Localized Acanthosis Nigricans at the Site of Repetitive Insulin Injections

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Localized Acanthosis Nigricans at the Site of Repetitive Insulin Injections

 

To the Editor:

Acanthosis nigricans (AN) is characterized by asymptomatic, hyperpigmented, velvety plaques that can occur anywhere on the body but most often present on the skin of the neck, axillae, groin, and other body folds.1-12 Although there are 5 subtypes, benign AN is the most common and is related to insulin resistance.1-4 Insulin can bind to insulinlike growth factor 1 (IGF-1) on keratinocytes, stimulating their proliferation. In type 2 diabetes mellitus, endogenous insulin levels are high enough to bind IGF-1 and activate keratinocytes, leading to the development of AN. Insulin injections have been associated with cutaneous side effects including lipoatrophy, lipohypertrophy, and postinflammatory hyperpigmentation.3 Acanthosis nigricans at insulin injection sites is a rare clinical condition.

A 64-year-old man presented for evaluation of a growing asymptomatic lesion on the abdomen of 6 years’ duration. He had a 17-year history of type 2 diabetes mellitus treated with insulin injections for 14 years after failing oral hypoglycemic agents. The patient reported injecting at the same site on the abdomen for the last 14 years. Physical examination revealed a lichenified, hyperpigmented, verrucous plaque on the lower abdomen under the umbilicus (Figure 1). No similar skin lesions were observed elsewhere on the body. A punch biopsy of the plaque showed hyperkeratosis, papillomatosis, acanthosis, and hyperpigmentation, which was consistent with AN (Figure 2). The patient was instructed to rotate injection sites and avoid the affected area. Over-the-counter ammonium lactate cream applied twice daily to the affected site also was recommended. After 2 months of treatment with this regimen, the patient reported softening and lightening of the lesion on the abdomen.

Figure 1. Localized acanthosis nigricans presenting as a lichenified, hyperpigmented, hyperkeratotic plaque at a recurring insulin injection site on the lower abdomen in a 64-year-old man with type 2 diabetes mellitus.

Figure 2. Histopathology demonstrated hyperkeratosis, papillomatosis, acanthosis, and hyperpigmentation (H&E, original magnification ×10).

A PubMed search of articles indexed for MEDLINE for all English-language studies with human participants using the terms acanthosis nigricans and insulin injections yielded 20 results. Of them, 13 discussed localized AN at insulin injection sites: 12 case reports (Table)1-12 and 1 observational study in a group of diabetic patients.13



In the observational study, 500 diabetic patients were examined for insulin injection-site dermatoses and only 2 had localized injection-site AN. No other information was provided for these 2 patients.13 In the 12 published case reports,1-12 all patients did not rotate sites for their insulin injections and repeatedly injected into the affected area. The abdomen was the most commonly affected site, seen in 83% (10/12) of cases, while 25% (3/12) involved the thighs. All but 1 patient had type 2 diabetes mellitus. In 2 patients, “amyloid” was noted on the biopsy report in addition to changes consistent with AN. At least 2 patients had clearance after rotating injection sites.3,12



It has been suggested that localized AN at insulin injection sites develops through similar mechanisms as benign AN. Contributing factors to the development of benign AN may be IGF-1, fibroblast growth factor, and epidermal growth factor.1-3 Insulin is similar in structure to IGF-1 and can bind to IGF-1 receptors at high enough concentrations. Insulinlike growth factor 1 receptors are present on keratinocytes and fibroblasts, which proliferate upon activation, leading to the development of AN.1-3 Localized AN is thought to occur when repetitive insulin at the injection site saturates IGF-1 receptors on local keratinocytes.

Based on our patient and prior reports in the literature, localized AN is an uncommon cutaneous complication of insulin injections. Physicians should ask about repetitive insulin injections in the same site when localized AN occurs in patients with diabetes mellitus on insulin therapy. They also should discuss the importance of rotating sites for insulin adminstration to prevent the development of cutaneous complications including AN.

