International Journal of Research in Dermatology

Kumar D et al. Int J Res Dermatol. 2016 Dec;2(4):64-68

http://www.ijord.com

Evaluation of general and cutaneous manifestations of hypothyroidism: a single center experience in Odisha

Dharmendra Kumar1, Ahmad Nadeem Aslami2*


1Department of Dermatology, Venerology & Leprosy, 2Department of Community Medicine, Narayan Medical College & Hospital, Sasaram, Bihar, India

Received: 21 September 2016

Accepted: 14 October 2016

*Correspondence:

Dr. Ahmad Nadeem Aslami,

E-mail: ahmadnadeemaslami@gmail.com

Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

ABSTRACT

Background: Endocrine diseases may induce manifestation through the skin. Hypothyroidism is known to cause a wide range of general and skin manifestations. Dermatologists may commonly see skin disorders that reflect an underlying hypothyroid state. The objective of the study was to evaluate varied general and cutaneous manifestations of hypothyroidism.

Methods: A hospital based descriptive clinical study was conducted in the department of Dermatology, Venerology and Leprosy, MKCG Medical College, Berhampur, Odisha. Diagnosed cases of hypothyroidism were included as the study subjects. An informed consent was taken from each patient. Institutional ethics committee of the college approved the Study.

Results: 320 patients of hypothyroidism were evaluated. Maximum patients 115 (35.9%) were among 31-40 years of age group. Male to female ratio was 1:5.7. The percentage of hypothyroid patients who complained of constipation, fatigue, Cold intolerance, weight gain and neck swelling was 75.0%, 57.2%, 50.9%, 35.9% and 31.9% respectively. Among females, 54.5% were having irregular menses. The most common cutaneous symptom was dry course skin (75.9%), followed by diffuse hair loss (50.9%), puffy oedema (48.1%), decreased sweating (11.9%) and yellow skin (9.1%). The most observed cutaneous sign was xerosis (66.9%), followed by alteration in skin texture (55.0%). Some patients showed more than one cutaneous signs. The most common hair changes in our patients were diffuse hair loss (55.9%), followed by course scalp hair (29.4%).

Conclusions: The interaction between hypothyroidism and skin is of profound clinical importance. So, dermatologists need to be alert of the ways in which these two organ systems interact, so that early diagnosis and management of hypothyroidism may ensue.

Keywords: Cutaneous manifestations, Hypothyroidism, Xerosis, Odisha

INTRODUCTION

Thyroid disorders involve all organ systems of body and the skin is no exception. “Thyroid skin connections” are a long recognized complex problem of dermato-endocrinology. Cutaneous manifestations may be the first presenting signs or may precede thyroid disease diagnosis by many years.1

Hypothyroidism is the most common pathological hormone deficiency. Worldwide, the most common cause of hypothyroidism is iodine deficiency.2 Almost one-third of the world’s population lives in areas of iodine deficiency.3 Hypothyroidism can be caused by either inadequate circulating levels of thyroid hormone or target cell resistance of hormonal action.

Primary hypothyroidism of autoimmune etiology is the most common cause.4 In the adults, the onset of hypothyroidism is usually so insidious that the typical manifestations may take months or years to go unnoticed by individual, family and friends.5

Hypothyroidism can manifest as asymptomatic subclinical condition to overt myxoedema. Several general and cutaneous manifestations can be present. Other than these, many organ systems are also affected.6 Hypothyroidism shows many non-specific cutaneous manifestation and many individuals without a thyroid disease may exhibit them. So, these do not allow definite diagnosis without Thyroid function test.7

There is a paucity of data in Berhampur district of Odisha regarding the hypothyroidism. So, the present study was done to evaluate varied general and cutaneous manifestations of hypothyroidism.

METHODS

The study was a hospital based descriptive clinical study conducted in the department of Dermatology, Venerology and Leprosy with the collaboration of department of Endocrinology, MKCG Medical College & hospital, Behrampur, Odisha. The duration of the study was two years.

