*Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand, **Michigan Health Clinics, Saginaw, Michigan, USA.
ABSTRACT
Results: A total of 197 participants, mainly general practitioners, were included. The highest percentage of correct diagnoses were benign erythematous, eczematous lesions (35.5%, senile purpura; 36.0%, xerotic eczema), and malignant diseases (35.5%, basal cell carcinoma; 27.4%, squamous cell carcinoma; 11.7%, subungual melanoma; 24.4%, acral lentiginous melanoma). In contrasts, the lowest percentage of correct diagnosis were premalignant diseases (0.5%, arsenical keratosis; 4.6%, actinic keratosis; 1.0% Bowen’s disease) and benign hypopigmented lesion (0.5%, stellate pseudoscar; 7.6%, idiopathic guttate hypomelanosis). Harmful treatment with systemic antifungal therapy was used in subungual melanoma (58.0%). Harmful management of senile comedone, subungual melanoma and acral lentiginous melanoma was significantly found in physicians given the incorrect diagnosis. (p = 0.027, p <0.001, p = 0.014, respectively). Conclusion: Most physicians recognized malignant lesions, benign erythematous or eczematous diseases in elderly skin. Surprisingly, almost all physicians couldn’t diagnose premalignant lesions and benign hypopigmented lesions.
INTRODUCTION
A major global trend in population aging is rapidly occurring. By 2050, the proportion of the world’s population aged 60 years will increase from 12% to 22%.1 Thailand has also become an aging society, with 18.24% of the population aged over 60 years in 2021.2 The emergence of senile dermatosis in the aging population is expected. Elderly skin goes through changes that are both intrinsic and extrinsic. Intrinsic changes result from chronological aging, such as thinning of the epidermis, reduction in the function of sweat and apocrine glands. Extrinsic changes result from UV and other environmental pollutants.
Both changes are responsible for the susceptibility of skin conditions in the elderly.3,4
Diagnosis and management of skin conditions in the elderly are challenging due to many aspects, such as ordinary physiologic change, atypical disease presentation, and multiple comorbidities. Yet, there was no prior assessment report on the knowledge of geriatric skin conditions among Thai physicians. This knowledge gap will help identify potential improvements in understanding skin conditions in the elderly. Many studies have shown an increase in diagnostic capabilities and proper referral in general practitioners after providing educated sessions.5,6
Corresponding author: Penvadee Pattanaprichakul E-mail: penvadee.pat@gmail.com
Received 3 August 2022 Revised 30 August 2022 Accepted 7 September 2022 ORCID ID:http://orcid.org/0000-0002-3293-7813 http://dx.doi.org/10.33192/smj.v75i1.260522
All material is licensed under terms of the Creative Commons Attribution 4.0 International (CC-BY-NC-ND 4.0) license unless otherwise stated.
For these reasons, this study aims to assess the knowledge of common geriatric skin conditions in Thai physicians.
MATERIALS AND METHODS
Study design
This retrospective study was conducted at the Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand. The protocol was approved by the Siriraj Institutional Review Board (COA no. Si 456/2012). The data includes knowledge of diagnosis and management of common dermatological conditions in the elderly, as seen in Table 2. We conducted a retrospective review of physicians’ demographic data and working experiences derived from records at the annual short dermatology course for general practitioners. Which was held by the dermatological society of Thailand from 2016 to 2019.
We compiled a reviewed list of differential diagnoses and management. Management was categorized as proper, disadvantageous, and harmful. Proper management was defined as necessary, beneficial actions for patients, such as tissue biopsy in premalignant or malignant lesions. Disadvantageous management was defined as the actions which provided no benefits, had no, or only minor adverse effects on patients. Such as the use of topical steroids in premalignant or malignant lesions, which might cause some delay in tissue diagnosis. Defining harmful management encompasses actions causing severe adverse reactions or worsening skin conditions.
