From Wikipedia, the free encyclopedia
Xanthelasma
Other namesxanthelasma palpebrarum; xanthoma palpebrarum
Pronunciation
Specialty Ophthalmology  Edit this on Wikidata

Xanthelasma is a sharply demarcated yellowish deposit of cholesterol underneath the skin. [1] It usually occurs on or around the eyelids (xanthelasma palpebrarum, abbreviated XP). [1] [2] While they are neither harmful to the skin nor painful, these minor growths may be disfiguring and can be removed. [1] There is a growing body of evidence for the association between xanthelasma deposits and blood low-density lipoprotein levels and increased risk of atherosclerosis. [3] [4]

A xanthelasma may be referred to as a xanthoma when becoming larger and nodular, assuming tumorous proportions. [5] Xanthelasma is often classified simply as a subtype of xanthoma. [6]

Diagnosis

Xanthelasma in the form of XP can be diagnosed from clinical impression, although in some cases it may need to be distinguished ( differential diagnosis) from other conditions, especially necrobiotic xanthogranuloma, syringoma, palpebral sarcoidosis, sebaceous hyperplasia, Erdheim–Chester disease, lipoid proteinosis ( Urbach–Wiethe disease), and the syndrome of adult-onset asthma and periocular xanthogranuloma (AAPOX). [2] Differential diagnosis can be accomplished by surgical excision followed by microscopic examination by a pathologist ( biopsy to determine histopathology). [2] The typical clinical impression of XP is soft, yellowish papules, plaques, or nodules, symmetrically distributed on the medial side of the upper eyelids; sometimes the lower eyelids are affected as well. [2]

Treatment

Xanthelasmata can be removed with a trichloroacetic acid peel, surgery, lasers or cryotherapy. [2] Removal may cause, although uncommon, scarring and pigment changes.

Prognosis

Recurrence is common: 40% of patients with XP had recurrence after primary surgical excision, 60% after secondary excision, and 80% when all four eyelids were involved. A possible cause might be insufficiently deep excisions. [2]

Epidemiology

Xanthelasma is a rare disorder in the general population, with a variable incidence of 0.56 to 1.5% in western developed countries. The age of onset ranges from 15 to 75, with a peak in the 4th to 5th decades of life. There also seems to be a greater prevalence in females, but this might be due to higher consciousness to cosmetic defects. [7]

Etymology

The word is derived from Greek xanthós, ξανθός 'yellow' and élasma, έλασμα, 'foil'. The plural is xanthelasmata.

See also

References

  1. ^ a b c Frew JW, Murrell DF, Haber RM (October 2015). "Fifty shades of yellow: a review of the xanthodermatoses". International Journal of Dermatology. 54 (10): 1109–1123. doi: 10.1111/ijd.12945. PMID  26227781.
  2. ^ a b c d e f Nair PA, Singhal R (2017-12-18). "Xanthelasma palpebrarum - a brief review". Clinical, Cosmetic and Investigational Dermatology. 11: 1–5. doi: 10.2147/CCID.S130116. PMC  5739544. PMID  29296091.
  3. ^ Ozdöl S, Sahin S, Tokgözoğlu L (August 2008). "Xanthelasma palpebrarum and its relation to atherosclerotic risk factors and lipoprotein (a)". International Journal of Dermatology. 47 (8): 785–9. doi: 10.1111/j.1365-4632.2008.03690.x. PMID  18717856. S2CID  25746456.
  4. ^ Chang, Hua-Ching; Sung, Chih-Wei; Lin, Ming-Hsiu (March 2020). "Serum lipids and risk of atherosclerosis in xanthelasma palpebrarum: A systematic review and meta-analysis". Journal of the American Academy of Dermatology. 82 (3): 596–605. doi: 10.1016/j.jaad.2019.08.082. PMID  31499151. S2CID  202413378.
  5. ^ Shields C, Shields J (2008). Eyelid, conjunctival and orbital tumors: atlas and textbook. Hagerstwon, MD: Lippincott Williams & Wilkins. ISBN  978-0-7817-7578-6.[ page needed]
  6. ^ Xanthelasma (8th ed.). 2009. Retrieved November 8, 2012. {{ cite book}}: |work= ignored ( help)
  7. ^ Jain A, Goyal P, Nigam PK, Gurbaksh H, Sharma RC (September 2007). "Xanthelasma Palpebrarum-clinical and biochemical profile in a tertiary care hospital of Delhi". Indian Journal of Clinical Biochemistry. 22 (2): 151–3. doi: 10.1007/BF02913335. PMC  3453794. PMID  23105704.