References
  1. Yahagi E, Mabuchi T, Nuruki H, et al. Case of exogenous insulin-derived acanthosis nigricans caused by insulin injections. Tokai J Exp Clin Med. 2014;39:5-9.
  2. Dhingra M, Garg G, Gupta M, et al. Exogenous insulin-derived acanthosis nigricans: could it be a cause of increased insulin requirement? Dermatol Online J. 2013;19:9.
  3. Buzási K, Sápi Z, Jermendy G. Acanthosis nigricans as a local cutaneous side effect of repeated human insulin injections. Diabetes Res Clin Pract. 2011;94:E34-E36.
  4. Mailler-Savage EA, Adams BB. Exogenous insulin-derived acanthosis nigricans. Arch Dermatol. 2008;144:126-127.
  5. Nandeesh BN, Rajalakshmi T, Shubha B. Cutaneous amyloidosis and insulin with coexistence of acanthosis nigricans. Indian J Pathol Microbiol. 2014;57:127-129.
  6. Kudo-Watanuki S, Kurihara E, Yamamoto K, et al. Coexistence of insulin-derived amyloidosis and an overlying acanthosis nigricans-like lesion at the site of insulin injection. Clin Exp Dermatol. 2013;38:25-29.
  7. Brodell JD Jr, Cannella JD, Helms SE. Case report: acanthosis nigricans resulting from repetitive same-site insulin injections. J Drugs Dermatol. 2012;11:E85-E87.
  8. Erickson L, Lipschutz DE, Wrigley W, et al. A peculiar cutaneous reaction to repeated injections of insulin. JAMA. 1969;209:934-935.
  9. Fleming MG, Simon SI. Cutaneous insulin reaction resembling acanthosis nigricans. Arch Dermatol. 1986;122:1054-1056.
  10. Pachon Burgos A, Chan Aguilar MP. Visual vignette. hyperpigmented hyperkeratotic cutaneous insulin reaction that resembles acanthosis nigricans with lipohypertrophy. Endocr Pract. 2008;14:514.
  11. Chapman SE, Bandino JP. A verrucous plaque on the abdomen: challenge. Am J Dermatopathol. 2017;39:E163.
  12. Huang Y, Hessami-Booshehri M. Acanthosis nigricans at sites of insulin injection in a man with diabetes. CMAJ. 2018;190:E1390.
  13. Sawatkar GU, Kanwar AJ, Dogra S, et al. Spectrum of cutaneous manifestations of type 1 diabetes mellitus in 500 South Asian patients. Br J Dermatol. 2014;171:1402-1406.
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From the Department of Dermatology, Wake Forest School of Medicine, Winston-Salem, North Carolina.

The authors report no conflict of interest.

Correspondence: Leonora Bomar, MD, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157-1071 (lculp@wakehealth.edu).

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From the Department of Dermatology, Wake Forest School of Medicine, Winston-Salem, North Carolina.

The authors report no conflict of interest.

Correspondence: Leonora Bomar, MD, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157-1071 (lculp@wakehealth.edu).

Author and Disclosure Information

From the Department of Dermatology, Wake Forest School of Medicine, Winston-Salem, North Carolina.

The authors report no conflict of interest.

Correspondence: Leonora Bomar, MD, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157-1071 (lculp@wakehealth.edu).

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To the Editor:

Acanthosis nigricans (AN) is characterized by asymptomatic, hyperpigmented, velvety plaques that can occur anywhere on the body but most often present on the skin of the neck, axillae, groin, and other body folds.1-12 Although there are 5 subtypes, benign AN is the most common and is related to insulin resistance.1-4 Insulin can bind to insulinlike growth factor 1 (IGF-1) on keratinocytes, stimulating their proliferation. In type 2 diabetes mellitus, endogenous insulin levels are high enough to bind IGF-1 and activate keratinocytes, leading to the development of AN. Insulin injections have been associated with cutaneous side effects including lipoatrophy, lipohypertrophy, and postinflammatory hyperpigmentation.3 Acanthosis nigricans at insulin injection sites is a rare clinical condition.

