Medscape is available in 5 Language Editions – Choose your Edition here.



  • Author: Robert A Schwartz, MD, MPH; Chief Editor: Dirk M Elston, MD  more...
Updated: Jun 07, 2016


Carotenemia is a clinical condition characterized by yellow pigmentation of the skin (xanthoderma) and increased beta-carotene levels in the blood. In most cases, the condition follows prolonged and excessive consumption of carotene-rich foods, such as carrots, squash, and sweet potatoes. Carotenemia is a common finding in children. The condition of carotenemia is harmless, but it can lead to a mistaken diagnosis of jaundice. (See the image below.)

Carotenoderma visible on nasolabial folds of young Carotenoderma visible on nasolabial folds of young child.

Carotene is a lipochrome that normally adds yellow color to the skin. With elevated blood levels of carotene, the prominence of this yellowing is increased. Carotenemia may be particularly evident when the stratum corneum is thickened or when the subcutaneous fat is strongly represented. The condition is more easily appreciated in light-complexioned people, and may present chiefly as yellowing of the palms and the soles in more darkly pigmented individuals.

Carotinemia was originally noted as xanthosis diabetica in 1904 by von Noorden, who observed it to be prominent in the nasolabial folds and on the palms and soles.[1]


Diet-induced carotenemia is observed most frequently in infants and young children. Mothers may induce the condition by giving their infants large amounts of carrots in commercial infant food preparations.[2]

In addition, vegetarians are more likely to develop carotenemia than nonvegetarians. The condition may also be associated with the ingestion of carotene-rich nutritional supplements.[3]

Diseases, including hypothyroidism,[4] diabetes mellitus,[5] hepatic disorders, anorexia nervosa, and renal diseases, may also give rise to carotenemia.[6]



Carotenoids are pigments of plant origin and are responsible for the yellow and orange color of fruits and vegetables. Carotenoids act as antioxidants, affect cell growth regulation, and modulate gene expression and immune response. Animals are incapable of synthesizing carotenoids. Carotenoids are among the nutrients most commonly linked with prenatal and neonatal health; avocados are high in carotenoids.[7]

Carotenes are the hydrocarbon component of carotenoids. Carotene derived from plant foods is the primary source of dietary vitamin A (retinol). Ingested carotenes, enclosed as crystals or amorphous solids within vegetable cells, are converted to vitamin A in the mucosal cells of the small intestine.

Approximately 10% of ingested carotene is absorbed unchanged and is carried directly to the liver by portal circulation. Factors influencing the absorption of carotene include the fiber content of the plant and the particulate size of the food. Pancreatic lipase, bile acids, fat, and, possibly, thyroid hormone aid in the absorption of carotene.

Cooking, pureeing, or mashing fruits and vegetables ruptures cell membranes, thereby increasing the bioavailability of carotene for absorption. Consumption of mashed or pureed food, which is common in infants, may account for an increased incidence of diet-induced carotenemia.

Carotene is excreted through the colon and epidermis. In the latter area, the horny layer of skin reabsorbs carotene if excretion is unusually heavy. In fact, carotenoids accumulate in the epidermis about 2 weeks after serum levels achieve equilibrium, and maximum accumulation occurs in areas with an abundance of sweat glands, such as the nasolabial folds, palms, and soles.

Carotene does not readily cross the placenta but is found in high concentrations in human milk. Consequently, infants who are breastfeeding have higher serum levels of carotene than do infants fed with formula.

Excessive ingestion of carotenoids is nontoxic. Although in dietary carotenemia, elevated serum carotene often is accompanied by a corresponding elevation in serum vitamin A levels, hypervitaminosis A is not observed, presumably because the conversion of carotenoids to vitamin A is regulated. In other causes of carotenemia, serum vitamin A levels are within reference ranges or low.

Intestinal disease and infections may impair the absorption of carotene. Ingestion of mineral oil also decreases absorption, whereas water dispersion agents enhance absorption. The conversion of beta-carotene (provitamin A) to vitamin A is accelerated by thyroxine and hyperthyroidism.



