Dermatoses Associated with Diabetes Mellitus

authors:

avatar Lyubomir Dourmishev ORCID 1 , * , avatar Joana Pozharashka 1

Department of Dermatology and Venereology, Medical University of Sofia, Sofia, Bulgaria

how to cite: Dourmishev L, Pozharashka J. Dermatoses Associated with Diabetes Mellitus. J Skin Stem Cell. 2019;6(4):e101180. https://doi.org/10.5812/jssc.101180.

Abstract

Context:

Diabetes is considered a major health problem, mainly due to its various debilitating complications, including blindness, renal failure, heart attack, stroke, limb amputation, and even death in millions of patients per year. Skin manifestations of diabetes are common in everyday clinical practice but often remain neglected. This review aims to highlight the pathogenetic mechanisms and clinical picture of skin conditions, associated with diabetes mellitus.

Evidence Acquisition:

The skin manifestations of diabetes mellitus are related to blood glucose levels. Initially, glycemia affects skin homeostasis by inhibiting keratinocyte proliferation and phagocytosis and inducing endothelial cell apoptosis, while in later stages, the involvement of the peripheral nervous system and vascular changes (micro and macroangiopathy) become the leading pathogenetic factors.

Results:

There are different classifications of skin changes in diabetes, depending on the frequency, the onset, or the type of diabetes. The most convenient classification from the practical point of view subdivides cutaneous manifestations into four categories: (A) cutaneous manifestation specific to diabetes; (B) compatible dermatosis not specific to diabetes; (C) skin infection associated with diabetes; and (D) skin manifestation due to antidiabetic therapy.

Conclusions:

Diabetes mellitus is associated with a wide range of dermatological disorders. Their recognition is important for the early diagnosis of diabetes and therefore might be helpful to reduce the complication rates.

1. Context

Dermatological manifestations of diabetes mellitus are common but often remain neglected, due to the heterogeneity of clinical signs, as well as the need for an interdisciplinary approach. Currently, diabetes is becoming more prevalent in developed countries (1). According to the WHO report, the number of people with diabetes worldwide increased four times in 25 years, from 108 million in 1980 to 422 million in 2014 (2). Diabetes may lead to serious consequences like blindness, renal failure, heart attack, stroke, and lower limb amputation if treated inadequately (1, 2). Approximately 1.6 million patients died in 2015, due to the complications of diabetes and 51% to 97% of diabetic patients presented with skin manifestations at the same time (2, 3). These facts highlight the importance of dermatologists for early detection of diabetes.

This review aims to highlight the pathogenetic mechanisms and clinical picture of skin conditions, associated with diabetes mellitus.

2. Evidence Acquisition

Skin manifestations of diabetes mellitus are related to increased glucose levels. Hyperglycemia affects skin homeostasis by inhibiting keratinocyte proliferation and phagocytosis, and inducing endothelial cell apoptosis. Later in the disease course, the involvement of the peripheral nervous system and vascular changes (micro and macroangiopathy) become the leading factors (3). Diabetic neuropathy is subdivided into sensory, motor, and autonomic forms. Sensory neuropathy is responsible for itching and paresthesia, as well as the reduced sensation of the skin. Motor neuropathy leads to changes in muscle tonus, causing foot deformities and development of the famous diabetic Charcot’s foot (4). Alterations in the autonomic nervous system can change sweat secretion, aggravating skin dryness and cause xerosis, hyperkeratosis, fissure formation, and compromised skin vascularization, resulting in diabetic dermopathy and sclerotic skin changes (5).

3. Results

There are different classifications of skin changes in diabetes, depending on the frequency (common or infrequent), the onset (early or late), and the type of diabetes. Skin manifestations are more common in insulin-dependent diabetes mellitus than in the insulin-independent variant (Box 1). As the majority of dermatoses occur in both types of diabetes, the most useful classification from the practical point of view is as follows: (1) cutaneous manifestation specific only to diabetes; (2) compatible dermatoses not specific to diabetes; (3) skin infection associated with diabetes; and (4) skin manifestation due to anti-diabetic therapy (6).

Box 1.

Skin Manifestations Depending on the Type of Diabetes Mellitus (Modified by Murphy-Chutorian et al. (5))

Skin Manifestations on the Type of Diabetes Mellitus
Type I
Bullosis diabeticorum
Necrobiosis lipoidica
Keratosis pilaris
Acquired ichthyosis
Vitiligo
Type II
Diabetic dermopathy
Acanthosis nigricans
Granuloma annulare
Scleredema adultorum (Buschke)
Erythema faciale

3.1. Cutaneous Manifestation Specific to Diabetes

Typical skin manifestations are largely associated with diabetes mellitus, although they may have a different etiology and pathogenesis in some patients. These dermatoses indicate either new-onset diabetes or poor glycemic control in already diagnosed diabetes.

