basal layer, and a horizontal demarcation of the dermoepidermal junction (Figure, B).

A biopsy of a papule showed hyperkeratosis, acanthosis, papillomatosis, and a flattened dermoepidermal junction with demarcated horizontal margin. Moderate lymphocytic infiltration in the upper dermis was noted (A)(H&E, original magnification ×100). A biopsy of the plaque showed acanthosis, several pseudohorn cysts, hyperpigmentation of the basal layer, and a horizontal demarcation of the dermoepidermal junction (B)(H&E, original magnification ×100).

Seborrheic keratosis is the most common benign epidermal tumor of the skin with variable appearance.1 It usually begins with well-circumscribed, dull, flat, tan or brown patches that then grow into waxy verrucous papules.1 There are many clinicopathologic variants of SK such as common SK, stucco keratosis, and dermatosis papulosa nigra in clinical variation, as well as acanthotic, hyperkeratotic, clonal, reticulated, irritated, and melanoacanthoma subtypes based on histological variation.2,3

Seborrheic keratosis is a tumor of keratinocytic origin. Although genetics, sun exposure,4 and human papillomavirus infection5 are thought to be causative factors, the precise etiology of SK is unknown.1

The histology of SK shows monotonous basaloid tumor cells without atypia. It generally is comprised of focal acanthosis and papillomatosis with a sharp flat base. Intraepithelial horn pseudocysts are notable features of SK and increased melanin often is seen.2,6

Irritated SK is a histologic variant of SK that has been mechanically or chemically irritated or is involved in immunologic responses. Histologically, the dermis underlying an SK lesion filled with a dense lymphocytic infiltration is characteristic.1,2

For symptomatic or cosmetically undesirable lesions, complete removal of the lesion is the preferred treatment. Cryotherapy, electrodesiccation followed by curettage, curettage followed by desiccation, laser ablation, and surgical excision are effective treatments.1

References
  1. Valencia DT, Nicholas RS, Ken KL, et al. Benign epithelial tumors, hamartomas, and hyperplasias. In: Goldsmith LA, Katz SI, Gilchrest BA, et al, eds. Fitzpatrick’s Dermatology in General Medicine. 8th ed. New York, NY: McGraw-Hill Professional; 2012:1319-1336.
  2. Kirkharn N. Tumors and cysts of the epidermis. In: Elder DE, Elenitsas R, Johnson BL Jr, eds. Lever’s Histopathology of the Skin. 10th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2009:791-850.
  3. Rajesh G, Thappa DM, Jaisankar TJ, et al. Spectrum of seborrheic keratoses in South Indians: a clinical and dermoscopic study. Indian J Dermatol Venereol Leprol. 2011;77:483-488.
  4. Yeatman JM, Kilkenny M, Marks R. The prevalence of seborrhoeic keratoses in an Australian population: does exposure to sunlight play a part in their frequency? Br J Dermatol. 1997;137:411-414.
  5. Li YH, Chen G, Dong XP, et al. Detection of epidermodysplasia verruciformis-associated human papillomavirus DNA in nongenital seborrhoeic keratosis. Br J Dermatol. 2004;151:1060-1065.
  6. Brinster NK, Liu V, Diwan AH, et al. Dermatopathology. Philadelphia, PA: Saunders/Elsevier; 2011.
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Correspondence: Young Min Park, MD, PhD, Department of Dermatology, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-Gu, Seoul, South Korea ([email protected]).

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Correspondence: Young Min Park, MD, PhD, Department of Dermatology, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-Gu, Seoul, South Korea ([email protected]).

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From the Department of Dermatology, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul.

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Correspondence: Young Min Park, MD, PhD, Department of Dermatology, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-Gu, Seoul, South Korea ([email protected]).