A 64-year-old man presented for evaluation of a growing asymptomatic lesion on the abdomen of 6 years’ duration. He had a 17-year history of type 2 diabetes mellitus treated with insulin injections for 14 years after failing oral hypoglycemic agents. The patient reported injecting at the same site on the abdomen for the last 14 years. Physical examination revealed a lichenified, hyperpigmented, verrucous plaque on the lower abdomen under the umbilicus (Figure 1). No similar skin lesions were observed elsewhere on the body. A punch biopsy of the plaque showed hyperkeratosis, papillomatosis, acanthosis, and hyperpigmentation, which was consistent with AN (Figure 2). The patient was instructed to rotate injection sites and avoid the affected area. Over-the-counter ammonium lactate cream applied twice daily to the affected site also was recommended. After 2 months of treatment with this regimen, the patient reported softening and lightening of the lesion on the abdomen.

Figure 1. Localized acanthosis nigricans presenting as a lichenified, hyperpigmented, hyperkeratotic plaque at a recurring insulin injection site on the lower abdomen in a 64-year-old man with type 2 diabetes mellitus.

Figure 2. Histopathology demonstrated hyperkeratosis, papillomatosis, acanthosis, and hyperpigmentation (H&E, original magnification ×10).

A PubMed search of articles indexed for MEDLINE for all English-language studies with human participants using the terms acanthosis nigricans and insulin injections yielded 20 results. Of them, 13 discussed localized AN at insulin injection sites: 12 case reports (Table)1-12 and 1 observational study in a group of diabetic patients.13



In the observational study, 500 diabetic patients were examined for insulin injection-site dermatoses and only 2 had localized injection-site AN. No other information was provided for these 2 patients.13 In the 12 published case reports,1-12 all patients did not rotate sites for their insulin injections and repeatedly injected into the affected area. The abdomen was the most commonly affected site, seen in 83% (10/12) of cases, while 25% (3/12) involved the thighs. All but 1 patient had type 2 diabetes mellitus. In 2 patients, “amyloid” was noted on the biopsy report in addition to changes consistent with AN. At least 2 patients had clearance after rotating injection sites.3,12



It has been suggested that localized AN at insulin injection sites develops through similar mechanisms as benign AN. Contributing factors to the development of benign AN may be IGF-1, fibroblast growth factor, and epidermal growth factor.1-3 Insulin is similar in structure to IGF-1 and can bind to IGF-1 receptors at high enough concentrations. Insulinlike growth factor 1 receptors are present on keratinocytes and fibroblasts, which proliferate upon activation, leading to the development of AN.1-3 Localized AN is thought to occur when repetitive insulin at the injection site saturates IGF-1 receptors on local keratinocytes.

Based on our patient and prior reports in the literature, localized AN is an uncommon cutaneous complication of insulin injections. Physicians should ask about repetitive insulin injections in the same site when localized AN occurs in patients with diabetes mellitus on insulin therapy. They also should discuss the importance of rotating sites for insulin adminstration to prevent the development of cutaneous complications including AN.

 

To the Editor:

Acanthosis nigricans (AN) is characterized by asymptomatic, hyperpigmented, velvety plaques that can occur anywhere on the body but most often present on the skin of the neck, axillae, groin, and other body folds.1-12 Although there are 5 subtypes, benign AN is the most common and is related to insulin resistance.1-4 Insulin can bind to insulinlike growth factor 1 (IGF-1) on keratinocytes, stimulating their proliferation. In type 2 diabetes mellitus, endogenous insulin levels are high enough to bind IGF-1 and activate keratinocytes, leading to the development of AN. Insulin injections have been associated with cutaneous side effects including lipoatrophy, lipohypertrophy, and postinflammatory hyperpigmentation.3 Acanthosis nigricans at insulin injection sites is a rare clinical condition.

A 64-year-old man presented for evaluation of a growing asymptomatic lesion on the abdomen of 6 years’ duration. He had a 17-year history of type 2 diabetes mellitus treated with insulin injections for 14 years after failing oral hypoglycemic agents. The patient reported injecting at the same site on the abdomen for the last 14 years. Physical examination revealed a lichenified, hyperpigmented, verrucous plaque on the lower abdomen under the umbilicus (Figure 1). No similar skin lesions were observed elsewhere on the body. A punch biopsy of the plaque showed hyperkeratosis, papillomatosis, acanthosis, and hyperpigmentation, which was consistent with AN (Figure 2). The patient was instructed to rotate injection sites and avoid the affected area. Over-the-counter ammonium lactate cream applied twice daily to the affected site also was recommended. After 2 months of treatment with this regimen, the patient reported softening and lightening of the lesion on the abdomen.