3.1.1. Diabetic dermopathy

Diabetic dermopathy is a common skin manifestation seen in more than half of diabetic patients. It is more common in men after the fifth decade of life. It occurs in the later stages of diabetes, often combined with nephropathy, neuropathy or retinopathy (7). Clinically, it presents with the appearance of well-demarcated hyperpigmented atrophic plaques on the anterior surface of the legs (7, 8). The pathogenesis of the disease includes trauma or peripheral angiopathy with subsequent accumulation of melanin and hemosiderin in the dermis. Diabetic dermopathy frequently associates with renal atherosclerosis (7). Differential diagnosis with skin manifestations of chronic venous insufficiency or nummular dermatitis have to be made.

3.1.2. Diabetic Foot Syndrome

Diabetic foot syndrome (Malum perforans) is a relatively common disease, affecting about 6% of the population (9). It occurs in 15% - 25% of diabetic patients, a little more often among those suffering from insulin-independent diabetes (10). Clinically, Malum perforans presents with hyperkeratosis, xerosis and callosity, which subsequently develops to an ulcer with callous edges and a necrotic, non-healing bottom (10). The pathogenesis of the disease is complex. It combines both chronic trauma and ischemic, neuropathic changes caused by diabetes (4). In the diabetic foot syndrome, the ulcer usually occurs on the skin overlying bony prominences, commonly over the third tarsometatarsal joint of the foot.

Patients with insulin-dependent diabetes and diabetic foot have more tendency towards infectious complications like gangrene and osteomyelitis, which may impose foot amputation (9). The development of diabetic neuro-osteoarthropathy, progressive bone and joint deformation, and the destruction of the foot, are described in the literature as the Charcot foot syndrome (11). The diabetic foot can also be combined with erythromelalgia with erythema, burning and pain on the foot provoked by warming. The differential diagnosis includes osteopathy with a different genesis: syringomyelia, alcoholic neuropathy, termed Acropathia ulcero-mutilans acquisita (Bureau-Barriere), etc. (12).

The treatment of the diabetic foot is complex and requires the following measures: chronic trauma prevention, daily hygiene, antiseptics/antibiotics inhibiting bacterial and mycotic colonization, hydrogels, epithelotonic agents, hyperbaric oxygen therapy, growth factors and surgery (4, 9).

3.1.3. Acanthosis Nigricans

Acanthosis nigricans is a dermatosis more common in insulin-independent diabetes, but also observed in patients with obesity, acromegaly, Cushing syndrome or neoplastic diseases (13). Hyperglycemia is found in more than half of the patients (14). It presents clinically with hyperpigmented verrucous linear plaques, mainly affecting skin folds (axillae, inguinal folds, and neck) (Figure 1). The role of insulin as an activator of IGF-1 receptors in keratinocytes and dermal fibroblasts is discussed in the pathogenesis of the disease (15).

Acanthosis nigricans in male patients with diabetes
Acanthosis nigricans in male patients with diabetes

3.1.4. Scleroderma-Like Skin Changes

Scleroderma-like skin changes include a heterogeneous group of syndromes with a common clinical presentation of skin tightening. Progressive finger skin thickening affects 8% - 50% of diabetic patients and is more common in type I diabetes mellitus (16). The changes resemble sclerodactyly in systemic sclerosis, lacking both respiratory and gastrointestinal tract involvement and without autoantibodies in the serum. However, sclerodactyly in diabetes is combined with a high risk of diabetic nephropathy and retinopathy. Diabetes is also common in Dupuytren’s contracture and stenosing tenosynovitis with the “trigger finger” symptom (17). Another important symptom is the “prayer sign” in which the patient is unable to press his palms tightly due to the tightening and flexion contracture of the fingers (18).

3.1.5. Scleredema Adultorum

Scleredema adultorum (Buschke) is a rare disease with a multi-etiological origin, first described in 1902 (19). There are three variants of scleredema: (1) scleredema in young or middle-aged women, occurring after infectious diseases; (2) slowly advancing scleredema in patients with monoclonal gammopathies/multiple myeloma; and (3) scleredema associated with diabetes mellitus (19). Only 2% - 15% of patients with diabetes develop scleredema adultorum. The disease is more common in obese, middle-aged men with uncontrolled glycemia. The ratio of insulin-dependent to insulin-independent diabetes is 6.5/1 (20). Clinically, the disease presents with erythema and skin thickening, covering mainly the chest, slowly progressing to the back of the neck, shoulders, face, and upper extremities (Figure 2). A case with symmetric periorbital edema and partial vision blockage was also described (21). Scleredema adultorum is usually treatment-resistant and the correction of hyperglycemia rarely ameliorates the condition.