Dietary sources

The health benefits of foods that contain retinoids may encourage their excessive intake, whether for the foods’ antioxidant vitamins[8] or to stimulate T cells.[9, 10] (The consumption of fresh fruits and vegetables, such as carrots, may be beneficial to patients with psoriasis and porphyria because of their high content of carotenoids.[11] )[12]

Carotenes occur in all pigmented fruits and vegetables, being synthesized as they ripen. In green vegetables, the color of carotene is often masked by the green color of chlorophyll. As a rule of thumb, the deeper the green or yellow of a fruit or vegetable, the more carotene it contains. Although often overlooked by parents, most strained baby foods on the market contain carrots. Ingestion of nutrient supplements is another source of carotenemia.

Human and cow milk also contain carotene. The occasional yellow color of milk is due to carotene content, and human milk provides a rich source of carotene, especially if maternal serum carotene levels are high. (The yellow color of colostrum is caused by carotene content.)

Diseases-related sources

Diabetes mellitus

Many individuals with diabetes have elevated serum carotene levels, but only 10% of these individuals exhibit yellowing of the skin. Carotenemia may be related to restricted dietary habits, hyperlipidemia, or a deficiency in the conversion of carotene into vitamin A by the liver.


The commonly accepted cause of carotenemia in hypothyroidism is a decrease in the conversion of carotene into vitamin A, as well as associated hyperlipidemia and hypercholesterolemia.

Thyroid hormone is antagonistic to vitamin A and controls its rate of consumption. In hypothyroidism, the consumption of vitamin A is decelerated, and the rate of conversion from carotene to vitamin A is reduced.

Anorexia nervosa

The association between carotenemia and anorexia nervosa is well documented. Carotenemia in patients with this disease is not thought to be associated with a high-carotene diet. It may instead be related to hypercholesterolemia, which is an occasional, albeit reversible, defect in the conversion of carotene to vitamin A, or it may result from a normal intake of dietary carotene in the presence of a decreased requirement.

Systemic amyloidosis

Systemic lambda-type AL amyloidosis may be associated with hyper–β-carotenemia with a prominent carotenoderma facilitating recognition of the diagnosis.[13]


Disorders associated with the development of carotenemia also include the following:

  • Liver disease - Primary hepatic injury may prevent the conversion of carotene to vitamin A
  • Kidney disease - Serum carotene levels may be markedly elevated in patients with chronic glomerulonephritis and nephrotic syndrome
  • Inborn errors of metabolism - Carotenemia may result from a failure to convert carotene into vitamin A due to an inborn error of metabolism
  • Familial conditions


A low-carotene diet leads to progressive disappearance of the yellow skin discoloration. Because of the lipophilic nature of carotenoids, however, sufficient amounts can remain in tissue for several months, causing yellow skin even after serum carotene levels return to normal.

Carotenemia is a benign condition. Complications are rare with diet-induced carotenemia; Vitamin A poisoning does not occur even with massive doses of carotene, because the conversion of carotene to vitamin A takes place slowly. (However, a man who had allegedly ingested 6-7 pounds of carrots per week was observed with constipation, hypercarotenemia, elevated liver enzyme levels, and possible vitamin A toxicity.[14] )

A correlation between metabolic carotenemia and biliary dyskinesia has been suggested. In patients with metabolic carotenemia, significant relationships were identified between the gall bladder contraction rate and the levels of serum carotene, vitamin A, and lipids.

Amenorrhea may be associated with carotenemia. This occurs in patients who consume a pure or predominantly vegetarian diet without red meat. Dietary modifications can reduce carotene levels, which, in turn, normalize the menstrual cycle.


Patient History

A history of excessive carotene intake consistent with the diagnosis of hypercarotenemia is usually present.

Metabolic carotenemia without a history of excessive carotene intake may be due to a genetic defect in the metabolism of carotenoids.