Patients diagnosed with hypothyroidism constituted the study subjects. The diagnosis of hypothyroidism was established after laboratory investigations on the basis of both clinical manifestations and laboratory reports of thyroid profile. Three hundred and twenty hypothyroid patients (TSH level >5.5 µIU/dl) were included in the study.

Exclusion criteria included all patients of thyroid ablation or thyroidectomy, co-existing infections, thyroid or other malignancies, other systemic illness like diabetes mellitus, cardiac, renal and liver failure etc., pregnancy and those already on thyroid hormone replacement therapy. Known cases of hypothyroidism who were on treatment but their serum TSH level was <5.5 µIU/dl were excluded from the study. It should also be noted that pathologies such as psoriasis, lichen, eczema, acrochordons, lentigines, and nevi evidenced and recorded at the physical examination of patients, have not been included in this work because, although they are common in daily dermatological practice, they are not related directly to hypothyroidism.

An informed consent was taken from each patient. A general physical examination, systemic examination and a detailed dermatological examination was carried out and the relevant details recorded and tabulated. Apart from routine laboratory investigations, thyroid function tests (TSH, T3 and T4) were also done by radioimmunoassay.

Institutional ethics committee of the college approved the Study. Statistical analysis of data was performed using statistical package for social sciences (SPSS Version 16) and inferences were drawn. 2-sample z-test was used to compare two sample proportions. P values were calculated for two-tailed comparisons. Asymptotic (normal approximation) confidence limits (95% CI) for the difference in proportion was also calculated.8 Data is expressed in absolute (n) and relative (%) figures.

RESULTS

Total 320 patients were analyzed for the study. The age of patients ranged from 16 to 45 years, with a mean of 33.42 (±9.31) years. Maximum patients (115; 35.9%) were among 31-40 years of age group. Among patients of hypothyroidism, 272 (85.0%) were females. Females outnumbered males significantly in each age group, with a total male to female ratio of 1:5.66 as shown in Table 1.

The general complaints in the history in our study group are depicted in Table 2. Total 240 (75.0%) patients presented with constipation while 183 (57.2%) patients complained of fatigue. Cold intolerance was present in 50.9% of patients while 35.9% perceived weight gain and 31.9% complained of neck swelling. Of the 272 hypothyroid females, 244 were menstruating. Among them, 111 (45.5%) had regular cycles and 133 (54.5%) had irregular periods. Oligomenorrhoea and menorrhagia were the most common features in the latter group.

Table 1: Age and sex distribution of hypothyroid cases (n=320).
Age Group (in years)Male (%)Female (%)Z95% CITotal (% of N)
<209 (14.8)52 (85.2)7.80.55- 0.8561 (19.1)
21-3013 (14.0)80 (86.0)9.80.57-0.8693 (29.1)
31-4013 (11.3)102 (88.7)11.70.65- 0.90115 (35.9)
>4013 (25.5)38 (74.5)4.90.29-0.6851 (15.9)
Total48 (15.0)272 (85.0)17.70.62-0.77320 (100)

*All P values are highly significant (<0.0001)

Table 3 exhibits the most common cutaneous symptom in hypothyroid patients as dry course skin, noticed by 243 (75.9%) patients, followed by diffuse hair loss, which was reported by 163 (50.9%) patients. 16.9% patients noticed hair loss in other sites like axillae, pubic and lateral eyebrows. Generalized pruritus was complained by 131 (40.9%) patients. Puffy edema as a cutaneous symptom was reported by 154 (48.1%) patients.

Decreased sweating was reported by 38 (11.9%) patients, whereas yellow skin was noticed by 29 (9.1%) patients.