Scleredema adultorum (Buschke) in diabetic patients
Scleredema adultorum (Buschke) in diabetic patients

3.1.6. Necrobiosis Lipoidica Diabeticorum

Necrobiosis lipoidica diabeticorum is an inflammatory granulomatous dermatosis with collagen degeneration and vascular involvement. The disease is more common in women after the age of 30. Necrobiosis lipoidica often associates with insulin-independent diabetes and does not correlate with glycemic control. It clinically manifests with symmetrical, yellow-brown scleroatrophic plaques, located on the anterior surface of the shins, tending to ulcerate in one-third of cases (Figure 3). In rare cases, skin lesions can affect the trunk, upper extremities, and even the scalp (22).

Necrobiosis lipoidica diabeticorum perforans in a 42-year-old patient with uncontrolled diabetes 22
Necrobiosis lipoidica diabeticorum perforans in a 42-year-old patient with uncontrolled diabetes 22

3.1.7. Bullosis Diabeticorum

Bullosis diabeticorum is a rare dermatological manifestation, affecting less than 0.5% of patients with diabetes. It was initially described by Kramer in 1930 and reported twice as often in males, between the ages of 50 and 70 (23). Clinically, patients present with tense sterile bullae that appear suddenly on unaltered skin, usually on the limbs and less often on the trunk (8, 23). The typical location raises the question of whether microtraumas take part in the pathogenesis of the disease. Usually, subjective symptoms are lacking. The lesions regress spontaneously for two to six weeks but can recur. Differential diagnosis is made with a bullous reaction from physical factors, bullous pemphigoid or porphyria.

3.2. Compatible Dermatosis not Specific only to Diabetes

This group includes skin manifestations often seen in several metabolic diseases, not exclusively diabetes.

3.2.1. Diabetes-Associated Pruritus

Diabetes-associated pruritus can be both disseminated and localized, most commonly on the scalp, ankles, inguinal folds, and genitalia. It may be a sign of skin infection or xerosis, but more often appears in unaffected skin (24).

3.2.2. Xerosis Cutis

Xerosis cutis occurs in about 44% of patients, considered one of the earliest manifestations of type I diabetes mellitus (25). Dry skin, however, is also a symptom of atopic dermatitis, psoriasis, acquired or congenital keratoderma and inflammatory or oncological diseases, as well as a manifestation of skin aging. The differential diagnosis is very wide, which determines the low diagnostic value of dry skin as a clinical sign.

3.2.3. Acquired Ichthyosis

Acquired ichthyosis is a relatively infrequent disease, affecting up to 25% of patients with insulin-independent diabetes (26). In addition to diabetes, neoplasms, infections, autoimmune diseases, and endocrinopathies are also important in the etiology of the disease (26). Ichthyosis mainly affects the lower legs and ankles, with dry, pigmented, polygonal scales. The disease is a manifestation of rapid skin aging and hyperkeratosis due to decreased corneocyte desquamation.

3.2.4. Keratosis Pilaris

Keratosis pilaris is seen in about 20% of patients with diabetes. The condition is considered one of the minor criteria for atopy and is common in children and adolescents with atopic dermatitis (27). The skin lesions are located on the lateral surfaces of the upper limbs, hips and face and are represented with keratotic follicular papules on erythematous or pigmented skin (28). The treatment with emollients and topical keratolytics has been successful although with temporary effect in the majority of patients.

3.2.5. Huntley Papules

Huntley papules are skin-colored, hyperkeratotic papules, grouped as “pebbles” on the extensor side of fingers (29). They are associated with type II diabetes and sometimes precede sclerotic finger changes and the “prayer sign”. Topical treatment is difficult and often ineffective.

3.2.6. Rubeosis Faciei Diabeticorum

Rubeosis faciei diabeticorum is facial erythema, affecting about half of the hospitalized diabetic patients (30). Rubeosis is a manifestation of suboptimal glycemic control, and associates with venous hyperemia and microangiopathy. The differential diagnosis is made with rosacea, malar rash in systemic lupus erythematosus or contact dermatitis. The strict control of blood glycemia leads to clinical improvement.