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The Diagnosis: Irritated Seborrheic Keratosis

Biopsies of one of the protruding papules and the underlying plaque were performed. The specimen from the papule showed hyperkeratosis, acanthosis, papillomatosis, and a flattened dermoepidermal junction with demarcated horizontal margin, which demonstrated apparent upward growth of the epidermis. Moderate lymphocytic infiltration in the upper dermis also was observed (Figure, A). The histologic findings of the plaque showed acanthosis, several pseudohorn cysts, hyperpigmentation of the basal layer, and a horizontal demarcation of the dermoepidermal junction (Figure, B).

A biopsy of a papule showed hyperkeratosis, acanthosis, papillomatosis, and a flattened dermoepidermal junction with demarcated horizontal margin. Moderate lymphocytic infiltration in the upper dermis was noted (A)(H&E, original magnification ×100). A biopsy of the plaque showed acanthosis, several pseudohorn cysts, hyperpigmentation of the basal layer, and a horizontal demarcation of the dermoepidermal junction (B)(H&E, original magnification ×100).

Seborrheic keratosis is the most common benign epidermal tumor of the skin with variable appearance.1 It usually begins with well-circumscribed, dull, flat, tan or brown patches that then grow into waxy verrucous papules.1 There are many clinicopathologic variants of SK such as common SK, stucco keratosis, and dermatosis papulosa nigra in clinical variation, as well as acanthotic, hyperkeratotic, clonal, reticulated, irritated, and melanoacanthoma subtypes based on histological variation.2,3

Seborrheic keratosis is a tumor of keratinocytic origin. Although genetics, sun exposure,4 and human papillomavirus infection5 are thought to be causative factors, the precise etiology of SK is unknown.1

The histology of SK shows monotonous basaloid tumor cells without atypia. It generally is comprised of focal acanthosis and papillomatosis with a sharp flat base. Intraepithelial horn pseudocysts are notable features of SK and increased melanin often is seen.2,6

Irritated SK is a histologic variant of SK that has been mechanically or chemically irritated or is involved in immunologic responses. Histologically, the dermis underlying an SK lesion filled with a dense lymphocytic infiltration is characteristic.1,2

For symptomatic or cosmetically undesirable lesions, complete removal of the lesion is the preferred treatment. Cryotherapy, electrodesiccation followed by curettage, curettage followed by desiccation, laser ablation, and surgical excision are effective treatments.1

The Diagnosis: Irritated Seborrheic Keratosis

Biopsies of one of the protruding papules and the underlying plaque were performed. The specimen from the papule showed hyperkeratosis, acanthosis, papillomatosis, and a flattened dermoepidermal junction with demarcated horizontal margin, which demonstrated apparent upward growth of the epidermis. Moderate lymphocytic infiltration in the upper dermis also was observed (Figure, A). The histologic findings of the plaque showed acanthosis, several pseudohorn cysts, hyperpigmentation of the basal layer, and a horizontal demarcation of the dermoepidermal junction (Figure, B).

A biopsy of a papule showed hyperkeratosis, acanthosis, papillomatosis, and a flattened dermoepidermal junction with demarcated horizontal margin. Moderate lymphocytic infiltration in the upper dermis was noted (A)(H&E, original magnification ×100). A biopsy of the plaque showed acanthosis, several pseudohorn cysts, hyperpigmentation of the basal layer, and a horizontal demarcation of the dermoepidermal junction (B)(H&E, original magnification ×100).

Seborrheic keratosis is the most common benign epidermal tumor of the skin with variable appearance.1 It usually begins with well-circumscribed, dull, flat, tan or brown patches that then grow into waxy verrucous papules.1 There are many clinicopathologic variants of SK such as common SK, stucco keratosis, and dermatosis papulosa nigra in clinical variation, as well as acanthotic, hyperkeratotic, clonal, reticulated, irritated, and melanoacanthoma subtypes based on histological variation.2,3

Seborrheic keratosis is a tumor of keratinocytic origin. Although genetics, sun exposure,4 and human papillomavirus infection5 are thought to be causative factors, the precise etiology of SK is unknown.1