Statistical analysis
The PASW Statistics for Windows, version 18 (SPSS Inc., Chicago, IL, USA), was used for data analysis. Categorical data, such as the numbers of physicians who answered correctly for diagnosis or differential diagnoses and the number of each management category, were described using frequency and percentage. Evaluating the relationship between physicians’ confidence level, the number of patients with skin conditions the physicians treated per week, and harmful management used a Chi- Squared analysis or Fisher’s exact test. The difference in the proportion of harmful management between those who had correct and incorrect diagnoses were evaluated using Chi-Squared tests or Fisher’s exact test.
RESULTS
Analysis of 197 physicians’ records with complete data was conducted. Approximately half of the physicians were between 26-30 years old, and most were general practitioners (83.0%). For the working setting, 66.7% of the physicians worked at public hospitals, while 20.3% and 19.8% worked at private hospitals and clinics,
respectively. Regarding the experience in treating patients with dermatologic conditions, most physicians (67.4%) treated 0 to 10 patients per week (Table 1).
Benign erythematous, eczematous, and malignant lesions represented the highest percentage of correct diagnoses (Table 2). Among benign erythematous lesions, 36% of physicians gave a correct diagnosis for xerotic eczema, followed by 35.5% for senile purpura. Malignant lesions showed only 35.5% of physicians made accurate diagnoses for basal cell carcinoma, 27.4% for squamous cell carcinoma, and 24.4% for acral lentiginous melanoma. However, less than 10% of physicians had the correct answers in premalignant and benign hypopigmented lesions.
Harmfultreatmentwascommonlyfoundinsubungual melanoma (58%). Principally, 174 physicians who had an incorrect diagnosis of this lesion, and 93 physicians (53%) misdiagnosed the lesions as onychomycosis. Therefore, many patients with melanoma were prescribed systemic antifungal therapy (Table 2).
Physicians with more than 30 patients per week recommended harmful management when diagnosing seborrheic keratosis and actinic keratosis, as seen in Table 3, which was significantly higher compared to physicians with 11-30 patients per week (11.8, 4.8, and 0.9%, respectively, with a p-value of 0.035 in seborrheic keratosis and 16.7, 8.6, and 3.3%, respectively with a p-value of 0.048 in actinic keratosis). In contrast, there was no difference in the percentage of harmful management among physicians with different confidence levels.
Table 4 compares the proportion of harmful management in correct and incorrect diagnoses. In all diseases, physicians with incorrect diagnoses tend to prescribe damaging solutions compared to correct diagnoses. There was no statistical significance between both groups except in senile comedone, subungual melanoma, and acral lentiginous melanoma.
DISCUSSION
This study shows that Thai general practitioners rarely recognize common skin conditions in the elderly. Additionally, premalignant skin lesions and benign hypopigmented lesions were the most common uncorrected diagnosis. The largest proportion of physicians recommended systemic antifungal therapy for subungual melanoma. For Thai general practitioners, these findings will improve their knowledge in recognizing skin conditions in the elderly.
In this study, physicians rarely recognized premalignant skin lesions compared to other benign and malignant skin lesions except for hypopigmented lesions. For premalignant lesions, actinic keratosis and Bowen
TABLE 1. Demographic data.
20 – 25 years old | 27/196 (13.8%) |
26 – 30 years old | 108/196 (55.1%) |
31 – 45 years old | 61/196 (31.1%) |
Female
137/196 (69.9%)
No | 164/168 (97.6%) |
Yes | 4/168 (2.4%) |
Status of the doctors | |
General practitioner | 161/194 (83.0%) |
Specialist other than dermatologists | 22/194 (11.3%) |
Diploma or M.Sc in dermatology | 3/194 (1.5%) |
Medical student | 3/194(1.5%) |
Others | 5/194 (2.6%) |
Workplace* | |
Public hospitals | 128/192 (66.7%) |
Private hospitals | 39/192 (20.3%) |
Private clinic | 38/192 (19.8%) |
0 – 10 patients/week
11 – 30 patients/week
> 30 patients/week
126/187 (67.4%)
42187 (22.5%)
19/187 (10.1 %)
Very low confidence | 53/194 (27.3%) |
Low confidence | 101/194 (52.1%) |
Moderate confidence to High confidence | 40/194 (20.6%) |
*One subject could have more than one work place
Abbreviation: M.Sc, Master of Science
TABLE 2. Pretest answers of participants at the beginning of dermatology short course training.