3.2.7. Palmar Erythema

Palmar erythema is usually symmetrical and accompanied by an elevated local temperature. It affects about 4% of patients with diabetes mellitus (31). Unlike erythromelalgia, the patients do not have any subjective symptoms in this condition. Palmar erythema is a symptom of venous hyperemia and microangiopathy. Differential diagnosis includes neoplastic erythema, rheumatoid arthritis, thyrotoxicosis, hepatic damage, drug-induced erythema and erythema in pregnancy.

3.2.8. Granuloma Annulare

Granuloma annulare is a rare, chronic, self-limiting annular dermatosis with multifactorial etiology. In addition to diabetes, etiologic factors include atopy, thyroiditis, connective tissue disease and neoplasia. It affects women twice as often as men (32). Clinically, granuloma annulare presents with papules that tend to conflate and form annular plaques with a raised edge and a flat center. It occurs more frequently on the limbs and at the sites of trauma, with lesions being erythematous or with skin color. The course is usually asymptomatic but itching or burning is reported in some cases. The generalized variant of granuloma annulare (Figure 4) is associated with diabetes in 15% (32) to 33% of cases (33). Except for cases of spontaneous regressions, granuloma annulare is resistant to therapy. Retinoids and phototherapy have clinical effects in some patients.

Granuloma annulare in a 49-year-old patient with diabetes
Granuloma annulare in a 49-year-old patient with diabetes

3.2.9. Lichen Planus

Lichen planus is an inflammatory psychosomatic disorder, affecting mucous membranes and the skin. In a study, diabetes or impaired glucose tolerance was detected in about 25% of patients (34). The etiology is multifactorial, mainly associated with psychiatric, infectious, autoimmune or drug factors. The clinical picture includes erythematous or livid polygonal papules or plaques overlying the extensor surfaces of the limbs and the trunk. Wickham striae are usually observed on the closer inspection of the lesions. Leukokeratotic plaques or erosions on the oral and genital mucosa are also common findings. The triad of hypertension, oral lichen, and diabetes is known as Grinspan’s syndrome (35).

3.2.10. Vitiligo

Vitiligo is a chronic disease that occurs suddenly with the appearance of hypopigmented or a pigmented macule around the eyes, lips, elbows, knees, genitalia or trunk as a result of autoimmune melanocyte destruction in the skin. It affects about 1% of the population, more often women (36) and is most commonly associated with insulin-independent diabetes. The association of vitiligo, diabetes, thyroiditis, Addison's disease, myasthenia gravis, idiopathic thrombopenic purpura is known as multiple autoimmune syndrome (37).

Some authors stated that several dermatoses like hidradenitis suppurativa (38), glucagonoma (39), eruptive xanthoma (40), lipoid proteinosis (41), Kyrle disease (42), carotenoderma, and psoriasis vulgaris are more common in diabetes. The latter remains a controversy but these diseases represent metabolic disturbances. An interesting clinical observation in patients with diabetes is a discordance between the color of the hair, which turns gray with age, and that of the eyebrows, which remains darker in color (43).

3.3. Diabetes-Associated Skin Infections

Patients with diabetes are significantly more susceptible to bacterial and mycotic infections than the rest of the population. Infectious dermatoses are observed in about 20% of patients with diabetes (44), with mycotic infections being prevalent in frequency in comparison with bacterial and viral ones (45). Diabetes-associated infections are characterized by chronic recurrent course therapeutic resistance and a higher incidence of potentially life-threatening complications. Some authors propose that systemic mycotic infections caused by Zygomycetes spp. are typical for patients with uncontrolled diabetes (46). Viral, bacterial and mycotic infections most frequently associated with diabetes are summarized in Box 2.

Box 2.

Common Infections in Patients with Diabetes

Common Infections
Viral infections
Herpes simplex
Herpes zoster
Bacterial Infections
Erysipelas
Cellulitis
Necrotic fasciitis
Fournier gangrene
Staphylococcal folliculitis
Furunculosis
Carbunculosis
Erythrasma
External otitis
Mycotic Infections
Yeast infections
Candida stomatitis
Candida balanoposthitis
Vulvovaginitis
Intertrigo
Erosio interdigitorum
Onychomycosis
Dermatophytic infections
Tinea
Onychomycosis
Systemic mycotic infections
Mucormycosis

3.4. Skin Manifestations Triggered by Anti-Diabetic Therapy

The current treatment of diabetes is carried out with two groups of medicines: insulin and oral antidiabetic agents. Insulin is administered subcutaneously. It may be related, although very rarely, to acute hypersensitivity side effects, including urticaria, angioneurotic edema and anaphylactic shock and may sometimes be life-threatening. Lipodystrophy (lipohypertrophy or lipoatrophy) might occur at the injection site. The latter not only is an aesthetic problem but also severely disrupts insulin pharmacokinetics. Therefore, the injection site should be changed if this side effect occurs (47).