As previously mentioned, amenorrhea may be associated with carotenemia. This occurs in patients who consume a pure or predominantly vegetarian diet without red meat. Dietary modifications can reduce carotene levels, which, in turn, normalize the menstrual cycle.

Patients may present with symptoms—such as pruritus, fatigue, abdominal pain, and weight loss—specific to one of the rare causes of carotenemia.


Physical Examination

Carotenemia is characterized by a yellow pigmentation of the skin that is more pronounced under artificial light.

Because carotene is excreted by sebaceous glands and is present in sweat, the yellow pigmentation is particularly noticeable in areas where sweating is marked.

Yellow pigmentation often appears first on the tip of the nose, palms, soles, and nasolabial folds, extending gradually over the entire body. However, the yellow pigmentation is most prominently displayed on the palms, soles, and nasolabial folds. The pigmentary change results from deposition of carotene in the fat-soluble stratum corneum.

The sclerae are always spared, which readily distinguishes carotenemia from jaundice; however, carotenemia occasionally may present with coloration of the palate. Note that the conjunctivae and oral mucosa are areas lacking stratum corneum.

Children who present with rare causes of carotenemia that are not related to diet may have physical signs specific to that disease process.


Differential Diagnosis

Differential diagnosis in carotenemia includes the following:

  • Excess ingestion or percutaneous absorption of chemicals - Eg, quinacrine, mepacrine, dinitrophenol, saffron, tetryl, picric acid, canthaxanthin
  • Sorafenib - Yellow skin discoloration can be associated with use of the oral, multitargeted tyrosine kinase inhibitor sorafenib for treatment of metastatic renal cell carcinoma [15]
  • Lycopenemia - Appears as an orange-yellow skin discoloration resulting from the ingestion of large amounts of tomatoes or other fruits containing lycopene
  • Type III hyperlipoproteinemia - A rare form of dyslipidemia, this condition was described with lycopenemia; it includes orange discoloration of xanthomas following serum lycopene elevation unassociated with excessive dietary intake [16]
  • Riboflavinemia
  • Diabetes mellitus
  • Hypothyroidism
  • Anorexia nervosa
  • Liver disease
  • Kidney disease
  • Inborn errors of metabolism
  • Familial conditions - May be associated with carotenemia


Laboratory studies

Laboratory studies are not generally indicated in the evaluation of diet-induced carotenemia. If studies are made, carotenemia can be verified by a high serum beta-carotene level, normal liver function test results, and a normal or slightly elevated vitamin A level. (The serum beta-carotene level can be increased 3-4 times the normal value and still be associated with a normal or only slightly elevated vitamin A level.) Accumulation of beta-carotene in the skin is delayed by up to 2 weeks, in contrast to the serum.

Elevated serum carotene levels range between 250-500 µg/dL. Multiple authors have reported wide variations in reference range values of serum carotene, making the interpretation of such values difficult.

Measuring carotene levels in skin may be facilitated by use of Resonance Raman spectroscopy and reflection spectroscopy, both noninvasive optical quantitative methods for the measurement of carotenoid antioxidant levels in human skin in vivo. Skin carotenoid status may be a good way to predict plasma carotenoid status.[17, 18]

Histologic findings

A skin biopsy specimen may show autofluorescence in the superficial horny layer and a pemphiguslike pattern of intracellular autofluorescence.


Dietary Treatment

Reassure parents of pediatric patients that diet-induced carotenemia is a benign condition that requires no treatment. If extreme parental anxiety is present, physicians can inform parents which foods are rich in carotene, and the child can be placed on a carotene-deficient diet.

With elimination of the intake of carotene-rich foods, serum carotene levels drop sharply within a week and the yellow discoloration of the skin gradually disappears over several weeks to months. Medications are not indicated for the treatment of diet-induced carotenemia.

Inform parents that many green vegetables, such as spinach and green beans, are rich in carotene.[6]

Other causes of carotenemia are extremely rare in children. When suspected, direct appropriate investigation and treatment toward the underlying etiology.