Table 2: General symptoms among hypothyroid cases (n=320).
Table reproduced from source PDF page 3
Table 3: Various skin manifestations (symptoms) among hypothyroid cases (n=320).
Table reproduced from source PDF page 3

The most observed cutaneous sign was xerosis, seen in a total of 214 (66.9%) patients. This was followed by alteration in skin texture, which was seen in 176 (55.0%) patients. The least common cutaneous sign in our patients was xanthalesma palpebrum, which was noticed in 9 (2.8%) of our patients. Some patients showed more than one cutaneous signs as presented in Table 4.

Table 4: Cutaneous signs among hypothyroid cases (n=320).
Table reproduced from source PDF page 3

The most common hair changes in our patients was diffuse hair loss, seen in 179 (55.9%) patients, followed by course scalp hair, seen in 94 (29.4%) patients. Least common hair changes were madarosis, seen in only 17 (5.3%) cases. No hair changes were seen in 110 (34.4%) patients.

Figure 1: Hair changes in hypothyroid patients (n=320). | 179 (55.9%) 60.0% 50.0% 94 (29.4%) 40.0% 30.0% 17 20.0% (5.3%) 10.0% 0.0% Diffuse Coarse Madarosis hair loss hair
Figure 1: Hair changes in hypothyroid patients (n=320).

In this study, Vitiligo was seen in 40 patients while 22 patients had melasma. The other associated cutaneous diseases were also noted including Acanthosis nigrans (8), systemic sclerosis (6), discoid lupus erythematosus (5), alopecia areata (5) and psoriasis (4).

DISCUSSION

In our study group of 320 patients, the mean age of patients was 33.42 years, which corresponds with other studies.9,10 There were 272 (85.0%) females and just 48 (15.0%) males. Female preponderance may be due to increased association of autoimmune disorders including autoimmune thyroiditis in females.11,12

The most common general symptom complained by patients was constipation. Gastrointestinal system disorders are usually ignored in hypothyroidism because of certain systemic symptoms of cardiovascular, neuromuscular, and ocular disorders with thyroid dysfunctions.13 Constipation in hypothyroidism may occur due to changes in the motor activities of the digestive systems.14 Limited number of studies has found that hypothyroid patients show significant reduction in gastric emptying.15,16

57.2% of hypothyroid patients complained of fatigue in day to day activities, mostly by older patients. Many hypothyroid patients experience persistent fatigue and fatigue-related symptoms, as well as poor performance on various domains of neurocognitive functioning. A more sensitive TSH receptor (TSHR-Glu 727) increases the ability of neurons to adjust intracellular thyroid hormone levels, thereby affecting neuropsychological functioning.17-19 Among menstruating females, 54.5% had irregular periods with complaints of oligomenorrhoea as well as menorrhagea. Both hyper and hypothyroidism may result in menstrual disturbances. In hypothyroidism, polymenorrhoea is more common due to defects in hemostatis. Fertility is also reduced in hypothyroidism.

Menstrual irregularity tends to be more frequent in severe hypothyroidism in comparison to mild cases.20,21 A study done in Meerut showed oligomenorrheoa as the most common menstrual abnormality in hypothyroid female patients.22

The predominant cutaneous symptom in our patients was dry skin, followed by diffuse hair loss and puffy edema. Similar observations were made by Jabbour et al and Hueston et al., in their studies.23,24 Other cutaneous symptoms in our study were very similar to studies conducted by other authors.9-12 Generalized pruritus was complained by many patients as it is related to dry and course skin.

Classical myxoedema, formerly used as a synonym for hypothyroidism is rarely seen today.5 Although puffiness in hands, face and eyelids was complained by nearly half of our patients. This might have occurred due to increased glycosaminoglycan deposition in skin. Hyaluronic acid, a mucopolysaccharide may also be deposited. These materials are hygroscopic and they produce mucinous oedema, responsible for the mucinous features and puffy appearance with hypothyroidism.5

The dryness of hypothyroid skin may result from decreased eccrine gland secretion. The mechanism for decreased sweating is not clear although the hypothyroid glands are atrophic on histological examination. A role may also be played by periodic acid-Schiff (PAS)-positive material that can accumulate in hypothyroid patients.25