Oral antidiabetic agents are a growing heterogeneous group of drugs. Allergic skin reactions and photosensitivity are relatively more common in the group of sulfonylureas, chlorpropamide and tolbutamide. In combination with alcohol, chlorpropamide causes disulfiram-like reactions (facial flushing, headaches and nausea). In recent years, an increasing number of reports have been published on bullous pemphigoid (48-50) or mucous membrane pemphigoid (51), induced by dipeptidyl peptidase 4 inhibitors (vildagliptin, linagliptin and sitagliptin). Generalized skin eruption, urticaria and eczema were reported after the initiation of sodium-glucose cotransporters (ipragliflozin, dapagliflozin, canagliflozin, and empagliflozin) for diabetes (52).

4. Conclusions

Diabetes mellitus is associated with a wide range of dermatological disorders. The recognition of the cutaneous sins of diabetes is important for its early diagnosis and can help with adequate disease control. On the other hand, an active search for initial changes, such as xerosis, hyperkeratosis or skin infections and their appropriate management could help reduce the late, often severe complications of diabetes.

Although most dermatological conditions require specific treatment, a key rule is to improve glycemic control. Patient education and lifestyle change are essential for improving the quality of life of diabetic patients.

References

  • 1.

    Almourani R, Chinnakotla B, Patel R, Kurukulasuriya LR, Sowers J. Diabetes and cardiovascular disease: An Update. Curr Diab Rep. 2019;19(12):161. [PubMed ID: 31828525]. https://doi.org/10.1007/s11892-019-1239-x.

  • 2.

    WHO. Global report on diabetes. 2016. Available from: http://apps.who.int/iris/bitstream/handle/10665/204871/9789241565257_eng.pdf?sequence=1.

  • 3.

    de Macedo GM, Nunes S, Barreto T. Skin disorders in diabetes mellitus: An epidemiology and physiopathology review. Diabetol Metab Syndr. 2016;8(1):63. [PubMed ID: 27583022]. [PubMed Central ID: PMC5006568]. https://doi.org/10.1186/s13098-016-0176-y.

  • 4.

    Bandyk DF. The diabetic foot: Pathophysiology, evaluation, and treatment. Semin Vasc Surg. 2018;31(2-4):43-8. [PubMed ID: 30876640]. https://doi.org/10.1053/j.semvascsurg.2019.02.001.

  • 5.

    Murphy-Chutorian B, Han G, Cohen SR. Dermatologic manifestations of diabetes mellitus: A review. Endocrinol Metab Clin North Am. 2013;42(4):869-98. [PubMed ID: 24286954]. https://doi.org/10.1016/j.ecl.2013.07.004.

  • 6.

    Romano G, Moretti G, Di Benedetto A, Giofre C, Di Cesare E, Russo G, et al. Skin lesions in diabetes mellitus: Prevalence and clinical correlations. Diabetes Res Clin Pract. 1998;39(2):101-6. [PubMed ID: 9597379]. https://doi.org/10.1016/s0168-8227(97)00119-8.

  • 7.

    McCash S, Emanuel PO. Defining diabetic dermopathy. J Dermatol. 2011;38(10):988-92. [PubMed ID: 21762390]. https://doi.org/10.1111/j.1346-8138.2011.01251.x.

  • 8.

    Brzezinski P, Chiriac AE, Pinteala T, Foia L, Chiriac A. Diabetic dermopathy ("shin spots") and diabetic bullae ("bullosis diabeticorum") at the same patient. Pak J Med Sci. 2015;31(5):1275-6. [PubMed ID: 26649029]. [PubMed Central ID: PMC4641298]. https://doi.org/10.12669/pjms.315.7521.

  • 9.

    Amin N, Doupis J. Diabetic foot disease: From the evaluation of the "foot at risk" to the novel diabetic ulcer treatment modalities. World J Diabetes. 2016;7(7):153-64. [PubMed ID: 27076876]. [PubMed Central ID: PMC4824686]. https://doi.org/10.4239/wjd.v7.i7.153.

  • 10.

    Singh N, Armstrong DG, Lipsky BA. Preventing foot ulcers in patients with diabetes. JAMA. 2005;293(2):217-28. [PubMed ID: 15644549]. https://doi.org/10.1001/jama.293.2.217.

