Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jun 8;12(7):e220410.
doi: 10.1530/EC-22-0410. Print 2023 Jul 1.

Skin manifestations in rare types of diabetes and other endocrine conditions

Affiliations
Review

Skin manifestations in rare types of diabetes and other endocrine conditions

Felix Reschke et al. Endocr Connect. .

Abstract

As the most visible and vulnerable organ of the human organism, the skin can provide an impression of its state of health. Rare forms of diabetes and endocrinopathies are often diagnosed late or primarily misinterpreted due to their rarity. Skin peculiarities associated with these rare diseases may be indicative of the underlying endocrinopathy or form of diabetes. At the same time, rare skin changes in diabetes or endocrinopathies can also be a major challenge for dermatologists, diabetologists and endocrinologists in optimal patient and therapy management. Active collaboration between these different specialist groups can therefore lead to increased patient safety, better therapeutic success and more targeted diagnostics.

Keywords: cutaneous effects of rare diabetes; rare dermatologic changes in endocrine disorders; rare endocrinopathies; rare types of diabetes.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest that could be perceived as prejudicing the impartiality of this review article.

Figures

Figure 1
Figure 1
Skin changes in diabetes mellitus.
Figure 2
Figure 2
Skin changes in childhood diabetes. Skin irritation and scratching artefacts caused by a CGM sensor.
Figure 3
Figure 3
Skin changes in childhood diabetes. Typical skin lesions of necrobiosis lipoidica in a girl suffering from type 1 diabetes and low metabolic control.
Figure 4
Figure 4
Typical skin changes of acanthosis nigricans at cervical (A), axillary (A, B) and nuchal (C) localisation in a youth with paediatric diabetes and poor metabolic control.
Figure 5
Figure 5
Typical skin changes of striae distensae and accompanying hirsutism in a teenage girl with type 2 diabetes mellitus and polycystic ovarian syndrome.
Figure 6
Figure 6
Characteristic skin lesion in a girl with Cushing's syndrome. In addition to the facial mottling with incipient acne vulgaris, there is also an accumulation of fat in the neck area.
Figure 7
Figure 7
Classic skin changes that are indicative of hyperpigmentation, for example in the context of adrenal insufficiency. The hyperpigmentation can manifest itself all over the body. Here is an example on the hands (A), the gums (B), the nipple (C) and the tongue (D).

Similar articles

Cited by

References

    1. Quatrano NA & Loechner KJ. Dermatologic manifestations of endocrine disorders. Current Opinion in Pediatrics 201224487–493. (10.1097/MOP.0b013e328355a31b) - DOI - PubMed
    1. Commission European. Rare diseases. Brussels, Belgium: European Commission, Research and Innovation, 2022. (available at: https://ec.europa.eu/info/research-and-innovation/research-area/health/r...)
    1. Filetti S. Rare endocrine disease: still a long and a winding road. Endocrine 202171535–536. (10.1007/s12020-021-02656-7) - DOI - PMC - PubMed
    1. Webb SM Kristensen J Vitali D van Klink S van Beuzekom C Santos A & Nordenström A. EndoERN patient survey on their perception of health care experience and of unmet needs for rare endocrine diseases. Endocrine 202171569–577. (10.1007/s12020-021-02625-0) - DOI - PubMed
    1. Kallali W, Messiaen C, Saïdi R, Lessim S, Viaud M, Dulon J, Nedelcu M, Samara D, Houang M, Donadille B, et al.Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseases. Orphanet Journal of Rare Diseases 202116 469. (10.1186/s13023-021-02099-3) - DOI - PMC - PubMed