Necrolytic acral erythema

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Necrolytic acral erythema
Other namesZinc-responsive necrolytic acral erythema[1]
SpecialtyDermatology

Necrolytic acral erythema is a cutaneous condition that is a manifestation of hepatitis C viral infection or zinc deficiency.[2] In the early stages, bullae, erosions, and erythematous or violaceous papules are its defining characteristics. Well-defined plaques with erythema on the outer rim, lichenification, secondary hyperpigmentation, and fine desquamation on the surface begin to appear in the late phase.[3]

Signs and symptoms[edit]

Traditionally, necrolytic acral erythema manifests as distinct, dark red hyperkeratotic plaques with a keratotic border that are usually found on the dorsum of the foot and toes. Ankles, legs, and knees may also be affected in some cases.[4] On occasion, lesions may appear on the buttocks, genitalia, hands, and elbows. It has been documented that the nails, palms, and soles, features typically thought of as distinguishing characteristics against necrolytic acral erythema, are affected.[5] Necrolytic acral erythema can show clinically as either acute or chronic. Flaccid blisters, erosions at the margins, and noticeable erythema are the symptoms of acute lesions. The hyperkeratotic surface, moderate erythema, and dark red border are seen in the chronic lesions. Edema may be present in conjunction.[4] The illness may have been present for two to one hundred and sixty months at the time of presentation.[6]

Three stages characterize the evolution of necrolytic acral erythema lesions: early, well-developed, and late. Scaly, erythematous papules or plaques with a distinctively dark or worn center first emerge. When the lesions reach a well-developed stage, they combine to create a thick, hyperpigmented plaque that is clearly defined and has adhering scales. Sometimes there might be pustules.[4] In the later stages, the lesions become thinner, more confined, and more pigmented.[7] Lesions usually show a spontaneous remission and relapse pattern throughout time.[5]

Causes[edit]

As of yet, the precise etiology of necrolytic acral erythema remains unknown. Numerous causes, including hepatic dysfunction, hypoglucagonemia, hypoalbimunemia, hypoaminoacidemia, zinc deficiency, and diabetes with or without an underlying hepatitis C viral infection, have been postulated as part of the multifactorial pathophysiology of necrolytic acral erythema.[4]

Diagnosis[edit]

The biopsy site and illness stage are reflected in the histological characteristics. Early lesions from the margin display upper epidermal necrosis that has detached from the surrounding tissue in the form of blisters. Acanthosis, spongiosis, and a superficial dermal infiltration mimicking nummular dermatitis are observed in the epidermis. The well-developed lesions exhibit necrotic keratinocytes, psoriasiform hyperplasia, subcorneal pustules, significant papillomatosis, and parakeratosis. A fissure may occur in the top epidermis as a result of necrotic keratinocytes converging.[4]

Treatment[edit]

The most successful course of treatment to date has been oral zinc therapy.[4]

Epidemiology[edit]

Both sexes are equally affected by the illness; 46.2% of males and 53.8% of females are affected, respectively. Patients with necrolytic acral erythema fall into the 19–58 year age range, with a mean age of 44±11.3 and a median age of 50.[6]

See also[edit]

References[edit]

  1. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Zinc responsive necrolytic acral erythema". www.orpha.net. Retrieved 16 May 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
  3. ^ Botelho, Luciane Francisca Fernandes; Enokihara, Milvia Maria Simões e Silva; Enokihara, Mauro Yoshiaki (2016). "Necrolytic acral erythema: a rare skin disease associated with hepatitis C virus infection". Anais Brasileiros de Dermatologia. 91 (5). FapUNIFESP (SciELO): 649–651. doi:10.1590/abd1806-4841.20164203. ISSN 0365-0596.
  4. ^ a b c d e f Inamadar, Arun; Shivanna, Ragunatha; Ankad, Balachandra S. (2020). "Necrolytic Acral Erythema: Current Insights". Clinical, Cosmetic and Investigational Dermatology. 13. Informa UK Limited: 275–281. doi:10.2147/ccid.s189175. ISSN 1178-7015. PMC 7147628.
  5. ^ a b Bentley, Danette; Andea, Aleodor; Holzer, Aton; Elewski, Boni (2009). "Lack of classic histology should not prevent diagnosis of necrolytic acral erythema". Journal of the American Academy of Dermatology. 60 (3). Elsevier BV: 504–507. doi:10.1016/j.jaad.2008.08.046. ISSN 0190-9622. PMC 2708073.
  6. ^ a b El-Darouti, Mohammad A.; Mashaly, Heba M.; El-Nabarawy, Eman; Eissa, Amal M.; Abdel-Halim, Mona R.E.; Fawzi, Marwa M.T.; El-Eishi, Nermine H.; Tawfik, Sherine O.; Zaki, Naglaa S.; Zidan, Anoud Z.; Fawzi, Marwa; Abdelaziz, Mohammad; Fawzi, Mai M.T.; Shaker, Olfat G. (2010). "Leukocytoclastic vasculitis and necrolytic acral erythema in patients with hepatitis C infection: Do viral load and viral genotype play a role?". Journal of the American Academy of Dermatology. 63 (2). Elsevier BV: 259–265. doi:10.1016/j.jaad.2009.07.050. ISSN 0190-9622.
  7. ^ Abdallah, Mahmoud A.; Ghozzi, Mohamed Y.; Monib, Hoda A.; Hafez, Aisha M.; Hiatt, Kim M.; Smoller, Bruce R.; Horn, Thomas D. (2005). "Necrolytic acral erythema: A cutaneous sign of hepatitis C virus infection". Journal of the American Academy of Dermatology. 53 (2). Elsevier BV: 247–251. doi:10.1016/j.jaad.2005.04.049. ISSN 0190-9622.

Further reading[edit]

  • Abdallah, Mahmoud A.; Hull, Cheryl; Horn, Thomas D. (2005-01-01). "Necrolytic Acral Erythema: A Patient From the United States Successfully Treated With Oral Zinc". Archives of Dermatology. 141 (1). doi:10.1001/archderm.141.1.85. ISSN 0003-987X.
  • Kapoor, Roger; Johnson, Richard A. (2011-04-14). "Necrolytic Acral Erythema". New England Journal of Medicine. 364 (15): 1479–1480. doi:10.1056/NEJMc1101858. ISSN 0028-4793.

External links[edit]