  • 11.

    Jeffcoate WJ. Charcot foot syndrome. Diabet Med. 2015;32(6):760-70. [PubMed ID: 25818542]. https://doi.org/10.1111/dme.12754.

  • 12.

    Moretti G, Puglisi Guerra A, Schepis C. Acropathia ulcero-mutilans acquisita. J Eur Acad Dermatol Venereol. 2006;20(9):1141-3. [PubMed ID: 16987279]. https://doi.org/10.1111/j.1468-3083.2006.01638.x.

  • 13.

    Dourmishev LA, Draganov PV. Paraneoplastic dermatological manifestation of gastrointestinal malignancies. World J Gastroenterol. 2009;15(35):4372-9. [PubMed ID: 19764087]. [PubMed Central ID: PMC2747056]. https://doi.org/10.3748/wjg.15.4372.

  • 14.

    Panda S, Das A, Lahiri K, Chatterjee M, Padhi T, Rathi S, et al. Facial acanthosis nigricans: A morphological marker of metabolic syndrome. Indian J Dermatol. 2017;62(6):591-7. [PubMed ID: 29263532]. [PubMed Central ID: PMC5724306]. https://doi.org/10.4103/ijd.IJD_545_17.

  • 15.

    Yahagi E, Mabuchi T, Nuruki H, Manabe Y, Ikoma N, Ozawa A, et al. Case of exogenous insulin-derived acanthosis nigricans caused by insulin injections. Tokai J Exp Clin Med. 2014;39(1):5-9. [PubMed ID: 24733591].

  • 16.

    Brik R, Berant M, Vardi P. The scleroderma-like syndrome of insulin-dependent diabetes mellitus. Diabetes Metab Rev. 1991;7(2):120-8. [PubMed ID: 1794257].

  • 17.

    Vasiliadis AV, Itsiopoulos I. Trigger finger: An atraumatic medical phenomenon. J Hand Surg Asian Pac Vol. 2017;22(2):188-93. [PubMed ID: 28506168]. https://doi.org/10.1142/S021881041750023X.

  • 18.

    Raina S, Jaryal A, Sonnatakke T. Prayer sign. Indian Dermatol Online J. 2013;4(3):259. [PubMed ID: 23984257]. [PubMed Central ID: PMC3752499]. https://doi.org/10.4103/2229-5178.115545.

  • 19.

    Parmar RC, Bavdekar SB, Bansal S, Doraiswamy A, Khambadkone S. Scleredema adultorum. J Postgrad Med. 2000;46(2):91-3. [PubMed ID: 11013472].

  • 20.

    Meguerditchian C, Jacquet P, Beliard S, Benderitter T, Valero R, Carsuzza F, et al. Scleredema adultorum of Buschke: An under recognized skin complication of diabetes. Diabetes Metab. 2006;32(5 Pt 1):481-4. [PubMed ID: 17110904]. https://doi.org/10.1016/s1262-3636(07)70307-5.

  • 21.

    Mohamed M, Belhadjali H, Bechir AB, Moussa A, Zili J. Scleredema adultorum of Buschke with prominent periorbital edema in a Tunisian patient with diabetes mellitus: A case report. Int J Dermatol. 2016;55(2):e100-2. [PubMed ID: 26536602]. https://doi.org/10.1111/ijd.13128.

  • 22.

    Lozanova P, Dourmishev L, Vassileva S, Miteva L, Balabanova M. Perforating disseminated necrobiosis lipoidica diabeticorum. Case Rep Dermatol Med. 2013;2013:370361. [PubMed ID: 23533835]. [PubMed Central ID: PMC3596912]. https://doi.org/10.1155/2013/370361.

  • 23.

    Kurdi AT. Bullosis diabeticorum. Lancet. 2013;382(9907). e31. [PubMed ID: 23706658]. https://doi.org/10.1016/S0140-6736(13)60145-2.

  • 24.

    Tseng HW, Ger LP, Liang CK, Liou HH, Lam HC. High prevalence of cutaneous manifestations in the elderly with diabetes mellitus: An institution-based cross-sectional study in Taiwan. J Eur Acad Dermatol Venereol. 2015;29(8):1631-5. [PubMed ID: 25178455]. https://doi.org/10.1111/jdv.12664.

  • 25.

    Goyal A, Raina S, Kaushal SS, Mahajan V, Sharma NL. Pattern of cutaneous manifestations in diabetes mellitus. Indian J Dermatol. 2010;55(1):39-41. [PubMed ID: 20418975]. [PubMed Central ID: PMC2856371]. https://doi.org/10.4103/0019-5154.60349.

