Background: Autoimmune thyroid disorders frequently present with a wide range of dermatological manifestations. Identifying these cutaneous features may assist in early detection and better clinical management. This study assessed the prevalence and pattern of skin findings among patients with autoimmune thyroid dysfunction. Methods: A cross-sectional study was conducted among 50 patients diagnosed with autoimmune thyroid disorder. Demographic details, thyroid status, and anti-TPO antibody levels were documented. Each participant underwent a detailed dermatological examination. Findings were summarized using descriptive statistics, and the prevalence of skin changes was compared between hypothyroid and hyperthyroid groups. Results: Women constituted the majority of participants (84%), and the mean age was 38.6 ± 9.4 years. Hypothyroidism was observed in 76%, while 24% had hyperthyroidism. Elevated anti-TPO antibody levels were detected in 88%, confirming autoimmune etiology. Dermatological manifestations were common, with dry skin (62%) being the most frequent presentation, followed by hair changes (48%), urticaria (20%), and hyperpigmentation (18%). Less frequent findings included pruritus (14%), vitiligo (10%), alopecia areata (8%), and nail changes (6%). In total, 84% of participants exhibited at least one dermatological abnormality. Skin changes were slightly more prevalent in hypothyroid individuals (86.8%) compared with hyperthyroid patients (75%). Conclusion: Cutaneous manifestations were highly prevalent among patients with autoimmune thyroid disorder, with xerosis, hair abnormalities, and urticaria forming the predominant pattern. These findings highlight the importance of routine dermatological evaluation in individuals with suspected or confirmed thyroid dysfunction to facilitate timely diagnosis and comprehensive care.
Autoimmune thyroid disorders are among the most prevalent endocrine conditions, with a marked predominance in adult women and a well-established autoimmune basis involving Hashimoto thyroiditis and Graves disease [1]. These disorders arise from immune-mediated injury to thyroid tissue, leading to variable hormonal disturbances that influence multiple organ systems, including the skin. The skin is particularly sensitive to alterations in thyroid hormone levels because these hormones regulate epidermal turnover, follicular cycling, sweat gland activity, and melanocyte function [1,2].
Cutaneous manifestations in thyroid dysfunction span a wide clinical spectrum, ranging from xerosis and hair thinning to more specific autoimmune-associated findings such as vitiligo, urticaria, and alopecia areata [2,3]. Many of these features present early and may precede overt endocrine symptoms, making them valuable diagnostic clues for underlying thyroid disease [1,4]. Their recognition is especially important in routine outpatient practice, where subtle dermatological signs may be overlooked.
Despite their diagnostic relevance, dermatological features of autoimmune thyroid disorders often remain under-recognized. Population-based studies and clinical reports emphasize the need for heightened awareness of these manifestations to support earlier detection and comprehensive evaluation [3,5]. Understanding their frequency and pattern in local settings can also help refine screening strategies.
The present cross-sectional study aims to document the prevalence and spectrum of dermatological manifestations among patients with autoimmune thyroid disorders. By identifying the cutaneous profile of this population, the study highlights the importance of integrating dermatological assessment into routine thyroid disorder evaluation.
Study Design and Setting
This research was designed as a hospital-based cross-sectional study and was conducted in the Department of Dermatology, Government Medical College (GMC), Pulivendula. The study period extended from January 2024 to May 2024.
Study Population
A total of 50 patients diagnosed with autoimmune thyroid disorder were enrolled using consecutive sampling. Individuals aged 18 years and above, attending the dermatology or medicine outpatient clinics, and having confirmed autoimmune thyroid dysfunction based on thyroid function tests and anti-TPO antibody levels were eligible for inclusion.
Inclusion Criteria
Patients with newly diagnosed or known autoimmune thyroid disorder
Age ≥ 18 years
Elevated anti-TPO antibody levels supporting autoimmune etiology
Willingness to participate and provide written informed consent
Exclusion Criteria
Non-autoimmune thyroid disease
Chronic systemic illnesses (e.g., renal failure, chronic liver disease)
Pregnancy or lactation
Current use of medications known to produce dermatological side effects
Patients unwilling to undergo dermatological examination
Data Collection
A structured proforma was used to record demographic details, clinical history, thyroid status (hypothyroidism or hyperthyroidism), and laboratory markers. Each patient underwent a detailed dermatological examination under natural daylight conditions. Skin, hair, and nail findings were documented carefully, ensuring consistency across participants.
Laboratory Parameters
Thyroid function tests (TSH, T3, T4) and anti-TPO antibody levels were obtained from the hospital laboratory as part of routine evaluation.
Statistical Analysis
Data were entered and compiled using standard spreadsheet software. Descriptive statistics, including frequencies, percentages, and mean values, were used to summarize the findings. No inferential tests were performed due to the limited sample size.