Correct Diseases differential | Correct diagnosis | n | Proper | Disadvantageous | Harmful | |
diagnosis | n (%) | (%) | (%) | (%) | ||
n (%) | ||||||
Benign disease | ||||||
Hypopigmented lesion | ||||||
Stellate pseudoscar | 1 (0.5) | 1 (0.5) | 149 | 37 (24.8) | 84 (56.4) | 28 (18.8) |
Idiopathic guttate hypomelanosis | 15 (7.6) | 15 (7.6) | 131 | 32 (24.4) | 89 (67.9) | 10 (7.6) |
Erythematous/eczematous lesion | ||||||
Senile purpura | 81 (41.1) | 70 (35.5) | 143 | 121 (84.6) | 20 (14.0) | 2 (1.4) |
Xerotic eczema | 94 (47.7) | 71 (36.0) | 165 | 154 (93.3) | 8 (4.8) | 3 (1.8) |
Progressive pigmentary dermatosis | 4 (2.0) | 2 (1.0) | 130 | 59 (45.4) | 56 (43.1) | 15 (11.5) |
Lump and bump lesion (Tumor and plaque) | ||||||
Seborrheic keratosis | 51 (25.9) | 34 (17.3) | 176 | 168 (95.5) | 3 (1.7) | 5 (2.8) |
Solar lentigo | 20 (10.2) | 12 (6.1) | 141 | 56 (39.7) | 77 (54.6) | 8 (5.7) |
Senile comedone | 46 (23.4) | 41 (20.8) | 121 | 46 (38.0) | 59 (48.8) | 16 (13.2) |
Premalignant disease | ||||||
Arsenical keratosis | 3 (1.5) | 1 (0.5) | 163 | 78 (47.9) | 74 (45.4) | 11 (6.7) |
Actinic keratosis | 14 (7.1) | 9 (4.6) | 151 | 20 (13.2) | 122 (80.8) | 9 (6.0) |
Bowen’s disease | 3 (1.5) | 2 (1.0) | 137 | 36 (26.3) | 86 (62.8) | 15 (10.9) |
Malignant disease | ||||||
Basal cell carcinoma | 90 (45.7) | 70 (35.5) | 186 | 179 (96.2) | 5 (2.7) | 2 (1.1) |
Squamous cell carcinoma | 71 (36.0) | 54 (27.4) | 173 | 162 (93.6) | 9 (5.2) | 2 (1.2) |
Subungual melanoma | 30 (15.2) | 23 (11.7) | 162 | 35 (21.6) | 33 (20.4) | 94 (58.0) |
Acral lentiginous melanoma | 62 (31.5) | 48 (24.4) | 152 | 126 (82.9) | 13 (8.6) | 13 (8.6) |
disease typically present with an erythematous patch with a dry scale that sometimes resembles other skin conditions. As in this study, physicians mostly misdiagnosed premalignant lesions as psoriasis or chronic eczema. Similarly, a previous study showed general practitioners provided correct diagnosis of benign skin tumor lesions (seborrheic keratosis, melanocytic nervus) better than premalignant (actinic keratosis, nervous dysplasia).7 Most primary care physicians from selected countries provide acceptable diagnosis of basal cell carcinoma than actinic keratosis (90% VS 74%).8 Yet, both studies had significantly higher overall correct diagnoses, including premalignant skin lesions, compared to this study. This study highlights the need for educational intervention for Thai general practitioners who can’t recognize common skin lesions in the elderly. The need for intervention is
especially evident when diagnosing premalignant and benign hypopigmented lesions. Subungual melanoma is a severe subtype of acral lentiginous melanoma commonly presented with longitudinal melanonychia. The presence of Hutchinson’s sign, ulceration, and broad heterogenous band appearance suggested the diagnosis of subungual melanoma.9,10 Subungual melanoma is common among Asians and Blacks.11 Our study demonstrated a low correct diagnosis for these lesion types. Table 4 also shows that harmful management was concordant with misdiagnosis. Thus, Thai general practitioners need to recognize the alarming features for correct diagnosis to avoid delayed or harmful treatment.