  • 26.

    Sanli H, Akay BN, Sen BB, Kocak AY, Emral R, Bostanci S. Acquired ichthyosis associated with type 1 diabetes mellitus. Dermatoendocrinol. 2009;1(1):34-6. [PubMed ID: 20046586]. [PubMed Central ID: PMC2715201]. https://doi.org/10.4161/derm.1.1.7170.

  • 27.

    Hanifin JM. Diagnostic features of atopic dermatitis. Acta Derm Venereol (Suppl). 1980;92:44-7.

  • 28.

    Pavlovic MD, Milenkovic T, Dinic M, Misovic M, Dakovic D, Todorovic S, et al. The prevalence of cutaneous manifestations in young patients with type 1 diabetes. Diabetes Care. 2007;30(8):1964-7. [PubMed ID: 17519431]. https://doi.org/10.2337/dc07-0267.

  • 29.

    Guarneri C, Guarneri F, Borgia F, Vaccaro M. Finger pebbles in a diabetic patient: Huntley's papules. Int J Dermatol. 2005;44(9):755-6. [PubMed ID: 16135146]. https://doi.org/10.1111/j.1365-4632.2004.02580.x.

  • 30.

    Namazi MR, Jorizzo JL, Fallahzadeh MK. Rubeosis faciei diabeticorum: A common, but often unnoticed, clinical manifestation of diabetes mellitus. ScientificWorldJournal. 2010;10:70-1. [PubMed ID: 20062952]. [PubMed Central ID: PMC5763940]. https://doi.org/10.1100/tsw.2010.11.

  • 31.

    Serrao R, Zirwas M, English JC. Palmar erythema. Am J Clin Dermatol. 2007;8(6):347-56. [PubMed ID: 18039017]. https://doi.org/10.2165/00128071-200708060-00004.

  • 32.

    Erkek E, Karaduman A, Bukulmez G, Senturk N, Ozkaya O. An unusual form of generalized granuloma annulare in a patient with insulin-dependent diabetes mellitus. Acta Derm Venereol. 2001;81(1):48-50. [PubMed ID: 11411916]. https://doi.org/10.1080/00015550121061.

  • 33.

    Ben Mously R, el Euch D, Chakroun R, Mokni M, Cherif F, Azaiz MI, et al. [Granuloma annulare: Apropos of 18 cases]. Tunis Med. 2003;81(7):495-8. French. [PubMed ID: 14534961].

  • 34.

    Seyhan M, Ozcan H, Sahin I, Bayram N, Karincaoglu Y. High prevalence of glucose metabolism disturbance in patients with lichen planus. Diabetes Res Clin Pract. 2007;77(2):198-202. [PubMed ID: 17275122]. https://doi.org/10.1016/j.diabres.2006.12.016.

  • 35.

    Kokten N, Uzun L, Karadag AS, Zenginkinet T, Kalcioglu MT. Grinspan's syndrome: A rare case with malignant transformation. Case Rep Otolaryngol. 2018;2018:9427650. [PubMed ID: 29686919]. [PubMed Central ID: PMC5857307]. https://doi.org/10.1155/2018/9427650.

  • 36.

    Dourmishev A. Vitiligo. In: Dourmishev A, editor. Disorders of the skin pigmentation. Sofia: Med. i Fizk Publ. House; 1986. p. 59-6.

  • 37.

    Humbert P, Dupond JL. The multiple autoimmune syndromes (MAS). Br J Dermatol. 1997;136(3):468-9. [PubMed ID: 9115940]. https://doi.org/10.1111/j.1365-2133.1997.tb14972.x.

  • 38.

    Kluger N, Nuutinen P, Lybeck E, Ruohoalho T, Salava A. Type 2 diabetes mellitus in a cohort of Finnish patients with hidradenitis suppurativa. J Eur Acad Dermatol Venereol. 2020;34(2):e98-e100. [PubMed ID: 31596976]. https://doi.org/10.1111/jdv.16010.

  • 39.

    Koike N, Hatori T, Imaizumi T, Harada N, Fukuda A, Takasaki K, et al. Malignant glucagonoma of the pancreas diagnoses through anemia and diabetes mellitus. J Hepatobiliary Pancreat Surg. 2003;10(1):101-5. [PubMed ID: 12918465]. https://doi.org/10.1007/s10534-002-0791-y.

  • 40.