The most common cutaneous sign observed in our study was xerosis, followed by alteration in skin texture. Thyroid hormone is an important regulator of epidermal homeostasis. The skin in hypothyroids become rough and altered, sometimes covered with fine scales, notably on extensor extremities.26

Thyroid hormones also accelerate barrier formation by increasing the activity of enzymes in the cholesterol sulfate cycle. Thus, hypothyroidism may hinder the epidemiological barrier function too.27

Hypothyroidism also may affect the development of the lamellar granules (Odland bodies), which are vital in the establishment of a normal stratum corneum.28 In the upper spinous layer and stratum granulosum layer of the epidermis, lamellar bodies are secreted from keratinocytes. They form an impermeable, lipid-containing membrane that serve as a water barrier and is important for correct skin barrier function.

In this study, a variety of associated cutaneous diseases were noticed. Several studies have shown an association of hypothyroidism with these cutaneous diseases.12,29-32 Irrelevant diseases were not included in this study whose findings might be coincidental.

CONCLUSION

We conclude that the interrelationship between hypothyroidism and skin is dynamic and complex. Thus, it is critical to examine thoroughly any patient presenting with sign and symptom of hypothyroidism. Dermatologists must see skin lesions that reflect an underlying hypothyroid state. The early identification by laboratory test can lead to prompt treatment and reduce further complications.