Figure 1. Localized acanthosis nigricans presenting as a lichenified, hyperpigmented, hyperkeratotic plaque at a recurring insulin injection site on the lower abdomen in a 64-year-old man with type 2 diabetes mellitus.

Figure 2. Histopathology demonstrated hyperkeratosis, papillomatosis, acanthosis, and hyperpigmentation (H&E, original magnification ×10).

A PubMed search of articles indexed for MEDLINE for all English-language studies with human participants using the terms acanthosis nigricans and insulin injections yielded 20 results. Of them, 13 discussed localized AN at insulin injection sites: 12 case reports (Table)1-12 and 1 observational study in a group of diabetic patients.13



In the observational study, 500 diabetic patients were examined for insulin injection-site dermatoses and only 2 had localized injection-site AN. No other information was provided for these 2 patients.13 In the 12 published case reports,1-12 all patients did not rotate sites for their insulin injections and repeatedly injected into the affected area. The abdomen was the most commonly affected site, seen in 83% (10/12) of cases, while 25% (3/12) involved the thighs. All but 1 patient had type 2 diabetes mellitus. In 2 patients, “amyloid” was noted on the biopsy report in addition to changes consistent with AN. At least 2 patients had clearance after rotating injection sites.3,12



It has been suggested that localized AN at insulin injection sites develops through similar mechanisms as benign AN. Contributing factors to the development of benign AN may be IGF-1, fibroblast growth factor, and epidermal growth factor.1-3 Insulin is similar in structure to IGF-1 and can bind to IGF-1 receptors at high enough concentrations. Insulinlike growth factor 1 receptors are present on keratinocytes and fibroblasts, which proliferate upon activation, leading to the development of AN.1-3 Localized AN is thought to occur when repetitive insulin at the injection site saturates IGF-1 receptors on local keratinocytes.

Based on our patient and prior reports in the literature, localized AN is an uncommon cutaneous complication of insulin injections. Physicians should ask about repetitive insulin injections in the same site when localized AN occurs in patients with diabetes mellitus on insulin therapy. They also should discuss the importance of rotating sites for insulin adminstration to prevent the development of cutaneous complications including AN.