    Inoue-Nishimoto T, Hanafusa T, Hirohata A, Kiyohara-Mabuchi E, Mizoguchi N, Matsumoto K, et al. Eruptive xanthoma with acute pancreatitis in a patient with hypertriglyceridemia and diabetes. Ann Dermatol. 2016;28(1):136-7. [PubMed ID: 26848240]. [PubMed Central ID: PMC4737826]. https://doi.org/10.5021/ad.2016.28.1.136.

  • 41.

    Baykal C, Topkarci Z, Yazganoglu KD, Azizlerli G, Baykan B. Lipoid proteinosis: A case series from Istanbul. Int J Dermatol. 2007;46(10):1011-6. [PubMed ID: 17910705]. https://doi.org/10.1111/j.1365-4632.2007.03115.x.

  • 42.

    Lokesh V, Lakshmikantha A, Kannan S. Kyrle's disease: A cutaneous manifestation of diabetes mellitus. BMJ Case Rep. 2017;2017. [PubMed ID: 29092963]. [PubMed Central ID: PMC5695492]. https://doi.org/10.1136/bcr-2017-220023.

  • 43.

    Wollina U. Eyebrow colour in diabetics. Acta Dermatovenerol Alp Pannonica Adriat. 2005;14(4):157-60. [PubMed ID: 16435045].

  • 44.

    Bustan RS, Wasim D, Yderstraede KB, Bygum A. Specific skin signs as a cutaneous marker of diabetes mellitus and the prediabetic state - a systematic review. Dan Med J. 2017;64(1). [PubMed ID: 28007053].

  • 45.

    ElFangary MM, ElNemisy NM, Sanad EM, Sorour NE. Skin manifestations in Egyptian diabetic patients: A case series study. Egypt J Dermatol Venerol. 2013;33(2). https://doi.org/10.4103/1110-6530.123941.

  • 46.

    Afroze SN, Korlepara R, Rao GV, Madala J. Mucormycosis in a diabetic patient: A case report with an insight into its pathophysiology. Contemp Clin Dent. 2017;8(4):662-6. [PubMed ID: 29326525]. [PubMed Central ID: PMC5754995]. https://doi.org/10.4103/ccd.ccd_558_17.

  • 47.

    Gentile S, Strollo F, Della Corte T, Marino G, Guarino G. Insulin related lipodystrophic lesions and hypoglycemia: Double standards? Diabetes Metab Syndr. 2018;12(5):813-8. [PubMed ID: 29703450]. https://doi.org/10.1016/j.dsx.2018.04.023.

  • 48.

    Pasmatzi E, Monastirli A, Habeos J, Georgiou S, Tsambaos D. Dipeptidyl peptidase-4 inhibitors cause bullous pemphigoid in diabetic patients: Report of two cases. Diabetes Care. 2011;34(8). e133. [PubMed ID: 21788636]. [PubMed Central ID: PMC3142019]. https://doi.org/10.2337/dc11-0804.

  • 49.

    Attaway A, Mersfelder TL, Vaishnav S, Baker JK. Bullous pemphigoid associated with dipeptidyl peptidase IV inhibitors. A case report and review of literature. J Dermatol Case Rep. 2014;8(1):24-8. [PubMed ID: 24748908]. [PubMed Central ID: PMC3989094]. https://doi.org/10.3315/jdcr.2014.1166.

  • 50.

    Yoshiji S, Murakami T, Harashima SI, Ko R, Kashima R, Yabe D, et al. Bullous pemphigoid associated with dipeptidyl peptidase-4 inhibitors: A report of five cases. J Diabetes Investig. 2018;9(2):445-7. [PubMed ID: 28520234]. [PubMed Central ID: PMC5835473]. https://doi.org/10.1111/jdi.12695.

  • 51.

    Gaudin O, Seta V, Alexandre M, Bohelay G, Aucouturier F, Mignot-Grootenboer S, et al. Gliptin accountability in mucous membrane pemphigoid induction in 24 out of 313 patients. Front Immunol. 2018;9:1030. [PubMed ID: 29881377]. [PubMed Central ID: PMC5976795]. https://doi.org/10.3389/fimmu.2018.01030.

  • 52.

    Yabe D, Nishikino R, Kaneko M, Iwasaki M, Seino Y. Short-term impacts of sodium/glucose co-transporter 2 inhibitors in Japanese clinical practice: Considerations for their appropriate use to avoid serious adverse events. Expert Opin Drug Saf. 2015;14(6):795-800. [PubMed ID: 25851664]. https://doi.org/10.1517/14740338.2015.1034105.