Contributor Information and Disclosures

Robert A Schwartz, MD, MPH Professor and Head of Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, Rutgers New Jersey Medical School; Visiting Professor, Rutgers University School of Public Affairs and Administration

Robert A Schwartz, MD, MPH is a member of the following medical societies: Alpha Omega Alpha, New York Academy of Medicine, American Academy of Dermatology, American College of Physicians, Sigma Xi

Disclosure: Nothing to disclose.


Jack Grzybowski, MD Staff Physician, Department of Pediatrics, University of Medicine and Dentistry of New Jersey-New Jersey Medical School

Jack Grzybowski, MD is a member of the following medical societies: Sigma Xi

Disclosure: Nothing to disclose.

Chief Editor

Dirk M Elston, MD Professor and Chairman, Department of Dermatology and Dermatologic Surgery, Medical University of South Carolina College of Medicine

Dirk M Elston, MD is a member of the following medical societies: American Academy of Dermatology

Disclosure: Nothing to disclose.


Jatinder Bhatia, MBBS Professor of Pediatrics, Chief, Section of Neonatology, Department of Pediatrics, Medical College of Georgia

Jatinder Bhatia, MBBS is a member of the following medical societies: American Academy of Pediatrics, American Association for the Advancement of Science, American Dietetic Association, American Pediatric Society, American Society for Clinical Nutrition, American Society for Parenteral and Enteral Nutrition, Society for Pediatric Research, and Southern Society for Pediatric Research

Disclosure: Nothing to disclose.

David F Butler, MD Professor of Dermatology, Texas A&M University College of Medicine; Chair, Department of Dermatology, Director, Dermatology Residency Training Program, Scott and White Clinic, Northside Clinic

David F Butler, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American Medical Association, American Society for Dermatologic Surgery, American Society for MOHS Surgery, Association of Military Dermatologists, and Phi Beta Kappa

Disclosure: Nothing to disclose.

Mary Farley, MD Dermatologic Surgeon/Mohs Surgeon, Anne Arundel Surgery Center

Disclosure: Nothing to disclose.

Maria Rebello Mascarenhas, MBBS Associate Professor of Pediatrics, University of Pennsylvania School of Medicine; Section Chief of Nutrition, Division of Gastroenterology and Nutrition, Director, Nutrition Support Service, Children's Hospital of Philadelphia

Maria Rebello Mascarenhas, MBBS is a member of the following medical societies: American Gastroenterological Association, American Society for Parenteral and Enteral Nutrition, and North American Society for Pediatric Gastroenterology and Nutrition

Disclosure: Nothing to disclose.

Raymond D Pitetti, MD, MPH Associate Professor, Department of Pediatrics, Division of Pediatric Emergency Medicine, University of Pittsburgh School of Medicine; Associate Division Chief, Division of Pediatric Emergency Medicine; Associate Medical Director, Emergency Department; Medical Director, Sedation Services; Medical Director, Express Care; Medical Director, Patient Safety; Consulting Staff, University of Pittsburgh Physicians

Raymond D Pitetti, MD, MPH is a member of the following medical societies: Allegheny County Medical Society, American Academy of Pediatrics, Pennsylvania Medical Society, and Society for Pediatric Research

Disclosure: Nothing to disclose.

Maureen B Poh-Fitzpatrick, MD Professor Emerita of Dermatology and Special Lecturer, Columbia University College of Physicians and Surgeons; Professor of Medicine (Dermatology), University of Tennessee Health Science Center College of Medicine

Maureen B Poh-Fitzpatrick, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, and New York Academy of Medicine

Disclosure: Clinuvel Pharmaceuticals, Ltd. Honoraria Consulting

ary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

  1. Julka S, Jamdagni N, Verma S, Goyal R. Yellow palms and soles: A rare skin manifestation in diabetes mellitus. Indian J Endocrinol Metab. 2013 Oct. 17:S299-300. [Medline]. [Full Text].

  2. Karthik SV, Campbell-Davidson D, Isherwood D. Carotenemia in infancy and its association with prevalent feeding practices. Pediatr Dermatol. 2006 Nov-Dec. 23(6):571-3. [Medline].