Limitations of this retrospective study include collected data that may have some bias and missing data. Management was dependent on the diagnosis. Therefore,
P-value
TABLE 3. Comparison of harmful management among physicians with different level of experience according to the average numbers of dermatologic patients per week.
Diseases 0-10 patients n (%) | 11-30 patients n (%) | > 30 patients n (%) | ||
Benign disease | ||||
Hypopigmented lesion | ||||
Stellate pseudoscar | 19/88 (21.6) | 3/38 (7.9) | 4/16 (25) | 0.132 |
Idiopathic guttate hypomelanosis | 7/79 (8.9) | 2/33 (6.1) | 1/14 (7.1) | 1.000 |
Erythematous/eczematous lesion | ||||
Senile purpura | 1/88 (1.1) | 1/34 (2.9) | 0/17 (0.0) | 0.416 |
Xerotic eczema | 2/102 (2.0) | 1/37 (2.7) | 0/18 (0.0) | |
Progressive pigmentary dermatosis | 9/76 (11.8) | 4/33 (12.1) | 2/17 (11.8) | 1.000 |
Lump and bump lesion | ||||
Seborrheic keratosis | 1/110 (0.9) | 2/42 (4.8) | 2/17 (11.8) | 0.035* |
Solar lentigo | 5/90 (5.6) | 3/32 (9.4) | 0/15 (0.0) | 0.742 |
Senile comedone | 12/72 (16.7) | 2/30 (6.7) | 2/15 (13.3) | |
Premalignant | ||||
Arsenical keratosis | 7/101 (6.9) | 1/39 (2.6) | 2/17 (11.8) | 0.308 |
Actinic keratosis | 3/92 (3.3) | 3/35 (8.6) | 3/18 (16.7) | 0.048* |
Bowen’s disease | 8/81 (9.9) | 6/37 (16.2) | 1/14 (7.1) | 0.591 |
Malignant disease | ||||
Basal cell carcinoma | 2/116 (1.7) | 0/42 (0.0) | 0/19 (0.0) | 0.687 |
Squamous cell carcinoma | 1/108 (0.9) | 1/40 (2.5) | 0/18 (0.0) | 0.578 |
Subungual melanoma | 63/100 (63.0) | 19/39 (48.7) | 9/16 (56.3) | 0.294 |
Acral lentiginous melanoma | 6/94 (6.4) | 5/38 (13.2) | 2/16 (12.5) | 0.369 |
*A p-value less than 0.05 indicated statistical significance, Chi-squared test.
an incorrect diagnosis leads to inappropriate treatment. In reality, physicians should observe or refer patients to dermatologists for proper diagnosis. In conclusion, benign erythematous/eczematous diseases and malignant lesions, including xerotic eczema, basal cell carcinoma, senile purpura, squamous cell carcinoma, and acral lentiginous melanoma, were the elderly skin conditions that the physicians most recognized. In contrast, premalignant lesions and benign hypopigmented lesions couldn’t be diagnosed by almost all physicians.
REFERENCES
World Health Organization. Aging and Health [Internet]. Switzerland: World Health Organization; 2021 Oct [cited 2022 Mar 31]. Available from: https://www.who.int/news- room/fact-sheets/detail/ageing-and-health.
National Statistic Office. Demography population and housing branch [Internet]. Thailand: National Statistic Office; 2021 [cited 2022 Mar 31]. Available from: https://statbbi.nso.go.th/staticreport/ page/sector/en/01.aspx.
