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ULY CLINIC
ULY CLINIC
25 Septemba 2025, 01:36:42
Jellinek’s sign
Jellinek’s sign (also known as Rasin’s sign) refers to brownish pigmentation on the eyelids, typically more prominent on the upper eyelid than the lower. This cutaneous change is observed in patients with Graves’ disease, reflecting underlying autoimmune thyroid dysfunction.
Pathophysiology
Graves’ disease is an autoimmune hyperthyroidism caused by thyroid-stimulating immunoglobulins activating the thyroid gland.
Chronic thyroid hormone excess can lead to dermal melanocyte stimulation, causing localized pigmentation changes.
Eyelid skin, being thin and highly vascular, is particularly susceptible to this pigmentation.
The pigmentation may coincide with other ocular manifestations of Graves’ disease, such as exophthalmos, lid retraction, and periorbital edema.
Examination Technique
Patient positioning: Have the patient sit comfortably with eyes open and relaxed.
Inspection: Examine both upper and lower eyelids in good lighting.
Documentation: Note the distribution, intensity, and symmetry of pigmentation. Compare with surrounding facial skin.
Additional assessment: Evaluate for associated ophthalmopathy, including lid lag, retraction, and proptosis.
Clinical Features
Feature | Manifestation |
Eyelid pigmentation | Brownish discoloration, more prominent on upper eyelids |
Laterality | Usually bilateral but may be asymmetric |
Associated ocular signs | Lid retraction, lid lag, proptosis (Graves’ ophthalmopathy) |
Systemic association | Symptoms of hyperthyroidism: tachycardia, weight loss, tremors, heat intolerance |
Differential Diagnosis
Condition | Key Feature | Notes |
Graves’ disease | Brown eyelid pigmentation + hyperthyroid signs | Classic autoimmune hyperthyroidism |
Addison’s disease | Generalized hyperpigmentation | Often includes buccal mucosa and palmar creases |
Chronic sun exposure | Localized pigmentation | Usually photodistributed; no systemic symptoms |
Dermal melanocytosis | Blue-gray or slate pigmentation | Congenital or acquired; not associated with thyroid disease |
Pediatric considerations
Rare in children, as Graves’ disease is uncommon but can occur.
Pigmentation may be subtle and requires careful inspection.
Geriatric considerations
May be less noticeable due to age-related skin changes.
Consider differential diagnoses such as solar lentigines or drug-induced pigmentation.
Limitations
Pigmentation may be subtle or masked by skin tone.
Not specific for Graves’ disease; must correlate with other clinical and laboratory findings.
Patient counseling
Explain that the pigmentation reflects thyroid-related changes and is part of the autoimmune process.
Reassure that treatment of underlying hyperthyroidism may stabilize but not necessarily reverse pigmentation.
Advise regular follow-up with an endocrinologist for monitoring thyroid function and ocular health.
Conclusion
Jellinek’s sign is a clinical indicator of eyelid pigmentation often associated with Graves’ disease. It serves as a visible cue for underlying thyroid dysfunction and should prompt evaluation for systemic and ocular features of hyperthyroidism.
References
Bahn RS, et al. Hyperthyroidism and Other Causes of Thyrotoxicosis: Management Guidelines of the American Thyroid Association and American Association of Clinical Endocrinologists. Thyroid. 2011;21(6):593–646.
Wiersinga WM. Graves’ Ophthalmopathy: Pathophysiology, Natural History, and Treatment. Thyroid. 2012;22(6):615–625.
Ross DS, et al. Diagnosis and Management of Hyperthyroidism in Adults: A Clinical Review. JAMA. 2016;316(10):1047–1058.
Bahn RS. Clinical Review: Graves’ Ophthalmopathy. N Engl J Med. 2010;362:726–738.