External links

From Wikipedia, the free encyclopedia
Xanthelasma
Other namesxanthelasma palpebrarum; xanthoma palpebrarum
Pronunciation
Specialty Ophthalmology  Edit this on Wikidata

Xanthelasma is a sharply demarcated yellowish deposit of cholesterol underneath the skin. [1] It usually occurs on or around the eyelids (xanthelasma palpebrarum, abbreviated XP). [1] [2] While they are neither harmful to the skin nor painful, these minor growths may be disfiguring and can be removed. [1] There is a growing body of evidence for the association between xanthelasma deposits and blood low-density lipoprotein levels and increased risk of atherosclerosis. [3] [4]

A xanthelasma may be referred to as a xanthoma when becoming larger and nodular, assuming tumorous proportions. [5] Xanthelasma is often classified simply as a subtype of xanthoma. [6]

Diagnosis

Xanthelasma in the form of XP can be diagnosed from clinical impression, although in some cases it may need to be distinguished ( differential diagnosis) from other conditions, especially necrobiotic xanthogranuloma, syringoma, palpebral sarcoidosis, sebaceous hyperplasia, Erdheim–Chester disease, lipoid proteinosis ( Urbach–Wiethe disease), and the syndrome of adult-onset asthma and periocular xanthogranuloma (AAPOX). [2] Differential diagnosis can be accomplished by surgical excision followed by microscopic examination by a pathologist ( biopsy to determine histopathology). [2] The typical clinical impression of XP is soft, yellowish papules, plaques, or nodules, symmetrically distributed on the medial side of the upper eyelids; sometimes the lower eyelids are affected as well. [2]

Treatment

Xanthelasmata can be removed with a trichloroacetic acid peel, surgery, lasers or cryotherapy. [2] Removal may cause, although uncommon, scarring and pigment changes.

Prognosis

Recurrence is common: 40% of patients with XP had recurrence after primary surgical excision, 60% after secondary excision, and 80% when all four eyelids were involved. A possible cause might be insufficiently deep excisions. [2]

Epidemiology

Xanthelasma is a rare disorder in the general population, with a variable incidence of 0.56 to 1.5% in western developed countries. The age of onset ranges from 15 to 75, with a peak in the 4th to 5th decades of life. There also seems to be a greater prevalence in females, but this might be due to higher consciousness to cosmetic defects. [7]

Etymology

The word is derived from Greek xanthós, ξανθός 'yellow' and élasma, έλασμα, 'foil'. The plural is xanthelasmata.

See also

References

  1. ^ a b c Frew JW, Murrell DF, Haber RM (October 2015). "Fifty shades of yellow: a review of the xanthodermatoses". International Journal of Dermatology. 54 (10): 1109–1123. doi: 10.1111/ijd.12945. PMID  26227781.
  2. ^ a b c d e f Nair PA, Singhal R (2017-12-18). "Xanthelasma palpebrarum - a brief review". Clinical, Cosmetic and Investigational Dermatology. 11: 1–5. doi: 10.2147/CCID.S130116. PMC  5739544. PMID  29296091.
  3. ^ Ozdöl S, Sahin S, Tokgözoğlu L (August 2008). "Xanthelasma palpebrarum and its relation to atherosclerotic risk factors and lipoprotein (a)". International Journal of Dermatology. 47 (8): 785–9. doi: 10.1111/j.1365-4632.2008.03690.x. PMID  18717856. S2CID  25746456.
  4. ^ Chang, Hua-Ching; Sung, Chih-Wei; Lin, Ming-Hsiu (March 2020). "Serum lipids and risk of atherosclerosis in xanthelasma palpebrarum: A systematic review and meta-analysis". Journal of the American Academy of Dermatology. 82 (3): 596–605. doi: 10.1016/j.jaad.2019.08.082. PMID  31499151. S2CID  202413378.
  5. ^ Shields C, Shields J (2008). Eyelid, conjunctival and orbital tumors: atlas and textbook. Hagerstwon, MD: Lippincott Williams & Wilkins. ISBN  978-0-7817-7578-6.[ page needed]
  6. ^ Xanthelasma (8th ed.). 2009. Retrieved November 8, 2012. {{ cite book}}: |work= ignored ( help)
  7. ^ Jain A, Goyal P, Nigam PK, Gurbaksh H, Sharma RC (September 2007). "Xanthelasma Palpebrarum-clinical and biochemical profile in a tertiary care hospital of Delhi". Indian Journal of Clinical Biochemistry. 22 (2): 151–3. doi: 10.1007/BF02913335. PMC  3453794. PMID  23105704.

External links


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