Jafferany M, Huynh TV, Silverman MA, Zaidi Z. Geriatric dermatoses: a clinical review of skin diseases in an aging population. Int J Dermatol. 2012;51(5):509-22.
Zalaudek I, Lallas A, Longo C, Moscarella E, Tiodorovic-Zivkovic D, Ricci C, et al. Problematic lesions in the elderly. Dermatol Clin. 2013;31(4):549-64, vii-viii.
Beecher SM, Keogh C, Healy C. Dedicated general practitioner education sessions can improve diagnostic capabilities and may
TABLE 4. Comparison of harmful management in participants given correct and incorrect diagnosis.
Harmful management Diseases in correct diagnosis n (%) | Harmful management in incorrect diagnosis n (%) | P-value | ||
Benign disease | ||||
Hypopigmented lesion | ||||
Stellate pseudoscar | 0/1 (0.0) | 28/148 (18.9) | 1.000 | |
Idiopathic guttate hypomelanosis Erythematous/eczematous lesion | 0/13 (0.0) | 10/118 (8.5) | 0.275 | |
Senile purpura | 0/62 (0.0) | 2/81 (2.5) | 0.505 | |
Xerotic eczema | 0/67 (0.0) | 3/98 (3.1) | 0.272 | |
Progressive pigmentary | dermatosis | 0/2 (0.0) | 15/128 (11.7) | 1.000 |
Lump and bump lesion (Tumor and plaque) | ||||
Seborrheic keratosis | 0/30 (0.0) | 5/146 (3.4) | 0.590 | |
Solar lentigo | 0/9 (0.0) | 8/132 (6.1) | 0.447 | |
Senile comedone | 1/36 (2.8) | 15/85 (17.6) | 0.027* | |
Premalignant disease | ||||
Arsenical keratosis | 0/1 (0.0) | 11/162 (6.8) | 1.000 | |
Actinic keratosis | 0/8 (0.0) | 9/143 (6.3) | 0.464 | |
Bowen’s disease | 0/2 (0.0) | 15/135 (11.1) | 1.000 | |
Malignant disease | ||||
Basal cell carcinoma | 0/70 (0.0) | 2/116 (1.7) | 0.528 | |
Squamous cell carcinoma | 0/54 (0.0) | 2/119 (1.7) | 1.000 | |
Subungual melanoma | 1/23 (4.3) | 93/139 (66.9) | <0.001* | |
Acral lentiginous melanoma | 0/45 (0.0) | 13/107 (12.1) | 0.014* |
*A p-value less than 0.05 indicated statistical significance, Chi-squared test.
have a positive effect on referral patterns for common skin lesions. Ir J Med Sci. 2018;187(4):959-63.
Basarab T, Munn SE, Jones RR. Diagnostic accuracy and appropriateness of general practitioner referrals to a dermatology out-patient clinic. Br J Dermatol. 1996;135(1):70-3.
Paine SL, Cockburn J, Noy SM, Marks R. Early detection of skin cancer. Knowledge, perceptions and practices of general practitioners in Victoria. Med J Aust. 1994;161(3):188-9, 92-5.
Halpern AC, Hanson LJ. Awareness of, knowledge of and attitudes to nonmelanoma skin cancer (NMSC) and actinic
keratosis (AK) among physicians. Int J Dermatol. 2004;43(9): 638-42.
Ruben BS. Pigmented lesions of the nail unit: clinical and histopathologic features. Semin Cutan Med Surg. 2010;29(3):148- 58.
Cust AE. Prognostic features for acral lentiginous melanoma. Br J Dermatol. 2018;178(2):311-2.
da Silva DLF, Toribio JM, Cintra ML, Magalhaes RF, Padoveze EH. Subungual Acral Lentiginous Melanoma of the Fifth Toe. Skin Appendage Disord. 2019;5(6):401-4.