  3. Takita Y, Ichimiya M, Hamamoto Y, Muto M. A case of carotenemia associated with ingestion of nutrient supplements. J Dermatol. 2006 Feb. 33(2):132-4. [Medline].

  4. Aktuna D, Buchinger W, Langsteger W, Meister E, Sternad H, Lorenz O, et al. [Beta-carotene, vitamin A and carrier proteins in thyroid diseases]. Acta Med Austriaca. 1993. 20(1-2):17-20. [Medline].

  5. Stawiski MA, Voorhees JJ. Cutaneous signs of diabetes mellitus. Cutis. 1976 Sep. 18(3):415-21. [Medline].

  6. Sale TA, Stratman E. Carotenemia associated with green bean ingestion. Pediatr Dermatol. 2004 Nov-Dec. 21(6):657-9. [Medline].

  7. Comerford KB, Ayoob KT, Murray RD, Atkinson SA. The Role of Avocados in Maternal Diets during the Periconceptional Period, Pregnancy, and Lactation. Nutrients. 2016 May 21. 8 (5):[Medline].

  8. Nunez-Cordoba JM, Martínez-Gonzalez MA. Antioxidant Vitamins and Cardiovascular Disease. Curr Top Med Chem. 2011 Apr 21. [Medline].

  9. Darvin ME, Fluhr JW, Meinke MC, Zastrow L, Sterry W, Lademann J. Topical beta-carotene protects against infra-red-light-induced free radicals. Exp Dermatol. 2011 Feb. 20(2):125-9. [Medline].

  10. Vaishnava S, Hooper LV. Eat Your Carrots! T Cells Are RARing to Go. Immunity. 2011 Mar 25. 34(3):290-2. [Medline].

  11. Kaimal S, Thappa DM. Diet in dermatology: revisited. Indian J Dermatol Venereol Leprol. 2010 Mar-Apr. 76(2):103-15. [Medline].

  12. Jung S, Wu K, Giovannucci E, Spiegelman D, Willett WC, Smith-Warner SA. Carotenoid intake and risk of colorectal adenomas in a cohort of male health professionals. Cancer Causes Control. 2013 Feb 1. [Medline].

  13. Hulková H, Svojanovský J, Sevela K, Krusová D, Hanuš J, Vezda P, et al. Systemic AL amyloidosis with unusual cutaneous presentation unmasked by carotenoderma. Amyloid. 2014 Mar. 21(1):57-61. [Medline].

  14. Sansone RA, Sansone LA. Carrot man: A case of excessive beta-carotene ingestion. Int J Eat Disord. 2012 Mar 19. [Medline].

  15. Dasanu CA, Dutcher J, Alexandrescu DT. Yellow skin discoloration associated with sorafenib use for treatment of metastatic renal cell carcinoma. South Med J. 2007 Mar. 100(3):328-30. [Medline].

  16. Royer M, Bulai Livideanu C, Periquet B, Maybon P, Lamant L, Mazereeuw-Hautier J, et al. [Orange skin and xanthomas associated with lycopenaemia in a setting of type III dyslipoproteinemia]. Ann Dermatol Venereol. 2009 Jan. 136(1):42-5. [Medline].

  17. Nguyen LM, Scherr RE, Linnell JD, Ermakov IV, Gellermann W, Jahns L, et al. Evaluating the relationship between plasma and skin carotenoids and reported dietary intake in elementary school children to assess fruit and vegetable intake. Arch Biochem Biophys. 2015 Apr 15. 572:73-80. [Medline].

  18. Ermakov IV, Gellermann W. Optical detection methods for carotenoids in human skin. Arch Biochem Biophys. 2015 Apr 15. 572:101-11. [Medline].

Carotenoderma visible on nasolabial folds of young child.
All material on this website is protected by copyright, Copyright © 1994-2016 by WebMD LLC. This website also contains material copyrighted by 3rd parties.