The histology of SK shows monotonous basaloid tumor cells without atypia. It generally is comprised of focal acanthosis and papillomatosis with a sharp flat base. Intraepithelial horn pseudocysts are notable features of SK and increased melanin often is seen.2,6

Irritated SK is a histologic variant of SK that has been mechanically or chemically irritated or is involved in immunologic responses. Histologically, the dermis underlying an SK lesion filled with a dense lymphocytic infiltration is characteristic.1,2

For symptomatic or cosmetically undesirable lesions, complete removal of the lesion is the preferred treatment. Cryotherapy, electrodesiccation followed by curettage, curettage followed by desiccation, laser ablation, and surgical excision are effective treatments.1

References
  1. Valencia DT, Nicholas RS, Ken KL, et al. Benign epithelial tumors, hamartomas, and hyperplasias. In: Goldsmith LA, Katz SI, Gilchrest BA, et al, eds. Fitzpatrick’s Dermatology in General Medicine. 8th ed. New York, NY: McGraw-Hill Professional; 2012:1319-1336.
  2. Kirkharn N. Tumors and cysts of the epidermis. In: Elder DE, Elenitsas R, Johnson BL Jr, eds. Lever’s Histopathology of the Skin. 10th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2009:791-850.
  3. Rajesh G, Thappa DM, Jaisankar TJ, et al. Spectrum of seborrheic keratoses in South Indians: a clinical and dermoscopic study. Indian J Dermatol Venereol Leprol. 2011;77:483-488.
  4. Yeatman JM, Kilkenny M, Marks R. The prevalence of seborrhoeic keratoses in an Australian population: does exposure to sunlight play a part in their frequency? Br J Dermatol. 1997;137:411-414.
  5. Li YH, Chen G, Dong XP, et al. Detection of epidermodysplasia verruciformis-associated human papillomavirus DNA in nongenital seborrhoeic keratosis. Br J Dermatol. 2004;151:1060-1065.
  6. Brinster NK, Liu V, Diwan AH, et al. Dermatopathology. Philadelphia, PA: Saunders/Elsevier; 2011.
References
  1. Valencia DT, Nicholas RS, Ken KL, et al. Benign epithelial tumors, hamartomas, and hyperplasias. In: Goldsmith LA, Katz SI, Gilchrest BA, et al, eds. Fitzpatrick’s Dermatology in General Medicine. 8th ed. New York, NY: McGraw-Hill Professional; 2012:1319-1336.
  2. Kirkharn N. Tumors and cysts of the epidermis. In: Elder DE, Elenitsas R, Johnson BL Jr, eds. Lever’s Histopathology of the Skin. 10th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2009:791-850.
  3. Rajesh G, Thappa DM, Jaisankar TJ, et al. Spectrum of seborrheic keratoses in South Indians: a clinical and dermoscopic study. Indian J Dermatol Venereol Leprol. 2011;77:483-488.
  4. Yeatman JM, Kilkenny M, Marks R. The prevalence of seborrhoeic keratoses in an Australian population: does exposure to sunlight play a part in their frequency? Br J Dermatol. 1997;137:411-414.
  5. Li YH, Chen G, Dong XP, et al. Detection of epidermodysplasia verruciformis-associated human papillomavirus DNA in nongenital seborrhoeic keratosis. Br J Dermatol. 2004;151:1060-1065.
  6. Brinster NK, Liu V, Diwan AH, et al. Dermatopathology. Philadelphia, PA: Saunders/Elsevier; 2011.
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A 61-year-old man presented with a cluster of asymptomatic brown papules and a plaque on the left calf of several years’ duration. The lesion consisted of multiple, dark brown, hyperkeratotic papules on a well-demarcated light brown flat plaque. The patient reported no increase in the size or number of lesions. He did not have a history of trauma or a personal or family history of skin cancer.

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