Funding: No funding sources

Conflict of interest: None declared

Ethical approval: The study was approved by the institutional ethics committee

REFERENCES

  1. 1. Paus R. Exploring the “thyroid-skin connection”: concepts, questions, and clinical relevance. J Invest Dermatol. 2010;130:7-10.
  2. 2. Roberts CG, Ladenson PW. Hypothyroidism. Lancet. 2004;363:793-803.
  3. 3. Zimmerman MB. Iodine deficiency. Endocr Rev. 2009;30:376-408.
  4. 4. Leonhardt JM, Heymann WR. Thyroid disease and the skin. Dermatol Clin. 2002;20:473-81.
  5. 5. Brent GA, Larsen PR, Davies TF. Hypothyroidism and Thyroiditis. In: Kronenberg HM, Melmed S, Polonsky KS, Larsen, eds. Williams Textbook of Endocrinology. 11th ed. Philadelphia: Pa: Saunders Elsevier; 2008: 333-376.
  6. 6. Felz MW, Forren AC. Profound hypothyroidism-a clinical review with eight recent cases: is it right before eyes? South Med J. 2004;97:491.
  7. 7. Burman KD, McKinley-Grant L. Dermatological aspects of thyroid disease. Clin Dermatol. 2006;24:247-55.
  8. 8. Newcombe RG. “Two sided confidence intervals for the single proportion: comparison for seven methods”. Statistics in Medicine. 1998;17:857-72.
  9. 9. Khurram IM, Choudhry KS, Muhammad K, Islam N. Clinical presentation of hypothyroidism: a case control analysis. J Ayub Med Coll Abbottabad. 2003;15:45-9.
  10. 10. Dogra A, Dua A, Singh P. Throid and skin. Indian J Dermatol. 2006:51:96-9.
  11. 11. Indra R, Patil SS, Joshi R, Pai M, Kalantri SP. Accuracy of physical examination in the diagnosis of hypothyroidism: Across-sectional, double-blind study. J Postgrad Med. 2004;50:7-11.
  12. 12. Keen MA, Hassan I, Bhat MH. A clinical study of the cutaneous manifestations of hypothyroidism in Kashmir valley. Indian J Dermatol. 2013;58:326.
  13. 13. Wegener M, Wedmann B, Langhoff T, Schaffstein J, Adamek R. Effect of hyperthyroidism on the transit of a caloric solid-liquid meal through the stomach, the small intestine, and the colon in man. J Clin Endocrinol Metab. 1992;75:745-9.
  14. 14. Lu CL, Montgomery P, Zou X, Orr WC, Chen JD. Gastric myoelectric activity in patients with cervical spinal cord injury. Am J Gastroenterol. 1998;93:2391-6.
  15. 15. Gunsar F, Yilmaz S, Bor S, Kumanlioglu, Cetinkalp S, Kabalak T, et al. Effect of hypo- and hyperthyroidism on gastric myoelectric activity. Dig Dis Sci. 2003;48:706-12.
  16. 16. Kahraman H, Kaya N, Demircali A, Bernay I, Tanyeri F. Gastric emptying time in patients with primary hypothyroidism. Eur J Gastroenterol Hepatol. 1997;9:901-4.
  17. 17. Saravan P, Chau WF, Roberts N, Vedhara K, Greenwood R, Dayan CM. Psychological well-being in patients on ‘adequate’ doses of L-Thyroxine: results of a large, controlled community-based questionnaire study. Clin Endocrinol. 2002;57:577-85.
  18. 18. Wekking EM, Appelhof BC, Fliers E, Schene AH, Huyser J, Tijssen JG, et al. Cognitive functioning and well being in euthyroid patients on thyroxine replacement therapy for primary hypothyroidism. Eur J Endocrinol. 2005;153:747-53.
  19. 19. Louwerens M, Appelhof BC, Verloop H, Peeters RP, Visser TJ, Boelen, A et al. Fatigue and fatigue-related symptoms in patients treated for different causes of hypothyroidism. Eur J Endocrinol. 2012;167:809-15.
  20. 20. Koutras DA. Disturbances of menstruation in thyroid disease. ANN NY Acad Sci. 1997;816:280-4.
  21. 21. Krassas GE, Pontikides N, Kaltsas T, Papadopoulou P, Paunkovic J, Paunkovic N, et al. Disturbances of menstruation in hypothyroidism. Clin Endocrinol. 1999;50:655-9.
  22. 22. Saran S, Gupta BS, Philip R, Singh KS, Bende SA, Agroiya P, et al. Effect of hypothyroidism on female reproductive hormones. Indian J Endocrinol Metab. 2016;20:108-13.
  23. 23. Jabbour SA, Miller JL. Review article: Endocrinopathies and the skin. Int J Dermatol. 2000;39:88-99.
  24. 24. Hueston WJ. Treatment of hypothyroidism. Am Fam Physician. 2001;64:1717-24.
  25. 25. Safer JD. Thyroid hormone action on skin. Dermatoendocrinol. 2011;3:211-5.
  26. 26. Heyman WR. Cutaneous manifestations of thyroid disease. J Am Acad Dermatol. 1992;26:885-902.
  27. 27. Hanley K, Jiang Y, Katagiri C, Feingold KR, Williams ML. Epidermal steroid sulfatase and cholesterol sulfotransferase are regulated during late gestation in the fetal rat. J Invest Dermatol. 1997;108:871-5.
  28. 28. Hanley K, Devaskar UP, Hicks SJ, Jiang Y, Crumrine D, Elias PM, et al. Hypothyroidism delays fetal stratum corneum development in mice. Pediatr Res. 1997;42:610-4.
  29. 29. Sedighe M, Gholamhossein G. Thyroid dysfunction and thyroid antibodies in Iranian patients with vitiligo. Indian J Dermatol. 2008;53:9-11.
  30. 30. Gopal KV, Rama Rao GR, Kumar YH, Appa Rao MV, Vasudev P, Srikant. Vitiligo: A part of a systemic autoimmune process. Indian J Dermatol Venerol Leprol. 2007;73:162-5.
  31. 31. Kuroki R, Sadamoto Y, Imamura M, Abe Y, Higuchi K, Kato K, et al. Acanthosis nigricans with severe obesity, insulin resistance and hypothyroidism: Improvement by diet control. Dermatology. 1999;198:164-6.
  32. 32. Thomas EA, Kadyan RS. Alopecia areata and autoimmunity: A clinical study. Indian J Dermatol. 2008;53:70-4.