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Ophthalmic manifestations of endocrine disorders—endocrinology and the eye

Overview of attention for article published in Translational Pediatrics, October 2017
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Title
Ophthalmic manifestations of endocrine disorders—endocrinology and the eye
Published in
Translational Pediatrics, October 2017
DOI 10.21037/tp.2017.09.08
Pubmed ID
Authors

Michael Lause, Alisha Kamboj, Esteban Fernandez Faith

Abstract

The skin serves as a window for clinicians to understand, diagnose, and monitor endocrine disease. Dermatologic manifestations of endocrinopathies contribute significantly to an individual's health and quality of life. In this review, we outline various disorders of the hypothalamic-pituitary axis, thyroid gland, pancreas, adrenal gland, and androgen axis as well as hereditary endocrine syndromes. In acromegaly, glycosaminoglycan deposition contributes to a thickening of skin and soft tissue, which manifests as coarsening and enlargement of facial and acral structures. Stimulation of the thyrotropin receptor in hyperthyroidism results in mesenchymal tissue proliferation and consequent pretibial myxedema; other associated cutaneous features include onycholysis, and hyperhidrosis. Individuals with hypothyroidism exhibit cold, dry skin and brittle hair as well as a jaundice-like appearance due to carotene excess. The cutaneous features of diabetes mellitus (DM), mediated to a large extent by hyperglycemia and hyperinsulinemia, include necrobiosis lipoidica diabeticorum (NLD), diabetic dermopathy, and acanthosis nigricans. Pediatric patients with Cushing's syndrome almost invariably present with truncal obesity and growth retardation; disruption of collagen formation and the catabolic effects of hypercortisolism result in skin atrophy and purple abdominal striae. In patients with Addison's disease, generalized hyperpigmentation, secondary to elevated levels of melanocyte-stimulating hormone (MSH), is most prominent in sun-exposed areas. Due to hyperandrogenism, individuals with polycystic ovarian syndrome (PCOS) often exhibit hirsutism, acne vulgaris, and androgenetic alopecia. In multiple endocrine neoplasia (MEN) syndromes, specific gene mutations may lead to angiofibromas, lichen amyloidosis, and ganglioneuromas. Disruptions of immune regulation result in autoimmune polyglandular syndromes (APS) and associated clinical features including chronic mucocutaneous candidiasis, vitiligo, and alopecia areata. This paper highlights the underlying pathophysiology, dermatologic manifestations, and treatment of the aforementioned endocrine disorders.

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The data shown below were compiled from readership statistics for 262 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 <1%
Bangladesh 1 <1%
Unknown 260 99%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 37 14%
Student > Master 31 12%
Student > Postgraduate 20 8%
Other 15 6%
Student > Doctoral Student 15 6%
Other 53 20%
Unknown 91 35%
Readers by discipline Count As %
Medicine and Dentistry 92 35%
Nursing and Health Professions 21 8%
Biochemistry, Genetics and Molecular Biology 14 5%
Unspecified 8 3%
Pharmacology, Toxicology and Pharmaceutical Science 5 2%
Other 27 10%
Unknown 95 36%