References
  1. Yahagi E, Mabuchi T, Nuruki H, et al. Case of exogenous insulin-derived acanthosis nigricans caused by insulin injections. Tokai J Exp Clin Med. 2014;39:5-9.
  2. Dhingra M, Garg G, Gupta M, et al. Exogenous insulin-derived acanthosis nigricans: could it be a cause of increased insulin requirement? Dermatol Online J. 2013;19:9.
  3. Buzási K, Sápi Z, Jermendy G. Acanthosis nigricans as a local cutaneous side effect of repeated human insulin injections. Diabetes Res Clin Pract. 2011;94:E34-E36.
  4. Mailler-Savage EA, Adams BB. Exogenous insulin-derived acanthosis nigricans. Arch Dermatol. 2008;144:126-127.
  5. Nandeesh BN, Rajalakshmi T, Shubha B. Cutaneous amyloidosis and insulin with coexistence of acanthosis nigricans. Indian J Pathol Microbiol. 2014;57:127-129.
  6. Kudo-Watanuki S, Kurihara E, Yamamoto K, et al. Coexistence of insulin-derived amyloidosis and an overlying acanthosis nigricans-like lesion at the site of insulin injection. Clin Exp Dermatol. 2013;38:25-29.
  7. Brodell JD Jr, Cannella JD, Helms SE. Case report: acanthosis nigricans resulting from repetitive same-site insulin injections. J Drugs Dermatol. 2012;11:E85-E87.
  8. Erickson L, Lipschutz DE, Wrigley W, et al. A peculiar cutaneous reaction to repeated injections of insulin. JAMA. 1969;209:934-935.
  9. Fleming MG, Simon SI. Cutaneous insulin reaction resembling acanthosis nigricans. Arch Dermatol. 1986;122:1054-1056.
  10. Pachon Burgos A, Chan Aguilar MP. Visual vignette. hyperpigmented hyperkeratotic cutaneous insulin reaction that resembles acanthosis nigricans with lipohypertrophy. Endocr Pract. 2008;14:514.
  11. Chapman SE, Bandino JP. A verrucous plaque on the abdomen: challenge. Am J Dermatopathol. 2017;39:E163.
  12. Huang Y, Hessami-Booshehri M. Acanthosis nigricans at sites of insulin injection in a man with diabetes. CMAJ. 2018;190:E1390.
  13. Sawatkar GU, Kanwar AJ, Dogra S, et al. Spectrum of cutaneous manifestations of type 1 diabetes mellitus in 500 South Asian patients. Br J Dermatol. 2014;171:1402-1406.
References
  1. Yahagi E, Mabuchi T, Nuruki H, et al. Case of exogenous insulin-derived acanthosis nigricans caused by insulin injections. Tokai J Exp Clin Med. 2014;39:5-9.
  2. Dhingra M, Garg G, Gupta M, et al. Exogenous insulin-derived acanthosis nigricans: could it be a cause of increased insulin requirement? Dermatol Online J. 2013;19:9.
  3. Buzási K, Sápi Z, Jermendy G. Acanthosis nigricans as a local cutaneous side effect of repeated human insulin injections. Diabetes Res Clin Pract. 2011;94:E34-E36.
  4. Mailler-Savage EA, Adams BB. Exogenous insulin-derived acanthosis nigricans. Arch Dermatol. 2008;144:126-127.
  5. Nandeesh BN, Rajalakshmi T, Shubha B. Cutaneous amyloidosis and insulin with coexistence of acanthosis nigricans. Indian J Pathol Microbiol. 2014;57:127-129.
  6. Kudo-Watanuki S, Kurihara E, Yamamoto K, et al. Coexistence of insulin-derived amyloidosis and an overlying acanthosis nigricans-like lesion at the site of insulin injection. Clin Exp Dermatol. 2013;38:25-29.
  7. Brodell JD Jr, Cannella JD, Helms SE. Case report: acanthosis nigricans resulting from repetitive same-site insulin injections. J Drugs Dermatol. 2012;11:E85-E87.
  8. Erickson L, Lipschutz DE, Wrigley W, et al. A peculiar cutaneous reaction to repeated injections of insulin. JAMA. 1969;209:934-935.
  9. Fleming MG, Simon SI. Cutaneous insulin reaction resembling acanthosis nigricans. Arch Dermatol. 1986;122:1054-1056.
  10. Pachon Burgos A, Chan Aguilar MP. Visual vignette. hyperpigmented hyperkeratotic cutaneous insulin reaction that resembles acanthosis nigricans with lipohypertrophy. Endocr Pract. 2008;14:514.
  11. Chapman SE, Bandino JP. A verrucous plaque on the abdomen: challenge. Am J Dermatopathol. 2017;39:E163.
  12. Huang Y, Hessami-Booshehri M. Acanthosis nigricans at sites of insulin injection in a man with diabetes. CMAJ. 2018;190:E1390.
  13. Sawatkar GU, Kanwar AJ, Dogra S, et al. Spectrum of cutaneous manifestations of type 1 diabetes mellitus in 500 South Asian patients. Br J Dermatol. 2014;171:1402-1406.
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Practice Points

  • Benign acanthosis nigricans (AN) is most often related to insulin resistance and presents as asymptomatic, hyperpigmented, velvety plaques on the neck, axillae, groin, and other body folds.
  • Benign AN related to insulin resistance occurs when insulin binds to insulinlike growth factor 1 on keratinocytes and stimulates proliferations.
  • Although insulin injections have been associated with several cutaneous side effects, including lipoatrophy, lipohypertrophy, and postinflammatory hyperpigmentation, localized AN is an uncommonly reported cutaneous adverse effect.
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