Approval for the study was obtained from the concerned authorities before starting study. Written informed consent was collected from all participants before enrollment
A total of 50 individuals with autoimmune thyroid disorder were included in the analysis. The demographic pattern showed a clear female predominance, with 84% women and 16% men, and the mean age was 38.6 ± 9.4 years (Table 1). More than half of the participants were between 30 and 45 years of age.
| Variable | Category | n (%) |
| Gender | Female | 42 (84%) |
| Male | 8 (16%) | |
| Age (years) | Mean ± SD | 38.6 ± 9.4 |
| Age Group | < 30 years | 8 (16%) |
| 30–45 years | 28 (56%) | |
| > 45 years | 14 (28%) |
Regarding thyroid status, hypothyroidism emerged as the most frequent presentation, affecting 76% of the cohort, while 24% had hyperthyroidism. Anti-TPO antibodies were elevated in 44 patients (88%), confirming autoimmune involvement in the majority (Table 2).
| Variable | Category | n (%) |
| Thyroid Disorder Type | Hypothyroidism | 38 (76%) |
| Hyperthyroidism | 12 (24%) | |
| Anti-TPO Antibody | Elevated | 44 (88%) |
| Normal/Low | 6 (12%) |
Figure 1: Thyroid Status and Autoimmune Markers
Dermatological abnormalities were widespread in the study population. Dry skin was the leading manifestation, documented in 62%, followed by hair changes in 48%, and urticaria in 20% of participants. Other findings such as hyperpigmentation, pruritus, vitiligo, alopecia areata, and nail changes appeared with lower frequency (Table 3).
| Dermatological Finding | n | % |
| Dry skin (Xerosis) | 31 | 62% |
| Hair changes (thinning/brittle) | 24 | 48% |
| Urticaria | 10 | 20% |
| Hyperpigmentation | 9 | 18% |
| Pruritus | 7 | 14% |
| Vitiligo | 5 | 10% |
| Alopecia areata | 4 | 8% |
| Nail changes | 3 | 6% |
Overall, 84% of the patients demonstrated at least one cutaneous feature linked to autoimmune thyroid dysfunction. The burden of skin involvement was slightly higher among individuals with hypothyroidism (86.8%) compared with those who were hyperthyroid (75%), as summarized in Table 4.
| Thyroid Status | Total Patients | With Skin Findings (n) | With Skin Findings (%) |
| Hypothyroidism | 38 | 33 | 86.8% |
| Hyperthyroidism | 12 | 9 | 75.0% |
| Overall | 50 | 42 | 84% |
The present study demonstrates that dermatological manifestations are remarkably common among individuals with autoimmune thyroid disorders, a finding that echoes longstanding observations linking thyroid dysfunction with a broad spectrum of cutaneous changes [6,7]. In our cohort, 84% of patients exhibited at least one skin, hair, or nail abnormality, underscoring the central role of thyroid hormones in maintaining epidermal turnover, hair cycling, and sweat gland activity, as highlighted in earlier dermatologic and endocrine reviews [6,11].
Xerosis was the most frequent finding, noted in 62% of participants, consistent with descriptions of diminished eccrine gland activity and slowed epidermal renewal in hypothyroid states [7,11]. Hair abnormalities were also common, occurring in nearly half of the study population. This mirrors previous reports noting that disruptions in thyroid hormone signaling can shift follicles toward telogen and impair keratin synthesis, resulting in diffuse thinning and brittle texture [6,8].
Autoimmune-associated manifestations such as vitiligo and alopecia areata appeared in a smaller yet important subset of patients. Their presence aligns with evidence that autoimmune thyroid disease frequently coexists with other organ-specific autoimmune conditions due to shared immunological pathways [8,9]. The occurrence of urticaria in 20% of cases also supports earlier findings linking chronic urticaria with thyroid-related autoantibodies and autoimmune activation [12].
Dermatological involvement was slightly higher in hypothyroid individuals than in those with hyperthyroidism, a pattern also observed in comparative analyses evaluating autoimmune and non-autoimmune thyroid cohorts [10]. This trend is clinically relevant because hypothyroidism often develops subtly, and early cutaneous clues may prompt expedited endocrine evaluation, particularly in settings where laboratory testing may be delayed.
Although limited by a modest sample size and single-center design, the findings of this study closely parallel established literature and reaffirm the importance of incorporating dermatological assessment into routine thyroid disorder evaluation. Early recognition of cutaneous manifestations not only supports timely diagnosis but also enhances comprehensive patient management.
This study highlights the strong association between autoimmune thyroid disorders and a broad range of dermatological manifestations. A striking 84% of patients exhibited at least one cutaneous change, with xerosis, hair abnormalities, urticaria, and hyperpigmentation appearing most frequently. Autoimmune-related findings such as vitiligo and alopecia areata were also documented, reflecting the shared immunological pathways between these conditions. Skin involvement was slightly higher in hypothyroid individuals, suggesting that cutaneous clues may help in early recognition of thyroid dysfunction. Routine dermatological evaluation should therefore be an integral component of clinical assessment, enabling timely diagnosis and more comprehensive management of autoimmune thyroid disease.